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	<id>https://chemwiki.ch.ic.ac.uk/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Ghb05</id>
	<title>ChemWiki - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="https://chemwiki.ch.ic.ac.uk/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Ghb05"/>
	<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/wiki/Special:Contributions/Ghb05"/>
	<updated>2026-08-11T15:54:46Z</updated>
	<subtitle>User contributions</subtitle>
	<generator>MediaWiki 1.43.8</generator>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=8044</id>
		<title>It:Histrionicotoxin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=8044"/>
		<updated>2006-12-11T16:58:53Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin is a poison.  In 1823 Captain Charles Stuart Cochrane discovered tribes of Indians native to Colombia using it for hunting.  They used the poison for the tips of their arrows and blowguns.  He discovered that the poison was extracted from small yellow brightly coloured frogs called Dendrobates histrionicus.&lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
&lt;br /&gt;
They have been found to be potent inhibitors of the acetyl choline receptor channel and as such constitute important synthetic targets.&lt;br /&gt;
&lt;br /&gt;
[[Image:Mech_his.JPG|thumb|left|250|Synthesis of Histrionicotoxin]]&lt;br /&gt;
&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;&amp;quot;&lt;br /&gt;
! {{chembox header}}  colspan=&amp;quot;3&amp;quot; |Histrionicotoxin &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;3&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:Histrionicotoxin.JPG|Histrionicotoxin]]&lt;br /&gt;
&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;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; 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;REMARK   MSI WebLab Viewer PDB file&lt;br /&gt;
REMARK   Created:  Thu Nov 23 14:47:40 GMT Standard Time 2006&lt;br /&gt;
ATOM      1  C1  MOL     1      14.947  14.885  -0.721  1.00  0.00              &lt;br /&gt;
ATOM      2  C2  MOL     1      16.156  15.570  -0.617  1.00  0.00              &lt;br /&gt;
ATOM      3  C3  MOL     1      14.108  13.403  -0.478  1.00  0.00              &lt;br /&gt;
ATOM      4  C4  MOL     1      17.591  15.314  -0.182  1.00  0.00              &lt;br /&gt;
ATOM      5  C5  MOL     1      14.694  12.027   0.398  1.00  0.00              &lt;br /&gt;
ATOM      6  C6  MOL     1      12.725  13.693   0.143  1.00  0.00              &lt;br /&gt;
ATOM      7  C7  MOL     1      18.732  15.072   0.163  1.00  0.00              &lt;br /&gt;
ATOM      8  N8  MOL     1      15.466  10.987  -0.454  1.00  0.00              &lt;br /&gt;
ATOM      9  C9  MOL     1      15.434  12.307   1.635  1.00  0.00              &lt;br /&gt;
ATOM     10  C10 MOL     1      13.504  11.247   1.015  1.00  0.00              &lt;br /&gt;
ATOM     11  O11 MOL     1      12.060  14.761  -0.533  1.00  0.00              &lt;br /&gt;
ATOM     12  C12 MOL     1      11.819  12.384  -0.183  1.00  0.00              &lt;br /&gt;
ATOM     13  C13 MOL     1      16.929  11.123  -0.659  1.00  0.00              &lt;br /&gt;
ATOM     14  C14 MOL     1      16.833  12.744   1.201  1.00  0.00              &lt;br /&gt;
ATOM     15  C15 MOL     1      12.478  11.003   0.056  1.00  0.00              &lt;br /&gt;
ATOM     16  C16 MOL     1      17.857  10.365   0.310  1.00  0.00              &lt;br /&gt;
ATOM     17  C17 MOL     1      17.221  12.421  -0.376  1.00  0.00              &lt;br /&gt;
ATOM     18  C18 MOL     1      19.305  10.605  -0.123  1.00  0.00              &lt;br /&gt;
ATOM     19  C19 MOL     1      20.308  10.532   0.749  1.00  0.00              &lt;br /&gt;
ATOM     20  C20 MOL     1      21.649  10.483   0.263  1.00  0.00              &lt;br /&gt;
ATOM     21  C21 MOL     1      22.767  10.394  -0.181  1.00  0.00              &lt;br /&gt;
