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ChemicalBook--->CAS DataBase List--->11021-13-9

11021-13-9

11021-13-9 Structure

11021-13-9 Structure
IdentificationMore
[Name]

GINSENOSIDE RB2
[CAS]

11021-13-9
[Synonyms]

GINSENOSIDE RB2
beta-d-glucopyranoside,(3-beta,12-beta)-20-((6-o-alpha-l-arabinopyranosyl-beta
-d-glucopyranosyl)oxy)-12-hydroxydammar-24-en-3-yl2-o-beta-d-glucopyranosyl-
ginsenosidec
20-[(6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranosyl)oxy]-12beta-hydroxydammar-24-en-3beta-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside
GINSENOSIDE Rb2 hplc
GINSENOSIDE RB2 WITH HPLC
arabinopyranosyl-β-D-glucopyranosyl)oxy]-12-
β-D-Glucopyranoside,(3β,12β)-20-[(6-O-α-L-
20-((6-O-alpha-L-Arabinopyranosyl-beta-D-glucopyranosyl)oxy)-12beta-hydroxydammar-24-en-3beta-yl 2-O-beta-D-glucopyranosyl-beta-D-glucopyranoside
[EINECS(EC#)]

234-251-4
[Molecular Formula]

C53H90O22
[MDL Number]

MFCD00221755
[Molecular Weight]

1079.27
[MOL File]

11021-13-9.mol
Chemical PropertiesBack Directory
[Melting point ]

197~199℃
[Boiling point ]

1117.1±65.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly, Sonicated)
[form ]

neat
[pka]

12.85±0.70(Predicted)
[color ]

White to Off-White
[Detection Methods]

NMR,HPLC
[Stability:]

Hygroscopic
[LogP]

4.730 (est)
[CAS DataBase Reference]

11021-13-9(CAS DataBase Reference)
Safety DataBack Directory
[Risk Statements ]

R22:Harmful if swallowed.
[Safety Statements ]

S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[WGK Germany ]

3
[RTECS ]

LZ5779240
[HS Code ]

29389090
Hazard InformationBack Directory
[Uses]

Ginsenoside Rb2 inhibits the catecholamines secretory responses activated by nicotinic stimulation and by direct membrane depolarization from isolated perfused rat adrenal medulla.
[Definition]

ChEBI: Ginsenoside Rb2 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, in which the hydroxy groups at positions 3 and 20 have been converted to the corresponding beta-D-glucopyranosyl-(1->2)-beta-D-glucopyranoside and alpha-L-arabinopyranosyl-(1->6)-beta-D-glucopyranoside respectively, and in which a double bond has been introduced at the 24-25 position. It has a role as a plant metabolite, an antiviral agent and a hypoglycemic agent. It is a 12beta-hydroxy steroid, a beta-D-glucoside, a disaccharide derivative, a ginsenoside and a tetracyclic triterpenoid. It derives from a hydride of a dammarane.
[storage]

4°C, protect from light
Spectrum DetailBack Directory
[Spectrum Detail]

GINSENOSIDE RB2(11021-13-9)MS
GINSENOSIDE RB2(11021-13-9)1HNMR
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