Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractExpression and evolution of delta9 and delta11 desaturase genes in the moth Spodoptera littoralis    Next AbstractA mechanistic model for mercury capture with in situ-generated titania particles: role of water vapor »

Insect Biochem Mol Biol


Title:"Inhibition of the acyl-CoA desaturases involved in the biosynthesis of Spodoptera littoralis sex pheromone by analogs of 10,11-methylene-10-tetradecenoic acid"
Author(s):Rodriguez S; Camps F; Fabrias G;
Address:"Departamento de Quimica Organica Biologica, Instituto de Investigaciones Quimicas y Ambientales de Barcelona, CSIC, Jordi Girona 18, 08034 Barcelona, Spain"
Journal Title:Insect Biochem Mol Biol
Year:2004
Volume:34
Issue:3
Page Number:283 - 289
DOI: 10.1016/j.ibmb.2003.11.003
ISSN/ISBN:0965-1748 (Print) 0965-1748 (Linking)
Abstract:"The desaturase inhibitory activity of the cyclopropenyl alcohols 9,10-methylene-9-tetradecen-1-ol (9-MTOL), 10,11-methylene-10-tetradecen-1-ol (10-MTOL) and 11,12-methylene-11-tetradecen-1-ol (11-MTOL), which are structural analogs of 10,11-methylene-10-tetradecenoic acid (10-MTA), is reported. At equimolar ratios with respect to the different substrates, the three compounds completely inhibited the three desaturation reactions involved in the biosynthesis of Spodoptera littoralis sex pheromone. The dose-dependence of inhibition was determined for 10-MTA and its alcohol derivative. Both compounds inhibited the transformation of perdeuterated palmitic acid into perdeuterated (Z)-11-hexadecenoic acid and that of (E)-11-tridecenoic acid into (Z,E)-9,11-tridecadienoic acid with similar IC(50) values. The overall results presented in this work support scattered data that neither the free carboxyl groups nor their acyl-CoA esters are a requisite for inhibition of desaturases. Since the synthesis of cyclopropenols is much more convenient than that of cyclopropene fatty acids, this finding is of economical relevance regarding the putative use of cyclopropene derivatives in pest control"
Keywords:"Animals Fatty Acid Desaturases/*antagonists & inhibitors/metabolism Fatty Acids, Unsaturated/chemistry/*pharmacology Gas Chromatography-Mass Spectrometry Kinetics Sex Attractants/*biosynthesis/chemistry Spodoptera/*metabolism;"
Notes:"MedlineRodriguez, Sergio Camps, Francisco Fabrias, Gemma eng Research Support, Non-U.S. Gov't England 2004/02/12 Insect Biochem Mol Biol. 2004 Mar; 34(3):283-9. doi: 10.1016/j.ibmb.2003.11.003"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 17-11-2024