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Details

Stereochemistry ACHIRAL
Molecular Formula C16H12O6
Molecular Weight 300.2629
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-O-METHYLLUTEOLIN

SMILES

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

InChI

InChIKey=RRRSSAVLTCVNIQ-UHFFFAOYSA-N
InChI=1S/C16H12O6/c1-21-9-5-12(19)16-13(20)7-14(22-15(16)6-9)8-2-3-10(17)11(18)4-8/h2-7,17-19H,1H3

HIDE SMILES / InChI

Molecular Formula C16H12O6
Molecular Weight 300.2629
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A weakly antimalarial biflavanone from Rhus retinorrhoea.
2001 Oct
Antioxidant activity of chemical components from sage (Salvia officinalis L.) and thyme (Thymus vulgaris L.) measured by the oil stability index method.
2002 Mar 27
Acasiane A and B and farnesirane A and B, diterpene derivatives from the roots of Acacia farnesiana.
2009 Feb
[Studies on the chemical constituents from Lobelia chinensis].
2010 Nov
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:34:34 GMT 2023
Edited
by admin
on Fri Dec 15 18:34:34 GMT 2023
Record UNII
732GA1Z079
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-O-METHYLLUTEOLIN
Common Name English
3'-HYDROXYGENKWANIN
Common Name English
4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-7-METHOXY-
Systematic Name English
LUTEOLIN 7-METHYL ETHER
Common Name English
Code System Code Type Description
CAS
20243-59-8
Created by admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
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EPA CompTox
DTXSID50942365
Created by admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
PRIMARY
PUBCHEM
5318214
Created by admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
PRIMARY
FDA UNII
732GA1Z079
Created by admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
PRIMARY