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April 15, 2026Russian Journal of Organic Chemistry0 citations

Synthesis, Characterization, and Biological Evaluation of Substituted (Z) -1-Benzyl-3-3- (4-nitrophenyl) -1-phenyl-1H-pyrazol-4-ylmethylidenepyrrolidine-2, 5-diones

HMH. A. ModiDPD. V. PathakPSP. D. Suradiya

Key Points

  • The aim is to synthesize and evaluate the antimicrobial properties of substituted pyrrolidine derivatives.
  • Synthesize a series of substituted (Z)-1-benzyl-3-{[3-(4-nitrophenyl)-1-phenyl-1H-pyrazol-4-yl]methylidene}pyrrolidine-2,5-diones.
  • Characterize synthesized compounds for structural properties.
  • Test antimicrobial activity against specific Gram-positive and Gram-negative bacteria, as well as fungi.
  • Conduct in silico molecular docking to analyze interactions with bacterial and fungal protein targets.
  • Compounds 8d and 8i showed significant antibacterial activity compared to other derivatives.
  • In vitro studies demonstrated varying levels of antimicrobial effectiveness.
  • Molecular docking provided insights into the potential mechanisms of action against targets.

Abstract

A series of substituted (Z) -1-benzyl-3-3- (4-nitrophenyl) -1-phenyl-1H-pyrazol-4-ylmethylidene­pyrrolidine-2, 5-dione derivatives 8a–8j were synthesized and characterized. Their in vitro antimicrobial activity was evaluated against Gram-positive bacteria (Staphylococcus aureus, Streptococcus pyogenes), Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa), and fungal species (Candida albicans, Aspergillus clavatus, Aspergillus niger). Compounds 8d and 8i exhibited significant antibacterial activity compared with the other derivatives. The antimicrobial activity was assessed by measuring zones of inhibition and compared with standard drugs. Furthermore, in silico molecular docking studies were performed to analyze the binding interactions of the synthesized compounds with selected bacterial (PDB IDs: 1JIJ, 4ROT, 1KZN, 4JVI) and fungal (PDB IDs: 5C5G, 1IYL, 1UKC) target proteins in order to elucidate their potential mechanism of action.

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Cite This Study

Modi et al. (2026) studied this question.

synapsesocial.com/papers/69df2a4be4eeef8a2a6af7fchttps://doi.org/10.1134/s1070428025602924
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