| Identification | Back Directory | [Name]
3,5,4''-TRIHYDROXY-7-METHOXYFLAVONE | [CAS]
569-92-6 | [Synonyms]
7-Methylkaempferol
Kaempferol 7-methyl ether
4H-1-Benzopyran-4-one, 3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy- | [Molecular Formula]
C16H12O6 | [MDL Number]
MFCD03419285 | [MOL File]
569-92-6.mol | [Molecular Weight]
300.26 |
| Chemical Properties | Back Directory | [Melting point ]
225-227℃ | [Boiling point ]
571.9±50.0 °C(Predicted) | [density ]
1.538 | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Soluble in methan | [form ]
powder | [pka]
6.18±0.40(Predicted) | [color ]
Yellow | [Major Application]
food and beverages | [InChI]
InChI=1S/C16H12O6/c1-21-10-6-11(18)13-12(7-10)22-16(15(20)14(13)19)8-2-4-9(17)5-3-8/h2-7,17-18,20H,1H3 | [InChIKey]
MQSZRBPYXNEFHF-UHFFFAOYSA-N | [SMILES]
C1(C2=CC=C(O)C=C2)OC2=CC(OC)=CC(O)=C2C(=O)C=1O |
| Hazard Information | Back Directory | [Uses]
food and beverages | [Definition]
ChEBI: A monomethoxyflavone that is the 7-methyl ether derivative of kaempferol. | [in vivo]
After oral administration of A. complanatus extract (10 mL/kg) to rats (equivalent to 17.6 mg/kg Rhamnocitrin), blood (approximately 0.3 mL) is collected from the ocular vein for analysis at 0, 0.083, 0.167, 0.25, 0.333, 0.5, 0.75, 1, 2, 4, 6, 9, and 12 hours after administration under ether anesthesia. The results shows that the plasma concentration of Rhamnocitrin reached its maximum at 0.65 hours, with an average Cmax of 29.57 ng/mL[1]. | [target]
HO-1 | ERK | MEK | p38MAPK | Immunology & Inflammation related |
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