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IMPPAT Phytochemical information:
trans-Piperitone epoxide
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY015096
Phytochemical name:
trans-Piperitone epoxide
Synonymous chemical names:
trans-piperitone epoxide
External chemical identifiers:
CID:12492569
,
FDASRS:Y4ZF10N3DK
Chemical structure information
SMILES:
CC([C@H]1CC[C@@]2([C@H](C1=O)O2)C)C
InChI:
InChI=1S/C10H16O2/c1-6(2)7-4-5-10(3)9(12-10)8(7)11/h6-7,9H,4-5H2,1-3H3/t7-,9+,10-/m1/s1
InChIKey:
IAFONZHDZMCORS-FKTZTGRPSA-N
DeepSMILES:
CC[C@H]CC[C@@][C@H]C6=O))O3))C)))))C
Functional groups:
C[C@@]1(C)O[C@H]1C(C)=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCCC2OC12
Scaffold Graph/Node level:
OC1CCCC2OC12
Scaffold Graph level:
CC1CCCC2CC12
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Oxepanes
NP Classifier Biosynthetic pathway:
Terpenoids
NP Classifier Superclass:
Monoterpenoids
NP Classifier Class:
Menthane monoterpenoids, Monocyclic monoterpenoids
NP-Likeness score:
3.039
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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