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ChemicalBook--->CAS DataBase List--->51011-05-3

51011-05-3

51011-05-3 Structure

51011-05-3 Structure
IdentificationBack Directory
[Name]

6''-O-MALONYLGENISTIN
[CAS]

51011-05-3
[Synonyms]

Genistin malonate
6''-O-MALONYLGENISTIN
Genistin 6''-O-Malonate
O-Malonylgenistin, 6''-
6-O-Malonylgenistin, free acid
6''-O-MALONYLGENISTIN USP/EP/BP
7-O-Glucosyl-6''-Malonyl Genistein
6''-O-Malonylgenistin (Malonylgenistin
Genistein-7-O-beta-D-glucosyl-6''-O-malonate
5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-O-(car...
5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-O-(carboxyacetyl)-beta-D-glucopyranoside
7-[[6-O-(Carboxyacetyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,7-[[6-O-(carboxyacetyl)-b-D-glucopyranosyl]oxy]-5-hydroxy-3-(4-hydroxyphenyl)-
4H-1-Benzopyran-4-one, 7-[[6-O-(carboxyacetyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-3-(4-hydroxyphenyl)-
4H-1-Benzopyran-4-one, 7-6-O-(carboxyacetyl)-.beta.-D-glucopyranosyloxy-5-hydroxy-3-(4-hydroxyphenyl)-
[Molecular Formula]

C24H22O13
[MDL Number]

MFCD02684045
[MOL File]

51011-05-3.mol
[Molecular Weight]

518.42
Chemical PropertiesBack Directory
[Boiling point ]

880.2±65.0 °C(Predicted)
[density ]

1.654±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20
[form ]

Solid
[pka]

2.70±0.32(Predicted)
[color ]

White to light yellow
[LogP]

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


GHS05,GHS07,GHS02
[Signal word ]

Danger
[Hazard statements ]

H302+H312+H332-H314-H225
[Precautionary statements ]

P501-P261-P270-P240-P210-P233-P243-P241-P242-P271-P264-P280-P370+P378-P362+P364-P303+P361+P353-P301+P330+P331-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P403+P235-P405
[HS Code ]

2932990090
Hazard InformationBack Directory
[Uses]

A metabolite of isoflavone derivatives. A derivative of Genistin (G350020). Inhibitor.
[Definition]

ChEBI: Malonylgenistin is a glycosyloxyisoflavone that is genistin in which the hydroxy hydrogen at position 6'' has been replaced by a malonyl group. It has a role as a plant metabolite. It is a glycosyloxyisoflavone, a hydroxyisoflavone, a malonate ester, a monosaccharide derivative and a beta-D-glucoside. It is functionally related to a genistein 7-O-beta-D-glucoside.
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