Structure via PubChem · Public domain (PubChem)
(−)-methyl jasmonate
Sign in to saveAlso known as methyl 2-[(1R,2R)-3-oxidanylidene-2-[(Z)-pent-2-enyl]cyclopentyl]ethanoate, methyl 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetate, 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid methyl ester, 2-(3-keto-2-pent-2-enyl-cyclopentyl)acetic acid methyl ester, 2-(3-oxo-2-pent-2-enylcyclopentyl)acetic acid methyl ester, methyl 2-(3-oxo-2-pent-2-enyl-cyclopentyl)acetate, methyl 2-(3-oxo-2-pent-2-enyl-cyclopentyl)ethanoate, methyl 2-(3-oxo-2-pent-2-enylcyclopentyl)acetate
chemical compound
In the Vinony graph
Within Vinony's link graph, (−)-methyl jasmonate is referenced by 31 other articles, and connects out to flower, hydrogen and oxygen.
It sits within the topics Acetate esters, Alkene derivatives and Chembox image size set.
Its subject is documented across 18 Wikipedia language editions.
Chemical data
- Formula
- C13H20O3
- Molecular weight
- 224.3 g/mol
- IUPAC name
- methyl 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetate
- SMILES
- CC/C=C\C[C@@H]1[C@H](CCC1=O)CC(=O)OC
- InChIKey
- GEWDNTWNSAZUDX-WQMVXFAESA-N
- XLogP
- 1.9
- Polar surface area
- 43.4 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
4,608 papers- The roles of methyl jasmonate to stress in plants.Functional plant biology : FPB · 2019
- Methyl jasmonate: a phytohormone with potential for the treatment of inflammatory bowel diseases.The Journal of pharmacy and pharmacology · 2018
- Reactive Carbonyl Species Mediate Methyl Jasmonate-Induced Stomatal Closure.Plant & cell physiology · 2020
- Methyl jasmonate alleviates arsenic toxicity in rice.Plant cell reports · 2020
- Methyl jasmonate improves rubber production and quality in Lactuca Serriola.Scientific reports · 2024
via PubMed
Wikidata facts
- Mass
- 224.141245
Show 6 more facts
- found in taxon
- Persicaria hydropiperoides
- canonical SMILES
- CCC=CCC1C(CCC1=O)CC(=O)OC
- chemical formula
- C₁₃H₂₀O₃
- isomeric SMILES
- CC/C=C\C[C@@H]1[C@H](CCC1=O)CC(=O)OC
- subject has role
- primary metabolite
- Commons category
- Methyl jasmonate
Sources (5)
via Wikidata · CC0