Virtual Screening, Selection and Development of a Benzindolone Structural Scaffold for Inhibition of Lumazine Synthase

Virtual screening of a library of commercially available compounds vs. the structure of Mycobacterium tuberculosis lumazine synthase identified 2-(2-oxo-1,2-dihydrobenzo[cd]indole-6-sulfonamido)acetic acid (9) as a possible lead compound. Compound 9 proved to be an effective inhibitor of M. tubercul...

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Detalhes bibliográficos
Main Authors: Talukdar, Arindam, Morgunova, Ekaterina, Duan, Jianxin, Meining, Winfried, Foloppe, Nicolas, Nilsson, Lennart, Bacher, Adelbert, Illarionov, Boris, Fischer, Markus, Ladenstein, Rudolf, Cushman, Mark
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2868945/
https://ncbi.nlm.nih.gov/pubmed/20430628
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2010.03.072
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