Results 201 to 210 of about 33,001 (251)

Genome-wide identification and integrated analysis of the WNK kinase gene family and expression analysis of PgWNK genes under methyl jasmonate treatment in Panax ginseng. [PDF]

BMC Plant Biol
Zhang K, Wang A, Shi L, Liu J, Zhang Y, Jiang Y, Zhang M, Wang Y, Zhao M, Wang K.   +9 more
europepmc   +1 more source

Comparative Effects of Putrescine, Salicylic Acid, Citric Acid, and Methyl Jasmonate on Postharvest Quality and Storage Life of <i>Pleurotus ostreatus</i>. [PDF]

Food Sci Nutr
Şahin B, Kibar B, Kibar H.
europepmc   +1 more source

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Fragrance material review on methyl jasmonate

Food and Chemical Toxicology, 2012
A toxicologic and dermatologic review of methyl jasmonate when used as a fragrance ingredient is presented. Methyl jasmonate is a member of the fragrance structural group Ketones Cyclopentanones and Cyclopentenones. The common characteristic structural element of the group members is a cyclopentanone or cyclopentenone ring with a straight or branched ...
A M Api
exaly   +3 more sources

Synthesis of (Z)-jasmone and methyl jasmonate.

Agricultural and Biological Chemistry, 1980
(1980). Synthesis of (Z)-Jasmone and Methyl Jasmonate. Agricultural and Biological Chemistry: Vol. 44, No. 3, pp. 687-688.
Yoshinobu Naoshima, Kazuhiko Nishimoto, Shoji Wakabayashi, Shûichi Hayashi   +3 more
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Methyl jasmonate as a vital substance in plants

Trends in Genetics, 2003
The plant floral scent methyl jasmonate (MeJA) has been identified as a vital cellular regulator that mediates diverse developmental processes and defense responses against biotic and abiotic stresses. The pleiotropic effects of MeJA have raised numerous questions about its regulation for biogenesis and mode of action.
Jong-Joo, Cheong, Yang Do, Choi
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The roles of methyl jasmonate to stress in plants

Functional Plant Biology, 2018
Plants are constantly exposed to various stresses, which can degrade their health. The stresses can be alleviated by the application of methyl jasmonate (MeJA), which is a hormone involved in plant signalling. MeJA induces synthesis of defensive compounds and initiates the expression of pathogenesis-related genes involved in systemic acquired ...
Xiaxia Yu, Wenjin Zhang, Yu Zhang, Xiaojia Zhang, Duoyong Lang, Xinhui Zhang   +5 more
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Jasmonic acid, methyl jasmonate and methyl dihydrojasmonate as active compounds of topical formulations

Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2018
Abstract Jasmonates are plant hormones that may positively affect the appearance, condition and health of human skin. They have anti-parasitic and anti-tumor activity, stimulate dermis desquamation and reduce discolorations. The aim of this study was to obtain and characterize topical formulations containing jasmonic acid/methyl jasmonate or methyl ...
Anna Olejnik, Alicja Sliwowska, Izabela Nowak   +2 more
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Rice Allelopathy Induced by Methyl Jasmonate and Methyl Salicylate

Journal of Chemical Ecology, 2007
Methyl jasmonate (MeJA) and methyl salicylate (MeSA) are important signaling molecules that induce plant defense against insect herbivores and microbial pathogens. We tested the hypothesis that allelopathy is an inducible defense mechanism, and that the JA and SA signaling pathways may activate allelochemicals release. Exogenous application of MeJA and
Hai Hong, Bi, Ren Sen, Zeng, Li Ming, Su, Min, An, Shi Ming, Luo   +4 more
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An Expeditious Synthesis of Methyl Jasmonate

Helvetica Chimica Acta, 2006
AbstractWe present an efficient three‐step, two‐pot synthesis of methyl jasmonate (trans‐1) based on Diels–Alder cycloaddition of cyclopent‐2‐enone (2) and chloroprene (= 2‐chlorobuta‐1,3‐diene; 3d) in either CHCl3 or CH2Cl2, catalyzed by SnCl4 (0.2 mol‐equiv.) at 20° (75% yield).
Christian Chapuis, Carole Cantatore, Jean‐Yves de Saint Laumer   +2 more
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(–)‐Methyl Cucurbate and (–)‐Methyl Jasmonate by Kinetic Resolution

Liebigs Annalen, 1996
AbstractThe kinetic resolution of a malonate‐substituted cyclopentenone gave rise to the formation of an enantiopure Diels‐Alder adduct which was converted into methyl dehydrocucurbate 2 by diastereoselective alkylation with (Z)‐1‐bromo‐2‐pentene and subsequent borohydride reduction.
Claudia Borm, Ekkehard Winterfeldt
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