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	<id>https://chemwiki.ch.ic.ac.uk/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Xj06</id>
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	<updated>2026-04-04T04:39:20Z</updated>
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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14209</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14209"/>
		<updated>2007-12-07T18:28:24Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;350&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
=Indications &amp;amp; Dosage=&lt;br /&gt;
Amoxicillin can be used to treat infections of the ear, nose, and throat, the genitourinary tract, the skin and skin structure, and the lower respiratory tract due to susceptible (only b-lactamase-negative) strains of Streptococcus spp. (a- and b-hemolytic strains only), S. pneumoniae, Staphylococcus spp., H. influenzae, E. coli, P. mirabilis, or E. faecalis. Also for the treatment of acute, uncomplicated gonorrhea (ano-genital and urethral infections) due to N. gonorrhoeae (males and females).#[http://redpoll.pharmacy.ualberta.ca/drugbank/cgi-bin/getCard.cgi?CARD=APRD00248.txt]&lt;br /&gt;
&lt;br /&gt;
Amoxicillin can be taken as Capsule (250 mg or 500 mg), Powder for solution, Powder for suspension, Suspension and Tablet (500 mg or 875 mg). Capsules and tablets should be taken with a glass of water.  &lt;br /&gt;
The usual dosage for adult is 500 mg every 12 hours or 250 mg every 8 hours for ear, nose or throat infection.  For a severe infection, the dosage will be 875 mg every 12 hours or 500 mg every 8 hours. It can be taken with or without meals.&lt;br /&gt;
=Side effect=&lt;br /&gt;
Serious toxicity may not occur after taking large dose of Amoxicillin. However, nausea, vomiting or diarrhea may occur.&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14208</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14208"/>
		<updated>2007-12-07T18:26:13Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
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 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
=Indications &amp;amp; Dosage=&lt;br /&gt;
Amoxicillin can be used to treat infections of the ear, nose, and throat, the genitourinary tract, the skin and skin structure, and the lower respiratory tract due to susceptible (only b-lactamase-negative) strains of Streptococcus spp. (a- and b-hemolytic strains only), S. pneumoniae, Staphylococcus spp., H. influenzae, E. coli, P. mirabilis, or E. faecalis. Also for the treatment of acute, uncomplicated gonorrhea (ano-genital and urethral infections) due to N. gonorrhoeae (males and females).#[http://redpoll.pharmacy.ualberta.ca/drugbank/cgi-bin/getCard.cgi?CARD=APRD00248.txt]&lt;br /&gt;
&lt;br /&gt;
Amoxicillin can be taken as Capsule (250 mg or 500 mg), Powder for solution, Powder for suspension, Suspension and Tablet (500 mg or 875 mg). Capsules and tablets should be taken with a glass of water.  &lt;br /&gt;
The usual dosage for adult is 500 mg every 12 hours or 250 mg every 8 hours for ear, nose or throat infection.  For a severe infection, the dosage will be 875 mg every 12 hours or 500 mg every 8 hours. It can be taken with or without meals.&lt;br /&gt;
=Side effect=&lt;br /&gt;
Serious toxicity may not occur after taking large dose of Amoxicillin. However, nausea, vomiting or diarrhea may occur.&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14206</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14206"/>
		<updated>2007-12-07T18:20:01Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
=Indications &amp;amp; Dosage=&lt;br /&gt;
Amoxicillin can be used to treat infections of the ear, nose, and throat, the genitourinary tract, the skin and skin structure, and the lower respiratory tract due to susceptible (only b-lactamase-negative) strains of Streptococcus spp. (a- and b-hemolytic strains only), S. pneumoniae, Staphylococcus spp., H. influenzae, E. coli, P. mirabilis, or E. faecalis. Also for the treatment of acute, uncomplicated gonorrhea (ano-genital and urethral infections) due to N. gonorrhoeae (males and females).#[http://redpoll.pharmacy.ualberta.ca/drugbank/cgi-bin/getCard.cgi?CARD=APRD00248.txt]&lt;br /&gt;
&lt;br /&gt;
Amoxicillin can be taken as Capsule (250 mg or 500 mg), Powder for solution, Powder for suspension, Suspension and Tablet (500 mg or 875 mg). Capsules and tablets should be taken with a glass of water.  &lt;br /&gt;
The usual dosage for adult is 500 mg every 12 hours or 250 mg every 8 hours for ear, nose or throat infection.  For a severe infection, the dosage will be 875 mg every 12 hours or 500 mg every 8 hours. It can be taken with or without meals.&lt;br /&gt;
=Side effect=&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14204</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14204"/>
		<updated>2007-12-07T18:11:46Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
=Indications &amp;amp; Dosage=&lt;br /&gt;
Amoxicillin can be taken as tablets, chewable tablets or capsules. Capsules and tablets should be taken with a glass of water.  &lt;br /&gt;
The usual dosage for adult is 500 mg every 12 hours or 250 mg every 8 hours for ear, nose or throat infection.  For a severe infection, the dosage will be 875 mg every 12 hours or 500 mg every 8 hours.&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14203</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14203"/>
		<updated>2007-12-07T18:11:23Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
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 28 29  1&lt;br /&gt;
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 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
=Indications &amp;amp; Dosage&lt;br /&gt;
Amoxicillin can be taken as tablets, chewable tablets or capsules. Capsules and tablets should be taken with a glass of water.  &lt;br /&gt;
The usual dosage for adult is 500 mg every 12 hours or 250 mg every 8 hours for ear, nose or throat infection.  For a severe infection, the dosage will be 875 mg every 12 hours or 500 mg every 8 hours. =&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14200</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14200"/>
		<updated>2007-12-07T17:53:56Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
Amoxicillin, (also called amoxicillin) is an antibiotic in the penicillin group. It is used to treat a variety of infections bacteria. The oral route of taking amoxicillin and the easily absorbed character makes it a better choice than other antibiotics in beta-lactam antibiotics. &lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
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 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
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 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14179</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14179"/>
		<updated>2007-12-07T17:38:01Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14177</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14177"/>
		<updated>2007-12-07T17:36:59Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14176</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14176"/>
		<updated>2007-12-07T17:36:41Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14166</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14166"/>
		<updated>2007-12-07T17:28:10Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;300&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14163</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14163"/>
		<updated>2007-12-07T17:27:45Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxicillin-3D.png |250px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin-3D.png&amp;diff=14159</id>
		<title>File:Amoxicillin-3D.png</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin-3D.png&amp;diff=14159"/>
