ChemWiki - User contributions [en]

It:Ethenzamide

2006-12-07T16:32:22Z

Asd105: /* References */

==Ethenzamide==

Ethenzamide has become widely used in cold and flu medications due to its anit-inflammatory and analgesic properties.

== Structure and properties == 

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure],
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
12 12 0 0 0 0 0 0 0 0999 V2000
4.4194 -3.0500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4182 -3.8773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1331 -4.2902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8495 -3.8769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8466 -3.0463 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1313 -2.6372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1292 -1.8083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8417 -1.3958 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.4139 -1.3972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5667 -2.6250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2875 -3.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0000 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6 1 1 0 0 0 0
1 2 2 0 0 0 0
6 7 1 0 0 0 0
3 4 2 0 0 0 0
7 8 1 0 0 0 0
7 9 2 0 0 0 0
4 5 1 0 0 0 0
5 10 1 0 0 0 0
2 3 1 0 0 0 0
10 11 1 0 0 0 0
5 6 2 0 0 0 0
11 12 1 0 0 0 0

M END</inlineContents>
</jmolApplet>
</jmol>


|-
| [2D structure]
|[[Image:Third structure.JPG|thumb|Description]] 
|-
| [IR spectrum]
| [[Image:IR THREE.JPG|thumb|Description]] 
|-
| [UV spectrum]
| [[Image:Uv third and final.JPG|thumb|Description]] 
|-
| [Retention time]
| 5.18 
|-
| [Melting point]
| 129-134 
|-

| [SMILES]
| CCOC1=CC=CC=C1C(N)=O 
|-
| [FW]
| 165.19184 
|-
|}

== References == 

Uv link http://chrom.tutms.tut.ac.jp/JINNO/DRUGDATA/14ethenzamide.html

http://www.freepatentsonline.com/5419915.html

www.chemexper.com

It:Ethenzamide

2006-12-07T16:31:29Z

Asd105: /* Structure and properties */

It:Ethenzamide

2006-12-07T16:29:49Z

Asd105: /* Ethenzamide */

It:Ethenzamide

2006-12-07T16:07:07Z

Asd105:

==Ethenzamide==
== Structure and properties == 

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure],
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
12 12 0 0 0 0 0 0 0 0999 V2000
4.4194 -3.0500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4182 -3.8773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1331 -4.2902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8495 -3.8769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8466 -3.0463 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1313 -2.6372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1292 -1.8083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8417 -1.3958 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.4139 -1.3972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5667 -2.6250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2875 -3.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0000 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6 1 1 0 0 0 0
1 2 2 0 0 0 0
6 7 1 0 0 0 0
3 4 2 0 0 0 0
7 8 1 0 0 0 0
7 9 2 0 0 0 0
4 5 1 0 0 0 0
5 10 1 0 0 0 0
2 3 1 0 0 0 0
10 11 1 0 0 0 0
5 6 2 0 0 0 0
11 12 1 0 0 0 0

M END</inlineContents>
</jmolApplet>
</jmol>


|-
| [2D structure]
|[[Image:Third structure.JPG|thumb|Description]] 
|-
| [IR spectrum]
| [[Image:IR THREE.JPG|thumb|Description]] 
|-
| [UV spectrum]
| [[Image:Uv third and final.JPG|thumb|Description]] 
|-
| [Retention time]
| 5.18 
|-
| [Melting point]
| 129-134 
|-

| [SMILES]
| CCOC1=CC=CC=C1C(N)=O 
|-
| [FW]
| 165.19184 
|-
|}

It:Ethenzamide

2006-12-07T16:02:48Z

Asd105:

==Ethenzamide==
== Structure and properties == 

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure],
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
12 12 0 0 0 0 0 0 0 0999 V2000
4.4194 -3.0500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4182 -3.8773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1331 -4.2902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8495 -3.8769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8466 -3.0463 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1313 -2.6372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1292 -1.8083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8417 -1.3958 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.4139 -1.3972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5667 -2.6250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2875 -3.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0000 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6 1 1 0 0 0 0
1 2 2 0 0 0 0
6 7 1 0 0 0 0
3 4 2 0 0 0 0
7 8 1 0 0 0 0
7 9 2 0 0 0 0
4 5 1 0 0 0 0
5 10 1 0 0 0 0
2 3 1 0 0 0 0
10 11 1 0 0 0 0
5 6 2 0 0 0 0
11 12 1 0 0 0 0

M END</inlineContents>
</jmolApplet>
</jmol>


|-
| [2D structure]
|[[Image:Third structure.JPG|thumb|Description]] 
|-
| [IR spectrum]
| [[Image:IR THREE.JPG|thumb|Description]] 
|-
| [UV spectrum]
| [[Image:Uv third and final.JPG|thumb|Description]] 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

File:Third structure.JPG

2006-12-07T16:01:46Z

Asd105:

It:Ethenzamide

2006-12-07T15:56:36Z

Asd105:

==Ethenzamide==
== Structure and properties == 

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure],
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
12 12 0 0 0 0 0 0 0 0999 V2000
4.4194 -3.0500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4182 -3.8773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1331 -4.2902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8495 -3.8769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8466 -3.0463 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1313 -2.6372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1292 -1.8083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8417 -1.3958 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.4139 -1.3972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5667 -2.6250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2875 -3.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0000 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6 1 1 0 0 0 0
1 2 2 0 0 0 0
6 7 1 0 0 0 0
3 4 2 0 0 0 0
7 8 1 0 0 0 0
7 9 2 0 0 0 0
4 5 1 0 0 0 0
5 10 1 0 0 0 0
2 3 1 0 0 0 0
10 11 1 0 0 0 0
5 6 2 0 0 0 0
11 12 1 0 0 0 0

M END</inlineContents>
</jmolApplet>
</jmol>


|-
| [2D structure]
|? 
|-
| [IR spectrum]
| [[Image:IR THREE.JPG|thumb|Description]] 
|-
| [UV spectrum]
| [[Image:Uv third and final.JPG|thumb|Description]] 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

File:Uv third and final.JPG

2006-12-07T15:55:34Z

Asd105:

It:Ethenzamide

2006-12-07T15:55:06Z

Asd105:

==Ethenzamide==
== Structure and properties == 

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure],
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
12 12 0 0 0 0 0 0 0 0999 V2000
4.4194 -3.0500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4182 -3.8773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1331 -4.2902 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8495 -3.8769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8466 -3.0463 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1313 -2.6372 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1292 -1.8083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8417 -1.3958 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.4139 -1.3972 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.5667 -2.6250 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2875 -3.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0000 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6 1 1 0 0 0 0
1 2 2 0 0 0 0
6 7 1 0 0 0 0
3 4 2 0 0 0 0
7 8 1 0 0 0 0
7 9 2 0 0 0 0
4 5 1 0 0 0 0
5 10 1 0 0 0 0
2 3 1 0 0 0 0
10 11 1 0 0 0 0
5 6 2 0 0 0 0
11 12 1 0 0 0 0

M END</inlineContents>
</jmolApplet>
</jmol>


|-
| [2D structure]
|? 
|-
| [IR spectrum]
| [[Image:IR THREE.JPG|thumb|Description]] 
|-
| [UV spectrum]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

It:Ethenzamide

2006-12-07T15:51:37Z

Asd105:

File:IR THREE.JPG

2006-12-07T15:50:20Z

Asd105:

It:Ethenzamide

2006-12-07T15:49:40Z

Asd105:

It:Ethenzamide

2006-12-07T15:45:18Z

Asd105:

==Ethenzamide==

It:projects

2006-12-07T15:44:51Z

Asd105: /* Supplemental Project Page */

__FORCETOC__

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| bgcolor="#CCFF00" |01
| bgcolor="#CCFF00" | [[it:Lignocaine|Lignocaine (used in dentistry as a "local")]]
|-
| bgcolor="#CCFF00" |02
| bgcolor="#66FF99" | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]
|-
| bgcolor="#CCFF00" |03
| bgcolor="#CCFF00" | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]
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| bgcolor="#CCFF00" |04
| bgcolor="#66FF99" | [[it:Gossypol|Gossypol (male birth control)]]
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| bgcolor="#CCFF00" |13
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| bgcolor="#CCFF00" | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]
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| bgcolor="#CCFF00" |24
| bgcolor="#66FF99" | [[it:Sertraline|Sertraline HCl (anti-depression)]]
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| bgcolor="#CCFF00" |25
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| bgcolor="#CCFF00" |26
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| bgcolor="#CCFF00" |27
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[[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-name|parameter}}, 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!
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)

----
[[Template:Chem-Data]]

[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables

[[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]]

[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]

[[R & S Phrases]]

It:projects

2006-12-07T15:41:57Z

Asd105: /* Supplemental Project Page */

__FORCETOC__

'''''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.'''''
== Sandbox (Play-Pen) ==

This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button '''on the right''' and '''not''' at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet ''cheat sheet''] summary of how to create a Wiki page. It's a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: Α, α, β Δ, δ
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 '''Show Preview'''. No not use '''Save Page''' so as to leave this area uncluttered for others.
----
{|
|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. Sorry about the delay in getting this working, but the cause was pretty unobvious.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC)
<center><jmol>
<jmolApplet>
<title>Pentahelicene</title><color>yellow</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents>
</jmolApplet>
<jmolMenu>
<item><text>Start spinning</text><script>spin on</script></item>
<item><text>Stop spinning</text><script>spin off</script></item>
<menuHeight>-1</menuHeight>
</jmolMenu>
<jmolButton>
<script>console</script>
<text>open a console window</text>
</jmolButton>
</jmol></center>
-----
<center><jmol><jmolAppletButton><title>Show Pentahelicene in popup window</title><color>cyan</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents></jmolAppletButton>
</jmol></center>

