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IMPPAT Phytochemical information:
Pentanoic acid, 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY007858
Phytochemical name:
Pentanoic acid, 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester
Synonymous chemical names:
curassavine
External chemical identifiers:
CID:155104
Chemical structure information
SMILES:
CCC(C(C(=O)OCC1CCN2C1CCC2)(C(O)C)O)C
InChI:
InChI=1S/C16H29NO4/c1-4-11(2)16(20,12(3)18)15(19)21-10-13-7-9-17-8-5-6-14(13)17/h11-14,18,20H,4-10H2,1-3H3
InChIKey:
VBLBKKUAYMFOAG-UHFFFAOYSA-N
DeepSMILES:
CCCCC=O)OCCCCNC5CCC5)))))))))))CO)C))O))C
Functional groups:
CN(C)C, CO, COC(C)=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1CC2CCCN2C1
Scaffold Graph/Node level:
C1CC2CCCN2C1
Scaffold Graph level:
C1CC2CCCC2C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Pyrrolizidines
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Ornithine alkaloids
NP Classifier Class:
Pyrrolizidine alkaloids
NP-Likeness score:
1.049
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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