		<updated>2007-12-07T17:24:39Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14153</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14153"/>
		<updated>2007-12-07T17:18:21Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
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 14 19  1&lt;br /&gt;
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 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
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 19 22  1&lt;br /&gt;
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 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14134</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14134"/>
		<updated>2007-12-07T17:09:54Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Amoxicillin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid={{{PubChem}}} Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://www.emolecules.com/cgi-bin/search?t=ss&amp;amp;q= OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1]&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14127</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14127"/>
		<updated>2007-12-07T17:00:31Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  {{{Box_Name}}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid={{{PubChem}}} Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://www.emolecules.com/cgi-bin/search?t=ss&amp;amp;q= OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1]&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14126</id>
		<title>It07:Amoxicillin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Amoxicillin&amp;diff=14126"/>
		<updated>2007-12-07T16:59:38Z</updated>

		<summary type="html">&lt;p&gt;Xj06: New page: {| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot; ! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgco...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  {{{Box_Name}}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Amoxocillin.JPG |250px|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| 7-[2-amino-2-(4-hydroxyphenyl) -acetyl]amino-3,3-dimethyl-6-oxo -2-thia-5-azabicyclo[3.2.0]heptane -4-carboxylic acid&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| J01CA04&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 26787-78-0&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/PubChem PubChem (CID)]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid={{{PubChem}}} Substance: 175459 &lt;br /&gt;
Compound: 33613&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|[http://www.emolecules.com/cgi-bin/search?t=ss&amp;amp;q= OC1=CC=C([C@H](C(N[C@@H]2C(N([C@@H]([C@](O)=O)C(C)(C)S3)[C@]32[H])=O)=O)N)C=C1]&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| C16H19N3O5S  &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 365.4 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 95% oral&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Approximately 20% protein-bound in blood serum&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Less than 30% biotransformed in liver&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| 61.3 minutes&lt;br /&gt;
 |-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Renal&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| A(AU) B(US)&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| POM(UK)&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| Oral, intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk -25;frame 0;MultipleBonds ON; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;&lt;br /&gt;
http://www.mol-net.com/tmp/14108.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 44 46  0  0  0&lt;br /&gt;
 5.927     2.498     0.639     O &lt;br /&gt;
 5.064     1.541     0.208     C &lt;br /&gt;
 4.012     1.881     -0.63     C &lt;br /&gt;
 3.136     0.906     -1.066999 C &lt;br /&gt;
 3.3079998 -0.407    -0.67     C &lt;br /&gt;
 2.3509998 -1.468999 -1.148    C &lt;br /&gt;
 1.833     -1.116    -2.04     H &lt;br /&gt;
 1.3439999 -1.762    -0.065    C &lt;br /&gt;
 0.29      -0.941000 0.115     N &lt;br /&gt;
 -0.688    -1.226000 1.168     C &lt;br /&gt;
 -0.267999 -1.814999 1.9830002 H &lt;br /&gt;
 -1.990000 -1.777000 0.6410000 C &lt;br /&gt;
 -2.567999 -0.564    0.869     N &lt;br /&gt;
 -2.978    0.19      -0.320000 C &lt;br /&gt;
 -2.463    -0.213000 -1.192    H &lt;br /&gt;
 -4.465    0.035     -0.513    C &lt;br /&gt;
 -5.019    0.3060000 -1.705    O &lt;br /&gt;
 -5.158    -0.333    0.4060000 O &lt;br /&gt;
 -2.642    1.7010001 -0.187    C &lt;br /&gt;
 -2.454    2.3579998 -1.556    C &lt;br /&gt;
 -3.692    2.44      0.6450000 C &lt;br /&gt;
 -1.038    1.548     0.7199999 S &lt;br /&gt;
 -1.444999 0.01      1.641     C &lt;br /&gt;
 -1.581000 0.128     2.716     H &lt;br /&gt;
 -2.363    -2.843999 0.202     O &lt;br /&gt;
 1.482     -2.737    0.6430000 O &lt;br /&gt;
 3.097     -2.692999 -1.466999 N &lt;br /&gt;
 4.3560004 -0.749    0.1649999 C &lt;br /&gt;
 5.238     0.222     0.6       C &lt;br /&gt;
 5.567     2.8479998 1.4649999 H &lt;br /&gt;
 3.8769999 2.9060001 -0.940000 H &lt;br /&gt;
 2.316     1.1700001 -1.719    H &lt;br /&gt;
 0.18      -0.162    -0.450999 H &lt;br /&gt;
 -5.973    0.206     -1.828    H &lt;br /&gt;
 -3.372    2.26      -2.136    H &lt;br /&gt;
 -2.22     3.4150002 -1.423    H &lt;br /&gt;
 -1.636    1.8689998 -2.085    H &lt;br /&gt;
 -3.733    2.007     1.645     H &lt;br /&gt;
 -3.424    3.494     0.717     H &lt;br /&gt;
 -4.667    2.345     0.168     H &lt;br /&gt;
 3.823     -2.429000 -2.116    H &lt;br /&gt;
 3.5579998 -2.982    -0.617000 H &lt;br /&gt;
 4.488     -1.775000 0.473     H &lt;br /&gt;
 6.056     -0.044999 1.252     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 30  1&lt;br /&gt;
  2 29  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 31  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 32  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 28  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6  8  1&lt;br /&gt;
  6 27  1&lt;br /&gt;
  8  9  1&lt;br /&gt;
  8 26  1&lt;br /&gt;
  9 10  1&lt;br /&gt;
  9 33  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 10 23  1&lt;br /&gt;
 10 12  1&lt;br /&gt;
 12 13  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 13 14  1&lt;br /&gt;
 13 23  1&lt;br /&gt;
 14 15  1&lt;br /&gt;
 14 16  1&lt;br /&gt;
 14 19  1&lt;br /&gt;
 16 17  1&lt;br /&gt;
 16 18  1&lt;br /&gt;
 17 34  1&lt;br /&gt;
 19 20  1&lt;br /&gt;
 19 21  1&lt;br /&gt;
 19 22  1&lt;br /&gt;
 20 35  1&lt;br /&gt;
 20 36  1&lt;br /&gt;
 20 37  1&lt;br /&gt;
 21 38  1&lt;br /&gt;
 21 39  1&lt;br /&gt;
 21 40  1&lt;br /&gt;
 22 23  1&lt;br /&gt;
 23 24  1&lt;br /&gt;
 27 41  1&lt;br /&gt;
 27 42  1&lt;br /&gt;
 28 29  1&lt;br /&gt;
 28 43  1&lt;br /&gt;
 29 44  1  &lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=14125</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=14125"/>
		<updated>2007-12-07T16:58:55Z</updated>

		<summary type="html">&lt;p&gt;Xj06: /* Supplemental  Project Page */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	&lt;br /&gt;
 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek:&amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. Do not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|NEW: This demonstrates the use of  Jmol loading discrete molecule files (rather than having to paste them into the wiki page).  Upload the molecule file, and invoke it as shown here. Use it for eg loading large proteins etc.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC) and --[[User:Rzepa|Rzepa]] 07:41, 16 October 2007 (BST) and  --[[User:Rzepa|Rzepa]] 15:56, 18 October 2007 (BST)&lt;br /&gt;
&lt;br /&gt;
If no rotatable molecule appears to the right there my be a problem in the browser cache - reload the page bypassing the cache using ctrl+F5. If this doesn&#039;t work check that  [http://www.java.com/en/download/help/testvm.xml Java] is correctly functioning on your system.&lt;br /&gt;
