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Details

Stereochemistry ACHIRAL
Molecular Formula C17H14O6
Molecular Weight 314.2895
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ERMANIN

SMILES

COC1=CC=C(C=C1)C2=C(OC)C(=O)C3=C(O2)C=C(O)C=C3O

InChI

InChIKey=RJCJVIFSIXKSAH-UHFFFAOYSA-N
InChI=1S/C17H14O6/c1-21-11-5-3-9(4-6-11)16-17(22-2)15(20)14-12(19)7-10(18)8-13(14)23-16/h3-8,18-19H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Polymethylated myricetin in trichomes of the wild tomato species Solanum habrochaites and characterization of trichome-specific 3'/5'- and 7/4'-myricetin O-methyltransferases.
2011-04
Anti-HIV-1 diterpenoids from leaves and twigs of Polyalthia sclerophylla.
2010-05
In vitro antileishmanial, antiplasmodial and cytotoxic activities of phenolics and triterpenoids from Baccharis dracunculifolia D. C. (Asteraceae).
2009-12
Modulation of P-glycoprotein-mediated resistance by kaempferol derivatives isolated from Zingiber zerumbet.
2007-06
Prostaglandin inhibitory and antioxidant components of Cistus laurifolius, a Turkish medicinal plant.
2006-12-06
Inhibition of inducible nitric oxide synthase and cyclooxygenase-2 expression by flavonoids isolated from Tanacetum microphyllum.
2006-11
Antimycobacterial agents from selected Mexican medicinal plants.
2005-09
Flavonoids and aromatic compounds from the rhizomes of Zingiber zerumbet.
2004-04
Flavonoids and a sesquiterpene lactone from Tanacetum microphyllum inhibit anti-inflammatory mediators in LPS-stimulated mouse peritoneal macrophages.
2004-01
Phytotoxic compounds from Flourensia cernua.
2003-09
Antimycobacterial flavones from Haplopappus sonorensis.
2003-04
Antipoliovirus flavonoids from Psiadia dentata.
2001-09
Samioside, a new phenylethanoid glycoside with free-radical scavenging and antimicrobial activities from Phlomis samia.
2001-08
Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds.
1994-08-03
Differential inhibitory effects of various flavonoids on the activities of reverse transcriptase and cellular DNA and RNA polymerases.
1990-07-05
Patents

Patents

Name Type Language
ERMANIN
Common Name English
NSC-31882
Preferred Name English
5,7-DIHYDROXY-3,4'-DIMETHOXYFLAVONE
Systematic Name English
5,7-DIHYDROXY-3-METHOXY-2-(4-METHOXYPHENYL)CHROMEN-4-ONE
Systematic Name English
KAEMPFEROL 3,4'-DI-O-METHYL ETHER
Common Name English
5,7-DIHYDROXY-3-METHOXY-2-(4-METHOXYPHENYL)-4-BENZOPYRONE
Systematic Name English
Code System Code Type Description
CHEBI
146142
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
WIKIPEDIA
ERMANIN
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
NSC
31882
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
244-093-8
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
CAS
20869-95-8
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
PUBCHEM
5352001
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
FDA UNII
850D90YJN3
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID90174986
Created by admin on Mon Mar 31 18:58:19 GMT 2025 , Edited by admin on Mon Mar 31 18:58:19 GMT 2025
PRIMARY