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IMPPAT Phytochemical information:
2-((3,3-Dimethyloxiran-2-yl)methyl)-3-methylfuran
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY009211
Phytochemical name:
2-((3,3-Dimethyloxiran-2-yl)methyl)-3-methylfuran
Synonymous chemical names:
rose furan epoxide, rosefuran epoxide, rosefurane epoxide, rosenfuran epoxide
External chemical identifiers:
CID:6428926
Chemical structure information
SMILES:
Cc1ccoc1CC1OC1(C)C
InChI:
InChI=1S/C10H14O2/c1-7-4-5-11-8(7)6-9-10(2,3)12-9/h4-5,9H,6H2,1-3H3
InChIKey:
BVTAIXWVSMPSFL-UHFFFAOYSA-N
DeepSMILES:
Ccccoc5CCOC3C)C
Functional groups:
CC1OC1(C)C, coc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1coc(CC2CO2)c1
Scaffold Graph/Node level:
C1COC(CC2CO2)C1
Scaffold Graph level:
C1CCC(CC2CC2)C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Heteroaromatic compounds
NP Classifier Biosynthetic pathway:
Terpenoids
NP Classifier Superclass:
Monoterpenoids
NP Classifier Class:
Acyclic monoterpenoids
NP-Likeness score:
2.1
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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