&lt;br /&gt;
===References ===&lt;br /&gt;
This shows how citations&amp;lt;ref&amp;gt;Example of adding a citation {{DOI|10.1021/ja9825332}}&amp;lt;/ref&amp;gt; can be added to &lt;br /&gt;
text&amp;lt;ref&amp;gt;adding a further citation {{DOI|10.1021/ja9825332}}&amp;lt;/ref&amp;gt; to produce a nice effect.&lt;br /&gt;
&lt;br /&gt;
===Multiple uses of the same footnote ===&lt;br /&gt;
&lt;br /&gt;
The code for citing multiple quotes from the same source can be found [http://www.mediawiki.org/wiki/Extension:Cite/Cite.php here]. This stops the same reference being stated multiple times at the bottom of the page when you try to reference more than one item from the same source.&lt;br /&gt;
&lt;br /&gt;
=== Collected citations appear below here ===&lt;br /&gt;
&amp;lt;references /&amp;gt;--[[User:Rzepa|Rzepa]] 15:18, 25 October 2007 (BST)&lt;br /&gt;
|&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;title&amp;gt;Pentahelicene&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;yellow&amp;lt;/color&amp;gt;&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;uploadedFileContents&amp;gt;Pentahelicene.mol&amp;lt;/uploadedFileContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;jmolMenu&amp;gt;&lt;br /&gt;
&amp;lt;item&amp;gt;&amp;lt;text&amp;gt;Start spinning&amp;lt;/text&amp;gt;&amp;lt;script&amp;gt;spin on&amp;lt;/script&amp;gt;&amp;lt;/item&amp;gt;&lt;br /&gt;
&amp;lt;item&amp;gt;&amp;lt;text&amp;gt;Stop spinning&amp;lt;/text&amp;gt;&amp;lt;script&amp;gt;spin off&amp;lt;/script&amp;gt;&amp;lt;/item&amp;gt;&lt;br /&gt;
&amp;lt;menuHeight&amp;gt;-1&amp;lt;/menuHeight&amp;gt;&lt;br /&gt;
&amp;lt;/jmolMenu&amp;gt;&lt;br /&gt;
&amp;lt;jmolButton&amp;gt;&lt;br /&gt;
    &amp;lt;script&amp;gt;console&amp;lt;/script&amp;gt;&lt;br /&gt;
    &amp;lt;text&amp;gt;open a console window&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolAppletButton&amp;gt;&amp;lt;title&amp;gt;Show CIYSIM.cif in popup window&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;cyan&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;uploadedFileContents&amp;gt;CIYSIM.cif&amp;lt;/uploadedFileContents&amp;gt;&amp;lt;/jmolAppletButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;URGENT Announcement&#039;&#039;&#039;&#039;&#039;  &lt;br /&gt;
&lt;br /&gt;
Whilst the  Wiki itself is pretty robust, and although it is difficult to break a page on it, this did happen a few days ago to project 12.  What seems to have happened is that some  &#039;&#039;bad&#039;&#039; code (HTML or XML) was copied from another Web page, and pasted into the  project 12 page.  The Wiki system could not cope with this particular bad code, and sulked.  Fortunately, by invoking appropriate magic, the page has now been restored to its state prior to the breakage, and  I have learnt a valuable lesson in how to fix it if this happens again. So this serves as a warning;  if you are copying/pasting blind from other web pages (which in general you should not be doing), you do run the risk of breaking the page.  Hopefully, the break will be detected during the preview, and serves to remind that you should  &#039;&#039;always&#039;&#039; preview before saving to detect any such breaks. --[[User:Rzepa|Rzepa]] 10:21, 28 November 2007 (UTC)&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07a:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:wilkinson|Wilkinson&#039;s catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |21	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Schrock|Schrock metathesis catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |22	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:knots|Molecular-scale knots (nanoscale devices)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
|bgcolor=&amp;quot;#CCFF00&amp;quot; |23	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |24	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Sertraline|Sertraline HCl (anti-depression)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |25	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |26	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[i07t:Zithromycin|Zithromycin (anti-infective)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |27	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Lipitor|Lipitor (Cholesterol reducing agent)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |28	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Cyameluric Acid|Cyameluric acid (Linus Pauling&#039;s last idea!)]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it07:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it07:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
#[[it07:sitagliptin_page|An example entry- in edit mode, please copy this line and paste below to add to this list]]&lt;br /&gt;
#[[it07:Limonene|Limonene]]&lt;br /&gt;
#[[it07:name_of_project|Vitamin C ]]&lt;br /&gt;
#[[it07:Cylcophosphamide|Cyclophosphamide]]&lt;br /&gt;
#[[it07:Terbutaline Sulphate|Terbutaline Sulphate]]&lt;br /&gt;
#[[it07:Caffeine|Caffeine]]&lt;br /&gt;
#[[it07:Mefloquine|Mefloquine]]&lt;br /&gt;
#[[it07:Cadaverine|Cadaverine]]&lt;br /&gt;
#[[it07:Cyanidin|Cyanidin]]&lt;br /&gt;
#[[it07:Ezetimibe|Ezetimibe]]&lt;br /&gt;
#[[it07:Octanitrocubane|Octanitrocubane]]&lt;br /&gt;
#[[it07:Azadirachtin|Azadirachtin]]&lt;br /&gt;
#[[it07:Nicotine|Nicotine]]&lt;br /&gt;
#[[it07:Cyclopentasiloxane|Cyclopentasiloxane]]&lt;br /&gt;
#[[it07:Trinitrotoluene|Trinitrotoluene]]&lt;br /&gt;
#[[it07:Hydroxychloroquine|Hydroxychloroquine]]&lt;br /&gt;
#[[it07:Aspartame|Aspartame]]&lt;br /&gt;
#[[it07:Azulene|Azulene]]&lt;br /&gt;
#[[it07:Chlorine Trifluoride|Chlorine Trifluoride]]&lt;br /&gt;
#[[it07:Cholesterol|Cholesterol]]&lt;br /&gt;
#[[it07:Vitamin E|Vitamin E]]&lt;br /&gt;
#[[it07:Phenothiazine|Phenothiazine]]&lt;br /&gt;
#[[it07:linalool|linalool]]&lt;br /&gt;
#[[it07:Glutamic acid|Glutamic acid]]&lt;br /&gt;
#[[it07:N-(4-hydroxyphenyl)ethanamide|N-(4-hydroxyphenyl)ethanamide]]&lt;br /&gt;
#[[it07:Epinephrine|Epinephrine]]&lt;br /&gt;
#[[it07:Sodium Valproate|Sodium Valproate]]&lt;br /&gt;
#[[it07:Hyaluronic acid |Hyaluronic acid  ]]&lt;br /&gt;
#[[it07:Methylenedioxymethamphetamine |Methylenedioxymethamphetamine ]]&lt;br /&gt;
#[[it07:salicylic acid |salicylic acid ]]&lt;br /&gt;
#[[it07:Morphine|Morphine]]&lt;br /&gt;
#[[Cetirizine]]&lt;br /&gt;
#[[it07:Bisacodyl|Bisacodyl]]&lt;br /&gt;
#[[it07:Rivaroxaban|Rivaroxaban]]&lt;br /&gt;
#[[it07:Sodium Lauryl Sulfate|Sodium Lauryl Sulfate]]&lt;br /&gt;
#[[it07:Silicon Dioxide|Silicon Dioxide]]&lt;br /&gt;
#[[it07:Vanillin|Vanillin]]&lt;br /&gt;
#[[it07:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
#[[it07:Capsaicin|Capsaicin]]&lt;br /&gt;
#[[it07:Menthol|Menthol]]&lt;br /&gt;
#[[it07:Tamoxifen|Tamoxifen]]&lt;br /&gt;
#[[it07:Copper arsenate|Scheele&#039;s Green]]&lt;br /&gt;
#[[it07:Strychnine|Strychnine]]&lt;br /&gt;
#[[it07:Testosterone|Testosterone]]&lt;br /&gt;
#[[it07:Monosodium glutamate|Monosodium glutamate]]&lt;br /&gt;
#[[it07:Taurine|Taurine]]&lt;br /&gt;
#[[it07:Phenethylamine|Phenethylamine]]&lt;br /&gt;
#[[it07:Verbenone|Verbenone]]&lt;br /&gt;
#[[it07:Salbutamol|Salbutamol]]&lt;br /&gt;
#[[it07:Lactic acid|Lactic acid]]&lt;br /&gt;
#[[it07:Aspirin|Aspirin]]&lt;br /&gt;
#[[it07:EDTA|EDTA]]&lt;br /&gt;
#[[it07:Heroin|Heroin]]&lt;br /&gt;
#[[it07:Cocaine|Cocaine]]&lt;br /&gt;
#[[it07:Myristicin|Myristin (The hallucinogen in nutmeg)]]&lt;br /&gt;
#[[it07:Encefabol|Encefabol]]&lt;br /&gt;
#[[it07:Sarin|Sarin]]&lt;br /&gt;
#[[Thebaine]]&lt;br /&gt;
#[[Nitroglycerin]]&lt;br /&gt;
#[[it07:Methamphetamine|Methamphetamine]]&lt;br /&gt;
#[[it07:Sildenafil|Sildenafil]]&lt;br /&gt;
#[[Grubbs&#039; Catalyst]]&lt;br /&gt;
#[[it07:Warfarin|Warfarin]]&lt;br /&gt;
