英哈
吡咯烷
结核分枝杆菌
化学
肺结核
立体化学
组合化学
医学
病理
作者
Tetiana Matviiuk,Jan Madacki,Giorgia Mori,Béatrice Silvia Orena,Christophe Menendez,Andrii I. Kysil,Christiane André-Barrès,Frédéric Rodriguez,Jana Korduláková,Sonia Mallet−Ladeira,Zoia Voitenko,Maria Rosalia Pasca,Christian Lherbet,Michel Baltas
标识
DOI:10.1016/j.ejmech.2016.07.028
摘要
A series of GEQ analogues bearing pyrrolidinone or pyrrolidine cores were synthesized and evaluated against InhA, essential target for Mycobacterium tuberculosis (M.tb) survival. The compounds were also evaluated against M.tb H37Rv growth. Interestingly, some of the compounds, not efficient as InhA inhibitors, are active against M.tb with MICs up to 1.4 μM. In particular, compound 4b was screened with different M.tb mutated strains in order to identify the cellular target, but without success, suggesting a new possible mode of action.
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