CAS 2034-65-3 | 4H-1-Benzopyran-4-one, 3,7-dihydroxy-2-(4-hydroxyphenyl)- | CAS Number 2034-65-3

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2034-65-3 | 4H-1-Benzopyran-4-one, 3,7-dihydroxy-2-(4-hydroxyphenyl)-

CAS No: 2034-65-3 Catalog No: AG0028VH MDL No:

Product Description

Catalog Number:

AG0028VH

Chemical Name:

4H-1-Benzopyran-4-one, 3,7-dihydroxy-2-(4-hydroxyphenyl)-

CAS Number:

2034-65-3

Molecular Formula:

C15H10O5

Molecular Weight:

270.2369

IUPAC Name:

3,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

InChI:

InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)15-14(19)13(18)11-6-5-10(17)7-12(11)20-15/h1-7,16-17,19H

InChI Key:

OBWHQJYOOCRPST-UHFFFAOYSA-N

SMILES:

Oc1ccc(cc1)c1oc2cc(O)ccc2c(=O)c1O

Properties

Complexity:

422

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

270.053g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

270.24g/mol

Monoisotopic Mass:

270.053g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

87A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

2.7

Literature

Title	Journal
Synthesis and biological evaluation of novel flavonols as potential anti-prostate cancer agents.	European journal of medicinal chemistry 20120801
The flavonoid scaffold as a template for the design of modulators of the vascular Ca(v) 1.2 channels.	British journal of pharmacology 20111101
Fuscacarpans A-C, new pterocarpans from the stems of Erythrina fusca.	Fitoterapia 20100901
Flavonoids with DNA strand-scission activity from Rhus javanica var. roxburghiana.	Fitoterapia 20080101
Copper-induced peroxidation of phosphatidylserine-containing liposomes is inhibited by nanomolar concentrations of specific antioxidants.	Chemistry and physics of lipids 20071201
Comparative molecular field analysis of flavonoid inhibitors of the PIM-1 kinase.	Bioorganic & medicinal chemistry 20071001
Vasorelaxant and antioxidant activity of flavonols and flavones: structure-activity relationships.	Journal of cardiovascular pharmacology 20050901
Inhibitory effects of some flavonoids on the activity of mushroom tyrosinase.	Biochemistry. Biokhimiia 20030401