| Literature DB >> 24556148 |
Yaling Gong1, Selin Somersan Karakaya2, Xiaoyong Guo1, Purong Zheng1, Ben Gold3, Yao Ma1, David Little3, Julia Roberts3, Thulasi Warrier3, Xiuju Jiang3, Maneesh Pingle3, Carl F Nathan4, Gang Liu5.
Abstract
Tuberculosis remains one of the deadliest infectious diseases, killing 1.4 million people annually and showing a rapid increase in cases resistant to multiple drugs. New antibiotics against tuberculosis are urgently needed. Here we describe the design, synthesis and structure-activity relationships of a series of benzimidazole-based compounds with activity against Mycobacterium tuberculosis (Mtb) in a replicating state, a physiologically-induced non-replicating state, or both. Compounds 49, 67, 68, 69, 70, and 72, which shared a 5-nitrofuranyl moiety, exhibited high potency and acceptable selectivity indices (SI). As illustrated by compound 70 (MIC90 < 0.049 μg/mL, SI > 512), the 5-nitrofuranyl group was compatible with minimal cytotoxicity and good intra-macrophage killing, although it lacked non-replicating activity when assessed by CFU assays. Compound 70 had low mutagenic potential by SOS Chromotest assay, making this class of compounds good candidates for further evaluation and target identification.Entities:
Keywords: Benzimidazole; Drug; Mycobacterium tuberculosis; Nitrofuran; Tuberculosis
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Year: 2014 PMID: 24556148 DOI: 10.1016/j.ejmech.2014.01.039
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514