Synthesis, Characterization, and Evaluation of Some Quinoline Derivatives as Possible Anti-Bacterial Agents

Four quinoline derivatives are synthesized by reflux reaction of isatin with beta keto ester. The studies of docking results show good hydrogen bonding using Molegro virtual docker software (MVD). Mentioned compounds exhibit Mol dock score between the range -78.3595 to -124.166 more as compare with standard ligand chloramphenicol i.e., -99.4262. Synthesized compounds were then characterized by 1H- NMR and FTIR and tested in-vitro. The synthesized compounds show good antibacterial activity against bacteria (E. coli, Staphylococcus aureus, S. typhi, B. subtilis).

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Publication Details

Journal
Asian Journal of Pharmacy and Technology
Published
2025-03-05
DOI
https://doi.org/10.52711/2231-5713.2025.00001
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00
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article

Synthesis, Characterization, and Evaluation of Some Quinoline Derivatives as Possible Anti-Bacterial Agents

Vikrant Dalwal, Shivali Shivali, Shilpa Thakur, Rahul Khatri et al.
Asian Journal of Pharmacy and Technology
Synthesis and biological activity
article

Synthesis, Characterization, and Evaluation of Some Quinoline Derivatives as Possible Anti-Bacterial Agents

Vikrant Dalwal, Shivali Shivali, Shilpa Thakur, Rahul Khatri, Monika Devi, Palvi Sharma
article en

Abstract

Four quinoline derivatives are synthesized by reflux reaction of isatin with beta keto ester. The studies of docking results show good hydrogen bonding using Molegro virtual docker software (MVD). Mentioned compounds exhibit Mol dock score between the range -78.3595 to -124.166 more as compare with standard ligand chloramphenicol i.e., -99.4262. Synthesized compounds were then characterized by 1H- NMR and FTIR and tested in-vitro. The synthesized compounds show good antibacterial activity against bacteria (E. coli, Staphylococcus aureus, S. typhi, B. subtilis).

Asian Journal of Pharmacy and Technology
Hindu College of Pharmacy (IN)
Openalex Percentile: Top 94%
Synthesis and biological activity
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