U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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 PECTOLINARINGENIN

SMILES

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

InChI

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

HIDE SMILES / InChI

Molecular Formula C17H14O6
Molecular Weight 314.2895
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of two candidate flavone 8-O-methyltransferases suggests the existence of two potential routes to nevadensin in sweet basil.
2013-08
Antidiabetic effect of flavones from Cirsium japonicum DC in diabetic rats.
2010-03
Anti-inflammatory activity of pectolinarigenin and pectolinarin isolated from Cirsium chanroenicum.
2008-11
Anti-inflammatory and immunosuppressive effect of flavones isolated from Artemisia vestita.
2008-10-30
In vitro biological evaluation of novel 7-O-dialkylaminoalkyl cytotoxic pectolinarigenin derivatives against a panel of human cancer cell lines.
2008-10-15
Pectolinarin and Pectolinarigenin of Cirsium setidens Prevent the Hepatic Injury in Rats Caused by D-Galactosamine via an Antioxidant Mechanism.
2008-04
5,7-Dihydroxy-6,4'-dimeth-oxyflavone.
2007-12-06
Anticancer activity and quantitative analysis of flavone of Cirsium japonicum DC.
2007-08
Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio.
2004-07
Iridoids from Globularia dumulosa.
2003-04-25
Antiproliferative constituents in plants 10. Flavones from the leaves of Lantana montevidensis Briq. and consideration of structure-activity relationship.
2002-07
Spasmolytic effects of baccharis conferta and some of its constituents.
2002-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:44 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:44 GMT 2025
Record UNII
4U3UZ1K35N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PECTOLINARINGENIN
Common Name English
PECTOLINARIGENIN
MI  
Preferred Name English
4H-1-BENZOPYRAN-4-ONE, 5,7-DIHYDROXY-6-METHOXY-2-(4-METHOXYPHENYL)-
Systematic Name English
5,7-DIHYDROXY-4',6-DIMETHOXYFLAVONE
Systematic Name English
6-METHOXYACACETIN
Common Name English
NSC-106403
Code English
5,7-DIHYDROXY-6-METHOXY-2-(4-METHOXYPHENYL)-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
PECTOLINARIGENIN [MI]
Common Name English
Code System Code Type Description
PUBCHEM
5320438
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
MERCK INDEX
m8440
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
Pectolinarigenin
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID20199960
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
CHEBI
81336
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
NSC
106403
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
CAS
520-12-7
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
MESH
C079207
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-286-0
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY
FDA UNII
4U3UZ1K35N
Created by admin on Mon Mar 31 18:51:44 GMT 2025 , Edited by admin on Mon Mar 31 18:51:44 GMT 2025
PRIMARY