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New anti-infective derivatives, processes for their preparation, use of the derivatives in pharmaceutical compositions containing them, and therapeutic

机译:新的抗感染衍生物,其制备方法,该衍生物在含有它们的药物组合物中的用途以及治疗性

摘要

The present invention relates to bi-substrate inhibitor molecules combining (i) a pyridine, pyridinium or dihydropyridine-type structure allied to active metabolites of isoniazide, or related structures, and (ii) a hydrophobic substituent. The invention also relates to the method for preparing said molecules, to the pharmaceutical compositions containing said molecules, and to the use thereof as inhibitors of enoyl reductase for the preparation of a drug, especially an anti-infective drug for the treatment of tuberculosis.
机译:本发明涉及双底物抑制剂分子,其结合了(i)与异烟肼的活性代谢物或相关结构相关联的吡啶,吡啶鎓或二氢吡啶型结构,以及(ii)疏水取代基。本发明还涉及制备所述分子的方法,涉及包含所述分子的药物组合物,以及其作为烯酰还原酶的抑制剂在制备药物,特别是用于治疗结核病的抗感染药中的用途。

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