#[[it07:Angelic Acid|Angelic Acid]]&lt;br /&gt;
#[[it07:Melem (Melon) |Melem]]&lt;br /&gt;
#[[it07:oxazaborolidines|Chiral Oxazaborolidines as Catalysts]]&lt;br /&gt;
#[[it07:RDX|RDX (chemical in plastic explosives)]]&lt;br /&gt;
#[[it07:Lysergic Acid|Lysergic Acid]]&lt;br /&gt;
#[[it07:Oseltamivir Phosphate|Oseltamivir Phosphate(Tamiflu)]]&lt;br /&gt;
#[[Fluoxetine Hydrochloride (Prozac)]]&lt;br /&gt;
#[[Dimethylmercury]]&lt;br /&gt;
#[[it07:Sorafenib(Nexavar®)|Sorafenib (Nexavar®)]]&lt;br /&gt;
#[[Rapamycin]]&lt;br /&gt;
#[[Rohypnol]]&lt;br /&gt;
#[[it07:Vitamin A|Vitamin A (Retinol)]]&lt;br /&gt;
#[[it07:THC|Tetrahydrocannabinol]]&lt;br /&gt;
#[[2,4-Dinitrophenylhydrazine|2,4-Dinitrophenylhydrazine]]&lt;br /&gt;
#[[Acetylcholine]]&lt;br /&gt;
#[[it07:Phenolphthalein|Phenolphthalein]]&lt;br /&gt;
#[[Carbon Dioxide]]&lt;br /&gt;
#[[Domoic Acid]]&lt;br /&gt;
#[[Kevlar]]&lt;br /&gt;
#[[it07:Erythromycin|Erythromycin]]&lt;br /&gt;
#[[it07:DIBAL|DIBAL]]&lt;br /&gt;
#[[Ephedrine]]&lt;br /&gt;
#[[it07:Lactose|Lactose]]&lt;br /&gt;
#[[it07:Thyjone|Thyjone]]&lt;br /&gt;
#[[Levothyroxine]]&lt;br /&gt;
#[[it07:Tropinone|Tropinone]]&lt;br /&gt;
#[[it07:Ozone|Ozone]]&lt;br /&gt;
#[[it07:Indinavir|Indinavir (Crixivan®)]]&lt;br /&gt;
#[[it07:Tetrodotoxin|Tetrodotoxin]]&lt;br /&gt;
#[[it07:Astaxanthin|Astaxanthin]]&lt;br /&gt;
#[[Methane]]&lt;br /&gt;
#[[it07:2 – Chlorobenzalmalononitrile|2 – Chlorobenzalmalononitrile (CS Gas)]]&lt;br /&gt;
#[[it07:Dichloro-Diphenyl-Trichloroethane|Dichloro-Diphenyl-Trichloroethane]]&lt;br /&gt;
#[[it07:Ketamine|Ketamine]]&lt;br /&gt;
#[[it07:Ethylene Glycol|Ethylene Glycol]]&lt;br /&gt;
#[[it07:HMX|HMX]]&lt;br /&gt;
#[[it07:Psilocybin|Psilocybin (magic mushrooms)]]&lt;br /&gt;
#[[it07:Dopamine|Dopamine]]&lt;br /&gt;
#[[it07:Mefenamic Acid|Mefenamic Acid]]&lt;br /&gt;
#[[it07:Sesamin|Sesamin]]&lt;br /&gt;
#[[it07:Riboflavin|Riboflavin (Vitamin B2)]]&lt;br /&gt;
#[[it07:Coniine|Coniine]]&lt;br /&gt;
#[[it07:Capecitabine|Capecitabine]]&lt;br /&gt;
#[[it07:Atenolol|Atenolol]]&lt;br /&gt;
#[[it07:Simvastatin|Simvastatin]]&lt;br /&gt;
#[[it07:Ammonia|Ammonia]]&lt;br /&gt;
#[[it07:Tetrodotoxin|Tetrodotoxin]]&lt;br /&gt;
#[[it07:Halomon|Halomon]]&lt;br /&gt;
#[[it07:Hexyl Cinnamal|Hexyl Cinnamal]]&lt;br /&gt;
#[[it07:Humulene|Humulene]]&lt;br /&gt;
#[[it07:PETN|PETN]]&lt;br /&gt;
#[[it07:Lipoic Acid|Lipoic Acid]]&lt;br /&gt;
#[[it07:Amoxicillin|Amoxicillin]]&lt;br /&gt;
&lt;br /&gt;
== Wiki Templates ==&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use. Many other templates exist, often to be found on e.g. Wikipedia pages. You may decide one of these is of particular use, or of interest. If so, you can install it on the wiki here for you and others to use. Add below a line that looks like Template:Template-name, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others! --Rzepa 14:41, 20 October 2006 (BST) &lt;br /&gt;
&lt;br /&gt;
[[Template:Chem-Data]]&lt;br /&gt;
&lt;br /&gt;
[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables&lt;br /&gt;
&lt;br /&gt;
[[Template:Chembox supplement]] - to be linked to from the supplementary section of the table in the template above, for usage see [[Template_talk:chembox_supplement|here]]&lt;br /&gt;
&lt;br /&gt;
[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]&lt;br /&gt;
&lt;br /&gt;
[[R &amp;amp; S Phrases]]&lt;br /&gt;
&lt;br /&gt;
[[Template:Chembox new]]&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14118</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14118"/>
		<updated>2007-12-07T16:52:19Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14117</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14117"/>
		<updated>2007-12-07T16:51:44Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
=Jmol 3D structural views of molecule:=&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;=&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14116</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14116"/>
		<updated>2007-12-07T16:51:23Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
=Jmol 3D structural views of molecule:&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;=&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14112</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14112"/>
		<updated>2007-12-07T16:50:45Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
=&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;=&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14111</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14111"/>
		<updated>2007-12-07T16:49:54Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
&lt;br /&gt;
|-Jmol 3D structural views of molecule:&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14110</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14110"/>
		<updated>2007-12-07T16:49:17Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14109</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14109"/>
		<updated>2007-12-07T16:48:48Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Lipoic acid is also called alpha-lipoic acid, is a organic compound consists of a carboxylic acid and a cyclic disulfide. It is an antioxidant with solubility in both water and fat which is beneficial for health and beauty care.&lt;br /&gt;
{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14099</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14099"/>
		<updated>2007-12-07T16:37:11Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;380&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14093</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14093"/>
		<updated>2007-12-07T16:33:05Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html External MSDS]] &lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14091</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14091"/>
		<updated>2007-12-07T16:25:20Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic-acid.jpg |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.jpg&amp;diff=14082</id>
		<title>File:Lipoic-acid.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.jpg&amp;diff=14082"/>
		<updated>2007-12-07T16:19:17Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14081</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14081"/>
		<updated>2007-12-07T16:18:53Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |300px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14079</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14079"/>
		<updated>2007-12-07T16:18:01Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: LEPIC_ACID.gif |200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:LEPIC_ACID.gif&amp;diff=14078</id>
		<title>File:LEPIC ACID.gif</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:LEPIC_ACID.gif&amp;diff=14078"/>
		<updated>2007-12-07T16:17:38Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14074</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14074"/>
		<updated>2007-12-07T16:11:20Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic_acid.gif |200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;http://www.mol-net.com/tmp/14459.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14073</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14073"/>
		<updated>2007-12-07T16:08:59Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic_acid.gif |200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;‎&lt;br /&gt;
http://www.mol-net.com/tmp/14061.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14072</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14072"/>
		<updated>2007-12-07T16:08:14Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic_acid.gif |200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
|&lt;br /&gt;
1.	1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jmol 3D structural views of molecule:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;black&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;Lipoic-acid.pdb‎&lt;br /&gt;
