2013•Research and reviews : journal of chemistryRequires access

Synthesis of Some Newer Nalidixic Acid Derivatives as Potent Antimicrobial Agents

Fathi H. Assaleh, B. G. S. RAO, Ramalingam Peraman, Prakash Katakam

Open publisher page 1 citations

Abstract

A molecular manipulation efforts were made at β carbon of α, β unsaturated site of nalidixic acid by Michael addition, in expectation to get newer chemimanipulated derivatives with potent/modified antimicrobial spectrum. At the ends of chemimanipulative work, totally 5 derivatives were synthesized and characterized by spectral data. All the derivatives were screened for its antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Pseudomonas aureginosa, and Proteus vulgaris at a concentration of 100μg/disc with the same dose of nalidixic acid as control by agar plate disc diffusion method. The results revealed that hydrazine substituted tricyclic derivatives exhibited potent antibacterial activity gram +ve rather than against gram –ve, however, potentiation were found to be against gram +ve and gram –ve bacteria.

About this research paper

What this paper is about

A molecular manipulation efforts were made at β carbon of α, β unsaturated site of nalidixic acid by Michael addition, in expectation to get newer chemimanipulated derivatives with potent/modified antimicrobial spectrum. At the ends of chemimanipulative work, totally 5 derivatives were synthesized and characterized by spectral data. All the derivatives were screened for its antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Pseudomonas aureginosa, and Proteus vulgaris at a concentration of 100μg/disc with the same dose of nalidixic acid as control by agar plate disc diffusion method. The results revealed that hydrazine substituted tricyclic derivatives exhibited potent antibacterial activity gram +ve rather than against gram –ve, however, potentiation were found to be against gram +ve and gram –ve bacteria.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A molecular manipulation efforts were made at β carbon of α, β unsaturated site of nalidixic acid by Michael addition, in expectation to get newer chemimanipulated derivatives with potent/modified antimicrobial spectrum. At the ends of chemimanipulative work, totally 5 derivatives were synthesized and characterized by spectral data. All the derivatives were screened for its antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Pseudomonas aureginosa, and Proteus vulgaris at a concentration of 100μg/disc with the same dose of nalidixic acid as control by agar plate disc diffusion method. The results revealed that hydrazine substituted tricyclic derivatives exhibited potent antibacterial activity gram +ve rather than against gram –ve, however, potentiation were found to be against gram +ve and gram –ve bacteria.

Key concepts: Nalidixic acid, Antimicrobial, Proteus vulgaris, Bacillus subtilis, Chemistry, Agar diffusion test, Antibacterial activity, Proteus

Related papers

Back to paper searchBrowse research topicsOriginal source
Synthesis of Some Newer Nalidixic Acid Derivatives as Potent Antimicrobial Agents — Research Paper | ScholarLens