== Main Project Page ==
'''Please do not edit this page itself'''. Click on one of the titles to start editing.
{| summary="CIT Project Titles" border="1"
! bgcolor="cyan" |Project<br /> Number
! bgcolor="cyan" |General Keywords
|-
| bgcolor="#CCFF00" |01
| bgcolor="#CCFF00" | [[it:Lignocaine|Lignocaine (used in dentistry as a "local")]]
|-
| bgcolor="#CCFF00" |02
| bgcolor="#66FF99" | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]
|-
| bgcolor="#CCFF00" |03
| bgcolor="#CCFF00" | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]
|-
| bgcolor="#CCFF00" |04
| bgcolor="#66FF99" | [[it:Gossypol|Gossypol (male birth control)]]
|-
| bgcolor="#CCFF00" |05
| bgcolor="#CCFF00" | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]
|-
| bgcolor="#CCFF00" |06
| bgcolor="#66FF99" | [[it:Herceptin|Herceptin (topical anticancer drug)]]
|-
| bgcolor="#CCFF00" |07
| bgcolor="#CCFF00" | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]
|-
| bgcolor="#CCFF00" |08
| bgcolor="#66FF99" | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]
|-
| bgcolor="#CCFF00" |09
| bgcolor="#CCFF00" | [[it:Bufotoxin|Bufotoxin (active component of the toad ''Bufo vulgaris'')]]
|-
| bgcolor="#CCFF00" |10
| bgcolor="#66FF99" | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]
|-
| bgcolor="#CCFF00" |11
| bgcolor="#CCFF00" | [[it:Sibutramine|Sibutramine (appetite suppresor)]]
|-
| bgcolor="#CCFF00" |12
| bgcolor="#66FF99" | [[it:Anandamide|Anandamide (the "feel-good" factor in chocolate)]]
|-
| bgcolor="#CCFF00" |13
| bgcolor="#CCFF00" | [[it:h3nbh3|Ammonia-borane: H<sub>3</sub>N-BH<sub>3</sub> (Hydrogen storage molecule?)]]
|-
| bgcolor="#CCFF00" |14
| bgcolor="#66FF99" | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]
|-
| bgcolor="#CCFF00" |15
| bgcolor="#CCFF00" | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]
|-
| bgcolor="#CCFF00" |16
| bgcolor="#66FF99" | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]
|-
| bgcolor="#CCFF00" |17
| bgcolor="#CCFF00" | [[it:wilkinson|Wilkinson's catalyst]]
|-
| bgcolor="#CCFF00" |18
| bgcolor="#66FF99" | [[it:Jacobsen|Jacobsen's epoxidation catalyst]]
|-
| bgcolor="#CCFF00" |19
| bgcolor="#CCFF00" | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]
|-
| bgcolor="#CCFF00" |20
| bgcolor="#66FF99" | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]
|-
| bgcolor="#CCFF00" |21
| bgcolor="#CCFF00" | [[it:Schrock|Schrock metathesis catalyst]]
|-
| bgcolor="#CCFF00" |22
| bgcolor="#66FF99" | [[it:knots|Molecular-scale knots (nanoscale devices)]]
|-
|bgcolor="#CCFF00" |23
| bgcolor="#CCFF00" | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]
|-
| bgcolor="#CCFF00" |24
| bgcolor="#66FF99" | [[it:Sertraline|Sertraline HCl (anti-depression)]]
|-
| bgcolor="#CCFF00" |25
| bgcolor="#CCFF00" | [[it:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]
|-
| bgcolor="#CCFF00" |26
| bgcolor="#66FF99" | [[it:Zithromycin|Zithromycin (anti-infective)]]
|-
| bgcolor="#CCFF00" |27
| bgcolor="#CCFF00" | [[it:Lipitor|Lipitor (Cholesterol reducing agent)]]
|-
| bgcolor="#CCFF00" |28
| bgcolor="#66FF99" | [[it:Cyameluric Acid|Cyameluric acid (Linus Pauling's last idea!)]]
|}

== Supplemental Project Page ==

This area is for people who wish to create their own projects if none of the above appeal to them. Click on the '''Edit''' button to the right to open up an editable page,
then add an entry below as follows

*<nowiki> [[it:name_of_project|Descriptive name of intended project]]</nowiki>
*This will produce the effect: [[it:name_of_project|Descriptive name of intended project]]
----
*[[it:sitagliptin_page|Sitagliptin]]
*[[it:Retinal|Retinal, molecule of sight]]
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]
*[[it:Morphine|Morphine, painkiller]]
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]
*[[it:Propanil|Propanil, weedkiller]]
*[[it:Ranitidine|Ranitidine, antiulcerative]]
*[[it:chlorphentermine|chlorphentermine, anorectic]]
*[[it:Serotonin|Serotonin, The 'HAPPY' Drug]]
*[[it:Amphidinolide T1|Amphidinolide T1]]
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]
*[[it:Furosemide|Furosemide]]
*[[it:Tryptophan|Tryptophan]]
*[[it:methylpentynol|methylpentynol, tranquilliser.]]
*[[it:Ferrocene|Ferrocene]]
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]
*[[it:Psilocin|Psilocin]]
*[[it:Epibatidine|Epibatidine]]
*[[it:Beta Carotene|Beta Carotene]]
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]
*[[it:Linalool|Linalool(A component of essential oil)]]
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]
*[[it:Acrolein|Acrolein]]
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]
*[[it:Vanillin|Vanillin, flavouring used in food]]
*[[it:Gingerol|Gingerol, precursor of Zingerone]]
*[[it:MSG|MSG; because everyone loves the flavour]]
*[[it:DDT|DDT, Pesticide]]
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]
*[[it:Caffeine|Caffeine]]
*[[it:Fullerene]]
*[[it:Histrionicotoxin]]
*[[it:limonene]]
*[[it:Capsanthin]]
*[[it:Safrole|Safrole: A formerly popular food and drinks additive]]
*[[it:Adenosine_Triphosphate|Adenosine Triphosphate (ATP), Energy source in muscles]]
*[[it:Aspartame|Aspartame: Artificial sweetener]]
*[[it:Astemizole|Astemizole:non-sedating anti-histamine]]
*[[it:Flucloxacillin|Flucloxacillin:antibiotic]]
*[[it:Quinine|Quinine: The Perfect Tonic for Any Fever]]
*[[it:Caramel|Caramel]]
*[[it:Azithromycin|Azithromycin]]
*[[it:Artemisinin|Artemisinin: An antimalarial drug]]
*[[it:Bradykinin|Bradykinin]]
*[[it:Carminic_acid|Carminic acid, Red colouring agent]]
*[[it:Oxytocin|Oxytocin: The Hormone of Love]]
*[[it:Carmoisine|Carmoisine]]
*[[it:Ziegler-Natta|Ziegler-Natta]]
*[[it:Cyclamate|Cyclamate]]
*[[it:Polyurethane|Polyurethane]]
*[[it:sexithiophene|sexithiophene]]
*[[it:Polydimethylsiloxane|Polydimethylsiloxane: Silicon-based organic polymer]]
*[[it:Lycopene|Lycopene: the red antioxidant molecule]]
*[[it:Crystal Meth|Crystal Meth]]
*[[it:Mustard Gas|Mustard Gas]]
*[[it:Saxitoxin|Shellfish Poison]]
*[[it:Luminol|Luminol: Chemiluminescence Reactions]]
*[[it:Tumor Necrosis Factor|Tumour Necrosis Factor]]
*[[it:Tamiflu|Tamiflu: Antiviral]]
*[[it:Warfarin|Warfarin: Blood thinner]]
*[[it:Vitamin C|Ascorbic acid: Vitamin C]]
*[[it:Hexahelicene|Hexahelicene]]
*[[it:Cocaine|Cocaine]]
*[[it:Eucalyptol|Eucalyptol: The main component of eucalyptus oil]]
*[[it:dichlorodifluromethane| Dichlorodifluromethane]]
*[[it:Theobromine| Theobromine]]
*[[it:Maraviroc|Maraviroc: A Potent CCR5 Antagonist for treatment of HIV]]
*[[it:Aspirin]]
*[[it:DEET|DEET]]
*[[it:PhenylButazone|PhenylButazone]]
*[[it:Epinephrine|Epinephrine]]
*[[it:Phenylmercury Acetate|Phenylmurcury Acetate]]
*[[it:Methyltestosterone|Methyltestosterone]]
*[[it:Carboplatin|Carboplatin]]
*[[it:Osmium Tetroxide|Osmium Tetroxide]]
*[[it:TNT|TNT]]
*[[it:Ethenzamide|Ethenzamide]

== Wiki Utillities ==
Utilities have been written to help the conversion of material from HTML.

# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]

No wiki2html converter suitable for use has yet been identified.
=== Wiki Templates ===

[[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-name|parameter}}, 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!
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)

----
[[Template:Chem-Data]]

[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables

[[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]]

[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]

[[R & S Phrases]]

It:Methyltestosterone

2006-12-07T15:15:56Z

Asd105: /* References */

{| border="1" cellspacing="0" cellpadding="3" style="float: right; clear: right; margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} |
Methyltestosterone

Structure and properties
|-
| [3D structure]
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
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-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
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12 6 1 0 0 0 0
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16 13 1 0 0 0 0
17 15 2 0 0 0 0
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2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

|-
| [Structure]
|[[Image:New m structure.JPG|thumb|Description]] 
|-
| [IR Spectrum of Methyltestoserone]
| [[Image:New ir.JPG|thumb|Description]] 
|-
| Molecular Formula
|C20H30O2
|-
|Molecular Weight
|302.45
|-
|Other Names
|
Methyltestosterone

Mesterone

17β-Hydroxy-17α-methyl-4-androsten-3-one

17α-Methyl-4-androsten-17β-ol-3-one
|-
| CAS Number
|58-18-4
|-
|mp
|162-168 °C
|-
|Form
|Crystal
|-
|Colour
|White
|}
Methyltestosterone is an anabolic steroid.
Its legal use is for men with testosterone deficiencies, but because of the compounds “bulking” effect it has also been used as an illegal way to gain larger muscles. It can also be used as an aid for women with menopause problems and for treating breast cancer.

[http://www.sigmaaldrich.com/spectra/fnmr/FNMR008958.PDF NMR of Methyltestosterone]

[[Image:methyltestosterone.jpg]]

== References ==

http://www.sigmaaldrich.com/catalog/search/ProductDetail/FLUKA/69240

http://www.inchem.org/documents/pims/pharm/pim908.htm#SectionTitle:1.1%20%20Substance

www.chemexper.com

It:Methyltestosterone

2006-12-07T11:02:47Z

Asd105:

'''==Methyltestoserone=='''
----

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure]
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6974 1.5829 -0.2375 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3854 -2.0571 -0.1791 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7509 -1.8166 0.0642 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7904 -2.1552 0.4207 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7062 0.1553 -0.4992 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1080 -1.1910 -0.3126 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8203 0.0510 -1.0086 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
11 1 1 0 0 0 0
12 6 1 0 0 0 0
13 5 1 0 0 0 0
14 3 1 0 0 0 0
15 18 1 0 0 0 0
16 13 1 0 0 0 0
17 15 2 0 0 0 0
18 11 1 0 0 0 0
19 8 1 0 0 0 0
1 20 1 1 0 0 0
2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

|-
| [Structure]
|[[Image:New m structure.JPG|thumb|Description]] 
|-
| [IR Spectrum of Methyltestoserone]
| [[Image:New ir.JPG|thumb|Description]] 
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

It:Methyltestosterone

2006-12-07T11:01:49Z

Asd105:

'''==Methyltestoserone=='''
----

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure]
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6974 1.5829 -0.2375 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3854 -2.0571 -0.1791 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7509 -1.8166 0.0642 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7904 -2.1552 0.4207 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7062 0.1553 -0.4992 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1080 -1.1910 -0.3126 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8203 0.0510 -1.0086 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
11 1 1 0 0 0 0
12 6 1 0 0 0 0
13 5 1 0 0 0 0
14 3 1 0 0 0 0
15 18 1 0 0 0 0
16 13 1 0 0 0 0
17 15 2 0 0 0 0
18 11 1 0 0 0 0
19 8 1 0 0 0 0
1 20 1 1 0 0 0
2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

|-
| [Structure]
|[[Image:New m structure.JPG|thumb|Description]] 
|-
| [IR Spectrum of Methyltestoserone],| [[Image:New ir.JPG|thumb|Description]] IR spectrum of methyltestoserone
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

File:New m structure.JPG

2006-12-07T10:54:55Z

Asd105:

It:Methyltestosterone

2006-12-07T10:44:24Z

Asd105:

'''==Methyltestoserone=='''
----

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure]
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6974 1.5829 -0.2375 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3854 -2.0571 -0.1791 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7509 -1.8166 0.0642 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7904 -2.1552 0.4207 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7062 0.1553 -0.4992 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1080 -1.1910 -0.3126 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8203 0.0510 -1.0086 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
11 1 1 0 0 0 0
12 6 1 0 0 0 0
13 5 1 0 0 0 0
14 3 1 0 0 0 0
15 18 1 0 0 0 0
16 13 1 0 0 0 0
17 15 2 0 0 0 0
18 11 1 0 0 0 0
19 8 1 0 0 0 0
1 20 1 1 0 0 0
2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

|-
| [http://en.wikipedia.org/wiki/Abbe_number Abbe number]
|? 
|-
| [IR Spectrum of Methyltestoserone],| [[Image:New ir.JPG|thumb|Description]] IR spectrum of methyltestoserone
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

File:New ir.JPG

2006-12-07T10:40:59Z

Asd105:

It:Methyltestosterone

2006-12-07T10:40:27Z

Asd105:

'''==Methyltestoserone=='''
----

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [3D structure]
| <jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6974 1.5829 -0.2375 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3854 -2.0571 -0.1791 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7509 -1.8166 0.0642 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7904 -2.1552 0.4207 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7062 0.1553 -0.4992 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1080 -1.1910 -0.3126 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8203 0.0510 -1.0086 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
11 1 1 0 0 0 0
12 6 1 0 0 0 0
13 5 1 0 0 0 0
14 3 1 0 0 0 0
15 18 1 0 0 0 0
16 13 1 0 0 0 0
17 15 2 0 0 0 0
18 11 1 0 0 0 0
19 8 1 0 0 0 0
1 20 1 1 0 0 0
2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

|-
| [http://en.wikipedia.org/wiki/Abbe_number Abbe number]
|? 
|-
| [http://en.wikipedia.org/wiki/Dielectric_constant Dielectric constant], ε<sub>r</sub>
| ? ε<sub><small>0</small></sub> at ? °C 
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

It:Methyltestosterone

2006-12-07T10:32:21Z

Asd105:

'''==Methyltestoserone=='''
----
<jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
25 28 0 0 0 0 0 0 0 0999 V2000
-1.9324 0.4386 0.4762 C 0 0 1 0 0 0 0 0 0 0 0 0
2.5025 0.5559 0.2683 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.5870 -0.9018 0.1634 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4676 0.4541 -0.0646 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7477 -0.6966 -0.2390 C 0 0 2 0 0 0 0 0 0 0 0 0
0.3306 -0.8111 0.3673 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.8476 -1.0051 -0.2972 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9106 0.3431 -0.3689 C 0 0 2 0 0 0 0 0 0 0 0 0
1.7219 1.8054 -0.1889 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2738 1.7575 0.3498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6974 1.5829 -0.2375 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3854 -2.0571 -0.1791 C 0 0 0 0 0 0 0 0 0 0 0 0
2.7509 -1.8166 0.0642 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7904 -2.1552 0.4207 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7062 0.1553 -0.4992 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1080 -1.1910 -0.3126 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.8203 0.0510 -1.0086 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.2157 1.4934 -0.0373 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9502 1.0047 0.3564 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.9790 0.6588 2.0044 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6358 0.6010 1.8171 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9935 0.8027 -1.8390 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.5149 0.4457 -1.1465 H 0 0 0 0 0 0 0 0 0 0 0 0
1.6345 -0.6356 -1.3145 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3839 -0.8798 1.4451 H 0 0 0 0 0 0 0 0 0 0 0 0
2 9 1 0 0 0 0
3 1 1 0 0 0 0
4 1 1 0 0 0 0
5 6 1 0 0 0 0
6 4 1 0 0 0 0
7 3 2 0 0 0 0
8 2 1 0 0 0 0
9 10 1 0 0 0 0
10 4 1 0 0 0 0
11 1 1 0 0 0 0
12 6 1 0 0 0 0
13 5 1 0 0 0 0
14 3 1 0 0 0 0
15 18 1 0 0 0 0
16 13 1 0 0 0 0
17 15 2 0 0 0 0
18 11 1 0 0 0 0
19 8 1 0 0 0 0
1 20 1 1 0 0 0
2 21 1 1 0 0 0
8 22 1 6 0 0 0
4 23 1 6 0 0 0
5 24 1 6 0 0 0
6 25 1 1 0 0 0
12 14 1 0 0 0 0
15 7 1 0 0 0 0
2 5 1 0 0 0 0
8 16 1 0 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [http://en.wikipedia.org/wiki/Index_of_refraction Index of refraction], ''n''<sub>D</sub>
| ? 
|-
| [http://en.wikipedia.org/wiki/Abbe_number Abbe number]
|? 
|-
| [http://en.wikipedia.org/wiki/Dielectric_constant Dielectric constant], ε<sub>r</sub>
| ? ε<sub><small>0</small></sub> at ? °C 
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

It:Methyltestosterone

2006-12-07T10:27:03Z

Asd105:

'''==Methyltestoserone=='''
----

{| border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}} | Structure and properties
|-
| [http://en.wikipedia.org/wiki/Index_of_refraction Index of refraction], ''n''<sub>D</sub>
| ? 
|-
| [http://en.wikipedia.org/wiki/Abbe_number Abbe number]
|? 
|-
| [http://en.wikipedia.org/wiki/Dielectric_constant Dielectric constant], ε<sub>r</sub>
| ? ε<sub><small>0</small></sub> at ? °C 
|-
| [http://en.wikipedia.org/wiki/Bond_strength Bond strength]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_length Bond length]
| ? 
|-
| [http://en.wikipedia.org/wiki/Bond_angle Bond angle]
| ? 
|-
| [http://en.wikipedia.org/wiki/Magnetic_susceptibility Magnetic susceptibility]
| ? 
|-
|}

