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23666-13-9

23666-13-9 Structure

23666-13-9 Structure
IdentificationBack Directory
[Name]

VICENIN
[CAS]

23666-13-9
[Synonyms]

Vicenin-2
Vicenin-II
Apigenin 6,8-diglucoside
Apigenin 6,8-C-diglucoside
6,8-Di-C-β-D-glucopyranosylapigenin
Apigenin 6,8-C-di-β-D-glucopyranoside
Apigenin 6,8-di-C-glucoside (Vicenin-2)
4H-1-Benzopyran-4-one,6,8-di-b-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
6,8-Di(β-D-glucopyranosyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
2-(4-Hydroxyphenyl)-5,7-dihydroxy-6,8-bis(β-D-glucopyranosyl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 6,8-di-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
[Molecular Formula]

C27H30O15
[MDL Number]

MFCD08458851
[MOL File]

23666-13-9.mol
[Molecular Weight]

594.52
Chemical PropertiesBack Directory
[Melting point ]

>250 °C (decomp)
[Boiling point ]

974.7±65.0 °C(Predicted)
[density ]

1.758±0.06 g/cm3(Predicted)
[storage temp. ]

Hygroscopic, -20°C Freezer, Under inert atmosphere
[solubility ]

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

Solid
[pka]

5.68±0.40(Predicted)
[color ]

Light Yellow to Yellow
[Water Solubility ]

sparingly soluble in water
[Stability:]

Hygroscopic
[InChIKey]

FIAAVMJLAGNUKW-YFDIWHCFNA-N
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Desmodium sibiricum.
[Uses]

Vicenin 2 (CAS# 23666-13-9) is a biologically active compound extracted from Hypericum salsugineum and displays significant anti-cancer effects on breast carcinoma cell lines.
[Definition]

ChEBI: Isovitexin 8-C-beta-glucoside is a C-glycosyl compound that is isovitexin in which the hydrogen at position 8 is replaced by a beta-D-glucosyl residue. It has a role as a metabolite. It is a trihydroxyflavone and a C-glycosyl compound. It is functionally related to an isovitexin.
[Synthesis]

A method for simultaneous isolation of schaftoside, vicenin-2, and ecdysterone from Sagina japonica:
1. Ethanol extraction, followed by solvent partitioning to obtain an n-butanol extract.
2. The extract is fractionated on an AB-8 macroporous resin
[in vivo]

Vicenin 2 (50 mg/kg; orally administration; for 7 days) effectively reduces the MPO activity, attenuates the expression of pro-inflammatory cytokines and key inflammatory markers, in DSS-induced colitis mice[3].

Animal Model:Male C57BL/6J mice (25 g) treated with Dextran sulfate sodium (DSS)[3]
Dosage:50 mg/kg
Administration:Orally administration; for 7 days
Result:Effectively suppressed DSS-induced colitis by attenuating expressions of key inflammatory mediators.
[storage]

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

VICENIN(23666-13-9)1HNMR
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