Summary
SMILES: Oc1ccc(c(c1)O)C1COc2c(C1=O)c(O)cc(c2)OInChI: InChI=1S/C15H12O6/c16-7-1-2-9(11(18)3-7)10-6-21-13-5-8(17)4-12(19)14(13)15(10)20/h1-5,10,16-19H,6H2InChIKey: WNHXBLZBOWXNQO-UHFFFAOYSA-N
DeepSMILES: Occcccc6)O))CCOccC6=O))cO)ccc6)O
Scaffold Graph/Node/Bond level: O=C1c2ccccc2OCC1c1ccccc1
Scaffold Graph/Node level: OC1C(C2CCCCC2)COC2CCCCC21
Scaffold Graph level: CC1C2CCCCC2CCC1C1CCCCC1
Functional groups: cC(C)=O; cO; cOC
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: Isoflavanones
Synonymous chemical names:2,4,5,7-tetrahydroxyisoflavanone, 5,7,2',4'-tetrahydroxyisoflavanone, dalbergiodin, dalbergioiden, dalbergioidin
External chemical identifiers:CID:181994; ChEBI:65; MolPort-039-141-920
Chemical structure download