N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity
2-Furoyl-1-piperazine (1) was treated with a series of alkyl/aryl sulfonyl chlorides (2a-i) under benignant conditions to obtain its N-sulfonated derivatives (3a-i). These compounds were screened for their antibacterial potential against pathogenic bacteria. The low Minimum Inhibitory Concentration...
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Pakistan Journal of Pharmaceutical Sciences
2022
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2-s2.0-85129082085 Abbasi M.A.; Irshad M.; Aziz-Ur-Rehman; Siddiqui S.Z.; Shah S.A.A.; Shahid M. N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity 2022 Pakistan Journal of Pharmaceutical Sciences 35 2 10.36721/PJPS.2022.35.2.REG.579-585.1 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85129082085&doi=10.36721%2fPJPS.2022.35.2.REG.579-585.1&partnerID=40&md5=74e3ec50e089893dfa55a5cc8fc0dfa0 2-Furoyl-1-piperazine (1) was treated with a series of alkyl/aryl sulfonyl chlorides (2a-i) under benignant conditions to obtain its N-sulfonated derivatives (3a-i). These compounds were screened for their antibacterial potential against pathogenic bacteria. The low Minimum Inhibitory Concentration (MIC) values of these molecules, in comparison of ciprofloxacin, demonstrated their high antibacterial potential. Cytotoxic activities were ascertained through their hemolytic potential and mild hemolytic profiles of these compounds proved them to be promising compounds for drug designing and development. © 2022 Pakistan Journal of Pharmaceutical Sciences. All rights reserved. Pakistan Journal of Pharmaceutical Sciences 1011601X English Article |
author |
Abbasi M.A.; Irshad M.; Aziz-Ur-Rehman; Siddiqui S.Z.; Shah S.A.A.; Shahid M. |
spellingShingle |
Abbasi M.A.; Irshad M.; Aziz-Ur-Rehman; Siddiqui S.Z.; Shah S.A.A.; Shahid M. N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
author_facet |
Abbasi M.A.; Irshad M.; Aziz-Ur-Rehman; Siddiqui S.Z.; Shah S.A.A.; Shahid M. |
author_sort |
Abbasi M.A.; Irshad M.; Aziz-Ur-Rehman; Siddiqui S.Z.; Shah S.A.A.; Shahid M. |
title |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
title_short |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
title_full |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
title_fullStr |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
title_full_unstemmed |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
title_sort |
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity |
publishDate |
2022 |
container_title |
Pakistan Journal of Pharmaceutical Sciences |
container_volume |
35 |
container_issue |
2 |
doi_str_mv |
10.36721/PJPS.2022.35.2.REG.579-585.1 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85129082085&doi=10.36721%2fPJPS.2022.35.2.REG.579-585.1&partnerID=40&md5=74e3ec50e089893dfa55a5cc8fc0dfa0 |
description |
2-Furoyl-1-piperazine (1) was treated with a series of alkyl/aryl sulfonyl chlorides (2a-i) under benignant conditions to obtain its N-sulfonated derivatives (3a-i). These compounds were screened for their antibacterial potential against pathogenic bacteria. The low Minimum Inhibitory Concentration (MIC) values of these molecules, in comparison of ciprofloxacin, demonstrated their high antibacterial potential. Cytotoxic activities were ascertained through their hemolytic potential and mild hemolytic profiles of these compounds proved them to be promising compounds for drug designing and development. © 2022 Pakistan Journal of Pharmaceutical Sciences. All rights reserved. |
publisher |
Pakistan Journal of Pharmaceutical Sciences |
issn |
1011601X |
language |
English |
format |
Article |
accesstype |
|
record_format |
scopus |
collection |
Scopus |
_version_ |
1809677594432372736 |