Names | |
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IUPAC name
(24R)-3β,12β,25-Trihydroxy-20,24-epoxydammaran-6α-yl α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside
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Systematic IUPAC name
(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-1-({(1S,3aR,3bR,5S,5aR,7S,9aR,9bR,11R,11aR)-7,11-Dihydroxy-1-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-3a,3b,6,6,9a-pentamethylhexadecahydro-5H-cyclopenta[a]phenanthren-5-yl}oxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol | |
Other names
Ginsenoside A1
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Identifiers | |
3D model (JSmol)
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ECHA InfoCard | 100.208.747 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C42H72O14 | |
Molar mass | 801.024 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Pseudoginsenoside F11 is a chemical natural product found in American ginseng (Panax quinquefolius) but not in Asian ginseng (Panax ginseng), although it has similar properties to the Asian ginseng compound ginsenoside Rf.[1] The molecule is a triterpenoid saponin member of the dammarane family and contains a four-ring rigid skeleton.[1] Compounds in the ginsenoside family are found almost exclusively in plants of the genus Panax. A wide variety of difficult-to-characterize in vitro effects have been reported for the compounds in isolation.[2][3] Pseudoginsenoside F11 and its derivatives are sometimes referred to as having an ocotillol-type skeleton structure.[1][4]
Studies in mice have identified antagonistic effects on the actions of other well-characterized drugs, such as scopolamine,[5] morphine,[6][7] and methamphetamine.[8]