TER&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;3&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; |&lt;br /&gt;
|- &lt;br /&gt;
| [[Empirical formula]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot;| C19H25N1O1&lt;br /&gt;
|- &lt;br /&gt;
| [[calculated density]]&lt;br /&gt;
|colspan=&amp;quot;2&amp;quot;| 1.122 g/cm3&lt;br /&gt;
|-&lt;br /&gt;
| [[Other Name]]&lt;br /&gt;
|colspan=&amp;quot;2&amp;quot;|(-)-Histrionicotoxin]&lt;br /&gt;
|-&lt;br /&gt;
| [[Chemical formula|Molecular formula]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | C19H25N1O1&lt;br /&gt;
|-&lt;br /&gt;
| [[Molar mass]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; |283.414 g/mol&lt;br /&gt;
|-&lt;br /&gt;
| [[CAS registry number|CAS number]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | 13774-81-7&lt;br /&gt;
|-&lt;br /&gt;
| [[Appearance]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | yellow liquid&lt;br /&gt;
|-&lt;br /&gt;
! {{chembox header}} colspan=&amp;quot;3&amp;quot;| Properties&lt;br /&gt;
|-&lt;br /&gt;
| [[Density]] and [[Phase (matter)|phase]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; |  0.780 g/cm3&lt;br /&gt;
|-&lt;br /&gt;
| [[Solubility]] in [[Water_(molecule)|water (ph=7)]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | &lt;br /&gt;
|-&lt;br /&gt;
| [[Melting point]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | 15-17°C&lt;br /&gt;
|-&lt;br /&gt;
| [[Boiling point]]&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; | decomposes&lt;br /&gt;
|-&lt;br /&gt;
| [[Acid dissociation constant|Acidity]] (p&#039;&#039;Ka&#039;&#039;) &amp;lt;!-- omit if not a base. If several values, be clear --&amp;gt;&lt;br /&gt;
| colspan=&amp;quot;2&amp;quot; |&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=8043</id>
		<title>It:Histrionicotoxin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=8043"/>
		<updated>2006-12-11T16:41:27Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: Addation of synthesis&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin is a poison.  In 1823 Captain Charles Stuart Cochrane discovered tribes of Indians native to Colombia using it for hunting.  They used the poison for the tips of their arrows and blowguns.  He discovered that the poison was extracted from small yellow brightly coloured frogs called Dendrobates histrionicus.&lt;br /&gt;
&lt;br /&gt;
[[Image:Mech_his.JPG|thumb|left|250|Synthesis of Histrionicotoxin]]&lt;br /&gt;
&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;&amp;quot;&lt;br /&gt;
! {{chembox header}}  colspan=&amp;quot;3&amp;quot; |Histrionicotoxin &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;3&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:Histrionicotoxin.JPG|Histrionicotoxin]]&lt;br /&gt;
&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;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; 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;REMARK   MSI WebLab Viewer PDB file&lt;br /&gt;
REMARK   Created:  Thu Nov 23 14:47:40 GMT Standard Time 2006&lt;br /&gt;
ATOM      1  C1  MOL     1      14.947  14.885  -0.721  1.00  0.00              &lt;br /&gt;
ATOM      2  C2  MOL     1      16.156  15.570  -0.617  1.00  0.00              &lt;br /&gt;
ATOM      3  C3  MOL     1      14.108  13.403  -0.478  1.00  0.00              &lt;br /&gt;
ATOM      4  C4  MOL     1      17.591  15.314  -0.182  1.00  0.00              &lt;br /&gt;
ATOM      5  C5  MOL     1      14.694  12.027   0.398  1.00  0.00              &lt;br /&gt;
ATOM      6  C6  MOL     1      12.725  13.693   0.143  1.00  0.00              &lt;br /&gt;
ATOM      7  C7  MOL     1      18.732  15.072   0.163  1.00  0.00              &lt;br /&gt;
ATOM      8  N8  MOL     1      15.466  10.987  -0.454  1.00  0.00              &lt;br /&gt;
ATOM      9  C9  MOL     1      15.434  12.307   1.635  1.00  0.00              &lt;br /&gt;
