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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

SMILES

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

InChI

InChIKey=XMLSXPIVAXONDL-PLNGDYQASA-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

Description

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.

Originator

Approval Year

2021
470
Targets

Targets

Primary TargetPharmacologyConditionPotency
Activator
1430
 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

Patents

JP2002159565A
2
JP2003183689A
2
JP2004525163A
3
JP4266639B2
3
JP4739231B2
46
JPH08198863A
2
JPH11209797A
2
JPS53101335A
2
JPS5448707A
2
JPS5495535A
2
JPS554339A
2
JPS56115735A
2
JPS56127333A
2
JPS5634651A
2
JPS5639046A
2
JPS5735536A
2
JPS5738741A
3
JPS5764635A
2
JPS5772934A
2
JPS5799546A
2
JPS595138A
2
JPS60178841A
2
JPS62129237A
3
JPS62209073A
2
JPS62209074A
2
JPS63316776A
2
JPS6360982A
2

Sample Use Guides

In Vivo Use Guide
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 Fri Dec 15 17:44:53 GMT 2023
Edited
by admin
on Fri Dec 15 17:44:53 GMT 2023
Record UNII
RC4W0G9YUK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
JASMONE
FHFI   MI  
Common Name English
3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE
Systematic Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2-PENTENYL)-, (Z)-
Common Name English
JASMONE [MI]
Common Name English
FEMA NO. 3196
Code English
JASMONE [FHFI]
Common Name English
3-METHYL-2-N-PENTEN-2'-YLCYCLOPENTEN-2-ONE
Common Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2Z)-2-PENTEN-1-YL-
Systematic Name English
METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE, (Z)-, 3-
Systematic Name English
2-CYCLOPENTEN-1-ONE, 3-METHYL-2-(2Z)-2-PENTENYL-
Systematic Name English
3-METHYL-2-(2-CIS-PENTENYL)-2-CYCLOPENTEN-1-ONE
Systematic Name English
CIS-JASMONE
Common Name English
(Z)-JASMONE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
Code System Code Type Description
HSDB
8273
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
MERCK INDEX
m6577
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY Merck Index
CAS
488-10-8
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
RXCUI
2557370
Created by admin on Fri Dec 15 17:44:54 GMT 2023 , Edited by admin on Fri Dec 15 17:44:54 GMT 2023
PRIMARY
WIKIPEDIA
JASMONE
Created by admin on Fri Dec 15 17:44:54 GMT 2023 , Edited by admin on Fri Dec 15 17:44:54 GMT 2023
PRIMARY
JECFA MONOGRAPH
1046
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
SMS_ID
100000139593
Created by admin on Fri Dec 15 17:44:54 GMT 2023 , Edited by admin on Fri Dec 15 17:44:54 GMT 2023
PRIMARY
PUBCHEM
1549018
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
DAILYMED
RC4W0G9YUK
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-668-4
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
EPA CompTox
DTXSID4047092
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
FDA UNII
RC4W0G9YUK
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
EVMPD
SUB88355
Created by admin on Fri Dec 15 17:44:53 GMT 2023 , Edited by admin on Fri Dec 15 17:44:53 GMT 2023
PRIMARY
NIH
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