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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)C=C2OC(=CC(=O)C2=C1O)C3=CC(O)=C(O)C=C3

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
Eupafolin inhibits PGE2 production and COX2 expression in LPS-stimulated human dermal fibroblasts by blocking JNK/AP-1 and Nox2/p47(phox) pathway.
2014-09-01
Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy.
2012-06
An unusual dimeric guaianolide with antiprotozoal activity and further sesquiterpene lactones from Eupatoriumperfoliatum.
2011-05
Flavonoids and phenolic compounds from Rosmarinus officinalis.
2010-05-12
Chemical fingerprint and quantitative analysis of Salvia plebeia R.Br. by high-performance liquid chromatography.
2008-09-10
A novel daucosterol derivative and antibacterial activity of compounds from Arctotis arctotoides.
2007-08
Anti-inflammatory activity of flavonoids from Eupatorium arnottianum.
2007-07-25
Topical anti-inflammatory activity of flavonoids and a new xanthone from Santolina insularis.
2005-03-25
Cytotoxic activity of nepetin, a flavonoid from Eupatorium ballotaefolium HBK.
2004-12
Effects of natural flavones and flavonols on the kinase activity of Cdk5.
2004-03
A "flavone-polysaccharide" redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides.
2003-07
Iridoids from Globularia dumulosa.
2003-04-25
Flavonoids of Inula britannica protect cultured cortical cells from necrotic cell death induced by glutamate.
2002-04-01
Application of the electrotopological state index to QSAR analysis of flavone derivatives as HIV-1 integrase inhibitors.
1996-12
Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds.
1994-08-03
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:24:32 GMT 2025
Edited
by admin
on Mon Mar 31 20:24:32 GMT 2025
Record UNII
I3O7LF3GED
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-122416
Preferred Name English
EUPAFOLIN
Common Name 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 Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID10199959
Created by admin on Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
NSC
122416
Created by admin on Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
WIKIPEDIA
NEPETIN
Created by admin on Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
FDA UNII
I3O7LF3GED
Created by admin on Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
CAS
520-11-6
Created by admin on Mon Mar 31 20:24:32 GMT 2025 , Edited by admin on Mon Mar 31 20:24:32 GMT 2025
PRIMARY
Related Record Type Details
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