ATOM     10  C10 MOL     1      13.504  11.247   1.015  1.00  0.00              &lt;br /&gt;
ATOM     11  O11 MOL     1      12.060  14.761  -0.533  1.00  0.00              &lt;br /&gt;
ATOM     12  C12 MOL     1      11.819  12.384  -0.183  1.00  0.00              &lt;br /&gt;
ATOM     13  C13 MOL     1      16.929  11.123  -0.659  1.00  0.00              &lt;br /&gt;
ATOM     14  C14 MOL     1      16.833  12.744   1.201  1.00  0.00              &lt;br /&gt;
ATOM     15  C15 MOL     1      12.478  11.003   0.056  1.00  0.00              &lt;br /&gt;
ATOM     16  C16 MOL     1      17.857  10.365   0.310  1.00  0.00              &lt;br /&gt;
ATOM     17  C17 MOL     1      17.221  12.421  -0.376  1.00  0.00              &lt;br /&gt;
ATOM     18  C18 MOL     1      19.305  10.605  -0.123  1.00  0.00              &lt;br /&gt;
ATOM     19  C19 MOL     1      20.308  10.532   0.749  1.00  0.00              &lt;br /&gt;
ATOM     20  C20 MOL     1      21.649  10.483   0.263  1.00  0.00              &lt;br /&gt;
ATOM     21  C21 MOL     1      22.767  10.394  -0.181  1.00  0.00              &lt;br /&gt;
TER&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>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mech_his.JPG&amp;diff=8042</id>
		<title>File:Mech his.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Mech_his.JPG&amp;diff=8042"/>
		<updated>2006-12-11T16:39:13Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5962</id>
		<title>It:Histrionicotoxin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5962"/>
		<updated>2006-11-23T14:56:10Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: addition of 3d structure&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin is a poison.  In 1823 Captain Charles Stuart Cochrane discovered tribes of Indians native to Colombia using it for hunting.  They used the poison for the tips of their arrows and blowguns.  He discovered that the poison was extracted from small yellow brightly coloured frogs called Dendrobates histrionicus.&lt;br /&gt;
&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;&amp;quot;&lt;br /&gt;
! {{chembox header}}  colspan=&amp;quot;3&amp;quot; |Histrionicotoxin &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;3&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:Histrionicotoxin.JPG|Histrionicotoxin]]&lt;br /&gt;
&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;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; 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;REMARK   MSI WebLab Viewer PDB file&lt;br /&gt;
REMARK   Created:  Thu Nov 23 14:47:40 GMT Standard Time 2006&lt;br /&gt;
ATOM      1  C1  MOL     1      14.947  14.885  -0.721  1.00  0.00              &lt;br /&gt;
ATOM      2  C2  MOL     1      16.156  15.570  -0.617  1.00  0.00              &lt;br /&gt;
ATOM      3  C3  MOL     1      14.108  13.403  -0.478  1.00  0.00              &lt;br /&gt;
ATOM      4  C4  MOL     1      17.591  15.314  -0.182  1.00  0.00              &lt;br /&gt;
ATOM      5  C5  MOL     1      14.694  12.027   0.398  1.00  0.00              &lt;br /&gt;
ATOM      6  C6  MOL     1      12.725  13.693   0.143  1.00  0.00              &lt;br /&gt;
ATOM      7  C7  MOL     1      18.732  15.072   0.163  1.00  0.00              &lt;br /&gt;
ATOM      8  N8  MOL     1      15.466  10.987  -0.454  1.00  0.00              &lt;br /&gt;
ATOM      9  C9  MOL     1      15.434  12.307   1.635  1.00  0.00              &lt;br /&gt;
ATOM     10  C10 MOL     1      13.504  11.247   1.015  1.00  0.00              &lt;br /&gt;
ATOM     11  O11 MOL     1      12.060  14.761  -0.533  1.00  0.00              &lt;br /&gt;
ATOM     12  C12 MOL     1      11.819  12.384  -0.183  1.00  0.00              &lt;br /&gt;
ATOM     13  C13 MOL     1      16.929  11.123  -0.659  1.00  0.00              &lt;br /&gt;
ATOM     14  C14 MOL     1      16.833  12.744   1.201  1.00  0.00              &lt;br /&gt;
