Ginsenosides Rg1
Compound Structure: |
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Synonyms: | Ginsenoside RG;1 22427-39-0; Sanchinoside; C1 Panaxoside A ;Ginsenoside A2 | ||||||||||||||||||||||||||||||||||||||
Compound ID: | NMPC-1080 | ||||||||||||||||||||||||||||||||||||||
PubChem ID: | |||||||||||||||||||||||||||||||||||||||
Molecular Formula: | C42H72O14 | ||||||||||||||||||||||||||||||||||||||
Canonical SMILES: | CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C | ||||||||||||||||||||||||||||||||||||||
InChIKey: | YURJSTAIMNSZAE-HHNZYBFYSA-N | ||||||||||||||||||||||||||||||||||||||
About the compound: | Ginsenoside Rg1 is a ginsenoside found in Panax ginseng and Panaxjaponicus var. major that is dammarane which is substituted by hydroxy groups at the 3beta, 6alpha, 12beta and 20 pro-S positions, in which the hydroxy groups at positions 6 and 20 have been converted to the corresponding beta-D-glucopyranosides, and in which a double bond has been introduced at the 24-25 position. It has a role as a neuroprotective agent and a pro-angiogenic agent. It is a 12beta-hydroxy steroid, a beta-D-glucoside, a tetracyclic triterpenoid, a ginsenoside and a 3beta-hydroxy-4,4-dimethylsteroid. It derives from a hydride of a dammarane. Ginsenosides are a class of steroid glycosides, and triterpenesaponins, found exclusively in the plant genus Panax (ginseng). Ginsenosides have been the target of research, as they are viewed as the active compounds behind the claims of ginseng's efficacy. Because ginsenosides appear to affect multiple pathways, their effects are complex and difficult to isolate. Rg1 Appears to be most abundant in Panax ginseng (Chinese/Korean Ginseng). It improves spatial learning and increase hippocampal synaptophysin level in mice, plus demonstrates estrogen-like activity. GHS Hazard Statements H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral] |
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Properties: |
Chemical and Physical Properties
Source: PubChem |
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Source Species: |
Luffa cylindrica |