Summary
IMPPAT Phytochemical identifier: IMPPAT3_PHYID014153
Phytochemical name: Lisetin
Synonymous chemical names:Lisetin, lisetin
External chemical identifiers:CID:CID_44260098, ZINC:ZINC000059778183
Chemical structure information
SMILES:
COc1cc2c(c(c1O)CC=C(C)C)oc1c2c(=O)c2c(o1)cc(cc2O)OInChI:
InChI=1S/C21H18O7/c1-9(2)4-5-11-18(24)15(26-3)8-12-16-19(25)17-13(23)6-10(22)7-14(17)27-21(16)28-20(11)12/h4,6-8,22-24H,5H2,1-3H3InChIKey:
KOHGMAFQELVQRG-UHFFFAOYSA-NDeepSMILES:
COcccccc6O))CC=CC)C)))))occ5c=O)cco6)cccc6O)))OFunctional groups:
cOC, cO, CC=C(C)C, coc, c=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1c2ccccc2oc2oc3ccccc3c12Scaffold Graph/Node level:
OC1C2CCCCC2OC2OC3CCCCC3C21Scaffold Graph level:
CC1C2CCCCC2CC2CC3CCCCC3C21
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Isoflavonoids
ClassyFire Subclass: Isoflav-2-enes
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Isoflavonoids
NP Classifier Class: Coumaronochromones
NP-Likeness score: 2.183
Chemical structure download