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Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
[Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375095/ https://www.ncbi.nlm.nih.gov/pubmed/34423209 http://dx.doi.org/10.1021/acsomega.1c02614 |
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author | Twidle, Andrew M. Pilkington, Lisa I. Suckling, David M. Barker, David |
author_facet | Twidle, Andrew M. Pilkington, Lisa I. Suckling, David M. Barker, David |
author_sort | Twidle, Andrew M. |
collection | PubMed |
description | [Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-ene, (Z)-nonadec-12-en-9-amine, (Z)-11-methoxynonadec-7-ene, (Z)-1-(octylsulfinyl)-dec-3-ene, and (Z)-nonadec-12-en-9-ol. An imine analogue, N-((Z)-nonadec-12-en-9-ylidene)cyclopropanamine, was also synthesized but was too unstable for testing with the moths. None of the analogue compounds elicited significant responses from the male moth antennae. |
format | Online Article Text |
id | pubmed-8375095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83750952021-08-20 Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths Twidle, Andrew M. Pilkington, Lisa I. Suckling, David M. Barker, David ACS Omega [Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-ene, (Z)-nonadec-12-en-9-amine, (Z)-11-methoxynonadec-7-ene, (Z)-1-(octylsulfinyl)-dec-3-ene, and (Z)-nonadec-12-en-9-ol. An imine analogue, N-((Z)-nonadec-12-en-9-ylidene)cyclopropanamine, was also synthesized but was too unstable for testing with the moths. None of the analogue compounds elicited significant responses from the male moth antennae. American Chemical Society 2021-08-05 /pmc/articles/PMC8375095/ /pubmed/34423209 http://dx.doi.org/10.1021/acsomega.1c02614 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Twidle, Andrew M. Pilkington, Lisa I. Suckling, David M. Barker, David Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths |
title | Synthesis and Electrophysiological Testing of Carbonyl
Pheromone Analogues for Carposinid Moths |
title_full | Synthesis and Electrophysiological Testing of Carbonyl
Pheromone Analogues for Carposinid Moths |
title_fullStr | Synthesis and Electrophysiological Testing of Carbonyl
Pheromone Analogues for Carposinid Moths |
title_full_unstemmed | Synthesis and Electrophysiological Testing of Carbonyl
Pheromone Analogues for Carposinid Moths |
title_short | Synthesis and Electrophysiological Testing of Carbonyl
Pheromone Analogues for Carposinid Moths |
title_sort | synthesis and electrophysiological testing of carbonyl
pheromone analogues for carposinid moths |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375095/ https://www.ncbi.nlm.nih.gov/pubmed/34423209 http://dx.doi.org/10.1021/acsomega.1c02614 |
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