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 AbstractEvaluation of the Trapping Performance of Four Biogents AG Traps and Two Lures for the Surveillance of Aedes albopictus and Other Host-Seeking Mosquitoes    Next AbstractA Highly Selective and Sensitive Chiral Derivatization Method for High- Performance Liquid Chromatographic Determination of the Stereoisomer Composition of Natural Products With Chiral Branched Alkyl Chains »

Med Vet Entomol


Title:"Determination by HPLC fluorescence analysis of the natural enantiomers of sex pheromones in the New World screwworm fly, Cochliomyia hominivorax"
Author(s):Akasaka K; Carlson DA; Ohtaka T; Ohrui H; Mori K; Berkebile DR;
Address:"Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan"
Journal Title:Med Vet Entomol
Year:2009
Volume:23 Suppl 1
Issue:
Page Number:126 - 130
DOI: 10.1111/j.1365-2915.2008.00781.x
ISSN/ISBN:1365-2915 (Electronic) 0269-283X (Linking)
Abstract:"Bioassays of six racemic synthesized candidate sex pheromone compounds against male New World screwworm Cochliomyia hominivorax (Coquerel) flies showed that the most potent bioactivity was found with 6-acetoxy-19-methylnonacosane and 7-acetoxy-15-methylnonacosane compared with four other isomeric acetoxy nonacosanes and a larger aliphatic ketone. As all these methyl-branched compounds have two asymmetric carbons and four possible enantiomers, characterization of the natural enantiomers was essential. All four enantiomers for the two most bioactive isomers of the natural sex pheromone were synthesized for bioassay. Hydrolysis and derivatization of these enantiomers with different fluorescent reagents was followed by column-switched high-performance liquid chromatography. The use of two linked, reversed-phase columns of different polarity held at sub-ambient temperatures allowed good separation of each enantiomer. This analysis applied to natural material was successful, as (6R,19R)-6-acetoxy-19-methylnonanocosane, and (7R,15R)- and (7R,15S)-7-acetoxy-15-methylnonanocosane were detected in extracts of recently colonized female flies"
Keywords:"Alkanes/analysis Animals Anthracenes/analysis Chromatography, High Pressure Liquid Chromatography, Liquid Diptera/pathogenicity/*physiology Female Fluorescence Indicators and Reagents Male Screw Worm Infection/veterinary Sex Attractants/*chemistry/*isolat;"
Notes:"MedlineAkasaka, K Carlson, D A Ohtaka, T Ohrui, H Mori, K Berkebile, D R eng Research Support, Non-U.S. Gov't England 2009/04/02 Med Vet Entomol. 2009 Jun; 23 Suppl 1:126-30. doi: 10.1111/j.1365-2915.2008.00781.x"

 
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 26-12-2024