Summary
SMILES: CC(=CCc1c(O)cc2c(c1O)c(=O)c(co2)c1ccc(c2c1OC(C)(C)C(C2)O)O)CInChI: InChI=1S/C25H26O7/c1-12(2)5-6-14-18(27)10-19-21(22(14)29)23(30)16(11-31-19)13-7-8-17(26)15-9-20(28)25(3,4)32-24(13)15/h5,7-8,10-11,20,26-29H,6,9H2,1-4H3InChIKey: MSUIWRTZOBLKNX-UHFFFAOYSA-N
DeepSMILES: CC=CCccO)cccc6O))c=O)cco6))cccccc6OCC)C)CC6)O))))))O))))))))))))))C
Scaffold Graph/Node/Bond level: O=c1c(-c2cccc3c2OCCC3)coc2ccccc12
Scaffold Graph/Node level: OC1C2CCCCC2OCC1C1CCCC2CCCOC21
Scaffold Graph level: CC1C2CCCCC2CCC1C1CCCC2CCCCC21
Functional groups: CC=C(C)C; cO; c=O; coc; cOC; CO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Isoflavonoids
ClassyFire Subclass: Isoflavans
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Isoflavonoids
NP Classifier Class: Isoflavones
Synonymous chemical names:Lupinisolone C, lupinisolone c
External chemical identifiers:CID:CID_14237667
Chemical structure download