ATOM     15  C15 MOL     1      12.478  11.003   0.056  1.00  0.00              &lt;br /&gt;
ATOM     16  C16 MOL     1      17.857  10.365   0.310  1.00  0.00              &lt;br /&gt;
ATOM     17  C17 MOL     1      17.221  12.421  -0.376  1.00  0.00              &lt;br /&gt;
ATOM     18  C18 MOL     1      19.305  10.605  -0.123  1.00  0.00              &lt;br /&gt;
ATOM     19  C19 MOL     1      20.308  10.532   0.749  1.00  0.00              &lt;br /&gt;
ATOM     20  C20 MOL     1      21.649  10.483   0.263  1.00  0.00              &lt;br /&gt;
ATOM     21  C21 MOL     1      22.767  10.394  -0.181  1.00  0.00              &lt;br /&gt;
TER&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>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Histrionicotoxin_3d_structure.pdb&amp;diff=5960</id>
		<title>File:Histrionicotoxin 3d structure.pdb</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Histrionicotoxin_3d_structure.pdb&amp;diff=5960"/>
		<updated>2006-11-23T14:49:41Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: Histrionicotoxin_3d_&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin_3d_&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:3d_space_fill_Histrionicotoxin.pdb&amp;diff=5956</id>
		<title>File:3d space fill Histrionicotoxin.pdb</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:3d_space_fill_Histrionicotoxin.pdb&amp;diff=5956"/>
		<updated>2006-11-23T14:36:23Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5955</id>
		<title>It:Histrionicotoxin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5955"/>
		<updated>2006-11-23T14:31:42Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: Insert of chemdraw structure inside text box&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin is a poison.  In 1823 Captain Charles Stuart Cochrane discovered tribes of Indians native to Colombia using it for hunting.  They used the poison for the tips of their arrows and blowguns.  He discovered that the poison was extracted from small yellow brightly coloured frogs called Dendrobates histrionicus.&lt;br /&gt;
&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;&amp;quot;&lt;br /&gt;
! {{chembox header}}  colspan=&amp;quot;3&amp;quot; |Histrionicotoxin &lt;br /&gt;
|-&lt;br /&gt;
| align=&amp;quot;center&amp;quot; colspan=&amp;quot;3&amp;quot; bgcolor=&amp;quot;#ffffff&amp;quot; | [[Image:Histrionicotoxin.JPG|Histrionicotoxin]]&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Histrionicotoxin.JPG&amp;diff=5953</id>
		<title>File:Histrionicotoxin.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Histrionicotoxin.JPG&amp;diff=5953"/>
		<updated>2006-11-23T14:21:15Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: chem draw structure of Histrionicotoxin&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;chem draw structure of Histrionicotoxin&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5633</id>
		<title>It:Histrionicotoxin</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Histrionicotoxin&amp;diff=5633"/>
		<updated>2006-11-20T15:26:34Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: Introduction&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Histrionicotoxin is a poison.  In 1823 Captain Charles Stuart Cochrane discovered tribes of Indians native to Colombia using it for hunting.  They used the poison for the tips of their arrows and blowguns.  He discovered that the poison was extracted from small yellow brightly coloured frogs called Dendrobates histrionicus.&lt;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=5621</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=5621"/>
		<updated>2006-11-20T15:10:13Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: /* 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;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;. No 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;
&lt;br /&gt;
