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ChemicalBook--->CAS DataBase List--->161099-37-2

161099-37-2

161099-37-2 Structure

161099-37-2 Structure
IdentificationBack Directory
[Name]

4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy-
[CAS]

161099-37-2
[Synonyms]

3-[4,6-dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-7-hydroxychromen-4-one
4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy-
[Molecular Formula]

C21H20O6
[MDL Number]

MFCD34471608
[MOL File]

161099-37-2.mol
[Molecular Weight]

368.38
Chemical PropertiesBack Directory
[storage temp. ]

4°C, protect from light
[form ]

Solid
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

Glicoricone, a phenolic compound, is isolated from a species of licorice. Glicoricone is an inhibitor of monoamine oxidase (MAO), with an IC50 of 140 μM. Glicoricone binds to estrogen receptor (ER) and shows estrogen antagonist activity[1][2].
[Definition]

ChEBI: Glicoricone is a member of isoflavones.
[Biological Activity]

Glicoricone, a phenolic compound, is isolated from a species of licorice. Glicoricone is an inhibitor of monoamine oxidase (MAO), with an IC50 of 140 μM. Glicoricone binds to estrogen receptor (ER) and shows estrogen antagonist activity[1][2].
[storage]

4°C, protect from light
[References]

[1]. Hatano T, et, al. Phenolic constituents of licorice. III. Structures of glicoricone and licofuranone, and inhibitory effects of licorice constituents on monoamine oxidase. Chem Pharm Bull (Tokyo). 1991 May;39(5):1238-43.[2]. Boonmuen N, et, al. Licorice root components in dietary supplements are selective estrogen receptor modulators with a spectrum of estrogenic and anti-estrogenic activities. Steroids. 2016 Jan;105:42-9.
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