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article · Future Medicinal Chemistry

Synthesis and Biological Evaluation of 2-Aminothiazole-Thiazolidinone Conjugates as Potential Antitubercular Agents

Abstract

5-ethyl carboxylate derivative 6k revealed half antitubercular activity (minimal inhibitory concentration = 1.56 μg/ml) than the acetyl analog 6c (minimal inhibitory concentration = 0.78 μg/ml), however, it exhibited more potent broad spectrum antibacterial and antifungal activities in addition to its excellent safety profile with high selectivity toward M. tuberculosis over normal human lung cells. Collectively, these data suggested that compound 6k can be considered as an ideal lead compound for further optimization.

Research topics

  • Synthesis and biological activity
  • Synthesis and Characterization of Heterocyclic Compounds
  • Quinazolinone synthesis and applications

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DOI: 10.4155/fmc-2017-0327

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