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 AbstractA novel pheromone dispenser for mating disruption of the leafminer Phyllocnistis citrella (Lepidoptera: Gracillariidae)    Next AbstractIntentional coverage gaps reduce cost of mating disruption for Phyllocnistis citrella (Lepidoptera: Gracillariidae) in citrus »

J Chem Ecol


Title:Identification and synthesis of a male-produced pheromone for the neotropical root weevil Diaprepes abbreviatus
Author(s):Lapointe SL; Alessandro RT; Robbins PS; Khrimian A; Svatos A; Dickens JC; Otalora-Luna F; Kaplan F; Alborn HT; Teal PE;
Address:"Agriculture Research Service, United States Department of Agriculture, U. S. Horticultural Research Laboratory, 2001 South Rock Road, Fort Pierce, FL 34945, USA. stephen.lapointe@ars.usda.gov"
Journal Title:J Chem Ecol
Year:2012
Volume:20120321
Issue:4
Page Number:408 - 417
DOI: 10.1007/s10886-012-0096-8
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Print) 0098-0331 (Linking)
Abstract:"An unsaturated hydroxy-ester pheromone was isolated from the headspace and feces of male Diaprepes abbreviatus, identified, and synthesized. The pheromone, methyl (E)-3-(2-hydroxyethyl)-4-methyl-2-pentenoate, was discovered by gas chromatography-coupled electroantennogram detection (GC-EAD), and identified by gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR). The synthesis yielded an 86:14 mixture of methyl (E)-3-(2-hydroxyethyl)-4-methyl-2-pentenoate (active) and methyl (Z)-3-(2-hydroxyethyl)-4-methyl-2-pentenoate (inactive), along with a lactone breakdown product. The activity of the synthetic E-isomer was confirmed by GC-EAD, GC-MS, NMR, and bioassays. No antennal response was observed to the Z-isomer or the lactone. In a two-choice olfactometer bioassay, female D. abbreviatus moved upwind towards the synthetic pheromone or natural pheromone more often compared with clean air. Males showed no clear preference for the synthetic pheromone. This pheromone, alone or in combination with plant volatiles, may play a role in the location of males by female D. abbreviatus"
Keywords:"Animals Feces/chemistry Female Male Sex Attractants/*analysis/biosynthesis/*chemical synthesis/pharmacology Sexual Behavior, Animal/drug effects Weevils/*metabolism;"
Notes:"MedlineLapointe, Stephen L Alessandro, Rocco T Robbins, Paul S Khrimian, Ashot Svatos, Ales Dickens, Joseph C Otalora-Luna, Fernando Kaplan, Fatma Alborn, Hans T Teal, Peter E eng 2012/03/22 J Chem Ecol. 2012 Apr; 38(4):408-17. doi: 10.1007/s10886-012-0096-8. Epub 2012 Mar 21"

 
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 22-09-2024