Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides
The drug resistance phenomenon in microbes is resulting in the ineffectiveness of available drugs to treat the infections. Thus, there is a continued need to discover new molecules to combat the drug resistance phenomenon. Norfloxacin is a fluoroquinolone antibiotic that is used for the treatment of...
Published in: | Pakistan journal of pharmaceutical sciences |
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2-s2.0-85090108112 Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M. Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides 2020 Pakistan journal of pharmaceutical sciences 33 2 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090108112&partnerID=40&md5=c4f7466c4fc4e7f1f66042421b12713f The drug resistance phenomenon in microbes is resulting in the ineffectiveness of available drugs to treat the infections. Thus, there is a continued need to discover new molecules to combat the drug resistance phenomenon. Norfloxacin is a fluoroquinolone antibiotic that is used for the treatment of urinary tract infections. In this research work, norfloxacin is structurally modified by hybridizing with a range of substituted acetohydrazidic moieties through a multistep reaction. The first step involves the coupling of norfloxacin 1 with methyl chloroacetate followed by the treatment with hydrazine hydrate to result in corresponding acetohydrazide 3. A range of substituted benzaldehydes were reacted with the acetohydrazide to form the targeted series of norfloxacin derivatives 4a-i. The final compounds were screened for antimicrobial activity. Among the tested compounds, 4c, 4d, 4e and 4f displayed better antifungal activity against F.avenaceum, while compound 4c and 4e were active against F. bubigeum. NLM (Medline) 1011601X English Article |
author |
Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M. |
spellingShingle |
Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M. Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
author_facet |
Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M. |
author_sort |
Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M. |
title |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
title_short |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
title_full |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
title_fullStr |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
title_full_unstemmed |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
title_sort |
Synthesis, characterization and antimicrobial activity of norfloxacin based acetohydrazides |
publishDate |
2020 |
container_title |
Pakistan journal of pharmaceutical sciences |
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33 |
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2 |
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url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090108112&partnerID=40&md5=c4f7466c4fc4e7f1f66042421b12713f |
description |
The drug resistance phenomenon in microbes is resulting in the ineffectiveness of available drugs to treat the infections. Thus, there is a continued need to discover new molecules to combat the drug resistance phenomenon. Norfloxacin is a fluoroquinolone antibiotic that is used for the treatment of urinary tract infections. In this research work, norfloxacin is structurally modified by hybridizing with a range of substituted acetohydrazidic moieties through a multistep reaction. The first step involves the coupling of norfloxacin 1 with methyl chloroacetate followed by the treatment with hydrazine hydrate to result in corresponding acetohydrazide 3. A range of substituted benzaldehydes were reacted with the acetohydrazide to form the targeted series of norfloxacin derivatives 4a-i. The final compounds were screened for antimicrobial activity. Among the tested compounds, 4c, 4d, 4e and 4f displayed better antifungal activity against F.avenaceum, while compound 4c and 4e were active against F. bubigeum. |
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NLM (Medline) |
issn |
1011601X |
language |
English |
format |
Article |
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scopus |
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Scopus |
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1809677685610250240 |