Identification | Back Directory | [Name]
(+)-3-[1-[Bis(4-hydroxyphenyl)methyl]-2-oxo-2-(2,4,6-trihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one | [CAS]
93413-00-4 | [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 | [Molecular Formula]
C30H22O10 | [MDL Number]
MFCD27969124 | [MOL File]
93413-00-4.mol | [Molecular Weight]
542.49 |
Chemical Properties | Back Directory | [Boiling point ]
906.4±65.0 °C(Predicted) | [density ]
1.594±0.06 g/cm3(Predicted) | [form ]
Solid | [pka]
6.22±0.20(Predicted) | [color ]
Off-white to light yellow |
Hazard Information | Back Directory | [Uses]
Chamaechromone is a biflavonoid ingredient isolated from the roots of Stellera chamaejasme L. (Thymelaeaceae). Chamaechromone possesses anti-hepatitis B virus (HBV) effects against the surface antigen of HBV (HBsAg) secretion and has insecticidal activities[1]. | [References]
[1] Yan Lou, et al.Metabolites characterization of chamaechromone in vivo and in vitro by using ultra-performance liquid chromatography/Xevo G2 quadrupole time-of-flight tandem mass spectrometry. J Ethnopharmacol DOI:10.1016/j.jep.2013.10.027 |
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