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	<title>Bio Screening Industry News</title>
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	<pubDate>Fri, 29 Jan 2010 14:55:38 +0000</pubDate>
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		<title>Genipin</title>
		<link>http://www.bioscreening.net/glossary/genipin/</link>
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		<pubDate>Mon, 04 Jun 2007 21:26:12 +0000</pubDate>
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		<description><![CDATA[Genipin is the active compound found in the gardenia fruit extract, which is used in traditional Chinese medicine to relieve the symptoms of type 2 diabetes. Research conducted at the Beth Israel Deaconess Medical Center and Harvard Medical School indicated that the chemical is indeed effective.
Genipin is an aglycone derived from an iridoid glycoside called [...]]]></description>
			<content:encoded><![CDATA[<p><img align="left" title="Genipin chemical structure" alt="Genipin chemical structure" src="http://www.bioscreening.net/wp-content/files/Genipin.png" /><strong>Genipin</strong> is the active compound found in the gardenia fruit extract, which is used in traditional Chinese medicine to relieve the symptoms of type 2 diabetes. Research conducted at the Beth Israel Deaconess Medical Center and Harvard Medical School indicated that the chemical is indeed effective.</p>
<p>Genipin is an aglycone derived from an iridoid glycoside called <span class="new">geniposide</span> present in fruit of <em>Gardenia jasmindides Ellis</em>. Genipin is an excellent natural cross-linker for proteins, collagen, gelatin, and chitosan cross-linking. It has a low acute toxicity, with LD<sub>50</sub> i.v. 382 mg/kg in mice, therefore, much less toxic than glutaraldehyde and many other commonly used synthetic cross-linking regents. It is also used for pharmaceutical purposes, such as choleretic action for liver diseases control.</p>
<table width="583" border="1" style="height: 547px" class="toccolours">
<tr>
<td>IUPAC name</td>
<td>Methyl (<em>1R,2R,6S</em>)-2-hydroxy-9-(hydroxymethyl)- 3-oxabicyclo[4.3.0]nona-4,8-diene-5-carboxylate</td>
</tr>
<tr>
<th colspan="2" style="background: #f8eaba none repeat scroll 0% 50%; -moz-background-clip: -moz-initial; -moz-background-origin: -moz-initial; -moz-background-inline-policy: -moz-initial; text-align: center">Identifiers</th>
</tr>
<tr>
<td>CAS number</td>
<td>[6902-77-8]</td>
</tr>
<tr>
<td>PubChem</td>
<td>442424</td>
</tr>
<tr>
<td>SMILES</td>
<td>COC(=O)C1=CO[C@H]([C@H]2[C@@H]1CC=C2CO)O</td>
</tr>
<tr>
<th colspan="2" style="background: #f8eaba none repeat scroll 0% 50%; -moz-background-clip: -moz-initial; -moz-background-origin: -moz-initial; -moz-background-inline-policy: -moz-initial; text-align: center">Properties</th>
</tr>
<tr>
<td>Molecular formula</td>
<td>C<sub>11</sub>H<sub>14</sub>O<sub>5</sub></td>
</tr>
<tr>
<td>Molar mass</td>
<td>226.226 g/mol</td>
</tr>
<tr>
<td>Hydrogen Bonds Donors</td>
<td>2</td>
</tr>
<tr>
<td>Hydrogen Bonds Acceptors</td>
<td>5</td>
</tr>
<tr>
<td>Rotatable Bonds</td>
<td>3</td>
</tr>
<tr>
<td>Polar Surface Area</td>
<td>76</td>
</tr>
<tr>
<td>XLogP</td>
<td>-0.8</td>
</tr>
<tr>
<td>Exact Mass</td>
<td>226.084</td>
</tr>
<tr>
<td>MonoIsotopic Mass</td>
<td>226.084</td>
</tr>
<tr>
<td>Charge</td>
<td>0</td>
</tr>
<tr>
<td>Complexity</td>
<td>357</td>
</tr>
</table>
<p>Genipin Uses and Applications</p>
<ul>
<li><a href="http://www.bioscreening.net/glossary/genipin/genipin-and-diabetes/">Genipin for diabetes treatment</a></li>
<li><a href="http://www.bioscreening.net/glossary/genipin/genipin-for-liver-diseases-control/">Genipin for liver diseases control</a></li>
<li><a href="http://www.bioscreening.net/glossary/genipin/leather-industry/">Genipin for leather industry</a></li>
<li>Genipin as a natural cross-linker for proteins, collagen, gelatin, and chitosan</li>
<li>Genipin in forensic science</li>
</ul>
<p>Buy Genipin:</p>
<p><a href="http://www.timtec.net/genipin.html">Buy Genipin</a> from TimTec in mg, gram, and larger amounts
</p>
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