Synthesis, Characterization and Antihelminthic Activity of Some Pyrazole Derivative

Objective: The present study aimed to evaluate the antibacterial activity of different Pyrazole derivatives (4A–E) and screened against selected pathogenic microorganisms and to compare their efficacy with a standard antibiotic. Materials and Methods: The antibacterial activity of the developed formulations was assessed against Pseudomonas aeruginosa, Klebsiella pneumoniae, and Staphylococcus aureus using the zone of inhibition method. The results were compared with the standard drug tetracycline to determine relative efficacy. Results: Among all formulations, 5B and 5C demonstrated the highest antibacterial activity, exhibiting significant zones of inhibition against all tested microorganisms. Strong activity was particularly observed against Pseudomonas aeruginosa and Staphylococcus aureus, indicating broad-spectrum effectiveness. Other formulations showed moderate to low activity, while some exhibited no inhibition against Klebsiella pneumoniae.

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Publication Details

Journal
Iconic Research and Engineering Journals
Published
2026-05-08
DOI
https://doi.org/10.64388/irev9i11-1717424
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis, Characterization and Antihelminthic Activity of Some Pyrazole Derivative

Santosh Kumar Shukla, Bushra Taj
Iconic Research and Engineering Journals
Synthesis and biological activity
article

Synthesis, Characterization and Antihelminthic Activity of Some Pyrazole Derivative

Santosh Kumar Shukla, Bushra Taj
article en

Abstract

Objective: The present study aimed to evaluate the antibacterial activity of different Pyrazole derivatives (4A–E) and screened against selected pathogenic microorganisms and to compare their efficacy with a standard antibiotic. Materials and Methods: The antibacterial activity of the developed formulations was assessed against Pseudomonas aeruginosa, Klebsiella pneumoniae, and Staphylococcus aureus using the zone of inhibition method. The results were compared with the standard drug tetracycline to determine relative efficacy. Results: Among all formulations, 5B and 5C demonstrated the highest antibacterial activity, exhibiting significant zones of inhibition against all tested microorganisms. Strong activity was particularly observed against Pseudomonas aeruginosa and Staphylococcus aureus, indicating broad-spectrum effectiveness. Other formulations showed moderate to low activity, while some exhibited no inhibition against Klebsiella pneumoniae.

Iconic Research and Engineering JournalsVol. 9(11)
Openalex Percentile: Top 9%
Synthesis and biological activity
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