ChemicalBook--->CAS DataBase List--->52286-58-5

52286-58-5

52286-58-5 Structure

52286-58-5 Structure
IdentificationBack Directory
[Name]

Ginsenoside Rf
[CAS]

52286-58-5
[Synonyms]

PANAXOSIDE RF
RfGinsenoside
GINSENOSIDE RF
Ginsenoside Rf ,98%
GINSENOSIDE Rf hplc
GINSENOSIDE RF WITH HPLC
Ginsenoside Rf (Panaxoside Rf)
droxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-
β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihy
Ginsenoside Rf, 98%, from Panax ginseng C. A. Mey.
[3β,12β,20-Trihydroxydammar-24-en-6α-yl]2-O-(β-D-glucopyranosyl)-β-D-glucopyranoside
[3β,12β,20-Trihydroxy-5α-dammar-24-en-6α-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
(20S)-6α-(2-O-β-D-Glucopyranosyl-β-D-glucopyranosyloxy)-5α-dammara-24-ene-3β,20,12β-triol
(3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside
β-D-Glucopyranoside, (3β,6α,12β)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-β-D-glucopyranosyl-
b-D-Glucopyranoside, (3b,6a,12b)-3,12,20-trihydroxydammar-24-en-6-yl 2-O-b-D-glucopyranosyl-
(2S,3R,4S,5S,6R)-2-[[(2R,3R,4S,5S,6R)-2-[[(6R,10R,12S,13S,14R,17S)-3,12-dihydroxy-17-[(E,2S)-2-hydroxy-6-methyloct-5-en-2-yl]-4,4,10,14-tetramethyl-1,2,3,5,6,7,8,9,11,12,13,15,16,17-tetradecahydrocycl
(2S,3R,4S,5S,6R)-2-(((2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-((S)-2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthren-6-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H
[Molecular Formula]

C42H72O14
[MDL Number]

MFCD00210509
[MOL File]

52286-58-5.mol
[Molecular Weight]

801.01
Chemical PropertiesBack Directory
[Melting point ]

197~198℃
[Boiling point ]

912.3±65.0 °C(Predicted)
[density ]

1.33±0.1 g/cm3(Predicted)
[storage temp. ]

?20°C
[solubility ]

Methanol (Slightly), Pyridine (Slightly)
[form ]

neat
[pka]

12.85±0.70(Predicted)
[color ]

White to Off-White
[Major Application]

food and beverages
[InChIKey]

UZIOUZHBUYLDHW-CGJOLZHFNA-N
[LogP]

3.560 (est)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P501
[Hazard Codes ]

Xn
[Risk Statements ]

22
[Safety Statements ]

2-45-24/25
[WGK Germany ]

3
[RTECS ]

LY9536900
[HS Code ]

29389090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[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
Spectrum DetailBack Directory
[Spectrum Detail]

Ginsenoside Rf(52286-58-5)1HNMR
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