http://www.mol-net.com/tmp/14061.pdb&lt;br /&gt;
Jmol version 11.0.1  2007-02-27 23:36&lt;br /&gt;
EXTRACT: visible&lt;br /&gt;
 26 25  0  0  0&lt;br /&gt;
 5.72      -0.733    -0.213000 O &lt;br /&gt;
 4.598     -0.089    0.145     C &lt;br /&gt;
 3.285     -0.445    -0.503    C &lt;br /&gt;
 2.1739998 0.431     0.08      C &lt;br /&gt;
 0.841     0.07      -0.578    C &lt;br /&gt;
 -0.27     0.9460000 0.0050000 C &lt;br /&gt;
 -1.603    0.585     -0.653000 C &lt;br /&gt;
 -1.511    0.6530000 -1.737    H &lt;br /&gt;
 -2.093999 -1.127    -0.174    S &lt;br /&gt;
 -3.977    -0.683    0.611     S &lt;br /&gt;
 -4.145    0.986     -0.179    C &lt;br /&gt;
 -2.701    1.537     -0.162    C &lt;br /&gt;
 4.641     0.7759999 0.9880000 O &lt;br /&gt;
 6.562     -0.505    0.2030000 H &lt;br /&gt;
 3.353     -0.277    -1.578000 H &lt;br /&gt;
 3.0579998 -1.494    -0.313    H &lt;br /&gt;
 2.106     0.264     1.155     H &lt;br /&gt;
 2.401     1.48      -0.11     H &lt;br /&gt;
 0.9090000 0.238     -1.653    H &lt;br /&gt;
 0.614     -0.979000 -0.387999 H &lt;br /&gt;
 -0.338    0.778     1.08      H &lt;br /&gt;
 -0.042999 1.9950001 -0.185    H &lt;br /&gt;
 -4.507    0.8919999 -1.202    H &lt;br /&gt;
 -4.806    1.624     0.407     H &lt;br /&gt;
 -2.462000 1.828     0.86      H &lt;br /&gt;
 -2.675    2.4350002 -0.78     H &lt;br /&gt;
  1  2  1&lt;br /&gt;
  1 14  1&lt;br /&gt;
  2  3  1&lt;br /&gt;
  2 13  1&lt;br /&gt;
  3  4  1&lt;br /&gt;
  3 15  1&lt;br /&gt;
  3 16  1&lt;br /&gt;
  4  5  1&lt;br /&gt;
  4 17  1&lt;br /&gt;
  4 18  1&lt;br /&gt;
  5  6  1&lt;br /&gt;
  5 19  1&lt;br /&gt;
  5 20  1&lt;br /&gt;
  6  7  1&lt;br /&gt;
  6 21  1&lt;br /&gt;
  6 22  1&lt;br /&gt;
  7  8  1&lt;br /&gt;
  7 12  1&lt;br /&gt;
  7  9  1&lt;br /&gt;
 10 11  1&lt;br /&gt;
 11 12  1&lt;br /&gt;
 11 23  1&lt;br /&gt;
 11 24  1&lt;br /&gt;
 12 25  1&lt;br /&gt;
 12 26  1&lt;br /&gt;
Jmol script terminated&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14064</id>
		<title>It07:Lipoic Acid</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Lipoic_Acid&amp;diff=14064"/>
		<updated>2007-12-07T15:59:52Z</updated>

		<summary type="html">&lt;p&gt;Xj06: New page: {| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot; ! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not id...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{| class=&amp;quot;toccolours&amp;quot; border=&amp;quot;1&amp;quot; style=&amp;quot;float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse; width: 100px&amp;quot;&lt;br /&gt;
! {{chembox header}} | {{PAGENAME}} &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image: Lipoic_acid.gif |200px|{{PAGENAME}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | General&lt;br /&gt;
|- &lt;br /&gt;
| [http://en.wikipedia.org/wiki/IUPAC Systematic name]&lt;br /&gt;
| 5-dithiolan-3-ylpentanoic acid&lt;br /&gt;
&lt;br /&gt;
|-&lt;br /&gt;
| Brand Names/Synonyms&lt;br /&gt;
1.	| 1,2-Dithiolane-3R-pentanoic acid &lt;br /&gt;
2.	Lipoate &lt;br /&gt;
3.	Thioctic acid &lt;br /&gt;
4.	Thioctic acid (JAN) &lt;br /&gt;
5.	alpha-Lipoic acid &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| C8H14O2S2 &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Chemical_file_format SMILES] &amp;lt;!-- mostly for organic compounds, omit otherwise --&amp;gt;&lt;br /&gt;
| OC(CCCC[C@H]1SSCC1)=O&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Molar_mass Molar mass]&lt;br /&gt;
| 206.317 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| Appearance&lt;br /&gt;
| Yellow crystalline powder&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/CAS_registry_number CAS number]&lt;br /&gt;
| 62-46-4&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Properties&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Density Density] &amp;amp; [http://en.wikipedia.org/wiki/Phase_%28matter%29 phase]&lt;br /&gt;
| Do = 1.343 g.cm -3, solid&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Solubility Solubility in water]&lt;br /&gt;
| Insoluble in water. Soluble in Methanol, Alcohol and chloroform.&lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Melting_point Melting point]&lt;br /&gt;
| 333 – 335K &lt;br /&gt;
|-&lt;br /&gt;
| [http://en.wikipedia.org/wiki/Boiling_point Boiling point]&lt;br /&gt;
| 433 - 438K&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} | Hazards &amp;lt;!--  Summary only- MSDS entry provides more complete information --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| [[Material safety data sheet|MSDS]]&lt;br /&gt;
| [[{{PAGENAME}} (data page)#Material Safety Data Sheet|External MSDS]] http://redpoll.pharmacy.ualberta.ca/drugbank/drugBank/drugFile/msds/NUTR00035.html&lt;br /&gt;
|-&lt;br /&gt;
| [[RTECS]] number&lt;br /&gt;
| JP1192000&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=14060</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=14060"/>
		<updated>2007-12-07T15:54:04Z</updated>

		<summary type="html">&lt;p&gt;Xj06: /* Supplemental  Project Page */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	&lt;br /&gt;
 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek:&amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. Do not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|NEW: This demonstrates the use of  Jmol loading discrete molecule files (rather than having to paste them into the wiki page).  Upload the molecule file, and invoke it as shown here. Use it for eg loading large proteins etc.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC) and --[[User:Rzepa|Rzepa]] 07:41, 16 October 2007 (BST) and  --[[User:Rzepa|Rzepa]] 15:56, 18 October 2007 (BST)&lt;br /&gt;
&lt;br /&gt;
If no rotatable molecule appears to the right there my be a problem in the browser cache - reload the page bypassing the cache using ctrl+F5. If this doesn&#039;t work check that  [http://www.java.com/en/download/help/testvm.xml Java] is correctly functioning on your system.&lt;br /&gt;
&lt;br /&gt;
===References ===&lt;br /&gt;
This shows how citations&amp;lt;ref&amp;gt;Example of adding a citation {{DOI|10.1021/ja9825332}}&amp;lt;/ref&amp;gt; can be added to &lt;br /&gt;
text&amp;lt;ref&amp;gt;adding a further citation {{DOI|10.1021/ja9825332}}&amp;lt;/ref&amp;gt; to produce a nice effect.&lt;br /&gt;
&lt;br /&gt;
===Multiple uses of the same footnote ===&lt;br /&gt;
&lt;br /&gt;
The code for citing multiple quotes from the same source can be found [http://www.mediawiki.org/wiki/Extension:Cite/Cite.php here]. This stops the same reference being stated multiple times at the bottom of the page when you try to reference more than one item from the same source.&lt;br /&gt;
&lt;br /&gt;
=== Collected citations appear below here ===&lt;br /&gt;
&amp;lt;references /&amp;gt;--[[User:Rzepa|Rzepa]] 15:18, 25 October 2007 (BST)&lt;br /&gt;
|&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;title&amp;gt;Pentahelicene&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;yellow&amp;lt;/color&amp;gt;&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;uploadedFileContents&amp;gt;Pentahelicene.mol&amp;lt;/uploadedFileContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;jmolMenu&amp;gt;&lt;br /&gt;
&amp;lt;item&amp;gt;&amp;lt;text&amp;gt;Start spinning&amp;lt;/text&amp;gt;&amp;lt;script&amp;gt;spin on&amp;lt;/script&amp;gt;&amp;lt;/item&amp;gt;&lt;br /&gt;
&amp;lt;item&amp;gt;&amp;lt;text&amp;gt;Stop spinning&amp;lt;/text&amp;gt;&amp;lt;script&amp;gt;spin off&amp;lt;/script&amp;gt;&amp;lt;/item&amp;gt;&lt;br /&gt;
&amp;lt;menuHeight&amp;gt;-1&amp;lt;/menuHeight&amp;gt;&lt;br /&gt;
&amp;lt;/jmolMenu&amp;gt;&lt;br /&gt;
&amp;lt;jmolButton&amp;gt;&lt;br /&gt;
    &amp;lt;script&amp;gt;console&amp;lt;/script&amp;gt;&lt;br /&gt;
