Chemical Formula: C41H70O12
Chemical Formula C41H70O12
Found 12 metabolite its formula value is C41H70O12
Chikusetsusaponin Ia
Chikusetsusaponin Ia is found in tea. Chikusetsusaponin Ia is a constituent of Panax japonicum (Japanese ginseng) Constituent of Panax japonicum (Japanese ginseng). Chikusetsusaponin Ia is found in tea. D002491 - Central Nervous System Agents
Ginsenoside Mc
Ginsenoside Mc is considered to be practically insoluble (in water) and acidic
Mutalomycin
A polyether antibiotic produced by a strain of Streptomyces mutabilis NRRL 8088.
(20S,24R)-epoxydammarane 3beta,12beta,25-trihydroxy-12-O-beta-D-quinovopyranosyl-3-O-alpha-L-arabinopyranoside
ginsenoside Mx
Ginsenoside Mx is a ginsenoside found in Panax ginseng that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions and in which the hydroxy group at position 20 has been converted to the corresponding beta-D-xylopyranosyl-beta-D-glucopyranoside. It has a role as an antineoplastic agent and a plant metabolite. It is a ginsenoside, a tetracyclic triterpenoid, a beta-D-glucoside, a disaccharide derivative and a 3beta-hydroxy-4,4-dimethylsteroid. It is functionally related to a (20S)-protopanaxadiol. It derives from a hydride of a dammarane. ginsenoside Mx is a natural product found in Gynostemma pentaphyllum, Fusarium sacchari, and Centella asiatica with data available. A ginsenoside found in Panax ginseng that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions and in which the hydroxy group at position 20 has been converted to the corresponding beta-D-xylopyranosyl-beta-D-glucopyranoside. Gypenoside XIII is belonging to the gypenosides. Gypenosides, extracted from Gynostemma pentaphyllum, have various pharmacological properties and protect against cardiovascular diseases, especially atherosclerosis[1].
Ginsenoside C-Y
A ginsenoside found in Panax species that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions, in which the hydroxy group at position 20 has been converted to the corresponding alpha-L-arabinopyranosyl-(1->6)-beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position.
Ginsenoside Mc
A ginsenoside found in Panax notoginseng that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions and in which the hydroxy group at position 20 has been converted to the corresponding alpha-L-arabinofuranosyl-beta-D-glucopyranoside.