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 AbstractAsymmetric synthesis of (-)-dehydro-exo-brevicomin with a photoisomerisation-intramolecular acetalisation sequence    Next AbstractInhibitors of calling behavior of Plodia interpunctella »

Pest Manag Sci


Title:Identification of novel inhibitors of calling and in vitro [14C]acetate incorporation by pheromone glands of Plodia interpunctella
Author(s):Hirashima A; Eiraku T; Watanabe Y; Kuwano E; Taniguchi E; Eto M;
Address:"Department of Applied Genetics and Pest Management, Faculty of Agriculture, Graduate School, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan. ahirasim@agr.kyushu-u.ac.jp"
Journal Title:Pest Manag Sci
Year:2001
Volume:57
Issue:8
Page Number:713 - 720
DOI: 10.1002/ps.345
ISSN/ISBN:1526-498X (Print) 1526-498X (Linking)
Abstract:"Some octopamine agonists were found to suppress in vitro biosynthesis of the calling pheromone of the Indian meal moth, Plodia interpunctella. Isolated pheromone-gland preparations incorporated sodium [14C]acetate at a linear rate for 3 h when incubated with the pheromone biosynthesis activating neuropeptide (PBAN). This incorporation was dependent on the dose of PBAN (up to 0.5 microM). Thin-layer chromatography of a pheromone-gland extract revealed quantitative incorporation of radioactivity into a product exhibiting the same mobility as (Z,E)-9,12-tetradecadienyl acetate, the main component of the calling pheromone of P interpunctella. Twenty-seven octopamine agonists were initially screened using a calling behaviour bioassay of female P interpunctella. Four derivatives with activity in the nanomolar range were identified which were, in order of decreasing pheromonostatic activity: 2-(2,6-diethylphenylimino)thiazolidine > 2-(2,6-diethylphenylimino)oxazolidine > 2-(2,6-dimethylphenylimino)thiazolidine > 2-(2-ethylphenylimino)oxazolidine. These compounds also showed in vitro inhibitory activity in intracellular de novo pheromone biosynthesis. The results of the present study indicate that these derivatives could provide useful information in the characterization and differentiation of octopaminergic receptor types and subtypes"
Keywords:"Adenylyl Cyclases/metabolism Adrenergic alpha-Agonists/pharmacology Adrenergic alpha-Antagonists/pharmacology Animals Carbon Radioisotopes Dose-Response Relationship, Drug Female Male Moths/*drug effects/physiology Neuropeptides/pharmacology Octopamine/ag;"
Notes:"MedlineHirashima, A Eiraku, T Watanabe, Y Kuwano, E Taniguchi, E Eto, M eng Research Support, Non-U.S. Gov't England 2001/08/24 Pest Manag Sci. 2001 Aug; 57(8):713-20. doi: 10.1002/ps.345"

 
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 05-12-2024