PHARMACOLOGICAL EVALUATION OF SYNTHETIC DERIVATIVES OF HALOGENATED SCHIFF BASE FOR ITS ANTIMICROBIAL, ANTIOXIDANT, AND ANTI-INFLAMMATORY ACTIVITIES

Background: Microbial drug resistance is an emerging worldwide issue affecting developed and developing countries. In order to counter this challenge, scientists are working to synthesize new molecules that are safe and effective and specifically tailored to target resistant microorganisms. Halogenated Schiff bases, in particular, have demonstrated significant antimicrobial activity against various bacterial and fungal strains, along with anti-inflammatory and antioxidant properties. Objectives: The main objective of study was to investigate the anti-bacterial and anti-fungal effect of new synthetic derivatives of halogenated schiff base E-N-1- bis (4 chlorophenyl) –methaninmine (Sw7) and (E)-N-(4-chlorophenyl)-1-(2,6-dichlorophenyl) methaninmine) (Sw9) against pathogenic bacteria and fungi. Additionally, their anti-inflammatory and antioxidant activities were assessed. Methodology: In the current study, antimicrobial potentials of E-N-1-bis (4 chlorophenyl) – methaninmine) and (E)-N-(4-chlorophenyl)-1-(2,6-dichlorophenyl) methaninmine) against different bacterial strains and fungal strains were evaluated by disc-diffusion method. Their anti-inflammatory and antioxidant activities were also analyzed using carrageenan-induced paw oedema assay and DPPH assays respectively. Results: The current study revealed that the tested new synthetic halogenated Schiff bases are sensitive against Escherichia coli at the highest 100 µg/mL concentration. The compounds (E–N-1-bis (4-chlorophyl) -methenamine (Sw7) and (E)-N- (4 chlorophenyl)-1-(2,6- dichlorophenyl) methenamine) (Sw9) showed no anti-bacterial activity against the other tested strains of bacteria, including Pseudomonas aeruginosa, Streptococcus aureus, and Streptococcus pyogenes. New synthetic compounds (Sw7) and (Sw9) showed mild to moderate anti-fungal activity against Candida albicans but no activity against Aspergillus flavus. Conclusion: Results demonstrated that the synthetic halogenated Schiff bases, Sw7 and Sw9, exhibit selective antimicrobial and anti-fungal activity, with Sw7 showing sensitivity against E. coli and mild to moderate activity against C. albicans.

Authors

Institutions

Publication Details

Journal
International Journal of Pharmacy & Integrated Health Sciences
Published
2025-02-21
DOI
https://doi.org/10.56536/ijpihs.v6i1.229
Primary Topic
Organometallic Compounds Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

PHARMACOLOGICAL EVALUATION OF SYNTHETIC DERIVATIVES OF HALOGENATED SCHIFF BASE FOR ITS ANTIMICROBIAL, ANTIOXIDANT, AND ANTI-INFLAMMATORY ACTIVITIES

Fouzia Younis, Uzma Nisar, Muhammad Rashid, Manzoor Ahmad et al.
1 links
International Journal of Pharmacy & Integrated Health Sciences
Organometallic Compounds Synthesis and Characterization
article

PHARMACOLOGICAL EVALUATION OF SYNTHETIC DERIVATIVES OF HALOGENATED SCHIFF BASE FOR ITS ANTIMICROBIAL, ANTIOXIDANT, AND ANTI-INFLAMMATORY ACTIVITIES

Fouzia Younis, Uzma Nisar, Muhammad Rashid, Manzoor Ahmad, Rubina Mushtaq, Qirrat Sajjad, Azeem Iqbal, Hafeez Ullah Khan, Saliha Abrar, Nayab Sajid
article en

Abstract

Background: Microbial drug resistance is an emerging worldwide issue affecting developed and developing countries. In order to counter this challenge, scientists are working to synthesize new molecules that are safe and effective and specifically tailored to target resistant microorganisms. Halogenated Schiff bases, in particular, have demonstrated significant antimicrobial activity against various bacterial and fungal strains, along with anti-inflammatory and antioxidant properties. Objectives: The main objective of study was to investigate the anti-bacterial and anti-fungal effect of new synthetic derivatives of halogenated schiff base E-N-1- bis (4 chlorophenyl) –methaninmine (Sw7) and (E)-N-(4-chlorophenyl)-1-(2,6-dichlorophenyl) methaninmine) (Sw9) against pathogenic bacteria and fungi. Additionally, their anti-inflammatory and antioxidant activities were assessed. Methodology: In the current study, antimicrobial potentials of E-N-1-bis (4 chlorophenyl) – methaninmine) and (E)-N-(4-chlorophenyl)-1-(2,6-dichlorophenyl) methaninmine) against different bacterial strains and fungal strains were evaluated by disc-diffusion method. Their anti-inflammatory and antioxidant activities were also analyzed using carrageenan-induced paw oedema assay and DPPH assays respectively. Results: The current study revealed that the tested new synthetic halogenated Schiff bases are sensitive against Escherichia coli at the highest 100 µg/mL concentration. The compounds (E–N-1-bis (4-chlorophyl) -methenamine (Sw7) and (E)-N- (4 chlorophenyl)-1-(2,6- dichlorophenyl) methenamine) (Sw9) showed no anti-bacterial activity against the other tested strains of bacteria, including Pseudomonas aeruginosa, Streptococcus aureus, and Streptococcus pyogenes. New synthetic compounds (Sw7) and (Sw9) showed mild to moderate anti-fungal activity against Candida albicans but no activity against Aspergillus flavus. Conclusion: Results demonstrated that the synthetic halogenated Schiff bases, Sw7 and Sw9, exhibit selective antimicrobial and anti-fungal activity, with Sw7 showing sensitivity against E. coli and mild to moderate activity against C. albicans.

International Journal of Pharmacy & Integrated Health SciencesVol. 6(1)
University of Lahore (PK), University of Management and Technology (PK)
Openalex Percentile: Top 97%
Organometallic Compounds Synthesis and Characterization
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.