    &amp;lt;text&amp;gt;open a console window&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolAppletButton&amp;gt;&amp;lt;title&amp;gt;Show CIYSIM.cif in popup window&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;cyan&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;uploadedFileContents&amp;gt;CIYSIM.cif&amp;lt;/uploadedFileContents&amp;gt;&amp;lt;/jmolAppletButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Main Project Page ==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;URGENT Announcement&#039;&#039;&#039;&#039;&#039;  &lt;br /&gt;
&lt;br /&gt;
Whilst the  Wiki itself is pretty robust, and although it is difficult to break a page on it, this did happen a few days ago to project 12.  What seems to have happened is that some  &#039;&#039;bad&#039;&#039; code (HTML or XML) was copied from another Web page, and pasted into the  project 12 page.  The Wiki system could not cope with this particular bad code, and sulked.  Fortunately, by invoking appropriate magic, the page has now been restored to its state prior to the breakage, and  I have learnt a valuable lesson in how to fix it if this happens again. So this serves as a warning;  if you are copying/pasting blind from other web pages (which in general you should not be doing), you do run the risk of breaking the page.  Hopefully, the break will be detected during the preview, and serves to remind that you should  &#039;&#039;always&#039;&#039; preview before saving to detect any such breaks. --[[User:Rzepa|Rzepa]] 10:21, 28 November 2007 (UTC)&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Please do not edit this page itself&#039;&#039;&#039;.  Click on one of the titles to start editing.&lt;br /&gt;
{| summary=&amp;quot;CIT Project  Titles&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |Project&amp;lt;br /&amp;gt; Number&lt;br /&gt;
! bgcolor=&amp;quot;cyan&amp;quot; |General Keywords&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |01&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Lignocaine|Lignocaine (used in dentistry as a &amp;quot;local&amp;quot;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |02&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Piperine|Piperine (active ingredient of both black and white pepper)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |03&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Rapamycin|Rapamycin (prevents transplant rejection)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |04&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Gossypol|Gossypol (male birth control)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |05&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |06&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Herceptin|Herceptin (topical anticancer drug)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |07&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Gingerone|Zingerone (the characteristic smell of ginger)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |08&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Sucralose|Sucralose (non-metabolizable sweetening agent)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |09&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Bufotoxin|Bufotoxin (active component of the toad &#039;&#039;Bufo vulgaris&#039;&#039;)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |10&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Roaccutane|Roaccutane (treatment for severe acne)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |11&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Sibutramine|Sibutramine (appetite suppresor)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |12&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07a:Anandamide|Anandamide (the &amp;quot;feel-good&amp;quot; factor in chocolate)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |13&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:h3nbh3|Ammonia-borane: H&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;N-BH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (Hydrogen storage molecule?)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |14&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |17	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:wilkinson|Wilkinson&#039;s catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |18	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |19	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |20	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |21	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Schrock|Schrock metathesis catalyst]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |22	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:knots|Molecular-scale knots (nanoscale devices)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
|bgcolor=&amp;quot;#CCFF00&amp;quot; |23	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |24	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Sertraline|Sertraline HCl (anti-depression)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |25	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |26	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[i07t:Zithromycin|Zithromycin (anti-infective)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |27	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it07:Lipitor|Lipitor (Cholesterol reducing agent)]]	 &lt;br /&gt;
|-	 &lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |28	 &lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it07:Cyameluric Acid|Cyameluric acid (Linus Pauling&#039;s last idea!)]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Supplemental  Project Page ==&lt;br /&gt;
&lt;br /&gt;
This area is for people who wish to create their own projects if none of the above appeal to them. Click on the  &#039;&#039;&#039;Edit&#039;&#039;&#039;  button to the right to open up an editable page,&lt;br /&gt;
then add an entry below as follows&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;nowiki&amp;gt; [[it07:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it07:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
#[[it07:sitagliptin_page|An example entry- in edit mode, please copy this line and paste below to add to this list]]&lt;br /&gt;
#[[it07:Limonene|Limonene]]&lt;br /&gt;
#[[it07:name_of_project|Vitamin C ]]&lt;br /&gt;
#[[it07:Cylcophosphamide|Cyclophosphamide]]&lt;br /&gt;
#[[it07:Terbutaline Sulphate|Terbutaline Sulphate]]&lt;br /&gt;
#[[it07:Caffeine|Caffeine]]&lt;br /&gt;
#[[it07:Mefloquine|Mefloquine]]&lt;br /&gt;
#[[it07:Cadaverine|Cadaverine]]&lt;br /&gt;
#[[it07:Cyanidin|Cyanidin]]&lt;br /&gt;
#[[it07:Ezetimibe|Ezetimibe]]&lt;br /&gt;
#[[it07:Octanitrocubane|Octanitrocubane]]&lt;br /&gt;
#[[it07:Azadirachtin|Azadirachtin]]&lt;br /&gt;
#[[it07:Nicotine|Nicotine]]&lt;br /&gt;
#[[it07:Cyclopentasiloxane|Cyclopentasiloxane]]&lt;br /&gt;
#[[it07:Trinitrotoluene|Trinitrotoluene]]&lt;br /&gt;
#[[it07:Hydroxychloroquine|Hydroxychloroquine]]&lt;br /&gt;
#[[it07:Aspartame|Aspartame]]&lt;br /&gt;
#[[it07:Azulene|Azulene]]&lt;br /&gt;
#[[it07:Chlorine Trifluoride|Chlorine Trifluoride]]&lt;br /&gt;
#[[it07:Cholesterol|Cholesterol]]&lt;br /&gt;
#[[it07:Vitamin E|Vitamin E]]&lt;br /&gt;
#[[it07:Phenothiazine|Phenothiazine]]&lt;br /&gt;
#[[it07:linalool|linalool]]&lt;br /&gt;
#[[it07:Glutamic acid|Glutamic acid]]&lt;br /&gt;
#[[it07:N-(4-hydroxyphenyl)ethanamide|N-(4-hydroxyphenyl)ethanamide]]&lt;br /&gt;
#[[it07:Epinephrine|Epinephrine]]&lt;br /&gt;
#[[it07:Sodium Valproate|Sodium Valproate]]&lt;br /&gt;
#[[it07:Hyaluronic acid |Hyaluronic acid  ]]&lt;br /&gt;
#[[it07:Methylenedioxymethamphetamine |Methylenedioxymethamphetamine ]]&lt;br /&gt;
#[[it07:salicylic acid |salicylic acid ]]&lt;br /&gt;
#[[it07:Morphine|Morphine]]&lt;br /&gt;
#[[Cetirizine]]&lt;br /&gt;
#[[it07:Bisacodyl|Bisacodyl]]&lt;br /&gt;
#[[it07:Rivaroxaban|Rivaroxaban]]&lt;br /&gt;