== Main Project Page ==&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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it:Cyameluric|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; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
*[[it:Linalool|Linalool(A component of essential oil)]]&lt;br /&gt;
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]&lt;br /&gt;
*[[it:Acrolein|Acrolein]]&lt;br /&gt;
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]&lt;br /&gt;
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]&lt;br /&gt;
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]&lt;br /&gt;
*[[it:Vanillin|Vanillin, flavouring used in food]]&lt;br /&gt;
*[[it:Gingerol|Gingerol, precursor of Zingerone]]&lt;br /&gt;
*[[it:MSG|MSG; because everyone loves the flavour]]&lt;br /&gt;
*[[it:DDT|DDT, Pesticide]]&lt;br /&gt;
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]&lt;br /&gt;
*[[it:Caffeine|Caffeine]]&lt;br /&gt;
*[[it:Fullerene]]&lt;br /&gt;
*[[it:Histrionicotoxin]]&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
This takes you to an &#039;&#039;&#039;Export&#039;&#039;&#039; page. A backup of the Projects area can be made (in XML) if you want to keep your own &#039;&#039;snapshot&#039;&#039; of the project pages at any instant. After you Export the page you want (ie &#039;&#039;&#039;It:projects&#039;&#039;&#039; or &#039;&#039;&#039;It:Lignocaine&#039;&#039;&#039; for example) the XML encoding of it will appear in your browser Window. You should &#039;&#039;&#039;view source&#039;&#039;&#039; for this material, copy it to a text editor, and thence save it to disk.&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If someone else  starts editing a page at the same time as you,   the system will detect this and offer alternatives for you to deal with.  For example, it may suggest you copy the contents of the page you have been editing and merge it into the other person&#039;s page,&lt;br /&gt;
so that both the sets of edits are preserved.  Read the on-screen instructions carefully!&lt;br /&gt;
&lt;br /&gt;
Another precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. That way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)--[[User:Rzepa|Rzepa]] 08:31, 5 November 2006 (UTC)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&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-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!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&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;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=5619</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=5619"/>
		<updated>2006-11-20T15:09:34Z</updated>

		<summary type="html">&lt;p&gt;Ghb05: /* 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;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;. No 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;
&lt;br /&gt;
== Main Project Page ==&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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it: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; | [[it:Cyameluric|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; [[it:name_of_project|Descriptive name of intended project]]&amp;lt;/nowiki&amp;gt;&lt;br /&gt;
*This will produce the effect:  [[it:name_of_project|Descriptive name of intended project]]&lt;br /&gt;
----&lt;br /&gt;
*[[it:sitagliptin_page|Sitagliptin]]&lt;br /&gt;
*[[it:Retinal|Retinal, molecule of sight]]&lt;br /&gt;
*[[it:Tamoxifen|Tamoxifen, breast cancer treatment]]&lt;br /&gt;
*[[it:Morphine|Morphine, painkiller]]&lt;br /&gt;
*[[it:Pelargonidin|Pelargonidin, colouring in nature]]&lt;br /&gt;
*[[it:Propanil|Propanil, weedkiller]]&lt;br /&gt;
*[[it:Ranitidine|Ranitidine, antiulcerative]]&lt;br /&gt;
*[[it:chlorphentermine|chlorphentermine, anorectic]]&lt;br /&gt;
*[[it:Serotonin|Serotonin, The &#039;HAPPY&#039; Drug]]&lt;br /&gt;
