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[Species specificity and function of various insect pheromones]    Next Abstract"(Z,Z)-7,9-Dodecadienyl acetate, sex pheromone ofEpinotia tedella clerck (Lepidoptera: Tortricidae)" »

Z Naturforsch C Biosci


Title:Structure-response relationships in noctuid sex pheromone reception. An introductory report
Author(s):Priesner E; Jacobson M; Bestmann HJ;
Address:
Journal Title:Z Naturforsch C Biosci
Year:1975
Volume:30
Issue:2
Page Number:283 - 293
DOI: 10.1515/znc-1975-3-424
ISSN/ISBN:0341-0382 (Print) 0341-0382 (Linking)
Abstract:"Electroantennogram (EAG) data reflecting response spectra of male pheromone receptors have been analyzed for 16 species of Noctuidae (Lepidoptera). The test compounds included 100 pheromone analogues, altered in chain length, in position and configuration of double bond(s), and in the functional end groups. On comparison of amounts of substance required to elicit an equivalent EAG response, a single compound was determined to be most effective on a given species: these structures, either known or proposed as the natural sex pheromones of the species, were cis-7-dodecen-1-y1 acetate, cis-7-tetradecen-1-y1 acetate, cis-9-tetradecen-1-yu acetate, trans-9-tetradecen-1-y1 acetate, cis-11-hexadecen-1-y1 acetate, cis-9, trans-12-tetradecadien-1-y1 acetate, cis-9-tetradecen-1-y1 formate, and cis-9-tetradecen-1-ol, respectively. Elongation (shortening) of the chain by 1 or 2 methylene groups, the movement of a double bond 1 carbon from the optimum, a change to the opposite geometrical isomer, or the introduction of a second double bond invariably reduced EAG responses to 1.8 to 56 times below that observed with the most stimulating compound, in all 16 species. Further alterations in chain length or in double bond position caused even greater reduction in activity, as did certain in end group (Tables I and II). A set of distinct rules could be derived from these structure-response relationships; one of these rules concerns the optimum position of the double bond(s) in relation to chain length, and another one the ratios in activity values produced by end group variations, irrespective of chain length. The same rules described here for 16 noctuid species held also for the structure-response relationships observed within various additional groups of Lepidoptera. From EAG values determined in this study, an attempt has been made to calculate physicochemical propteries of underlying acceptor structures"
Keywords:Animals Lepidoptera/*physiology Male Moths/*physiology Olfactory Nerve/*physiology Pheromones/*physiology Sensory Receptor Cells/*physiology Structure-Activity Relationship;
Notes:"MedlinePriesner, E Jacobson, M Bestmann, H J eng Germany 1975/03/01 Z Naturforsch C Biosci. 1975 Mar-Apr; 30(2):283-93. doi: 10.1515/znc-1975-3-424"

 
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