| Company Name: |
Shanghai Tauto Biotech Co., Ltd.
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| Tel: |
021-51320588 |
| Email: |
tauto@tautobiotech.com |
| Products Intro: |
Product Name:Glicoricone
CAS:161099-37-2
Purity:98% Package:10mg;20mg;1gm;5gm;10gm;1KG
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| Company Name: |
Wuhan ChemFaces Biochemical Co., Ltd.
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| Tel: |
18607101326 15172504745 |
| Email: |
aileen@chemfaces.com |
| Products Intro: |
Product Name:Glicoricone
CAS:161099-37-2
Purity:>=98% Package:5mg ,10mg ,20mg ,50mg ,100mg; 200mg; 500mg or according to customer requirements Remarks:1908/5mg
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| | 4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy- Basic information |
| | 4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy- Chemical Properties |
| storage temp. | 4°C, protect from light |
| | 4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy- Usage And Synthesis |
| 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]. | | 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. |
| | 4H-1-Benzopyran-4-one,3-[4,6-dihydroxy-2-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-7-hydroxy- Preparation Products And Raw materials |
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