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IMPPAT Phytochemical information:
Flemistrictin D
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY008564
Phytochemical name:
Flemistrictin D
Synonymous chemical names:
flemistrictin d
External chemical identifiers:
CID:42607712
,
ZINC:ZINC000015216714
Chemical structure information
SMILES:
COc1c(C(=O)CCc2ccccc2)c(O)c2c(c1O)OC(C=C2)(C)C
InChI:
InChI=1S/C21H22O5/c1-21(2)12-11-14-17(23)16(20(25-3)18(24)19(14)26-21)15(22)10-9-13-7-5-4-6-8-13/h4-8,11-12,23-24H,9-10H2,1-3H3
InChIKey:
LJNJHJBBLPMBSN-UHFFFAOYSA-N
DeepSMILES:
COccC=O)CCcccccc6)))))))))cO)ccc6O))OCC=C6))C)C
Functional groups:
cC(C)=O, cC=CC, cO, cOC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C(CCc1ccccc1)c1ccc2c(c1)C=CCO2
Scaffold Graph/Node level:
OC(CCC1CCCCC1)C1CCC2OCCCC2C1
Scaffold Graph level:
CC(CCC1CCCCC1)C1CCC2CCCCC2C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Phenylpropanoids and polyketides
ClassyFire Class:
Linear 1,3-diarylpropanoids
ClassyFire Subclass:
Chalcones and dihydrochalcones
NP Classifier Biosynthetic pathway:
Shikimates and Phenylpropanoids
NP Classifier Superclass:
Flavonoids
NP Classifier Class:
Chalcones
NP-Likeness score:
1.935
Chemical structure download
2D:
2D MOL
2D MOL2
2D SDF
3D:
3D MOL
3D MOL2
3D SDF
3D PDB
3D PDBQT
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