IMPPAT: Indian Medicinal Plants, Phytochemistry And Therapeutics
a curated database
HOME
BROWSE
BASIC SEARCH
ADVANCED SEARCH
STATISTICS
ACKNOWLEDGEMENT
HELP
IMPPAT Phytochemical information:
Sophoronol
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY001572
Phytochemical name:
Sophoronol
Synonymous chemical names:
sophoronol
External chemical identifiers:
CID:15138471
,
ChEMBL:CHEMBL550446
Chemical structure information
SMILES:
COc1c2C=CC(Oc2ccc1C1(O)COc2c(C1=O)c(O)cc(c2)O)(C)C
InChI:
InChI=1S/C21H20O7/c1-20(2)7-6-12-15(28-20)5-4-13(18(12)26-3)21(25)10-27-16-9-11(22)8-14(23)17(16)19(21)24/h4-9,22-23,25H,10H2,1-3H3
InChIKey:
SYJLLCMGTNPNAB-UHFFFAOYSA-N
DeepSMILES:
COccC=CCOc6ccc%10CO)COccC6=O))cO)ccc6)O))))))))))))))C)C
Functional groups:
CO, cC(C)=O, cC=CC, cO, cOC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1c2ccccc2OCC1c1ccc2c(c1)C=CCO2
Scaffold Graph/Node level:
OC1C(C2CCC3OCCCC3C2)COC2CCCCC21
Scaffold Graph level:
CC1C2CCCCC2CCC1C1CCC2CCCCC2C1
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
NP-Likeness score:
2.643
Chemical structure download
2D:
2D MOL
2D MOL2
2D SDF
3D:
3D MOL
3D MOL2
3D SDF
3D PDB
3D PDBQT
Top