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		<title>6''-Malonoylginsenoside Rc - Revision history</title>
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		<updated>2026-06-09T15:30:20Z</updated>
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	<entry>
		<id>http://metabolomics.jp/mediawiki/index.php?title=6%27%27-Malonoylginsenoside_Rc&amp;diff=38266&amp;oldid=prev</id>
		<title>Toyama: New page: {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |SysName=(3beta,12beta)-20-[(6-O-alpha-L-Arabinofuranosyl-beta-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-[6-O-(carboxyacetyl)-beta-D-gl...</title>
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				<updated>2010-02-15T00:37:54Z</updated>
		
		<summary type="html">&lt;p&gt;New page: {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |SysName=(3beta,12beta)-20-[(6-O-alpha-L-Arabinofuranosyl-beta-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-[6-O-(carboxyacetyl)-beta-D-gl...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Hierarchy|{{PAGENAME}}}}&lt;br /&gt;
&lt;br /&gt;
{{Metabolite&lt;br /&gt;
|SysName=(3beta,12beta)-20-[(6-O-alpha-L-Arabinofuranosyl-beta-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-[6-O-(carboxyacetyl)-beta-D-glucopyranosyl]-beta-D-Glucopyranoside&lt;br /&gt;
|Common Name=&amp;amp;&amp;amp;Malonylginsenoside Rc&amp;amp;&amp;amp;Dammarane beta-D-glucopyranoside deriv.&amp;amp;&amp;amp;Ginsenoside mRc&amp;amp;&amp;amp;MG-Rc&amp;amp;&amp;amp;&lt;br /&gt;
|CAS=88140-36-7&lt;br /&gt;
|KNApSAcK=&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Spectroscopic Data==&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;width:80%&amp;quot;&lt;br /&gt;
&lt;br /&gt;
'''Free acid'''&lt;br /&gt;
|-&lt;br /&gt;
| '''M.P.''' || 150 - 152 °C &lt;br /&gt;
|-&lt;br /&gt;
| '''IR''' (KBr)|| 3381, 2934, 1733, 1631, 1381, 1071 cm&amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;width:80%&amp;quot;&lt;br /&gt;
'''Methyl ester'''&lt;br /&gt;
|-&lt;br /&gt;
| '''M.P.''' || 159 - 163 °C &lt;br /&gt;
|-&lt;br /&gt;
| '''&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H-NMR''' (C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;N)|| 0.80 (s, CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 0.96 (s, 3xCH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 1.12 (s, CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 1.32 (s, CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 1.63 (s), 1.67 (s, CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 3.65 (s, COOCH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;), 3.75 (s, OC-CH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-CO)&lt;br /&gt;
|-&lt;br /&gt;
| '''&amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;C-NMR''' (C&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;N, 22.5MHz)|| C-3) 89.3, (12) 70.3, (20) 83.4 '''Glc I''' (1) 104.8, (2) 84.1, (3) 77.9, (4) 72.1, (5) 77.9, (6) 62.6 '''Glc II''' (1) 106.0, (2) 76.6, (3) 78.8, (4) 70.9, (5) 75.1, (6) 65.4 '''Glc III''' (1) 98.1, (2) 75.0, (3) 78.4, (4) 71.4, (5) 76.4, (6) 68.4 '''Ara(f)''' (1) 110.0, (2) 83.1, (3) 79.0, (4) 86.0, (5) 62.6 '''Malonoyl''' (1) 167.2, (2) 41.6, (3) 167.2, (OCH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;) 52.2  &lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;small&amp;gt;Y. Nakagawa et al., Chem.Pharm.Bull., 37, 2961 (1989).&amp;lt;/small&amp;gt;&lt;/div&gt;</summary>
		<author><name>Toyama</name></author>	</entry>

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