5,4'-DIHYDROXY-7,3',5'-TRIMETHOXYFLAVONE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C18H16O7
Molecular Weight	344.3154
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 5,4'-DIHYDROXY-7,3',5'-TRIMETHOXYFLAVONE

Structure Search

SMILES

COC1=CC2=C(C(=O)C=C(O2)C3=CC(OC)=C(O)C(OC)=C3)C(O)=C1

InChI

InChIKey=VIKKUMIXGIDYKY-UHFFFAOYSA-N

InChI=1S/C18H16O7/c1-22-10-6-11(19)17-12(20)8-13(25-14(17)7-10)9-4-15(23-2)18(21)16(5-9)24-3/h4-8,19,21H,1-3H3

HIDE SMILES / InChI

Molecular Formula	C18H16O7
Molecular Weight	344.3154
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Iridoid glucosides and flavones from the aerial parts of Avicennia marina.	2006 Jul	17193312

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:33:32 GMT 2025` Edited by `admin` on `Mon Mar 31 23:33:32 GMT 2025`
Record UNII	A27NFM7JDA
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

4H-1-BENZOPYRAN-4-ONE, 5-HYDROXY-2-(4-HYDROXY-3,5-DIMETHOXYPHENYL)-7-METHOXY-

Preferred Name

English

5,4'-DIHYDROXY-7,3',5'-TRIMETHOXYFLAVONE

Systematic Name

English

Code System Code Type Description

PUBCHEM

15222911

Created by admin on Mon Mar 31 23:33:32 GMT 2025 , Edited by admin on Mon Mar 31 23:33:32 GMT 2025

PRIMARY

CHEBI

67647

Created by admin on Mon Mar 31 23:33:32 GMT 2025 , Edited by admin on Mon Mar 31 23:33:32 GMT 2025

PRIMARY

CAS

107316-94-9

Created by admin on Mon Mar 31 23:33:32 GMT 2025 , Edited by admin on Mon Mar 31 23:33:32 GMT 2025

PRIMARY

FDA UNII

A27NFM7JDA

Created by admin on Mon Mar 31 23:33:32 GMT 2025 , Edited by admin on Mon Mar 31 23:33:32 GMT 2025

PRIMARY

Related Record Type Details


					46AM2VJ0AW

ACAI

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

ORAC value expressed as umol TE/g for this compound is 4458.0 +/- 408.8. ORAC is a chemical antioxidant assay that is based on the inhibition of the peroxyl-radical induced oxidation initiated by thermal decomposition of AAPH.