6-HYDROXYFLAVANONE

OC1=CC=C2OC(CC(=O)C2=C1)C3=CC=CC=C3

InChIKey=XYHWPQUEOOBIOW-UHFFFAOYSA-N

InChI=1S/C15H12O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-8,15-16H,9H2

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

PubMed

Title	Date	PubMed
Optical isomer separation of flavanones and flavanone glycosides by nano-liquid chromatography using a phenyl-carbamate-propyl-beta-cyclodextrin chiral stationary phase.	2010-02-12	19699481
Microbial metabolism part 9. Structure and antioxidant significance of the metabolites of 5,7-dihydroxyflavone (chrysin), and 5- and 6-hydroxyflavones.	2008-04	18379084
Synthesis and immunosuppressive activity of L-rhamnopyranosyl flavonoids.	2006-06-21	16763696
Vasorelaxing effects of flavonoids: investigation on the possible involvement of potassium channels.	2004-10	15378228

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:38:47 GMT 2025` Edited by `admin` on `Mon Mar 31 20:38:47 GMT 2025`
Record UNII	1F174812MP
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

6-HYDROXYFLAVANONE

Systematic Name

English

(±)-6-HYDROXYFLAVANONE

Preferred Name

English

6-HYDROXY-2-PHENYLCHROMAN-4-ONE

Systematic Name

English

4H-1-BENZOPYRAN-4-ONE, 2,3-DIHYDRO-6-HYDROXY-2-PHENYL-

Systematic Name

English

6-HYDROXY-2-PHENYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE

Systematic Name

English

FLAVANONE, 6-HYDROXY-

Systematic Name

English

Code System Code Type Description

CAS

4250-77-5