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Supplier NameBOC Sciences
ContactLinna Green
Tel+16314854226
Mobile+16314854226
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Emailinfo@bocsci.com
Websitehttps://www.bocsci.com/
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LinkedInhttps://www.linkedin.com/company/boc-sciences
Product NameChamaechromone
Synonymsaechromone
Chamaechromone
(+)-Chamaechromone
3-[1,1-bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl]-5,7-dihydroxychromen-4-one
3-(1,1-Bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl)-5,7-dihydroxy-4H-chromen-4-one

Synonyms

aechromone
Chamaechromone
(+)-Chamaechromone
3-[1,1-bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl]-5,7-dihydroxychromen-4-one
3-(1,1-Bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl)-5,7-dihydroxy-4H-chromen-4-one
(+)-3-'1-'Bis(4-hydroxyphenyl)methyl-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl-5,7-dihydroxy-4H-1-benzopyran-4-one
(+)-3-[1-[Bis(4-hydroxyphenyl)methyl]-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one
CAS93413-00-4
EINECS
Chemical FormulaC30H22O10
Molecular Weight542.5
inchi
Package5 mg
Price$1,344
DescriptionsChamaechromone
Chamaechromone is isolated from the roots of Stellera chamaeja sme. Chamaechromone can undergo extensive phase I and phase II metabolism in rat. Chamaechromone has anti-HBV and insecticidal activity. The hydroxylation of Chamaechromone is inhibited by α-naphthoflavone, and predominantly catalyzed by recombinant human cytochrome P450 1A2.
Supplier Websitehttps://natuprod.bocsci.com/product/chamaechromone-cas-93413-00-4-266942.html
Last Update2025-04-30 11:27:47
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