It:Methyltestosterone

2006-12-07T10:14:03Z

Asd105:

{{Drug-Box |
| Box_Name =
| ImageFile =
| IUPACName =
| OtherName =
| CAS_No =
| ATC_Code =
| PubChem =
| SMILES = surround in nowiki script code '<' nowiki'>' insert SMILE here'</'nowiki'>'
| Formula =
| MolarMass =
| Bioavailability =
| Protein_binding
| Metabolism =
| Half_life =
| Excretion =
| Pregnancy_cat =
| Legal_status =
| Routes =
}}

It:projects

2006-12-07T10:11:44Z

Asd105: /* Supplemental Project Page */

__FORCETOC__

'''''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.'''''
== Sandbox (Play-Pen) ==

This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button '''on the right''' and '''not''' at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet ''cheat sheet''] summary of how to create a Wiki page. It's a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: Α, α, β Δ, δ
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 '''Show Preview'''. No not use '''Save Page''' so as to leave this area uncluttered for others.
----
{|
|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. Sorry about the delay in getting this working, but the cause was pretty unobvious.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC)
<center><jmol>
<jmolApplet>
<title>Pentahelicene</title><color>yellow</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents>
</jmolApplet>
<jmolMenu>
<item><text>Start spinning</text><script>spin on</script></item>
<item><text>Stop spinning</text><script>spin off</script></item>
<menuHeight>-1</menuHeight>
</jmolMenu>
<jmolButton>
<script>console</script>
<text>open a console window</text>
</jmolButton>
</jmol></center>
-----
<center><jmol><jmolAppletButton><title>Show Pentahelicene in popup window</title><color>cyan</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents></jmolAppletButton>
</jmol></center>

== Main Project Page ==
'''Please do not edit this page itself'''. Click on one of the titles to start editing.
{| summary="CIT Project Titles" border="1"
! bgcolor="cyan" |Project<br /> Number
! bgcolor="cyan" |General Keywords
|-
| bgcolor="#CCFF00" |01
| bgcolor="#CCFF00" | [[it:Lignocaine|Lignocaine (used in dentistry as a "local")]]
|-
| bgcolor="#CCFF00" |02
| bgcolor="#66FF99" | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]
|-
| bgcolor="#CCFF00" |03
| bgcolor="#CCFF00" | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]
|-
| bgcolor="#CCFF00" |04
| bgcolor="#66FF99" | [[it:Gossypol|Gossypol (male birth control)]]
|-
| bgcolor="#CCFF00" |05
| bgcolor="#CCFF00" | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]
|-
| bgcolor="#CCFF00" |06
| bgcolor="#66FF99" | [[it:Herceptin|Herceptin (topical anticancer drug)]]
|-
| bgcolor="#CCFF00" |07
| bgcolor="#CCFF00" | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]
|-
| bgcolor="#CCFF00" |08
| bgcolor="#66FF99" | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]
|-
| bgcolor="#CCFF00" |09
| bgcolor="#CCFF00" | [[it:Bufotoxin|Bufotoxin (active component of the toad ''Bufo vulgaris'')]]
|-
| bgcolor="#CCFF00" |10
| bgcolor="#66FF99" | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]
|-
| bgcolor="#CCFF00" |11
| bgcolor="#CCFF00" | [[it:Sibutramine|Sibutramine (appetite suppresor)]]
|-
| bgcolor="#CCFF00" |12
| bgcolor="#66FF99" | [[it:Anandamide|Anandamide (the "feel-good" factor in chocolate)]]
|-
| bgcolor="#CCFF00" |13
| bgcolor="#CCFF00" | [[it:h3nbh3|Ammonia-borane: H<sub>3</sub>N-BH<sub>3</sub> (Hydrogen storage molecule?)]]
|-
| bgcolor="#CCFF00" |14
| bgcolor="#66FF99" | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]
|-
| bgcolor="#CCFF00" |15
| bgcolor="#CCFF00" | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]
|-
| bgcolor="#CCFF00" |16
| bgcolor="#66FF99" | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]
|-
| bgcolor="#CCFF00" |17
| bgcolor="#CCFF00" | [[it:wilkinson|Wilkinson's catalyst]]
|-
| bgcolor="#CCFF00" |18
| bgcolor="#66FF99" | [[it:Jacobsen|Jacobsen's epoxidation catalyst]]
|-
| bgcolor="#CCFF00" |19
| bgcolor="#CCFF00" | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]
|-
| bgcolor="#CCFF00" |20
| bgcolor="#66FF99" | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]
|-
| bgcolor="#CCFF00" |21
| bgcolor="#CCFF00" | [[it:Schrock|Schrock metathesis catalyst]]
|-
| bgcolor="#CCFF00" |22
| bgcolor="#66FF99" | [[it:knots|Molecular-scale knots (nanoscale devices)]]
|-
|bgcolor="#CCFF00" |23
| bgcolor="#CCFF00" | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]
|-
| bgcolor="#CCFF00" |24
| bgcolor="#66FF99" | [[it:Sertraline|Sertraline HCl (anti-depression)]]
|-
| bgcolor="#CCFF00" |25
| bgcolor="#CCFF00" | [[it:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]
|-
| bgcolor="#CCFF00" |26
| bgcolor="#66FF99" | [[it:Zithromycin|Zithromycin (anti-infective)]]
|-
| bgcolor="#CCFF00" |27
| bgcolor="#CCFF00" | [[it:Lipitor|Lipitor (Cholesterol reducing agent)]]
|-
| bgcolor="#CCFF00" |28
| bgcolor="#66FF99" | [[it:Cyameluric Acid|Cyameluric acid (Linus Pauling's last idea!)]]
|}

== Supplemental Project Page ==

This area is for people who wish to create their own projects if none of the above appeal to them. Click on the '''Edit''' button to the right to open up an editable page,
then add an entry below as follows

*<nowiki> [[it:name_of_project|Descriptive name of intended project]]</nowiki>
*This will produce the effect: [[it:name_of_project|Descriptive name of intended project]]
----
*[[it:sitagliptin_page|Sitagliptin]]
*[[it:Retinal|Retinal, molecule of sight]]
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]
*[[it:Morphine|Morphine, painkiller]]
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]
*[[it:Propanil|Propanil, weedkiller]]
*[[it:Ranitidine|Ranitidine, antiulcerative]]
*[[it:chlorphentermine|chlorphentermine, anorectic]]
*[[it:Serotonin|Serotonin, The 'HAPPY' Drug]]
*[[it:Amphidinolide T1|Amphidinolide T1]]
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]
*[[it:Furosemide|Furosemide]]
*[[it:Tryptophan|Tryptophan]]
*[[it:methylpentynol|methylpentynol, tranquilliser.]]
*[[it:Ferrocene|Ferrocene]]
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]
*[[it:Psilocin|Psilocin]]
*[[it:Epibatidine|Epibatidine]]
*[[it:Beta Carotene|Beta Carotene]]
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]
*[[it:Linalool|Linalool(A component of essential oil)]]
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]
*[[it:Acrolein|Acrolein]]
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]
*[[it:Vanillin|Vanillin, flavouring used in food]]
*[[it:Gingerol|Gingerol, precursor of Zingerone]]
*[[it:MSG|MSG; because everyone loves the flavour]]
*[[it:DDT|DDT, Pesticide]]
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]
*[[it:Caffeine|Caffeine]]
*[[it:Fullerene]]
*[[it:Histrionicotoxin]]
*[[it:limonene]]
*[[it:Capsanthin]]
*[[it:Safrole|Safrole: A formerly popular food and drinks additive]]
*[[it:Adenosine_Triphosphate|Adenosine Triphosphate (ATP), Energy source in muscles]]
*[[it:Aspartame|Aspartame: Artificial sweetener]]
*[[it:Astemizole|Astemizole:non-sedating anti-histamine]]
*[[it:Flucloxacillin|Flucloxacillin:antibiotic]]
*[[it:Quinine|Quinine: The Perfect Tonic for Any Fever]]
*[[it:Caramel|Caramel]]
*[[it:Azithromycin|Azithromycin]]
*[[it:Artemisinin|Artemisinin: An antimalarial drug]]
*[[it:Bradykinin|Bradykinin]]
*[[it:Carminic_acid|Carminic acid, Red colouring agent]]
*[[it:Oxytocin|Oxytocin: The Hormone of Love]]
*[[it:Carmoisine|Carmoisine]]
*[[it:Ziegler-Natta|Ziegler-Natta]]
*[[it:Cyclamate|Cyclamate]]
*[[it:Polyurethane|Polyurethane]]
*[[it:sexithiophene|sexithiophene]]
*[[it:Polydimethylsiloxane|Polydimethylsiloxane: Silicon-based organic polymer]]
*[[it:Lycopene|Lycopene: the red antioxidant molecule]]
*[[it:Crystal Meth|Crystal Meth]]
*[[it:Mustard Gas|Mustard Gas]]
*[[it:Saxitoxin|Shellfish Poison]]
*[[it:Luminol|Luminol: Chemiluminescence Reactions]]
*[[it:Tumor Necrosis Factor|Tumour Necrosis Factor]]
*[[it:Tamiflu|Tamiflu: Antiviral]]
*[[it:Warfarin|Warfarin: Blood thinner]]
*[[it:Vitamin C|Ascorbic acid: Vitamin C]]
*[[it:Hexahelicene|Hexahelicene]]
*[[it:Cocaine|Cocaine]]
*[[it:Eucalyptol|Eucalyptol: The main component of eucalyptus oil]]
*[[it:dichlorodifluromethane| Dichlorodifluromethane]]
*[[it:Theobromine| Theobromine]]
*[[it:Maraviroc|Maraviroc: A Potent CCR5 Antagonist for treatment of HIV]]
*[[it:Aspirin]]
*[[it:DEET|DEET]]
*[[it:PhenylButazone|PhenylButazone]]
*[[it:Epinephrine|Epinephrine]]
*[[it:Phenylmercury Acetate|Phenylmurcury Acetate]]
*[[it:Methyltestosterone|Methyltestosterone]]

== Wiki Utillities ==
Utilities have been written to help the conversion of material from HTML.

# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]

No wiki2html converter suitable for use has yet been identified.
=== Wiki Templates ===

[[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-name|parameter}}, 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!
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)

----
[[Template:Chem-Data]]

[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables

[[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]]

[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]

[[R & S Phrases]]

It:PhenylButazone

2006-12-07T09:50:00Z

Asd105:

'''PhenylButazone'''

<jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
23 25 0 0 0 0 0 0 0 0999 V2000
0.1020 0.5214 -0.3987 N 0 0 0 0 0 0 0 0 0 1
-0.2149 -0.8923 -0.2482 N 0 0 0 0 0 0 0 0 0 2
1.4642 0.6456 -0.7455 C 0 0 0 0 0 0 0 0 0 3
0.9450 -1.6370 -0.5473 C 0 0 0 0 0 0 0 0 0 4
2.1019 -0.7189 -0.8165 C 0 0 0 0 0 0 0 0 0 5
-0.8166 1.5808 -0.0491 C 0 0 0 0 0 0 0 0 0 6
-1.5577 -1.3974 -0.0737 C 0 0 0 0 0 0 0 0 0 7
2.0074 1.7412 -0.9350 O 0 0 0 0 0 0 0 0 0 8
0.9581 -2.8731 -0.5869 O 0 0 0 0 0 0 0 0 0 9
3.1681 -0.9020 0.2757 C 0 0 0 0 0 0 0 0 0 10
-1.4410 1.5641 1.2038 C 0 0 0 0 0 0 0 0 0 11
-1.0742 2.6024 -0.9705 C 0 0 0 0 0 0 0 0 0 12
-2.5779 -0.9600 -0.9267 C 0 0 0 0 0 0 0 0 0 13
-1.8167 -2.3166 0.9492 C 0 0 0 0 0 0 0 0 0 14
4.4732 -0.1715 -0.0677 C 0 0 0 0 0 0 0 0 0 15
5.5029 -0.3629 1.0507 C 0 0 0 0 0 0 0 0 0 16
6.7974 0.3900 0.7252 C 0 0 0 0 0 0 0 0 0 17
-3.8691 -1.4469 -0.7463 C 0 0 0 0 0 0 0 0 0 18
-3.1119 -2.7966 1.1186 C 0 0 0 0 0 0 0 0 0 19
-1.9696 3.6123 -0.6312 C 0 0 0 0 0 0 0 0 0 20
-2.3350 2.5794 1.5306 C 0 0 0 0 0 0 0 0 0 21
-4.1363 -2.3629 0.2740 C 0 0 0 0 0 0 0 0 0 22
-2.5995 3.6012 0.6156 C 0 0 0 0 0 0 0 0 0 23
2 1 1 0 0 0
3 1 1 0 0 0
4 2 1 0 0 0
5 3 1 0 0 0
6 1 1 0 0 0
7 2 1 0 0 0
8 3 2 0 0 0
9 4 2 0 0 0
10 5 1 0 0 0
11 6 1 0 0 0
12 6 2 0 0 0
13 7 1 0 0 0
14 7 2 0 0 0
15 10 1 0 0 0
16 15 1 0 0 0
17 16 1 0 0 0
18 13 2 0 0 0
19 14 1 0 0 0
20 12 1 0 0 0
21 11 2 0 0 0
22 19 2 0 0 0
23 20 2 0 0 0
5 4 1 0 0 0
21 23 1 0 0 0
18 22 1 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

''Medical applications''

Phenylbutazone has been used to treat serious pain in dogs due to osteoarthritis as it is a fast effective painkiller and also an anti-inflammatory. However dogs receiving intensive phenylbutazone therapy to tolerate the pain of osteoarthritis usually have regular blood work and renal monitoring to accompany this treatment. This is because an overdose of this drug is known to cause renal failure and liver injury.
This drug is also used to treat horses for such problems as musculoskeletal problems, soft tissue injury and bone and joint problems. Phenylbutazone is a nonsterodial drug which provides fast acting pain relief one to two hours after initial introduction into the body. The drug can be taken either orally or intravenously to the blood.

Safety

This drug is harmful of swallowed in excess of the dosage prescribed, it is also irritating to both the skin and eyes and respiratory system. Another precaution when dealing with phenylbutazone is that it should not be given to animals that are pregnant or nursing young as research has indicated it’s harmful to embryos and young.
This drug must not be injected into the muscles directly or under the skin.

{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"
! {{chembox header}} colspan="3" |Structure of phenylbutazone
|-
| align="center" colspan="5" bgcolor="#ffffff" | [[Image:Drawing.JPG|thumb|Description]]
|-
! {{chembox header}} colspan="5" |IR Spectrum of Phenylbutazone
|-
| align="center" colspan="5" bgcolor="#ffffff" | [[Image:MyIR.jpg|thumb|Description]]
|-
| align="center" colspan="5" bgcolor="#ffffff" |
|-
| [[Systematic Name]]
| colspan="2"| 4-butyl-1,2-diphenyl-pyrazolidine-3,5-dione
|-
| [[Alternative Chemical Names]]
| colspan="3"| Phenylbutazone
|-
| [[Chemical formula|Molecular formula]]
| colspan="2" | C<sub>19</sub>H<sub>20</sub>N<sub>2</sub>O<sub>2
|-
| [[Molecular Weight]]
| colspan="2" | 308.38
|-
| [[Melting Points]]
| colspan="2" | 104-107
|-
== Structure ==
{| class="toccolours" border="1" style="fix: right; clear: left; margin: 1 1 1em 1em; border-collapse: collapse;"
|+ '''NMR of phenylbutazone'''
! [[Image:Nmr table.JPG|thumb|Description]] [[Image:Nmr pic.JPG|thumb|Description]] !!
<center><jmol>
|}</jmol>

==References==
http://jpet.aspetjournals.org/cgi/reprint/266/1/81.pdf

www.chemexper.com/

http://www.wedgewoodpharmacy.com/monographs/phenylbutazone.asp

http://www.sciencemag.org/cgi/content/abstract/159/3822/1479

It:PhenylButazone

2006-12-07T09:27:41Z

Asd105:

File:Nmr pic.JPG

2006-12-07T09:26:23Z

Asd105:

It:PhenylButazone

2006-12-07T09:26:13Z

Asd105:

'''PhenylButazone'''

<jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
23 25 0 0 0 0 0 0 0 0999 V2000
0.1020 0.5214 -0.3987 N 0 0 0 0 0 0 0 0 0 1
-0.2149 -0.8923 -0.2482 N 0 0 0 0 0 0 0 0 0 2
1.4642 0.6456 -0.7455 C 0 0 0 0 0 0 0 0 0 3
0.9450 -1.6370 -0.5473 C 0 0 0 0 0 0 0 0 0 4
2.1019 -0.7189 -0.8165 C 0 0 0 0 0 0 0 0 0 5
-0.8166 1.5808 -0.0491 C 0 0 0 0 0 0 0 0 0 6
-1.5577 -1.3974 -0.0737 C 0 0 0 0 0 0 0 0 0 7
2.0074 1.7412 -0.9350 O 0 0 0 0 0 0 0 0 0 8
0.9581 -2.8731 -0.5869 O 0 0 0 0 0 0 0 0 0 9
3.1681 -0.9020 0.2757 C 0 0 0 0 0 0 0 0 0 10
-1.4410 1.5641 1.2038 C 0 0 0 0 0 0 0 0 0 11
-1.0742 2.6024 -0.9705 C 0 0 0 0 0 0 0 0 0 12
-2.5779 -0.9600 -0.9267 C 0 0 0 0 0 0 0 0 0 13
-1.8167 -2.3166 0.9492 C 0 0 0 0 0 0 0 0 0 14
4.4732 -0.1715 -0.0677 C 0 0 0 0 0 0 0 0 0 15
5.5029 -0.3629 1.0507 C 0 0 0 0 0 0 0 0 0 16
6.7974 0.3900 0.7252 C 0 0 0 0 0 0 0 0 0 17
-3.8691 -1.4469 -0.7463 C 0 0 0 0 0 0 0 0 0 18
-3.1119 -2.7966 1.1186 C 0 0 0 0 0 0 0 0 0 19
-1.9696 3.6123 -0.6312 C 0 0 0 0 0 0 0 0 0 20
-2.3350 2.5794 1.5306 C 0 0 0 0 0 0 0 0 0 21
-4.1363 -2.3629 0.2740 C 0 0 0 0 0 0 0 0 0 22
-2.5995 3.6012 0.6156 C 0 0 0 0 0 0 0 0 0 23
2 1 1 0 0 0
3 1 1 0 0 0
4 2 1 0 0 0
5 3 1 0 0 0
6 1 1 0 0 0
7 2 1 0 0 0
8 3 2 0 0 0
9 4 2 0 0 0
10 5 1 0 0 0
11 6 1 0 0 0
12 6 2 0 0 0
13 7 1 0 0 0
14 7 2 0 0 0
15 10 1 0 0 0
16 15 1 0 0 0
17 16 1 0 0 0
18 13 2 0 0 0
19 14 1 0 0 0
20 12 1 0 0 0
21 11 2 0 0 0
22 19 2 0 0 0
23 20 2 0 0 0
5 4 1 0 0 0
21 23 1 0 0 0
18 22 1 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

''Medical applications''

Phenylbutazone has been used to treat serious pain in dogs due to osteoarthritis as it is a fast effective painkiller and also an anti-inflammatory. However dogs receiving intensive phenylbutazone therapy to tolerate the pain of osteoarthritis usually have regular blood work and renal monitoring to accompany this treatment. This is because an overdose of this drug is known to cause renal failure and liver injury.
This drug is also used to treat horses for such problems as musculoskeletal problems, soft tissue injury and bone and joint problems. Phenylbutazone is a nonsterodial drug which provides fast acting pain relief one to two hours after initial introduction into the body. The drug can be taken either orally or intravenously to the blood.

