Summary

IMPPAT Phytochemical identifier: IMPHY015794

Phytochemical name: Licoisoflavanone

Synonymous chemical names:
licoisoflavanone

External chemical identifiers:
CID:392443, MolPort-046-508-969

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Chemical structure information

SMILES:
Oc1cc(O)c2c(c1)OCC(C2=O)c1ccc2c(c1O)C=CC(O2)(C)C

InChI:
InChI=1S/C20H18O6/c1-20(2)6-5-12-15(26-20)4-3-11(18(12)23)13-9-25-16-8-10(21)7-14(22)17(16)19(13)24/h3-8,13,21-23H,9H2,1-2H3

InChIKey:
JNDPLDZUOFZXIG-UHFFFAOYSA-N

DeepSMILES:
OcccO)ccc6)OCCC6=O))cccccc6O))C=CCO6)C)C

Functional groups:
cC(C)=O, cC=CC, cO, cOC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1c2ccccc2OCC1c1ccc2c(c1)C=CCO2

Scaffold Graph/Node level:
OC1C(C2CCC3OCCCC3C2)COC2CCCCC21

Scaffold Graph level:
CC1C2CCCCC2CCC1C1CCC2CCCCC2C1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Isoflavonoids

ClassyFire Subclass: Isoflavans

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Isoflavonoids

NP Classifier Class: Isoflavanones, Isoflavones

NP-Likeness score: 2.678

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Chemical structure download