Abstract
A series of C-2 and C-6 substituted pyridines was synthesized and evaluated in vitro against Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus mutans and Candida albicans. Most of compounds exhibited a wide range of modest in vitro activity against the tested microorganisms.
Keywords: Substituted pyridines, Amide, Antimicrobial activity, Synthesis
Letters in Drug Design & Discovery
Title: Synthesis and Antimicrobial Activity of Pyridine Derivatives Substituted at C-2 and C-6 Positions
Volume: 4 Issue: 2
Author(s): Mauro Vieira De Almeida, Marcus Vinicius de Nora Souza, Nadia Rezende Barbosa, Frederico Pittella Silva, Giovanni Wilson Amarante and Sílvia Helena Cardoso
Affiliation:
Keywords: Substituted pyridines, Amide, Antimicrobial activity, Synthesis
Abstract: A series of C-2 and C-6 substituted pyridines was synthesized and evaluated in vitro against Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus mutans and Candida albicans. Most of compounds exhibited a wide range of modest in vitro activity against the tested microorganisms.
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Cite this article as:
Vieira De Almeida Mauro, Vinicius de Nora Souza Marcus, Rezende Barbosa Nadia, Pittella Silva Frederico, Wilson Amarante Giovanni and Helena Cardoso Sílvia, Synthesis and Antimicrobial Activity of Pyridine Derivatives Substituted at C-2 and C-6 Positions, Letters in Drug Design & Discovery 2007; 4 (2) . https://dx.doi.org/10.2174/157018007779422514
DOI https://dx.doi.org/10.2174/157018007779422514 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
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