Safety

This drug is harmful of swallowed in excess of the dosage prescribed, it is also irritating to both the skin and eyes and respiratory system. Another precaution when dealing with phenylbutazone is that it should not be given to animals that are pregnant or nursing young as research has indicated it’s harmful to embryos and young.
This drug must not be injected into the muscles directly or under the skin.

{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"
! {{chembox header}} colspan="3" |Structure of phenylbutazone
|-
| align="center" colspan="5" bgcolor="#ffffff" | [[Image:Drawing.JPG|thumb|Description]]
|-
! {{chembox header}} colspan="5" |IR Spectrum of Phenylbutazone
|-
| align="center" colspan="5" bgcolor="#ffffff" | [[Image:MyIR.jpg|thumb|Description]]
|-
| align="center" colspan="5" bgcolor="#ffffff" |
|-
| [[Systematic Name]]
| colspan="2"| 4-butyl-1,2-diphenyl-pyrazolidine-3,5-dione
|-
| [[Alternative Chemical Names]]
| colspan="3"| Phenylbutazone
|-
| [[Chemical formula|Molecular formula]]
| colspan="2" | C<sub>19</sub>H<sub>20</sub>N<sub>2</sub>O<sub>2
|-
| [[Molecular Weight]]
| colspan="2" | 308.38
|-
| [[Melting Points]]
| colspan="2" | 104-107
|-
== Structure ==
{| class="toccolours" border="1" style="fix: right; clear: left; margin: 1 1 1em 1em; border-collapse: collapse;"
|+ '''NMR of phenylbutazone'''
! [[Image:Nmr table.JPG|thumb|Description]] [[Image:Nmr table.JPG|thumb|Description]] !!
<center><jmol>
|- align="center"

|}</jmol>

File:Nmr table.JPG

2006-12-07T08:58:59Z

Asd105:

It:PhenylButazone

2006-12-06T18:37:27Z

Asd105:

File:My molecule 5.mol

2006-12-06T18:34:31Z

Asd105:

It:PhenylButazone

2006-12-06T18:33:13Z

Asd105:

It:PhenylButazone

2006-12-06T18:01:31Z

Asd105:

'''PhenylButazone'''

<jmol>
<jmolApplet>
<size>200</size>
<color>white</color>
<script>zoom 80; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;</script>
<inlineContents>phenylbutazone.mol
title1
title2
23 25 0 0 0 0 0 0 0 0999 V2000
0.1020 0.5214 -0.3987 N 0 0 0 0 0 0 0 0 0 1
-0.2149 -0.8923 -0.2482 N 0 0 0 0 0 0 0 0 0 2
1.4642 0.6456 -0.7455 C 0 0 0 0 0 0 0 0 0 3
0.9450 -1.6370 -0.5473 C 0 0 0 0 0 0 0 0 0 4
2.1019 -0.7189 -0.8165 C 0 0 0 0 0 0 0 0 0 5
-0.8166 1.5808 -0.0491 C 0 0 0 0 0 0 0 0 0 6
-1.5577 -1.3974 -0.0737 C 0 0 0 0 0 0 0 0 0 7
2.0074 1.7412 -0.9350 O 0 0 0 0 0 0 0 0 0 8
0.9581 -2.8731 -0.5869 O 0 0 0 0 0 0 0 0 0 9
3.1681 -0.9020 0.2757 C 0 0 0 0 0 0 0 0 0 10
-1.4410 1.5641 1.2038 C 0 0 0 0 0 0 0 0 0 11
-1.0742 2.6024 -0.9705 C 0 0 0 0 0 0 0 0 0 12
-2.5779 -0.9600 -0.9267 C 0 0 0 0 0 0 0 0 0 13
-1.8167 -2.3166 0.9492 C 0 0 0 0 0 0 0 0 0 14
4.4732 -0.1715 -0.0677 C 0 0 0 0 0 0 0 0 0 15
5.5029 -0.3629 1.0507 C 0 0 0 0 0 0 0 0 0 16
6.7974 0.3900 0.7252 C 0 0 0 0 0 0 0 0 0 17
-3.8691 -1.4469 -0.7463 C 0 0 0 0 0 0 0 0 0 18
-3.1119 -2.7966 1.1186 C 0 0 0 0 0 0 0 0 0 19
-1.9696 3.6123 -0.6312 C 0 0 0 0 0 0 0 0 0 20
-2.3350 2.5794 1.5306 C 0 0 0 0 0 0 0 0 0 21
-4.1363 -2.3629 0.2740 C 0 0 0 0 0 0 0 0 0 22
-2.5995 3.6012 0.6156 C 0 0 0 0 0 0 0 0 0 23
2 1 1 0 0 0
3 1 1 0 0 0
4 2 1 0 0 0
5 3 1 0 0 0
6 1 1 0 0 0
7 2 1 0 0 0
8 3 2 0 0 0
9 4 2 0 0 0
10 5 1 0 0 0
11 6 1 0 0 0
12 6 2 0 0 0
13 7 1 0 0 0
14 7 2 0 0 0
15 10 1 0 0 0
16 15 1 0 0 0
17 16 1 0 0 0
18 13 2 0 0 0
19 14 1 0 0 0
20 12 1 0 0 0
21 11 2 0 0 0
22 19 2 0 0 0
23 20 2 0 0 0
5 4 1 0 0 0
21 23 1 0 0 0
18 22 1 0 0 0
M END</inlineContents>
</jmolApplet>
</jmol>

''Medical applications''

Phenylbutazone has been used to treat serious pain in dogs due to osteoarthritis as it is a fast effective painkiller and also an anti-inflammatory. However dogs receiving intensive phenylbutazone therapy to tolerate the pain of osteoarthritis usually have regular blood work and renal monitoring to accompany this treatment. This is because an overdose of this drug is known to cause renal failure and liver injury.
This drug is also used to treat horses for such problems as musculoskeletal problems, soft tissue injury and bone and joint problems. Phenylbutazone is a nonsterodial drug which provides fast acting pain relief one to two hours after initial introduction into the body. The drug can be taken either orally or intravenously to the blood.

Safety

This drug is harmful of swallowed in excess of the dosage prescribed, it is also irritating to both the skin and eyes and respiratory system. Another precaution when dealing with phenylbutazone is that it should not be given to animals that are pregnant or nursing young as research has indicated it’s harmful to embryos and young.
This drug must not be injected into the muscles directly or under the skin.

[[Image:Drawing.JPG|thumb|Description]]
[[Image:MyIR.jpg|thumb|Description]]

File:Drawing.JPG

2006-12-06T17:58:05Z

Asd105:

File:MyIR.jpg

2006-12-06T17:46:58Z

Asd105:

File:MyIR.JPG

2006-12-06T17:42:48Z

Asd105:

It:PhenylButazone

2006-12-06T17:25:51Z

Asd105:

File:My molecule 4.mol

2006-12-06T17:16:43Z

Asd105:

It:PhenylButazone

2006-12-06T17:15:10Z

Asd105:

'''PhenylButazone'''

[[Image:Example.jpg]]

''Medical applications''

Phenylbutazone has been used to treat serious pain in dogs due to osteoarthritis as it is a fast effective painkiller and also an anti-inflammatory. However dogs receiving intensive phenylbutazone therapy to tolerate the pain of osteoarthritis usually have regular blood work and renal monitoring to accompany this treatment. This is because an overdose of this drug is known to cause renal failure and liver injury.
This drug is also used to treat horses for such problems as musculoskeletal problems, soft tissue injury and bone and joint problems. Phenylbutazone is a nonsterodial drug which provides fast acting pain relief one to two hours after initial introduction into the body. The drug can be taken either orally or intravenously to the blood.

Safety

This drug is harmful of swallowed in excess of the dosage prescribed, it is also irritating to both the skin and eyes and respiratory system. Another precaution when dealing with phenylbutazone is that it should not be given to animals that are pregnant or nursing young as research has indicated it’s harmful to embryos and young.
This drug must not be injected into the muscles directly or under the skin.

