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Ginsenoside Rf

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Ginsenoside Rf Basic information

Product Name:
Ginsenoside Rf
Synonyms:
  • GINSENOSIDE RF
  • PANAXOSIDE RF
  • GINSENOSIDE Rf hplc
  • GINSENOSIDE RF WITH HPLC
  • droxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-
  • β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihy
  • (3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside
  • (20S)-6α-(2-O-β-D-Glucopyranosyl-β-D-glucopyranosyloxy)-5α-dammara-24-ene-3β,12β,20-triol
CAS:
52286-58-5
MF:
C42H72O14
MW:
801.02
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Saponins
  • Ginsenoside series
Mol File:
52286-58-5.mol
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Ginsenoside Rf Chemical Properties

Melting point:
197~198℃
Boiling point:
912.3±65.0 °C(Predicted)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
Methanol (Slightly), Pyridine (Slightly)
form 
Solid
pka
12.85±0.70(Predicted)
color 
White to Off-White
InChIKey
UZIOUZHBUYLDHW-CGJOLZHFNA-N
LogP
3.560 (est)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
2-45-24/25
WGK Germany 
3
RTECS 
LY9536900
HS Code 
29389090
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Ginsenoside Rf Usage And Synthesis

Chemical Properties

White to off-white solid

Uses

Ginsenoside Rf is an anti-arthritic agent, attenuating collagen-induced arthritis in mice.

Definition

ChEBI: Ginsenoside Rf is a ginsenoside found in Panax ginseng and Panax japonicus 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 group at position 6 has been converted to the corresponding beta-D-glucopyranosyl-(1->2)-beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position. It has a role as a plant metabolite, an apoptosis inducer and an antineoplastic agent. It is a 12beta-hydroxy steroid, a 3beta-hydroxy steroid, a beta-D-glucoside, a disaccharide derivative, a ginsenoside, a tetracyclic triterpenoid, a 20-hydroxy steroid and a 3beta-hydroxy-4,4-dimethylsteroid. It derives from a hydride of a dammarane.

in vivo

Since inhibition of Ca2+ channels in sensory neurons contributes to antinociception by opioids, analgesic actions of Ginsenoside Rf are tested. Dose-dependent antinociception is found by systemic administration of Ginsenoside Rf in mice using two separate assays of tonic pain: in the acetic acid abdominal constriction test, the ED50 is 56±9 mg/kg, a concentration similar to those reported for aspirin and acetaminophen in the same assay; in the tonic phase of the biphasic formalin test, the ED50 is 129±32 mg/kg[2].

IC 50

N-type calcium channel

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