GINSENOSIDEF1
GINSENOSIDEF1 Basic information
- Product Name:
- GINSENOSIDEF1
- Synonyms:
-
- (20S)-20-(β-D-Glucopyranosyloxy)dammar-24-ene-3β,6α,12β-triol
- 3β,6α,12β-Trihydroxy-5α-dammar-24-en-20-yl β-D-glucopyranoside
- (3b,6a,12b)-3,6,12-Trihydroxydammar-24-ene-20-yl beta-D-glucopyranoside
- Ginsenoside F1
- GINSENOSIDE F1(P)
- 20(S)-Ginsenoside F1(3b,6a,12b)-3,6,12-Trihydroxydammar-24-ene-20-yl beta-D-glucopyranoside
- 20(S)-Ginsenoside F1
- Panaxoside Aprogenin
- CAS:
- 53963-43-2
- MF:
- C36H62O9
- MW:
- 638.87
- Product Categories:
-
- chemical reagent
- pharmaceutical intermediate
- phytochemical
- reference standards from Chinese medicinal herbs (TCM).
- standardized herbal extract
- Mol File:
- 53963-43-2.mol
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GINSENOSIDEF1 Chemical Properties
- Melting point:
- >165°C (dec.)
- Boiling point:
- 751.7±60.0 °C(Predicted)
- Density
- 1.23±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly )
- pka
- 12.94±0.70(Predicted)
- form
- powder
- color
- Pale Yellow
- Stability:
- Hygroscopic
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GINSENOSIDEF1 Usage And Synthesis
Uses
Ginsenoside F1 is a bioactive metabolite of the ginsenoside component of Panax ginseng with the ability to inhibit human cytochrome P450 enzymes. This has application in anti-cancer therapeutics as well as protective liver effects.
Definition
ChEBI: A ginsenoside found in Panax species that is dammarane which is substituted by hydroxy groups at the 3beta, 6alpha, 12beta and 20 pro-S positions, in which the hy roxy group at position 20 has been converted to the corresponding beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position.
GINSENOSIDEF1Supplier
Chembest Research Laboratories Limited
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