Summary
IMPPAT Phytochemical identifier: IMPHY000611
Phytochemical name: Daidzin
Synonymous chemical names:daidzein-7-glucoside, daidzin
External chemical identifiers:CID:107971, ChEMBL:CHEMBL486422, ChEBI:42202, ZINC:ZINC000004098610, FDASRS:4R2X91A5M5, SureChEMBL:SCHEMBL315373, MolPort-000-002-994
Chemical structure information
SMILES:
OC[C@H]1O[C@@H](Oc2ccc3c(c2)occ(c3=O)c2ccc(cc2)O)[C@@H]([C@H]([C@@H]1O)O)OInChI:
InChI=1S/C21H20O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,9,16,18-23,25-27H,8H2/t16-,18-,19+,20-,21-/m1/s1InChIKey:
KYQZWONCHDNPDP-QNDFHXLGSA-NDeepSMILES:
OC[C@H]O[C@@H]Occcccc6)occc6=O))cccccc6))O))))))))))))))[C@@H][C@H][C@@H]6O))O))OFunctional groups:
CO, c=O, cO, cO[C@@H](C)OC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1c(-c2ccccc2)coc2cc(OC3CCCCO3)ccc12Scaffold Graph/Node level:
OC1C(C2CCCCC2)COC2CC(OC3CCCCO3)CCC21Scaffold Graph level:
CC1C(C2CCCCC2)CCC2CC(CC3CCCCC3)CCC21
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Isoflavonoids
ClassyFire Subclass: Isoflavonoid o-glycosides
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Isoflavonoids
NP Classifier Class: Isoflavones
NP-Likeness score: 1.539
Chemical structure download