Description:
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.
- Molecular Weight:542.5
- Boiling Point:906.4±65.0 °C at 760 mmHg
- Purity:98.0%
Molecular Formula:
C30H22O10
Canonical SMILES:
C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=CC(=CC(=C4C3=O)O)O)C(=O)C5=C(C=C(C=C5O)O)O)O
InChI:
InChI=1S/C30H22O10/c31-16-5-1-14(2-6-16)25(15-3-7-17(32)8-4-15)26(30(39)27-21(35)9-18(33)10-22(27)36)20-13-40-24-12-19(34)11-23(37)28(24)29(20)38/h1-13,25-26,31-37H
InChIKey:
KLKLIUIRQAMTAJ-UHFFFAOYSA-N
Solubility:
In vitro: 10 mM in DMSO
Appearance:
Yellow powder
Storage: Store at -20°C
Synonyms:
3-[1,1-bis(4-hydroxyphenyl)-3-oxo-3-(2,4,6-trihydroxyphenyl)propan-2-yl]-5,7-dihydroxychromen-4-one Más detalles se encuentran
aquí