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Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products
In general, benzothiazole derivatives have attracted great interest due to their pharmaceutical and biological importance. New 2-amino-6-arylbenzothiazoles were synthesized in moderate to excellent yields via Suzuki cross coupling reactions using various aryl boronic acids and aryl boronic acid pina...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269778/ https://www.ncbi.nlm.nih.gov/pubmed/23892631 http://dx.doi.org/10.3390/molecules18088845 |
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author | Gull, Yasmeen Rasool, Nasir Noreen, Mnaza Nasim, Faiz-ul-Hassan Yaqoob, Asma Kousar, Shazia Rashid, Umer Bukhari, Iftikhar Hussain Zubair, Muhammad Islam, Md. Saiful |
author_facet | Gull, Yasmeen Rasool, Nasir Noreen, Mnaza Nasim, Faiz-ul-Hassan Yaqoob, Asma Kousar, Shazia Rashid, Umer Bukhari, Iftikhar Hussain Zubair, Muhammad Islam, Md. Saiful |
author_sort | Gull, Yasmeen |
collection | PubMed |
description | In general, benzothiazole derivatives have attracted great interest due to their pharmaceutical and biological importance. New 2-amino-6-arylbenzothiazoles were synthesized in moderate to excellent yields via Suzuki cross coupling reactions using various aryl boronic acids and aryl boronic acid pinacol esters and the antiurease and nitric oxide (NO) scavenging activity of the products were also examined. The most active compound concerning urease enzyme inhibition was 6-phenylbenzo[d]thiazole-2-amine 3e, with an IC(50) value of 26.35 µg/mL. Compound 3c, 6-(4-methoxyphenyl) benzo[d]thiazole-2-amine, exhibited the highest nitric oxide percentage scavenging at 100 µg/mL. |
format | Online Article Text |
id | pubmed-6269778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62697782018-12-18 Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products Gull, Yasmeen Rasool, Nasir Noreen, Mnaza Nasim, Faiz-ul-Hassan Yaqoob, Asma Kousar, Shazia Rashid, Umer Bukhari, Iftikhar Hussain Zubair, Muhammad Islam, Md. Saiful Molecules Article In general, benzothiazole derivatives have attracted great interest due to their pharmaceutical and biological importance. New 2-amino-6-arylbenzothiazoles were synthesized in moderate to excellent yields via Suzuki cross coupling reactions using various aryl boronic acids and aryl boronic acid pinacol esters and the antiurease and nitric oxide (NO) scavenging activity of the products were also examined. The most active compound concerning urease enzyme inhibition was 6-phenylbenzo[d]thiazole-2-amine 3e, with an IC(50) value of 26.35 µg/mL. Compound 3c, 6-(4-methoxyphenyl) benzo[d]thiazole-2-amine, exhibited the highest nitric oxide percentage scavenging at 100 µg/mL. MDPI 2013-07-25 /pmc/articles/PMC6269778/ /pubmed/23892631 http://dx.doi.org/10.3390/molecules18088845 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Gull, Yasmeen Rasool, Nasir Noreen, Mnaza Nasim, Faiz-ul-Hassan Yaqoob, Asma Kousar, Shazia Rashid, Umer Bukhari, Iftikhar Hussain Zubair, Muhammad Islam, Md. Saiful Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title | Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title_full | Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title_fullStr | Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title_full_unstemmed | Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title_short | Efficient Synthesis of 2-Amino-6-Arylbenzothiazoles via Pd(0) Suzuki Cross Coupling Reactions: Potent Urease Enzyme Inhibition and Nitric Oxide Scavenging Activities of the Products |
title_sort | efficient synthesis of 2-amino-6-arylbenzothiazoles via pd(0) suzuki cross coupling reactions: potent urease enzyme inhibition and nitric oxide scavenging activities of the products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269778/ https://www.ncbi.nlm.nih.gov/pubmed/23892631 http://dx.doi.org/10.3390/molecules18088845 |
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