ChemicalBook--->CAS DataBase List--->152-95-4

152-95-4

152-95-4 Structure

152-95-4 Structure
IdentificationMore
[Name]

Sophoricoside
[CAS]

152-95-4
[Synonyms]

5,7-dihydroxy-3-[4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
GENISTEIN-4'-GLUCOSIDE
GENISTEIN-4'-O-GLUCOSIDE
ISOGENISTIN
SOPHORICOSIDE
4'-beta-D-glucopyranosyloxy-5,7-dihydroxyisoflavone
5,7-Dihydroxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
4H-1-Benzopyran-4-one,3-[4-(β-
D-glucopyranosyloxy)phenyl]-5,7-dihydroxy-
Sophoricoside ,98%
3-[4-(β-D-Glucopyranosyloxy)phenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one
[Molecular Formula]

C21H20O10
[MDL Number]

MFCD01075138
[Molecular Weight]

432.38
[MOL File]

152-95-4.mol
Chemical PropertiesBack Directory
[Melting point ]

298°
[alpha ]

D20 -47° (pyridine); D20 -32° (10% aq pyridine)
[Boiling point ]

466.08°C (rough estimate)
[density ]

1.3597 (rough estimate)
[refractive index ]

1.5376 (estimate)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[solubility ]

Aqueous Base (Slightly), DMSO (Slightly, Heated), Pyridine (Slightly, Sonicated)
[form ]

Solid
[pka]

6.45±0.20(Predicted)
[color ]

White to Light Brown
[λmax]

271nm(MeOH)(lit.)
[Detection Methods]

HPLC,NMR
[Major Application]

metabolomics
vitamins, nutraceuticals, and natural products
[InChIKey]

ISQRJFLLIDGZEP-JNAFRSBINA-N
[SMILES]

C12C(O)=CC(O)=CC=1OC=C(C1C=CC(O[C@H]3[C@H](O)[C@H]([C@H](O)[C@@H](CO)O3)O)=CC=1)C2=O |&1:16,17,19,20,22,r|
[CAS DataBase Reference]

152-95-4(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[Safety Statements ]

22-24/25
[WGK Germany ]

WGK 3
[HS Code ]

29329990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

Light yellow solid
[Uses]

Genistein 4''-β-D-glucopyranoside is a metabolite of Genistein (G350000), which exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation.
[Definition]

ChEBI: Sophoricoside is an isoflavonoid and an acrovestone.
[Biological Activity]

Sophoricoside (SOP) improves lipopolysaccharides (LPS)-induced acute lung injury (ALI) in mice by activating the adenosine monophosphate-activated protein kinase (AMPK)/nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway. It also improves contact dermatitis by inhibiting the nuclear factor-kappa B (NF-KB) pathway in B cells in mice model.''Sophoricoside elicits anti-cancerimmunosuppressiveand anti-inflammatory activities. It inhibits proinflammatory cytokine production in human mast cells and has the potential to tre at allergic inflammation diseases.
[in vivo]

When the Sophoricoside is orally administered 1 h before compound 48/80 injections, the scratching behaviors is reduced. The inhibition rate of Sophoricoside (2 mg/kg) is approximately 41.21%. Orally administered Sophoricoside inhibits the scratching behaviors by 47.31%. When mice are treated for 2 weeks with Sophoricoside, the atopic dermatitis is recovered to a significant extent[1].

Spectrum DetailBack Directory
[Spectrum Detail]

Sophoricoside(152-95-4)1HNMR
Sophoricoside(152-95-4)IR1
Sophoricoside(152-95-4)IR2
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