IR spectrum of Phenylbutazone

[[Image:Example.jpg]]

It:projects

2006-12-06T17:14:46Z

Asd105: /* Supplemental Project Page */

__FORCETOC__

'''''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.'''''
== Sandbox (Play-Pen) ==

This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button '''on the right''' and '''not''' at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet ''cheat sheet''] summary of how to create a Wiki page. It's a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: Α, α, β Δ, δ
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 '''Show Preview'''. No not use '''Save Page''' so as to leave this area uncluttered for others.
----
{|
|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. Sorry about the delay in getting this working, but the cause was pretty unobvious.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC)
<center><jmol>
<jmolApplet>
<title>Pentahelicene</title><color>yellow</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents>
</jmolApplet>
<jmolMenu>
<item><text>Start spinning</text><script>spin on</script></item>
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<uploadedFileContents>Pentahelicene.mol</uploadedFileContents></jmolAppletButton>
</jmol></center>

== Main Project Page ==
'''Please do not edit this page itself'''. Click on one of the titles to start editing.
{| summary="CIT Project Titles" border="1"
! bgcolor="cyan" |Project<br /> Number
! bgcolor="cyan" |General Keywords
|-
| bgcolor="#CCFF00" |01
| bgcolor="#CCFF00" | [[it:Lignocaine|Lignocaine (used in dentistry as a "local")]]
|-
| bgcolor="#CCFF00" |02
| bgcolor="#66FF99" | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]
|-
| bgcolor="#CCFF00" |03
| bgcolor="#CCFF00" | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]
|-
| bgcolor="#CCFF00" |04
| bgcolor="#66FF99" | [[it:Gossypol|Gossypol (male birth control)]]
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| bgcolor="#CCFF00" |05
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|-
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| bgcolor="#66FF99" | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]
|-
| bgcolor="#CCFF00" |11
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|-
| bgcolor="#CCFF00" |12
| bgcolor="#66FF99" | [[it:Anandamide|Anandamide (the "feel-good" factor in chocolate)]]
|-
| bgcolor="#CCFF00" |13
| bgcolor="#CCFF00" | [[it:h3nbh3|Ammonia-borane: H<sub>3</sub>N-BH<sub>3</sub> (Hydrogen storage molecule?)]]
|-
| bgcolor="#CCFF00" |14
| bgcolor="#66FF99" | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]
|-
| bgcolor="#CCFF00" |15
| bgcolor="#CCFF00" | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]
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| bgcolor="#CCFF00" |17
| bgcolor="#CCFF00" | [[it:wilkinson|Wilkinson's catalyst]]
|-
| bgcolor="#CCFF00" |18
| bgcolor="#66FF99" | [[it:Jacobsen|Jacobsen's epoxidation catalyst]]
|-
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| bgcolor="#CCFF00" |20
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|-
| bgcolor="#CCFF00" |21
| bgcolor="#CCFF00" | [[it:Schrock|Schrock metathesis catalyst]]
|-
| bgcolor="#CCFF00" |22
| bgcolor="#66FF99" | [[it:knots|Molecular-scale knots (nanoscale devices)]]
|-
|bgcolor="#CCFF00" |23
| bgcolor="#CCFF00" | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]
|-
| bgcolor="#CCFF00" |24
| bgcolor="#66FF99" | [[it:Sertraline|Sertraline HCl (anti-depression)]]
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| bgcolor="#CCFF00" |25
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|-
| bgcolor="#CCFF00" |26
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| bgcolor="#CCFF00" |27
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|}

== Supplemental Project Page ==

This area is for people who wish to create their own projects if none of the above appeal to them. Click on the '''Edit''' button to the right to open up an editable page,
then add an entry below as follows

*<nowiki> [[it:name_of_project|Descriptive name of intended project]]</nowiki>
*This will produce the effect: [[it:name_of_project|Descriptive name of intended project]]
----
*[[it:sitagliptin_page|Sitagliptin]]
*[[it:Retinal|Retinal, molecule of sight]]
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]
*[[it:Morphine|Morphine, painkiller]]
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]
*[[it:Propanil|Propanil, weedkiller]]
*[[it:Ranitidine|Ranitidine, antiulcerative]]
*[[it:chlorphentermine|chlorphentermine, anorectic]]
*[[it:Serotonin|Serotonin, The 'HAPPY' Drug]]
*[[it:Amphidinolide T1|Amphidinolide T1]]
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]
*[[it:Furosemide|Furosemide]]
*[[it:Tryptophan|Tryptophan]]
*[[it:methylpentynol|methylpentynol, tranquilliser.]]
*[[it:Ferrocene|Ferrocene]]
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]
*[[it:Psilocin|Psilocin]]
*[[it:Epibatidine|Epibatidine]]
*[[it:Beta Carotene|Beta Carotene]]
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]
*[[it:Linalool|Linalool(A component of essential oil)]]
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]
*[[it:Acrolein|Acrolein]]
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]
*[[it:Vanillin|Vanillin, flavouring used in food]]
*[[it:Gingerol|Gingerol, precursor of Zingerone]]
*[[it:MSG|MSG; because everyone loves the flavour]]
*[[it:DDT|DDT, Pesticide]]
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]
*[[it:Caffeine|Caffeine]]
*[[it:Fullerene]]
*[[it:Histrionicotoxin]]
*[[it:limonene]]
*[[it:Capsanthin]]
*[[it:Safrole|Safrole: A formerly popular food and drinks additive]]
*[[it:Adenosine_Triphosphate|Adenosine Triphosphate (ATP), Energy source in muscles]]
*[[it:Aspartame|Aspartame: Artificial sweetener]]
*[[it:Astemizole|Astemizole:non-sedating anti-histamine]]
*[[it:Flucloxacillin|Flucloxacillin:antibiotic]]
*[[it:Quinine|Quinine: The Perfect Tonic for Any Fever]]
*[[it:Caramel|Caramel]]
*[[it:Azithromycin|Azithromycin]]
*[[it:Artemisinin|Artemisinin: An antimalarial drug]]
*[[it:Bradykinin|Bradykinin]]
*[[it:Carminic_acid|Carminic acid, Red colouring agent]]
*[[it:Oxytocin|Oxytocin: The Hormone of Love]]
*[[it:Carmoisine|Carmoisine]]
*[[it:Ziegler-Natta|Ziegler-Natta]]
*[[it:Cyclamate|Cyclamate]]
*[[it:Polyurethane|Polyurethane]]
*[[it:sexithiophene|sexithiophene]]
*[[it:Polydimethylsiloxane|Polydimethylsiloxane: Silicon-based organic polymer]]
*[[it:Lycopene|Lycopene: the red antioxidant molecule]]
*[[it:Crystal Meth|Crystal Meth]]
*[[it:Mustard Gas|Mustard Gas]]
*[[it:Saxitoxin|Shellfish Poison]]
*[[it:Luminol|Luminol: Chemiluminescence Reactions]]
*[[it:Tumor Necrosis Factor|Tumour Necrosis Factor]]
*[[it:Tamiflu|Tamiflu: Antiviral]]
*[[it:Warfarin|Warfarin: Blood thinner]]
*[[it:Vitamin C|Ascorbic acid: Vitamin C]]
*[[it:Hexahelicene|Hexahelicene]]
*[[it:Cocaine|Cocaine]]
*[[it:Eucalyptol|Eucalyptol: The main component of eucalyptus oil]]
*[[it:dichlorodifluromethane| Dichlorodifluromethane]]
*[[it:Theobromine| Theobromine]]
*[[it:Maraviroc|Maraviroc: A Potent CCR5 Antagonist for treatment of HIV]]
*[[it:Aspirin]]
*[[it:DEET|DEET]]
*[[it:PhenylButazone|PhenylButazone]]

== Wiki Utillities ==
Utilities have been written to help the conversion of material from HTML.

# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]

No wiki2html converter suitable for use has yet been identified.
=== Wiki Templates ===

[[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-name|parameter}}, 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!
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)

----
[[Template:Chem-Data]]

[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables

[[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]]

[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]

[[R & S Phrases]]

It:projects

2006-12-06T16:40:07Z

Asd105: /* Overlaps */

__FORCETOC__

'''''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.'''''
== Sandbox (Play-Pen) ==

This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button '''on the right''' and '''not''' at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet ''cheat sheet''] summary of how to create a Wiki page. It's a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: Α, α, β Δ, δ
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 '''Show Preview'''. No not use '''Save Page''' so as to leave this area uncluttered for others.
----
{|
|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. Sorry about the delay in getting this working, but the cause was pretty unobvious.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC)
<center><jmol>
<jmolApplet>
<title>Pentahelicene</title><color>yellow</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents>
</jmolApplet>
<jmolMenu>
<item><text>Start spinning</text><script>spin on</script></item>
<item><text>Stop spinning</text><script>spin off</script></item>
<menuHeight>-1</menuHeight>
</jmolMenu>
<jmolButton>
<script>console</script>
<text>open a console window</text>
</jmolButton>
</jmol></center>
-----
<center><jmol><jmolAppletButton><title>Show Pentahelicene in popup window</title><color>cyan</color>
<uploadedFileContents>Pentahelicene.mol</uploadedFileContents></jmolAppletButton>
</jmol></center>

