IMPPAT: Indian Medicinal Plants, Phytochemistry And Therapeutics
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IMPPAT Phytochemical information:
Pimpinellin
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY000745
Phytochemical name:
Pimpinellin
Synonymous chemical names:
pimpinellin
External chemical identifiers:
CID:4825
,
ChEMBL:CHEMBL1491809
,
ChEBI:8213
,
ZINC:ZINC000000898309
,
FDASRS:D419UK1B4L
,
SureChEMBL:SCHEMBL2255899
,
MolPort-000-881-658
Chemical structure information
SMILES:
COc1c(OC)c2occc2c2c1ccc(=O)o2
InChI:
InChI=1S/C13H10O5/c1-15-11-7-3-4-9(14)18-10(7)8-5-6-17-12(8)13(11)16-2/h3-6H,1-2H3
InChIKey:
BQPRWZCEKZLBHL-UHFFFAOYSA-N
DeepSMILES:
COccOC))coccc5cc9ccc=O)o6
Functional groups:
c=O, cOC, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=c1ccc2ccc3occc3c2o1
Scaffold Graph/Node level:
OC1CCC2CCC3OCCC3C2O1
Scaffold Graph level:
CC1CCC2CCC3CCCC3C2C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Phenylpropanoids and polyketides
ClassyFire Class:
Coumarins and derivatives
ClassyFire Subclass:
Furanocoumarins
NP Classifier Biosynthetic pathway:
Shikimates and Phenylpropanoids
NP Classifier Superclass:
Coumarins
NP Classifier Class:
Furocoumarins
NP-Likeness score:
1.356
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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