Summary

IMPPAT Phytochemical identifier: IMPHY011931

Phytochemical name: Hinokinin

Synonymous chemical names:
(+-)-hinokinin, (-) hinokinin, (-)-hinokinin, (-)hinokinin, hinkokinin, hinokinin

External chemical identifiers:
CID:442879, ChEMBL:CHEMBL242011, ChEBI:5722, ZINC:ZINC000001872258, SureChEMBL:SCHEMBL1121862, MolPort-039-338-821

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Chemical structure information

SMILES:
O=C1OC[C@@H]([C@H]1Cc1ccc2c(c1)OCO2)Cc1ccc2c(c1)OCO2

InChI:
InChI=1S/C20H18O6/c21-20-15(6-13-2-4-17-19(8-13)26-11-24-17)14(9-22-20)5-12-1-3-16-18(7-12)25-10-23-16/h1-4,7-8,14-15H,5-6,9-11H2/t14-,15+/m0/s1

InChIKey:
DDWGQGZPYDSYEL-LSDHHAIUSA-N

DeepSMILES:
O=COC[C@@H][C@H]5Ccccccc6)OCO5))))))))))Ccccccc6)OCO5

Functional groups:
COC(C)=O, c1cOCO1

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1OCC(Cc2ccc3c(c2)OCO3)C1Cc1ccc2c(c1)OCO2

Scaffold Graph/Node level:
OC1OCC(CC2CCC3OCOC3C2)C1CC1CCC2OCOC2C1

Scaffold Graph level:
CC1CCC(CC2CCC3CCCC3C2)C1CC1CCC2CCCC2C1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lignans, neolignans and related compounds

ClassyFire Class: Furanoid lignans

ClassyFire Subclass: Tetrahydrofuran lignans

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Lignans

NP Classifier Class: Dibenzylbutyrolactone lignans

NP-Likeness score: 1.096

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Chemical structure download