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Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments
An efficient method of producing quinine derivatives via reaction of acylation with 4,5-dichloroisothiazole-3-, 5-arylisoxazole-3-, adamantane- and hydrochlorides of pyridine-3- and pyridine-4-carbonyl chlorides was developed. All synthesized compounds were tested for antiviral, antimicrobial and an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182173/ https://www.ncbi.nlm.nih.gov/pubmed/35684414 http://dx.doi.org/10.3390/molecules27113476 |
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author | Mukusheva, Gulim K. Zhasymbekova, Aigerym R. Seidakhmetova, Roza B. Nurkenov, Oralgazy A. Akishina, Ekaterina A. Petkevich, Sergey K. Dikusar, Evgenij A. Potkin, Vladimir I. |
author_facet | Mukusheva, Gulim K. Zhasymbekova, Aigerym R. Seidakhmetova, Roza B. Nurkenov, Oralgazy A. Akishina, Ekaterina A. Petkevich, Sergey K. Dikusar, Evgenij A. Potkin, Vladimir I. |
author_sort | Mukusheva, Gulim K. |
collection | PubMed |
description | An efficient method of producing quinine derivatives via reaction of acylation with 4,5-dichloroisothiazole-3-, 5-arylisoxazole-3-, adamantane- and hydrochlorides of pyridine-3- and pyridine-4-carbonyl chlorides was developed. All synthesized compounds were tested for antiviral, antimicrobial and analgesic activity. The most pronounced antibacterial activity was shown by the compounds 2e, 3b, 3c and 3e with isoxazole and pyridine fragments. It was found that most of the tested compounds showed significant analgesic activity reducing the pain response of animals to the irritating effect of acetic acid. |
format | Online Article Text |
id | pubmed-9182173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91821732022-06-10 Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments Mukusheva, Gulim K. Zhasymbekova, Aigerym R. Seidakhmetova, Roza B. Nurkenov, Oralgazy A. Akishina, Ekaterina A. Petkevich, Sergey K. Dikusar, Evgenij A. Potkin, Vladimir I. Molecules Article An efficient method of producing quinine derivatives via reaction of acylation with 4,5-dichloroisothiazole-3-, 5-arylisoxazole-3-, adamantane- and hydrochlorides of pyridine-3- and pyridine-4-carbonyl chlorides was developed. All synthesized compounds were tested for antiviral, antimicrobial and analgesic activity. The most pronounced antibacterial activity was shown by the compounds 2e, 3b, 3c and 3e with isoxazole and pyridine fragments. It was found that most of the tested compounds showed significant analgesic activity reducing the pain response of animals to the irritating effect of acetic acid. MDPI 2022-05-27 /pmc/articles/PMC9182173/ /pubmed/35684414 http://dx.doi.org/10.3390/molecules27113476 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mukusheva, Gulim K. Zhasymbekova, Aigerym R. Seidakhmetova, Roza B. Nurkenov, Oralgazy A. Akishina, Ekaterina A. Petkevich, Sergey K. Dikusar, Evgenij A. Potkin, Vladimir I. Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title | Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title_full | Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title_fullStr | Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title_full_unstemmed | Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title_short | Quinine Esters with 1,2-Azole, Pyridine and Adamantane Fragments |
title_sort | quinine esters with 1,2-azole, pyridine and adamantane fragments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182173/ https://www.ncbi.nlm.nih.gov/pubmed/35684414 http://dx.doi.org/10.3390/molecules27113476 |
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