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Details

Stereochemistry ACHIRAL
Molecular Formula C16H12O7
Molecular Weight 316.2623
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EUPAFOLIN

SMILES

COC1=C(O)C2=C(OC(=CC2=O)C3=CC=C(O)C(O)=C3)C=C1O

InChI

InChIKey=FHHSEFRSDKWJKJ-UHFFFAOYSA-N
InChI=1S/C16H12O7/c1-22-16-11(20)6-13-14(15(16)21)10(19)5-12(23-13)7-2-3-8(17)9(18)4-7/h2-6,17-18,20-21H,1H3

HIDE SMILES / InChI

Molecular Formula C16H12O7
Molecular Weight 316.2623
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds.
1994 Aug 3
A "flavone-polysaccharide" redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides.
2003 Jul
Iridoids from Globularia dumulosa.
2003 Mar-Apr
Effects of natural flavones and flavonols on the kinase activity of Cdk5.
2004 Mar
Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy.
2012 Jun
Eupafolin inhibits PGE2 production and COX2 expression in LPS-stimulated human dermal fibroblasts by blocking JNK/AP-1 and Nox2/p47(phox) pathway.
2014 Sep 1
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 22:08:30 GMT 2023
Edited
by admin
on Fri Dec 15 22:08:30 GMT 2023
Record UNII
I3O7LF3GED
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EUPAFOLIN
Common Name English
NSC-122416
Code English
NEPETIN
Common Name English
FLAVONE, 3',4',5,7-TETRAHYDROXY-6-METHOXY-
Systematic Name English
4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-6-METHOXY-
Systematic Name English
5,7,3',4'-TETRAHYDROXY-6-METHOXY FLAVONE
Systematic Name English
6-METHOXYLUTEOLIN
Common Name English
Code System Code Type Description
PUBCHEM
5317284
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID10199959
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
NSC
122416
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
WIKIPEDIA
NEPETIN
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
FDA UNII
I3O7LF3GED
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
CAS
520-11-6
Created by admin on Fri Dec 15 22:08:30 GMT 2023 , Edited by admin on Fri Dec 15 22:08:30 GMT 2023
PRIMARY
Related Record Type Details
CONSTITUENT ALWAYS PRESENT -> PARENT