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N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide
To explore the potential of the N-cyano sulfilimine group as an amide bond isostere, a derivative of the blockbuster anthranilic diamide, chlorantramiliprole, was synthesized and evaluated with regard to its physicochemical properties, permeability, and biological activity. Given the combination of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832345/ https://www.ncbi.nlm.nih.gov/pubmed/36712628 http://dx.doi.org/10.1039/d2ra06988a |
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author | Kang, On-Yu Kim, Eunsil Lee, Won Hyung Ryu, Do Hyun Lim, Hwan Jung Park, Seong Jun |
author_facet | Kang, On-Yu Kim, Eunsil Lee, Won Hyung Ryu, Do Hyun Lim, Hwan Jung Park, Seong Jun |
author_sort | Kang, On-Yu |
collection | PubMed |
description | To explore the potential of the N-cyano sulfilimine group as an amide bond isostere, a derivative of the blockbuster anthranilic diamide, chlorantramiliprole, was synthesized and evaluated with regard to its physicochemical properties, permeability, and biological activity. Given the combination of N-cyano sulfilimine chlorantraniliprole 1 and its strong hydrogen bond acceptor character, high permeability, and excellent insecticidal activity, the N-cyano sulfilimine functional group could be considered as an amide bond isostere. |
format | Online Article Text |
id | pubmed-9832345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-98323452023-01-26 N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide Kang, On-Yu Kim, Eunsil Lee, Won Hyung Ryu, Do Hyun Lim, Hwan Jung Park, Seong Jun RSC Adv Chemistry To explore the potential of the N-cyano sulfilimine group as an amide bond isostere, a derivative of the blockbuster anthranilic diamide, chlorantramiliprole, was synthesized and evaluated with regard to its physicochemical properties, permeability, and biological activity. Given the combination of N-cyano sulfilimine chlorantraniliprole 1 and its strong hydrogen bond acceptor character, high permeability, and excellent insecticidal activity, the N-cyano sulfilimine functional group could be considered as an amide bond isostere. The Royal Society of Chemistry 2023-01-11 /pmc/articles/PMC9832345/ /pubmed/36712628 http://dx.doi.org/10.1039/d2ra06988a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Kang, On-Yu Kim, Eunsil Lee, Won Hyung Ryu, Do Hyun Lim, Hwan Jung Park, Seong Jun N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title |
N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title_full |
N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title_fullStr |
N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title_full_unstemmed |
N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title_short |
N-Cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
title_sort | n-cyano sulfilimine functional group as a nonclassical amide bond bioisostere in the design of a potent analogue to anthranilic diamide insecticide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832345/ https://www.ncbi.nlm.nih.gov/pubmed/36712628 http://dx.doi.org/10.1039/d2ra06988a |
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