| Weight | 224.3 g/mol |
|---|---|
| Formula | C13H20O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Methyl jasmonate
3-oxo-2-(2-pentenyl)cyclopentaneacetic acid methyl ester · methyl epijasmonate · jasmonic acid methyl ester
42536-97-0, 39924-52-2, 20073-13-6
Score:
#2015 in Biology
,
#2462 in Chemistry
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- Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. (Proceedings of the National Academy of Sciences of the United States of America, 1990)
- Arabidopsis Mutants Selected for Resistance to the Phytotoxin Coronatine Are Male Sterile, Insensitive to Methyl Jasmonate, and Resistant to a Bacterial Pathogen. (The Plant Cell, 1994)
- Hydrogen Peroxide Acts as a Second Messenger for the Induction of Defense Genes in Tomato Plants in Response to Wounding, Systemin, and Methyl Jasmonate (The Plant Cell, 2001)
- Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant (Proceedings of the National Academy of Sciences of the United States of America, 1992)
- Plant Defense Genes Are Synergistically Induced by Ethylene and Methyl Jasmonate. (The Plant Cell, 1994)
- Jasmonic acid/methyl jasmonate accumulate in wounded soybean hypocotyls and modulate wound gene expression. (Proceedings of the National Academy of Sciences of the United States of America, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-oxo-2-(2-pentenyl)cyclopentaneacetic acid methyl ester
- methyl epijasmonate
- jasmonic acid methyl ester
-
SMILESCCC=CCC1C(CCC1=O)CC(=O)OC
-
InChIKeyGEWDNTWNSAZUDX-UHFFFAOYSA-N
- Pubchem - Methyl jasmonate
- Wikipedia - methyl jasmonate
Methyl jasmonate (abbreviated MeJA) is a volatile organic compound used in plant defense and many diverse developmental pathways such as seed germination, root growth, flowering, fruit ripening, and senescence. Methyl jasmonate is derived from jasmonic acid and the reaction is catalyzed by S-adenosyl-L-methionine:jasmonic acid carboxyl methyltransferase. Plants produce jasmonic acid and methyl jasmonate in response to many biotic and abiotic stresses (in particular, herbivory and wounding), which build up in the damaged parts of the plant.
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Methyl jasmonate
(39924-52-2, 20073-13-6)
4 alternate names
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Methyl jasmonate
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4 alternate names
3 suppliers
Methyl jasmonate
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