IMPPAT Phytochemical information: 
cis-p-Mentha-1(7),8-dien-2-ol

cis-p-Mentha-1(7),8-dien-2-ol
Summary

IMPPAT Phytochemical identifier: IMPHY003675

Phytochemical name: cis-p-Mentha-1(7),8-dien-2-ol

Synonymous chemical names:
cis-p-mentha- 1(7),8-dien-2-ol, cis-p-mentha-1(7),8-dien-2-ol, cis-p-mentha-1(7),8-diene-2-ol, cis-p-menthe-1(7),8-dien-2-ol, p-cis-mentha-1(7),8-dien-2-ol

External chemical identifiers:
CID:6429040, ChEMBL:CHEMBL507840, SureChEMBL:SCHEMBL11876152
Chemical structure information

SMILES:
CC(=C)[C@H]1CCC(=C)[C@@H](C1)O

InChI:
InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h9-11H,1,3-6H2,2H3/t9-,10+/m0/s1

InChIKey:
PNVTXOFNJFHXOK-VHSXEESVSA-N

DeepSMILES:
CC=C)[C@H]CCC=C)[C@@H]C6)O

Functional groups:
C=C(C)C, CO
Molecular scaffolds

Scaffold Graph/Node/Bond level:
C=C1CCCCC1

Scaffold Graph/Node level:
CC1CCCCC1

Scaffold Graph level:
CC1CCCCC1
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Lipids and lipid-like molecules

ClassyFire Class: Prenol lipids

ClassyFire Subclass: Monoterpenoids

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Sesquiterpenoids, Monoterpenoids

NP Classifier Class: Germacrane sesquiterpenoids, Monocyclic monoterpenoids

NP-Likeness score: 3.084


Chemical structure download