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Synthesis and PreliminaryIn Vitro Evaluation of Antimycobacterial Activity of New Pyrrolo[1,2-a]quinoxaline-carboxylic Acid Hydrazide Derivatives
Authors:Jean Guillon  Robert C. Reynolds  Jean-Michel Leger  Marie-Aude Guie  Stephane Massip  Patrick Dallemagne
Affiliation:1. EA- Pharmacochimie, UFR des Sciences Pharmaceutiques, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076, Bordeaux Cedex, France;2. National Institute of Allergy and Infectious Diseases - TAACF, Southern Research Institute, 2000 Ninth Avenue South, Birmingham, AL, 35255, USA;3. Centre d'Etudes et de Recherche sur le Médicament de Normandie, UFR des Sciences Pharmaceutiques, 1 rue Vaubénard, 14032, Caen Cedex, France
Abstract:New pyrrolo[1,2-a]quinoxaline-2- or -4-carboxylic acid hydrazide derivatives were synthesized from nitroaniline or 1,2-phenylenediamine, and evaluated in vitro for their antimycobacterial activity as part of a TAACF TB screening program. Two compounds 7c and 13 showed an interesting activity at 6.25?μg/mL against Mycobacterium tuberculosis H37Rv, with a 94 and 100 percentage inhibition, respectively.
Keywords:Pyrrolo[1,2-a]quinoxaline-carboxylic acid hydrazide derivatives  Mycobacterium tuberculosis  Antimycobacterial agents  Tuberculosis
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