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Design, Synthesis, and Characterization of N-Oxide-Containing Heterocycles with in Vivo Sterilizing Antitubercular Activity.

Guilherme Felipe Dos Santos FernandesPaula Carolina de SouzaElsa Moreno-ViguriMery Santivañez-VelizRocio PaucarSilvia Pérez-SilanesKonstantin ChegaevStefano GuglielmoLoretta LazzaratoRoberta FrutteroChung Man ChinPatricia Bento da SilvaMarlus ChorilliMariana Cristina SolciaCamila Maríngolo RibeiroCaio Sander Paiva SilvaLeonardo Biancolino MarinoPriscila Longhin BosquesiDebbie M HuntLuiz Pedro S de CarvalhoCarlos Alberto de Souza CostaSang Hyun ChoYuehong WangScott Gary FranzblauFernando Rogério PavanJean Leandro Dos Santos
Published in: Journal of medicinal chemistry (2017)
Tuberculosis, caused by Mycobacterium tuberculosis (Mtb), is the infectious disease responsible for the highest number of deaths worldwide. Herein, 22 new N-oxide-containing compounds were synthesized followed by in vitro and in vivo evaluation of their antitubercular potential against Mtb. Compound 8 was found to be the most promising compound, with MIC90 values of 1.10 and 6.62 μM against active and nonreplicating Mtb, respectively. Additionally, we carried out in vivo experiments to confirm the safety and efficacy of compound 8; the compound was found to be orally bioavailable and highly effective, leading to a reduction of Mtb to undetectable levels in a mouse model of infection. Microarray-based initial studies on the mechanism of action suggest that compound 8 blocks translation. Altogether, these results indicate that benzofuroxan derivative 8 is a promising lead compound for the development of a novel chemical class of antitubercular drugs.
Keyphrases
  • mycobacterium tuberculosis
  • pulmonary tuberculosis
  • mouse model
  • infectious diseases
  • emergency department
  • hepatitis c virus
  • electronic health record