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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

Molecular Formula C11H16O
Molecular Weight 164.2441
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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
PubMed

PubMed

TitleDatePubMed
Nocturnal Plant Bugs Use cis-Jasmone to Locate Inflorescences of an Araceae as Feeding and Mating Site.
2016 Apr
The natural plant stress elicitor cis-jasmone causes cultivar-dependent reduction in growth of the stink bug, Euschistus heros and associated changes in flavonoid concentrations in soybean, Glycine max.
2016 Nov
Deletion of the Bombyx mori odorant receptor co-receptor (BmOrco) impairs olfactory sensitivity in silkworms.
2017 Jul
Design of larval chemical attractants based on odorant response spectra of odorant receptors in the cotton bollworm.
2017 May
Patents

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
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:07:55 GMT 2023
Edited
by admin
on Sat Dec 16 03:07:55 GMT 2023
Record UNII
7TCS3Y45DR
Record Status Validated (UNII)
Record Version
  • Download
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