Synthesis and Antimicrobial Potential of Substituted (Z)-5-Benzylidene-1,3-thiazolidine-2,4-diones with 1,3,4-Oxadiazole Functionalities

A variety of antimicrobials with distinct modes of action is vital for tackling the challenges associated with multidrug resistance. Herein, we have designed and synthesized novel thiazolidine-2,4-dione derivatives. These scaffolds have been analyzed for their potential antibacterial and antifungal activities. Among all, compound 6j exhibited excellent antibacterial activity with inhibition zone diameters ranging from 19 to 24 mm against pathogenic strains Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, and Pseudomonas aeruginosa. Compounds 6a and 6g showed moderate antifungal activity with inhibition zone diameters of 24 and 23 mm, respectively, against Aspergillus niger compared to the standard drug Nystatin. Furthermore, the molecular binding affinities of the synthesized thiazolidine-2,4-dione derivatives with proteins from various microorganisms have been assayed by molecular docking studies.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-12-01
DOI
https://doi.org/10.1134/s1070428024120133
Citations
2
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.50
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article

Synthesis and Antimicrobial Potential of Substituted (Z)-5-Benzylidene-1,3-thiazolidine-2,4-diones with 1,3,4-Oxadiazole Functionalities

Ghanshyam L. Jadav, Hanuman Narode, Debabrat Pathak, A. K. Mahida et al.
2 citations
Russian Journal of Organic Chemistry
Synthesis and biological activity
0.50
article

Synthesis and Antimicrobial Potential of Substituted (Z)-5-Benzylidene-1,3-thiazolidine-2,4-diones with 1,3,4-Oxadiazole Functionalities

Ghanshyam L. Jadav, Hanuman Narode, Debabrat Pathak, A. K. Mahida, H. A. Modi, Pooja D. Suradiya, Darshit B. Chhag
article en
2 citations

Abstract

A variety of antimicrobials with distinct modes of action is vital for tackling the challenges associated with multidrug resistance. Herein, we have designed and synthesized novel thiazolidine-2,4-dione derivatives. These scaffolds have been analyzed for their potential antibacterial and antifungal activities. Among all, compound 6j exhibited excellent antibacterial activity with inhibition zone diameters ranging from 19 to 24 mm against pathogenic strains Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, and Pseudomonas aeruginosa. Compounds 6a and 6g showed moderate antifungal activity with inhibition zone diameters of 24 and 23 mm, respectively, against Aspergillus niger compared to the standard drug Nystatin. Furthermore, the molecular binding affinities of the synthesized thiazolidine-2,4-dione derivatives with proteins from various microorganisms have been assayed by molecular docking studies.

Russian Journal of Organic ChemistryVol. 60(12)
Indrashil University (IN), M. P. Shah Medical College (IN)
Openalex Percentile: Top 37%
Synthesis and biological activity
0.50
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Synthesis and Antimicrobial Potential of Substituted (Z)-5-Benzylidene-1,3-thiazolidine-2,4-diones with 1,3,4-Oxadiazole Functionalities — Ghanshyam L. Jadav, Hanuman Narode, et al. · Russian Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS