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 Abstract"Homofarnesals: female sex attractant pheromone components of the southern cowpea weevil, Callosobruchus chinensis"    Next Abstract"Contact sex pheromone components of the seed beetle, Callosobruchus analis (F.)" »

J Chem Ecol


Title:"2,3-Dihydrohomofarnesal: female sex attractant pheromone component of Callosobruchus rhodesianus (Pic)"
Author(s):Shimomura K; Koshino H; Yajima A; Matsumoto N; Kagohara Y; Kamada K; Yajima S; Ohsawa K;
Address:"Department of Biosciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo 156-8502, Japan. k3shimom@nodai.ac.jp"
Journal Title:J Chem Ecol
Year:2010
Volume:20100706
Issue:8
Page Number:824 - 833
DOI: 10.1007/s10886-010-9824-0
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Linking)
Abstract:"Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is a pest of stored legumes through the Afro-tropical region. In laboratory bioassays, males of C. rhodesianus were attracted to volatiles collected from virgin females. Collections were purified by various chromatographic techniques, and the biologically active component isolated using gas chromatographic-electroantennographic detection analysis. Gas chromatography-mass spectrometry and NMR analyses suggested that the active compound was 2,3-dihydrohomofarnesal, i.e., 7-ethyl-3,11-dimethyl-6,10-dodecadienal. The structure was confirmed by non-stereoselective and enantioselective total synthesis. Using chiral gas chromatography, the absolute configuration of the natural compound was confirmed as (3S,6E)-7-ethyl-3,11-dimethyl-6,10-dodecadienal. Y-tube olfactomter assays showed that only the (S)-enantiomer attracted males of C. rhodesianus. The (R)-enantiomer and racemate did not attract males, suggesting that the (R)-enantiomer inhibits the activity of the natural compound. In combination with previous reports about sex attractant pheromones of congeners, we suggest that a saltational shift of the pheromone structure arose within the genus Callosobruchus"
Keywords:"Animals Chromatography, Gas Coleoptera/*chemistry/drug effects Farnesol/*analogs & derivatives/analysis/isolation & purification/pharmacology Female Male Mass Spectrometry Sex Attractants/*analysis/*isolation & purification/pharmacology;"
Notes:"MedlineShimomura, Kenji Koshino, Hiroyuki Yajima, Arata Matsumoto, Noriko Kagohara, Yuuma Kamada, Koichi Yajima, Shunsuke Ohsawa, Kanju eng 2010/07/08 J Chem Ecol. 2010 Aug; 36(8):824-33. doi: 10.1007/s10886-010-9824-0. Epub 2010 Jul 6"

 
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 21-11-2024