#[[it07:Sodium Lauryl Sulfate|Sodium Lauryl Sulfate]]&lt;br /&gt;
#[[it07:Silicon Dioxide|Silicon Dioxide]]&lt;br /&gt;
#[[it07:Vanillin|Vanillin]]&lt;br /&gt;
#[[it07:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
#[[it07:Capsaicin|Capsaicin]]&lt;br /&gt;
#[[it07:Menthol|Menthol]]&lt;br /&gt;
#[[it07:Tamoxifen|Tamoxifen]]&lt;br /&gt;
#[[it07:Copper arsenate|Scheele&#039;s Green]]&lt;br /&gt;
#[[it07:Strychnine|Strychnine]]&lt;br /&gt;
#[[it07:Testosterone|Testosterone]]&lt;br /&gt;
#[[it07:Monosodium glutamate|Monosodium glutamate]]&lt;br /&gt;
#[[it07:Taurine|Taurine]]&lt;br /&gt;
#[[it07:Phenethylamine|Phenethylamine]]&lt;br /&gt;
#[[it07:Verbenone|Verbenone]]&lt;br /&gt;
#[[it07:Salbutamol|Salbutamol]]&lt;br /&gt;
#[[it07:Lactic acid|Lactic acid]]&lt;br /&gt;
#[[it07:Aspirin|Aspirin]]&lt;br /&gt;
#[[it07:EDTA|EDTA]]&lt;br /&gt;
#[[it07:Heroin|Heroin]]&lt;br /&gt;
#[[it07:Cocaine|Cocaine]]&lt;br /&gt;
#[[it07:Myristicin|Myristin (The hallucinogen in nutmeg)]]&lt;br /&gt;
#[[it07:Encefabol|Encefabol]]&lt;br /&gt;
#[[it07:Sarin|Sarin]]&lt;br /&gt;
#[[Thebaine]]&lt;br /&gt;
#[[Nitroglycerin]]&lt;br /&gt;
#[[it07:Methamphetamine|Methamphetamine]]&lt;br /&gt;
#[[it07:Sildenafil|Sildenafil]]&lt;br /&gt;
#[[Grubbs&#039; Catalyst]]&lt;br /&gt;
#[[it07:Warfarin|Warfarin]]&lt;br /&gt;
#[[it07:Angelic Acid|Angelic Acid]]&lt;br /&gt;
#[[it07:Melem (Melon) |Melem]]&lt;br /&gt;
#[[it07:oxazaborolidines|Chiral Oxazaborolidines as Catalysts]]&lt;br /&gt;
#[[it07:RDX|RDX (chemical in plastic explosives)]]&lt;br /&gt;
#[[it07:Lysergic Acid|Lysergic Acid]]&lt;br /&gt;
#[[it07:Oseltamivir Phosphate|Oseltamivir Phosphate(Tamiflu)]]&lt;br /&gt;
#[[Fluoxetine Hydrochloride (Prozac)]]&lt;br /&gt;
#[[Dimethylmercury]]&lt;br /&gt;
#[[it07:Sorafenib(Nexavar®)|Sorafenib (Nexavar®)]]&lt;br /&gt;
#[[Rapamycin]]&lt;br /&gt;
#[[Rohypnol]]&lt;br /&gt;
#[[it07:Vitamin A|Vitamin A (Retinol)]]&lt;br /&gt;
#[[it07:THC|Tetrahydrocannabinol]]&lt;br /&gt;
#[[2,4-Dinitrophenylhydrazine|2,4-Dinitrophenylhydrazine]]&lt;br /&gt;
#[[Acetylcholine]]&lt;br /&gt;
#[[it07:Phenolphthalein|Phenolphthalein]]&lt;br /&gt;
#[[Carbon Dioxide]]&lt;br /&gt;
#[[Domoic Acid]]&lt;br /&gt;
#[[Kevlar]]&lt;br /&gt;
#[[it07:Erythromycin|Erythromycin]]&lt;br /&gt;
#[[it07:DIBAL|DIBAL]]&lt;br /&gt;
#[[Ephedrine]]&lt;br /&gt;
#[[it07:Lactose|Lactose]]&lt;br /&gt;
#[[it07:Thyjone|Thyjone]]&lt;br /&gt;
#[[Levothyroxine]]&lt;br /&gt;
#[[it07:Tropinone|Tropinone]]&lt;br /&gt;
#[[it07:Ozone|Ozone]]&lt;br /&gt;
#[[it07:Indinavir|Indinavir (Crixivan®)]]&lt;br /&gt;
#[[it07:Tetrodotoxin|Tetrodotoxin]]&lt;br /&gt;
#[[it07:Astaxanthin|Astaxanthin]]&lt;br /&gt;
#[[Methane]]&lt;br /&gt;
#[[it07:2 – Chlorobenzalmalononitrile|2 – Chlorobenzalmalononitrile (CS Gas)]]&lt;br /&gt;
#[[it07:Dichloro-Diphenyl-Trichloroethane|Dichloro-Diphenyl-Trichloroethane]]&lt;br /&gt;
#[[it07:Ketamine|Ketamine]]&lt;br /&gt;
#[[it07:Ethylene Glycol|Ethylene Glycol]]&lt;br /&gt;
#[[it07:HMX|HMX]]&lt;br /&gt;
#[[it07:Psilocybin|Psilocybin (magic mushrooms)]]&lt;br /&gt;
#[[it07:Dopamine|Dopamine]]&lt;br /&gt;
#[[it07:Mefenamic Acid|Mefenamic Acid]]&lt;br /&gt;
#[[it07:Sesamin|Sesamin]]&lt;br /&gt;
#[[it07:Riboflavin|Riboflavin (Vitamin B2)]]&lt;br /&gt;
#[[it07:Coniine|Coniine]]&lt;br /&gt;
#[[it07:Capecitabine|Capecitabine]]&lt;br /&gt;
#[[it07:Atenolol|Atenolol]]&lt;br /&gt;
#[[it07:Simvastatin|Simvastatin]]&lt;br /&gt;
#[[it07:Ammonia|Ammonia]]&lt;br /&gt;
#[[it07:Tetrodotoxin|Tetrodotoxin]]&lt;br /&gt;
#[[it07:Halomon|Halomon]]&lt;br /&gt;
#[[it07:Hexyl Cinnamal|Hexyl Cinnamal]]&lt;br /&gt;
#[[it07:Humulene|Humulene]]&lt;br /&gt;
#[[it07:PETN|PETN]]&lt;br /&gt;
#[[it07:Lipoic Acid|Lipoic Acid]]&lt;br /&gt;
&lt;br /&gt;
== Wiki Templates ==&lt;br /&gt;
&lt;br /&gt;
[[Template:DOI]] and [[Template:Doi-inline]] are providea as (protected) templates for your use. Many other templates exist, often to be found on e.g. Wikipedia pages. You may decide one of these is of particular use, or of interest. If so, you can install it on the wiki here for you and others to use. Add below a line that looks like Template:Template-name, save, and click on the red text to create the new template. If you prefer the task of adding useful templates to that of adding information about molecules, then you will be given full credit for performing this valuable service for others! --Rzepa 14:41, 20 October 2006 (BST) &lt;br /&gt;
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[[Template:Chem-Data]]&lt;br /&gt;
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[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables&lt;br /&gt;
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[[Template:Chembox new]]&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.pdb&amp;diff=14026</id>
		<title>File:Lipoic-acid.pdb</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.pdb&amp;diff=14026"/>
		<updated>2007-12-07T15:23:04Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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		<author><name>Xj06</name></author>
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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.mol&amp;diff=14020</id>
		<title>File:Lipoic-acid.mol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic-acid.mol&amp;diff=14020"/>
		<updated>2007-12-07T15:13:45Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
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		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin.mol&amp;diff=14019</id>
		<title>File:Amoxicillin.mol</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin.mol&amp;diff=14019"/>
		<updated>2007-12-07T15:10:52Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin.msv&amp;diff=14018</id>
		<title>File:Amoxicillin.msv</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxicillin.msv&amp;diff=14018"/>
		<updated>2007-12-07T15:09:01Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
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		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxocillin.JPG&amp;diff=14017</id>
		<title>File:Amoxocillin.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Amoxocillin.JPG&amp;diff=14017"/>
		<updated>2007-12-07T15:08:07Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic_acid.gif&amp;diff=14015</id>
		<title>File:Lipoic acid.gif</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Lipoic_acid.gif&amp;diff=14015"/>
		<updated>2007-12-07T15:02:28Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
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&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Herceptin&amp;diff=11409</id>
		<title>It07:Herceptin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It07:Herceptin&amp;diff=11409"/>
		<updated>2007-11-19T15:56:40Z</updated>

		<summary type="html">&lt;p&gt;Xj06: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Herceptin (also &#039;&#039;Trastuzumab&#039;&#039;) ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:800px-HerceptinFab.jpg]]&lt;br /&gt;
&lt;br /&gt;
{| style=&amp;quot;float: right; clear: right; margin: 0 0 0.5em 1em; background: #ffffff;&amp;quot; class=&amp;quot;toccolours&amp;quot; border=&amp;quot;0&amp;quot; cellpadding=&amp;quot;1&amp;quot; align=&amp;quot;right&amp;quot; width=&amp;quot;300&amp;quot;&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|  Herceptin &amp;lt;!-- replace if not identical with the article name --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;2&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image|{{{Box_Name}}}]] &amp;lt;!-- replace if not identical with the pagename --&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|IUPAC Systematic name&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| Systematic name&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Other Names&lt;br /&gt;
