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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...

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Autores principales: Kang, On-Yu, Kim, Eunsil, Lee, Won Hyung, Ryu, Do Hyun, Lim, Hwan Jung, Park, Seong Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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