作者:Joseph A. Maddry、Namita Bansal、Luiz E. Bermudez、Robert N. Comber、Ian M. Orme、William J. Suling、Larry N. Wilson、Robert C. Reynolds
DOI:10.1016/s0960-894x(98)00017-1
日期:1998.2
A series of hydrolytically-stable aza analogs of arabinofuranose was prepared and evaluated against Mycobacterium tuberculosis and M. avium. The compounds were designed to mimic the putative arabinose donor involved in biogenesis of the essential cell wall polysaccharide, arabinogalactan. Though most compounds displayed little activity in cell culture, one compound showed significant activity in infected
制备了一系列阿拉伯呋喃糖水解稳定的氮杂类似物,并针对结核分枝杆菌和鸟分枝杆菌进行了评估。设计这些化合物以模拟参与必需细胞壁多糖阿拉伯半乳聚糖的生物发生的推定的阿拉伯糖供体。尽管大多数化合物在细胞培养中显示很少的活性,但一种化合物在感染的巨噬细胞模型中显示了显着的活性。