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Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives
A series of thieno[2,3-b]thiophene moiety-containing bis-cyanopyrazoles 5a–c, bis-aminopyrazole 9 and bis-pyridazine derivatives 11 were synthesized and evaluated in vitro for their antimicrobial potential. The antimicrobial activity of some selected products was evaluated and showed good results. 5...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270460/ https://www.ncbi.nlm.nih.gov/pubmed/23603949 http://dx.doi.org/10.3390/molecules18044669 |
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author | Mabkhot, Yahia Nasser Kheder, Nabila Abdelshafy Farag, Ahmad M. |
author_facet | Mabkhot, Yahia Nasser Kheder, Nabila Abdelshafy Farag, Ahmad M. |
author_sort | Mabkhot, Yahia Nasser |
collection | PubMed |
description | A series of thieno[2,3-b]thiophene moiety-containing bis-cyanopyrazoles 5a–c, bis-aminopyrazole 9 and bis-pyridazine derivatives 11 were synthesized and evaluated in vitro for their antimicrobial potential. The antimicrobial activity of some selected products was evaluated and showed good results. 5,5'-(3,4-Dimethylthieno[2,3-b]thiophene-2,5-diyl)bis(3-acetyl-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile) (5d) was found to be more potent than the standard drug amphotericin B against Geotricum candidum and equipotent to amphotericin Bagainst Syncephalastrum racemosum. In addition, it was found to be equipotent to the standard drug Penicillin G against Staphylococcus aureus. Moreover, it was more potent than the standard drug streptomycin against Pseudomonas aeruginosa and Escherichia coli. |
format | Online Article Text |
id | pubmed-6270460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62704602018-12-14 Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives Mabkhot, Yahia Nasser Kheder, Nabila Abdelshafy Farag, Ahmad M. Molecules Article A series of thieno[2,3-b]thiophene moiety-containing bis-cyanopyrazoles 5a–c, bis-aminopyrazole 9 and bis-pyridazine derivatives 11 were synthesized and evaluated in vitro for their antimicrobial potential. The antimicrobial activity of some selected products was evaluated and showed good results. 5,5'-(3,4-Dimethylthieno[2,3-b]thiophene-2,5-diyl)bis(3-acetyl-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile) (5d) was found to be more potent than the standard drug amphotericin B against Geotricum candidum and equipotent to amphotericin Bagainst Syncephalastrum racemosum. In addition, it was found to be equipotent to the standard drug Penicillin G against Staphylococcus aureus. Moreover, it was more potent than the standard drug streptomycin against Pseudomonas aeruginosa and Escherichia coli. MDPI 2013-04-19 /pmc/articles/PMC6270460/ /pubmed/23603949 http://dx.doi.org/10.3390/molecules18044669 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 Mabkhot, Yahia Nasser Kheder, Nabila Abdelshafy Farag, Ahmad M. Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title | Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title_full | Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title_fullStr | Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title_full_unstemmed | Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title_short | Synthesis and Antimicrobial Activity of Some New Thieno[2,3-b]thiophene Derivatives |
title_sort | synthesis and antimicrobial activity of some new thieno[2,3-b]thiophene derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270460/ https://www.ncbi.nlm.nih.gov/pubmed/23603949 http://dx.doi.org/10.3390/molecules18044669 |
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