== Main Project Page ==
'''Please do not edit this page itself'''. Click on one of the titles to start editing.
{| summary="CIT Project Titles" border="1"
! bgcolor="cyan" |Project<br /> Number
! bgcolor="cyan" |General Keywords
|-
| bgcolor="#CCFF00" |01
| bgcolor="#CCFF00" | [[it:Lignocaine|Lignocaine (used in dentistry as a "local")]]
|-
| bgcolor="#CCFF00" |02
| bgcolor="#66FF99" | [[it:Piperine|Piperine (active ingredient of both black and white pepper)]]
|-
| bgcolor="#CCFF00" |03
| bgcolor="#CCFF00" | [[it:Rapamycin|Rapamycin (prevents transplant rejection)]]
|-
| bgcolor="#CCFF00" |04
| bgcolor="#66FF99" | [[it:Gossypol|Gossypol (male birth control)]]
|-
| bgcolor="#CCFF00" |05
| bgcolor="#CCFF00" | [[it:Gentamycin|Gentamicin A (aminoglycoside antibiotic)]]
|-
| bgcolor="#CCFF00" |06
| bgcolor="#66FF99" | [[it:Herceptin|Herceptin (topical anticancer drug)]]
|-
| bgcolor="#CCFF00" |07
| bgcolor="#CCFF00" | [[it:Gingerone|Zingerone (the characteristic smell of ginger)]]
|-
| bgcolor="#CCFF00" |08
| bgcolor="#66FF99" | [[it:Sucralose|Sucralose (non-metabolizable sweetening agent)]]
|-
| bgcolor="#CCFF00" |09
| bgcolor="#CCFF00" | [[it:Bufotoxin|Bufotoxin (active component of the toad ''Bufo vulgaris'')]]
|-
| bgcolor="#CCFF00" |10
| bgcolor="#66FF99" | [[it:Roaccutane|Roaccutane (treatment for severe acne)]]
|-
| bgcolor="#CCFF00" |11
| bgcolor="#CCFF00" | [[it:Sibutramine|Sibutramine (appetite suppresor)]]
|-
| bgcolor="#CCFF00" |12
| bgcolor="#66FF99" | [[it:Anandamide|Anandamide (the "feel-good" factor in chocolate)]]
|-
| bgcolor="#CCFF00" |13
| bgcolor="#CCFF00" | [[it:h3nbh3|Ammonia-borane: H<sub>3</sub>N-BH<sub>3</sub> (Hydrogen storage molecule?)]]
|-
| bgcolor="#CCFF00" |14
| bgcolor="#66FF99" | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]
|-
| bgcolor="#CCFF00" |15
| bgcolor="#CCFF00" | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]
|-
| bgcolor="#CCFF00" |16
| bgcolor="#66FF99" | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]
|-
| bgcolor="#CCFF00" |17
| bgcolor="#CCFF00" | [[it:wilkinson|Wilkinson's catalyst]]
|-
| bgcolor="#CCFF00" |18
| bgcolor="#66FF99" | [[it:Jacobsen|Jacobsen's epoxidation catalyst]]
|-
| bgcolor="#CCFF00" |19
| bgcolor="#CCFF00" | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]
|-
| bgcolor="#CCFF00" |20
| bgcolor="#66FF99" | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]
|-
| bgcolor="#CCFF00" |21
| bgcolor="#CCFF00" | [[it:Schrock|Schrock metathesis catalyst]]
|-
| bgcolor="#CCFF00" |22
| bgcolor="#66FF99" | [[it:knots|Molecular-scale knots (nanoscale devices)]]
|-
|bgcolor="#CCFF00" |23
| bgcolor="#CCFF00" | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]
|-
| bgcolor="#CCFF00" |24
| bgcolor="#66FF99" | [[it:Sertraline|Sertraline HCl (anti-depression)]]
|-
| bgcolor="#CCFF00" |25
| bgcolor="#CCFF00" | [[it:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]
|-
| bgcolor="#CCFF00" |26
| bgcolor="#66FF99" | [[it:Zithromycin|Zithromycin (anti-infective)]]
|-
| bgcolor="#CCFF00" |27
| bgcolor="#CCFF00" | [[it:Lipitor|Lipitor (Cholesterol reducing agent)]]
|-
| bgcolor="#CCFF00" |28
| bgcolor="#66FF99" | [[it:Cyameluric Acid|Cyameluric acid (Linus Pauling's last idea!)]]
|}

== Supplemental Project Page ==

This area is for people who wish to create their own projects if none of the above appeal to them. Click on the '''Edit''' button to the right to open up an editable page,
then add an entry below as follows

*<nowiki> [[it:name_of_project|Descriptive name of intended project]]</nowiki>
*This will produce the effect: [[it:name_of_project|Descriptive name of intended project]]
----
*[[it:sitagliptin_page|Sitagliptin]]
*[[it:Retinal|Retinal, molecule of sight]]
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]
*[[it:Morphine|Morphine, painkiller]]
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]
*[[it:Propanil|Propanil, weedkiller]]
*[[it:Ranitidine|Ranitidine, antiulcerative]]
*[[it:chlorphentermine|chlorphentermine, anorectic]]
*[[it:Serotonin|Serotonin, The 'HAPPY' Drug]]
*[[it:Amphidinolide T1|Amphidinolide T1]]
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]
*[[it:Furosemide|Furosemide]]
*[[it:Tryptophan|Tryptophan]]
*[[it:methylpentynol|methylpentynol, tranquilliser.]]
*[[it:Ferrocene|Ferrocene]]
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]
*[[it:Psilocin|Psilocin]]
*[[it:Epibatidine|Epibatidine]]
*[[it:Beta Carotene|Beta Carotene]]
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]
*[[it:Linalool|Linalool(A component of essential oil)]]
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]
*[[it:Acrolein|Acrolein]]
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]
*[[it:Vanillin|Vanillin, flavouring used in food]]
*[[it:Gingerol|Gingerol, precursor of Zingerone]]
*[[it:MSG|MSG; because everyone loves the flavour]]
*[[it:DDT|DDT, Pesticide]]
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]
*[[it:Caffeine|Caffeine]]
*[[it:Fullerene]]
*[[it:Histrionicotoxin]]
*[[it:limonene]]
*[[it:Capsanthin]]
*[[it:Safrole|Safrole: A formerly popular food and drinks additive]]
*[[it:Adenosine_Triphosphate|Adenosine Triphosphate (ATP), Energy source in muscles]]
*[[it:Aspartame|Aspartame: Artificial sweetener]]
*[[it:Astemizole|Astemizole:non-sedating anti-histamine]]
*[[it:Flucloxacillin|Flucloxacillin:antibiotic]]
*[[it:Quinine|Quinine: The Perfect Tonic for Any Fever]]
*[[it:Caramel|Caramel]]
*[[it:Azithromycin|Azithromycin]]
*[[it:Artemisinin|Artemisinin: An antimalarial drug]]
*[[it:Bradykinin|Bradykinin]]
*[[it:Carminic_acid|Carminic acid, Red colouring agent]]
*[[it:Oxytocin|Oxytocin: The Hormone of Love]]
*[[it:Carmoisine|Carmoisine]]
*[[it:Ziegler-Natta|Ziegler-Natta]]
*[[it:Cyclamate|Cyclamate]]
*[[it:Polyurethane|Polyurethane]]
*[[it:sexithiophene|sexithiophene]]
*[[it:Polydimethylsiloxane|Polydimethylsiloxane: Silicon-based organic polymer]]
*[[it:Lycopene|Lycopene: the red antioxidant molecule]]
*[[it:Crystal Meth|Crystal Meth]]
*[[it:Mustard Gas|Mustard Gas]]
*[[it:Saxitoxin|Shellfish Poison]]
*[[it:Luminol|Luminol: Chemiluminescence Reactions]]
*[[it:Tumor Necrosis Factor|Tumour Necrosis Factor]]
*[[it:Tamiflu|Tamiflu: Antiviral]]
*[[it:Warfarin|Warfarin: Blood thinner]]
*[[it:Vitamin C|Ascorbic acid: Vitamin C]]
*[[it:Hexahelicene|Hexahelicene]]
*[[it:Cocaine|Cocaine]]
*[[it:Eucalyptol|Eucalyptol: The main component of eucalyptus oil]]
*[[it:dichlorodifluromethane| Dichlorodifluromethane]]
*[[it:Theobromine| Theobromine]]
*[[it:Maraviroc|Maraviroc: A Potent CCR5 Antagonist for treatment of HIV]]
*[[it:Aspirin]]

'''PhenylButazone'''

[[Image:Example.jpg]]

''Medical applications''

Phenylbutazone has been used to treat serious pain in dogs due to osteoarthritis as it is a fast effective painkiller and also an anti-inflammatory. However dogs receiving intensive phenylbutazone therapy to tolerate the pain of osteoarthritis usually have regular blood work and renal monitoring to accompany this treatment. This is because an overdose of this drug is known to cause renal failure and liver injury.
This drug is also used to treat horses for such problems as musculoskeletal problems, soft tissue injury and bone and joint problems. Phenylbutazone is a nonsterodial drug which provides fast acting pain relief one to two hours after initial introduction into the body. The drug can be taken either orally or intravenously to the blood.

Safety

This drug is harmful of swallowed in excess of the dosage prescribed, it is also irritating to both the skin and eyes and respiratory system. Another precaution when dealing with phenylbutazone is that it should not be given to animals that are pregnant or nursing young as research has indicated it’s harmful to embryos and young.
This drug must not be injected into the muscles directly or under the skin.

IR spectrum of Phenylbutazone

[[Image:Example.jpg]]

== Wiki Utillities ==
Utilities have been written to help the conversion of material from HTML.

# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]

No wiki2html converter suitable for use has yet been identified.
=== Wiki Templates ===

[[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-name|parameter}}, 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!
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)

----
[[Template:Chem-Data]]

[[Template:Drug-Box]] - For pharmaceutical drugs just copy variable names and code generates tables

[[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]]

[[Template:NFPA_704]] - for notes on how to use, see [[Template_talk:NFPA_704|here]]

[[R & S Phrases]]