CAS 842-01-3
:7,8-dihydroxy-4-phenyl-2H-chromen-2-one
Description:
7,8-Dihydroxy-4-phenyl-2H-chromen-2-one, also known as flavone, is a naturally occurring compound belonging to the flavonoid class of phytochemicals. This substance features a chromone backbone with hydroxyl groups at the 7 and 8 positions and a phenyl group at the 4 position, contributing to its unique chemical properties. It is characterized by its yellow color and is soluble in organic solvents, while exhibiting limited solubility in water. The compound is known for its antioxidant properties, which can help in scavenging free radicals, and it may possess anti-inflammatory and antimicrobial activities. Additionally, it has been studied for its potential health benefits, including cardiovascular protection and anti-cancer effects. The presence of hydroxyl groups enhances its reactivity and ability to form hydrogen bonds, influencing its biological activity and interactions with other molecules. As a compound of interest in both medicinal chemistry and natural product research, 7,8-dihydroxy-4-phenyl-2H-chromen-2-one continues to be explored for its therapeutic potential.
Formula:C15H10O4
InChI:InChI=1/C15H10O4/c16-12-7-6-10-11(9-4-2-1-3-5-9)8-13(17)19-15(10)14(12)18/h1-8,16,18H
InChI key:JRVIIPJSVKTPBK-UHFFFAOYSA-N
SMILES:c1ccc(cc1)c1cc(=O)oc2c1ccc(c2O)O
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4-Phenyl-7,8-dihydroxycoumarin
CAS:4-Phenyl-7,8-dihydroxycoumarinFormula:C15H10O4Purity:99.5%Molecular weight:254.247,8-Dihydroxy-4-Phenyl-2H-Chromen-2-One
CAS:7,8-Dihydroxy-4-Phenyl-2H-Chromen-2-OneFormula:C15H10O4Purity:98%Molecular weight:254.247,8-Dihydroxy-4-Phenyl-2H-Chromen-2-One
CAS:Formula:C15H10O4Purity:98%Color and Shape:SolidMolecular weight:254.23754-Phenyl-7,8-dihydroxycoumarin
CAS:4-Phenyl-7,8-dihydroxycoumarin (7,8-Dihydroxy-4-phenylcoumarin) inhibits the activity of Staphylococcus aureus DNA helicaseFormula:C15H10O4Purity:99.5%Color and Shape:SolidMolecular weight:254.23757,8-Dihydroxy-4-phenylcoumarin
CAS:7,8-Dihydroxy-4-phenylcoumarin (7,8-DPC) is a coumarin derivative that inhibits human cytochrome P450 enzymes. It binds to the heme group of the enzyme and is reversible by hydroxylation. 7,8-DPC has been shown to inhibit catalytic activity in rat liver microsomes and recombinant human cytochrome P450 enzymes. This molecule has also been shown to be an irreversible inhibitor of human cytochrome P450 2C9. The carbonyl group found on the 7,8-DPC molecule's structure is responsible for its inhibitory activities.
Formula:C15H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:254.24 g/mol