|-&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| Trastuzumab&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;|Indentifiers&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;|[http://en.wikipedia.org/wiki/ATC_code ATC Code]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;| L01XC03 &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/CAS_number CAS number]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|180288-69-1&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Simplified_molecular_input_line_entry_specification SMILES]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Chemical Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Chemical_formula Molecular formula]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|C&amp;lt;sub&amp;gt;6470&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;10012&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;1726&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;2013&amp;lt;/sub&amp;gt;S&amp;lt;sub&amp;gt;42&amp;lt;/sub&amp;gt; &lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Molecular_weight Molar mass]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|145531.5 g/mol&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Pharmacokinetic Data&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Bioavailability Bioavailability]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Plasma_protein_binding Protein Binding]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Metabolism Metabolism]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|Unknown, possibly reticuloendothelial system&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Elimination_half-life Half life]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|2 - 12 days&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Excretion Excretion]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|?&lt;br /&gt;
|-&lt;br /&gt;
! colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot; bgcolor=&amp;quot;#dddddd&amp;quot;| Therapeutic considerations&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Pregnancy_category Pregnancy cat.]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|X&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Regulation_of_therapeutic_goods Legal status]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|&lt;br /&gt;
|-&lt;br /&gt;
! align=&amp;quot;left&amp;quot; bgcolor=&amp;quot;#ddeeff&amp;quot; width=&amp;quot;120&amp;quot;| [http://en.wikipedia.org/wiki/Route_of_administration Routes]&lt;br /&gt;
| align=&amp;quot;center&amp;quot;|Intravenous&lt;br /&gt;
|-&lt;br /&gt;
&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&amp;lt;noinclude&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== General ==&lt;br /&gt;
&lt;br /&gt;
&#039;Herceptin&#039; is the trade-name of a molecule called Trastuzumab, which is a humanized monoclonal antibody. It is particularly well known for its use as an anti-cancer agent, specifically in breast cancer.&lt;br /&gt;
&lt;br /&gt;
This molecule targets the HER2/neu receptor, and if too much of this receptor is produced, which occurs in some cases of breast cancer tumours, then Herceptin can be used to tre&lt;br /&gt;
&lt;br /&gt;
Herceptin cannot be taken orally, as it would be destroyed by the stomach. Instead, it is injected directly into the vein via a drip.&lt;br /&gt;
&lt;br /&gt;
== Using Herceptin ==&lt;br /&gt;
&lt;br /&gt;
Herceptin is most commonly used when there has been found to be an over-expression of the HER2 receptor. This over-expression can be detected by immunohistochemistry or either chromogenic or fluorescent in situ hybridisation. Alternative ways of detecting this over-expression include various polymerase chain reaction methods. &lt;br /&gt;
&lt;br /&gt;
Herceptin has been found to be unsuitable for patients with pre-existing heart problems, and has had unwanted cardiac effects on around 5% of patients used upon.&lt;br /&gt;
&lt;br /&gt;
After taking Herceptin, some patients suffered from unwanted side-effects, including nausea, vomiting, headaches and fatigue.&lt;br /&gt;
&lt;br /&gt;
== Pharmacological Action ==&lt;br /&gt;
&lt;br /&gt;
Herceptin acts in a different way to other standard treatments for cancer, including hormone replacement and chemotherapy. It is thought to have three main functions.&lt;br /&gt;
#In most cases of breast cancer the cancerous cells have too many copies of an oncogene, a gene which causes cells to rapidly grow and divide. The gene (part of the c-erbB-2 family) results in the expression of the HER2 receptor on the cell surface, thus allowing the cell to communicate and replicate. This receptor is targeted by Herceptin, which binds to it stopping communication and division.&lt;br /&gt;
#Once Herceptin is bound to the receptor it can be recognised by the body&#039;s Natural Killer immune cells (NK). These can then attack and destroy the unhealthy cells.&lt;br /&gt;
#Herceptin can be used in conjunction with chemotherapy, as the drugs work together and can be more effective than either treatment alone.&lt;br /&gt;
&lt;br /&gt;
== Herceptin&#039;s success ==&lt;br /&gt;
&lt;br /&gt;
Despite the unwanted side-effects, Herceptin has been found to be very useful in assisting the treatment of breast cancer. Recent clinical trials stated that Herceptin reduces the risk of relapse in breast cancer patients by 50% when given to them after breast cancer surgery, but before the cancer has spread any further, for one year.&lt;br /&gt;
&lt;br /&gt;
However, the fact that Herceptin can cause heart disease means that its use as an anti-cancer drug has become limited.&lt;br /&gt;
&lt;br /&gt;
== Side effects ==&lt;br /&gt;
&lt;br /&gt;
The Herceptin is believed to have several side effects for the women who had taken it. &lt;br /&gt;
&lt;br /&gt;
One significant complications of Herceptin is that is causes heart failure. Cardiac dysfunction is associated with herceptin in 2~7% [citation needed] of the cases. In very few cases, about 5% of the patients experienced stroke or life-threatening congestive heart failure—a condition in which the heart can&#039;t pump effectively. Therefore, 10% of the patients with pre-existing heart disease have limitations of tolerating this drug.  &lt;br /&gt;
&lt;br /&gt;
Another complication of Herceptin is the allergic-like reactions and lung reactions. According to the record from the company make Herceptin, 62 of the approximately 25,000 women who had taken Herceptin as of 2001 had a serious reaction to the medication. Symptoms of the allergic–like reactions included hives, wheezing, and trouble breathing because of swelling and muscle spasms of the airways. Lung reactions included swelling of the lung, low blood pressure, or pleural effusions.&lt;br /&gt;
&lt;br /&gt;
In most cases, about 40% of the women have the mild effects as flu-like symptom, which includes fever, chills, muscle aches and nausea in the first 24hour of the first dose. These effects usually become less severe after the first treatment. &lt;br /&gt;
&lt;br /&gt;
== Costs ==&lt;br /&gt;
&lt;br /&gt;
As well as Hercpetin&#039;s unwanted side-effects, its cost plays an important role in its issue to patients. It has been reported that Herceptin costs around £35,000 for a full course of treatment - a price that some public health services, including those of England and New Zealand, have been unwilling to pay for a drug with such major defects. However, after much campaigning, the Ontario Ministry of Health said in July 2005 that it would pay for the treatment.&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
#http://www.cancernet.co.uk/herceptin.htm&lt;br /&gt;
#http://www.breastcancer.org/treatment/targeted_therapies/herceptin/side_effects.jsp&lt;/div&gt;</summary>
		<author><name>Xj06</name></author>
	</entry>
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