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...

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Published in:Pakistan journal of pharmaceutical sciences
Main Author: Walayat K.; Ahmad M.; Rasul A.; Aslam S.; Anjum M.N.; Sultan S.; Iqbal M.
Format: Article
Language:English
Published: NLM (Medline) 2020
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090108112&partnerID=40&md5=c4f7466c4fc4e7f1f66042421b12713f
id 2-s2.0-85090108112
spelling 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
container_volume 33
container_issue 2
doi_str_mv
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.
publisher NLM (Medline)
issn 1011601X
language English
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