*[[it:Amphidinolide T1|Amphidinolide T1]]&lt;br /&gt;
*[[it:Rosiglitazone|Rosiglitazone, drug that is currently used to treat diabetes.]]&lt;br /&gt;
*[[it:Furosemide|Furosemide]]&lt;br /&gt;
*[[it:Tryptophan|Tryptophan]]&lt;br /&gt;
*[[it:methylpentynol|methylpentynol, tranquilliser.]]&lt;br /&gt;
*[[it:Ferrocene|Ferrocene]]&lt;br /&gt;
*[[it:Scopolamine|Scopolamine, the (Former) Truth Drug]]&lt;br /&gt;
*[[it:Camptothecin|Camptothecin,Anti-cancer agent ]]&lt;br /&gt;
*[[it:Salmeterol|Salmeterol, an agonist used to treat asthma]]&lt;br /&gt;
*[[it:Psilocin|Psilocin]]&lt;br /&gt;
*[[it:Epibatidine|Epibatidine]]&lt;br /&gt;
*[[it:Beta Carotene|Beta Carotene]]&lt;br /&gt;
*[[it:Thyroxine|Thyroxine, the Thyroid Hormone]]&lt;br /&gt;
*[[it:Tetrahydrocannabinol|Tetrahydrocannabinol]]&lt;br /&gt;
*[[it:Linalool|Linalool(A component of essential oil)]]&lt;br /&gt;
*[[it:Dihydroartemisinin| Dihydroartemisinin, An Active Anti-Malarial]]&lt;br /&gt;
*[[it:Acrolein|Acrolein]]&lt;br /&gt;
*[[it:Cinnamaldehyde|Cinnamaldehyde: The smell and taste in the spice cinnamon]]&lt;br /&gt;
*[[it:Melatonin|Melatonin: The All-Natural Nightcap]]&lt;br /&gt;
*[[it:Benzylpiperazine|Benzylpiperazine (BZP): Party Pills]]&lt;br /&gt;
*[[it:Vanillin|Vanillin, flavouring used in food]]&lt;br /&gt;
*[[it:Gingerol|Gingerol, precursor of Zingerone]]&lt;br /&gt;
*[[it:MSG|MSG; because everyone loves the flavour]]&lt;br /&gt;
*[[it:DDT|DDT, Pesticide]]&lt;br /&gt;
*[[it:Oseltamivir|Oseltamivir, neuraminidase inhibitor]]&lt;br /&gt;
*[[it:Caffeine|Caffeine]]&lt;br /&gt;
*[[it:Fullerene]]&lt;br /&gt;
*[[it:Histrionicotoxin}}&lt;br /&gt;
&lt;br /&gt;
== [[Special:Export|Export Pages]] ==&lt;br /&gt;
&lt;br /&gt;
This takes you to an &#039;&#039;&#039;Export&#039;&#039;&#039; page. A backup of the Projects area can be made (in XML) if you want to keep your own &#039;&#039;snapshot&#039;&#039; of the project pages at any instant. After you Export the page you want (ie &#039;&#039;&#039;It:projects&#039;&#039;&#039; or &#039;&#039;&#039;It:Lignocaine&#039;&#039;&#039; for example) the XML encoding of it will appear in your browser Window. You should &#039;&#039;&#039;view source&#039;&#039;&#039; for this material, copy it to a text editor, and thence save it to disk.&lt;br /&gt;
&lt;br /&gt;
== Overlaps ==&lt;br /&gt;
&lt;br /&gt;
If someone else  starts editing a page at the same time as you,   the system will detect this and offer alternatives for you to deal with.  For example, it may suggest you copy the contents of the page you have been editing and merge it into the other person&#039;s page,&lt;br /&gt;
so that both the sets of edits are preserved.  Read the on-screen instructions carefully!&lt;br /&gt;
&lt;br /&gt;
Another precaution you could take is to keep a copy of the contents of the page you are editing in eg Wordpad (or Word),&lt;br /&gt;
make the changes there, and then copy the entire lot to the  Wiki page to preview and then save. That way, if your contribution&lt;br /&gt;
is overlapped by someone else, you will still have a copy, and you can then resubmit it.&lt;br /&gt;
----&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 12:25, 19 October 2006 (BST)--[[User:Rzepa|Rzepa]] 08:31, 5 November 2006 (UTC)&lt;br /&gt;
&lt;br /&gt;
== Wiki Utillities ==&lt;br /&gt;
Utilities have been written to help the conversion of material from  HTML.&lt;br /&gt;
&lt;br /&gt;
# [http://diberri.dyndns.org/wikipedia/html2wiki/ A HTML2Wiki Converter]&lt;br /&gt;
&lt;br /&gt;
No wiki2html converter suitable for use has yet been identified.&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-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!&lt;br /&gt;
--[[User:Rzepa|Rzepa]] 14:41, 20 October 2006 (BST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
[[Template:Chem-Data]]&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;/div&gt;</summary>
		<author><name>Ghb05</name></author>
	</entry>
</feed>