http://metabolomics.jp/mediawiki/index.php?action=history&feed=atom&title=20S-Ginsenoside_Rg3 20S-Ginsenoside Rg3 - Revision history 2026-08-25T00:06:38Z Revision history for this page on the wiki MediaWiki 1.19.1 http://metabolomics.jp/mediawiki/index.php?title=20S-Ginsenoside_Rg3&diff=38261&oldid=prev Toyama: New page: {{Hierarchy|{{PAGENAME}}}} {{Metabolite |SysName=(3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside |Common Name=&&20(S)-Ginsenoside-Rg3&&Gin... 2010-02-15T02:43:02Z <p>New page: {{Hierarchy|{{PAGENAME}}}} {{Metabolite |SysName=(3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside |Common Name=&amp;&amp;20(S)-Ginsenoside-Rg3&amp;&amp;Gin...</p> <p><b>New page</b></p><div>{{Hierarchy|{{PAGENAME}}}}<br /> <br /> {{Metabolite<br /> |SysName=(3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside<br /> |Common Name=&amp;&amp;20(S)-Ginsenoside-Rg3&amp;&amp;Ginsenoside Rg3&amp;&amp;3beta-[(2-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-dammar-24-ene-12beta,20-diol&amp;&amp;Dammarane beta-D-glucopyranoside deriv.&amp;&amp;(20S)-Propanaxadiol&amp;&amp;(3beta,12beta)-12,20-Dihydroxydammar-24-en-3-yl O-beta-D-glucopyranosyl-(12)-beta-D-glucopyranoside&amp;&amp;<br /> |CAS=14197-60-5<br /> |KNApSAcK=<br /> }}<br /> <br /> <br /> ==Spectroscopic Data==<br /> <br /> {| class=&quot;wikitable&quot; style=&quot;width:80%&quot;<br /> |-<br /> | '''M.P.'''&lt;sup&gt;2&lt;/sup&gt; || 298 - 303 °C <br /> |-<br /> | '''IR''' (KBr)&lt;sup&gt;1&lt;/sup&gt;|| 3350, 1635, 1155, 1075, 1035, 1020, 985 cm&lt;sup&gt;-1&lt;/sup&gt;<br /> |-<br /> | '''&lt;sup&gt;1&lt;/sup&gt;H-NMR''' (C&lt;sub&gt;5&lt;/sub&gt;D&lt;sub&gt;5&lt;/sub&gt;N, 100 MHz)&lt;sup&gt;1&lt;/sup&gt;|| 0.86 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.00 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.11 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.31 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.40 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.65 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 1.68 (s, CH&lt;sub&gt;3&lt;/sub&gt;), 4.91 and 5.33 (each d, ''J''=7.0 Hz, 2 x anomeric H), 5.30 (m, H-24)<br /> |-<br /> | '''&lt;sup&gt;13&lt;/sup&gt;C-NMR''' (C&lt;sub&gt;5&lt;/sub&gt;D&lt;sub&gt;5&lt;/sub&gt;N, 25.15MHz)&lt;sup&gt;1&lt;/sup&gt;|| C-1) 39.4, (2) 26.9, (3) 89.2, (4) 39.9, (5) 56.6, (6) 18.6, (7) 35.4, (8) 40.2, (9) 50.6, (10) 37.2, (11) 32.3, (12) 71.0, (13) 49.4, (14) 51.9, (15) 31.6, (16) 26.9, (17) 50.8, (18) 16.0, (19) 16.5, (20) 73.2, (21) 22.8, (22) 43.4, (23) 22.8, (24) 126.2, (25) 130.8, (26) 25.9, (27) 17.8, (28) 28.3, (29) 16.7, (30) 17.5 '''Glc I''' (1) 105.1, (2) 83.5, (3) 78.1, (4) 71.9, (5) 78.1, (6) 63.1 '''Glc II''' (1) 106.0, (2) 77.0, (3) 78.5, (4) 72.0, (5) 78.1, (6) 63.1 <br /> |}<br /> &lt;small&gt;1) M. Okuhira et al., Yakugaku Zasshi, 103, 173 (1983)., 2) T. Taniyama et al., Yakugaku Zasshi, 103, 612 (1983).&lt;/small&gt;</div> Toyama