Summary
IMPPAT Phytochemical identifier: IMPHY008665
Phytochemical name: 2-(3,4-Dimethoxyphenyl)-7-hydroxy-4H-chromen-4-one
Synonymous chemical names:7-hydroxy-3',4'-dimethoxyflavone, flavone, 7-hydroxy-3',4'-dimethoxy
External chemical identifiers:CID:5378518, ChEMBL:CHEMBL345778, ZINC:ZINC000005640361, FDASRS:5JN0O0F1KZ, SureChEMBL:SCHEMBL4400168, MolPort-047-110-216
Chemical structure information
SMILES:
COc1cc(ccc1OC)c1cc(=O)c2c(o1)cc(cc2)OInChI:
InChI=1S/C17H14O5/c1-20-14-6-3-10(7-17(14)21-2)15-9-13(19)12-5-4-11(18)8-16(12)22-15/h3-9,18H,1-2H3InChIKey:
MEDOAKSPIIOKFU-UHFFFAOYSA-NDeepSMILES:
COcccccc6OC)))))ccc=O)cco6)cccc6))OFunctional groups:
c=O, cO, cOC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1cc(-c2ccccc2)oc2ccccc12Scaffold Graph/Node level:
OC1CC(C2CCCCC2)OC2CCCCC12Scaffold Graph level:
CC1CC(C2CCCCC2)CC2CCCCC12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Flavonoids
ClassyFire Subclass: O-methylated flavonoids
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Flavonoids
NP Classifier Class: Flavones
NP-Likeness score: 0.705
Chemical structure download