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Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery

Five-membered 1,2,4-oxadiazole heterocyclic ring has received considerable attention because of its unique bioisosteric properties and an unusually wide spectrum of biological activities. Thus, it is a perfect framework for the novel drug development. After a century since the 1,2,4-oxadiazole have...

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Autores principales: Biernacki, Karol, Daśko, Mateusz, Ciupak, Olga, Kubiński, Konrad, Rachon, Janusz, Demkowicz, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345688/
https://www.ncbi.nlm.nih.gov/pubmed/32485996
http://dx.doi.org/10.3390/ph13060111
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author Biernacki, Karol
Daśko, Mateusz
Ciupak, Olga
Kubiński, Konrad
Rachon, Janusz
Demkowicz, Sebastian
author_facet Biernacki, Karol
Daśko, Mateusz
Ciupak, Olga
Kubiński, Konrad
Rachon, Janusz
Demkowicz, Sebastian
author_sort Biernacki, Karol
collection PubMed
description Five-membered 1,2,4-oxadiazole heterocyclic ring has received considerable attention because of its unique bioisosteric properties and an unusually wide spectrum of biological activities. Thus, it is a perfect framework for the novel drug development. After a century since the 1,2,4-oxadiazole have been discovered, the uncommon potential attracted medicinal chemists’ attention, leading to the discovery of a few presently accessible drugs containing 1,2,4-oxadiazole unit. It is worth noting that the interest in a 1,2,4-oxadiazoles’ biological application has been doubled in the last fifteen years. Herein, after a concise historical introduction, we present a comprehensive overview of the recent achievements in the synthesis of 1,2,4-oxadiazole-based compounds and the major advances in their biological applications in the period of the last five years as well as brief remarks on prospects for further development.
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spelling pubmed-73456882020-07-09 Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery Biernacki, Karol Daśko, Mateusz Ciupak, Olga Kubiński, Konrad Rachon, Janusz Demkowicz, Sebastian Pharmaceuticals (Basel) Review Five-membered 1,2,4-oxadiazole heterocyclic ring has received considerable attention because of its unique bioisosteric properties and an unusually wide spectrum of biological activities. Thus, it is a perfect framework for the novel drug development. After a century since the 1,2,4-oxadiazole have been discovered, the uncommon potential attracted medicinal chemists’ attention, leading to the discovery of a few presently accessible drugs containing 1,2,4-oxadiazole unit. It is worth noting that the interest in a 1,2,4-oxadiazoles’ biological application has been doubled in the last fifteen years. Herein, after a concise historical introduction, we present a comprehensive overview of the recent achievements in the synthesis of 1,2,4-oxadiazole-based compounds and the major advances in their biological applications in the period of the last five years as well as brief remarks on prospects for further development. MDPI 2020-05-29 /pmc/articles/PMC7345688/ /pubmed/32485996 http://dx.doi.org/10.3390/ph13060111 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Biernacki, Karol
Daśko, Mateusz
Ciupak, Olga
Kubiński, Konrad
Rachon, Janusz
Demkowicz, Sebastian
Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title_full Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title_fullStr Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title_full_unstemmed Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title_short Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery
title_sort novel 1,2,4-oxadiazole derivatives in drug discovery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345688/
https://www.ncbi.nlm.nih.gov/pubmed/32485996
http://dx.doi.org/10.3390/ph13060111
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