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IMPPAT Phytochemical information:
(3R,5S)-3-methyl-5-[(1E)-3-methylbuta-1,3-dienyl]oxolan-2-one
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY004220
Phytochemical name:
(3R,5S)-3-methyl-5-[(1E)-3-methylbuta-1,3-dienyl]oxolan-2-one
Synonymous chemical names:
marmelolactone a
External chemical identifiers:
CID:101282726
,
ZINC:ZINC000196811093
Chemical structure information
SMILES:
CC(=C)/C=C/[C@H]1OC(=O)[C@@H](C1)C
InChI:
InChI=1S/C10H14O2/c1-7(2)4-5-9-6-8(3)10(11)12-9/h4-5,8-9H,1,6H2,2-3H3/b5-4+/t8-,9-/m1/s1
InChIKey:
VOJBXZDIFIJUKD-HOMPQPGZSA-N
DeepSMILES:
CC=C)/C=C/[C@H]OC=O)[C@@H]C5)C
Functional groups:
C=C(C)/C=C/C, COC(C)=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCCO1
Scaffold Graph/Node level:
OC1CCCO1
Scaffold Graph level:
CC1CCCC1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Lactones
ClassyFire Subclass:
Gamma butyrolactones
NP Classifier Biosynthetic pathway:
Terpenoids
NP-Likeness score:
3.021
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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