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Details

Stereochemistry ACHIRAL
Molecular Formula C11H16O
Molecular Weight 164.2441
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of JASMONE, (E)-

SMILES

CC\C=C\CC1=C(C)CCC1=O

InChI

InChIKey=XMLSXPIVAXONDL-SNAWJCMRSA-N
InChI=1S/C11H16O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h4-5H,3,6-8H2,1-2H3/b5-4+

HIDE SMILES / InChI
Jasmone is a natural organic compound extracted from the volatile portion of the oil from jasmine flowers. The natural extract contains only the cis form, while the synthetic material is often a mixture containing both forms, with the cis form predominating. Commercially it is used primarily in perfumes and cosmetics. Some studies on rodents had shown that cis-jasmine had a tranquillizing effect on the brain, possibly through the GABA-A receptors response.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.49 mM [Kd]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct

Sample Use Guides

in mice: The aroma of cis-jasmone or methyl jasmonate was generated by bubbling it with an air-pump. Air containing the fragrant compound (0.5 mM) was introduced into the cage. Male ddY strain male mice were exposed to the aroma 30 min prior to the administration of pentobarbital, because it possibly took some time before the aroma was absorbed into the blood through respiration.
Route of Administration: Irrigation
In Vitro Use Guide
Unknown
Name Type Language
JASMONE, (E)-
Common Name English
3-METHYL-2-(TRANS-2-PENTENYL)-2-CYCLOPENTEN-1-ONE
Systematic Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2E)-2-PENTENYL-
Systematic Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2E)-2-PENTEN-1-YL-
Systematic Name English
TRANS-JASMONE
Common Name English
JASMONE, TRANS-
Common Name English
(E)-JASMONE
Common Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2-PENTENYL)-, TRANS-
Common Name English
JASMONE TRANS-FORM [MI]
Common Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2-PENTENYL)-, (E)-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID50904403
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
228-410-7
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY
MERCK INDEX
m6577
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY Merck Index
CAS
6261-18-3
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY
PUBCHEM
1549019
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY
FDA UNII
7TCS3Y45DR
Created by admin on Sat Dec 16 03:07:55 GMT 2023 , Edited by admin on Sat Dec 16 03:07:55 GMT 2023
PRIMARY