Department of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, California 95064, USA.
J Med Chem. 2010 May 27;53(10):4187-97. doi: 10.1021/jm100265s.
Leishmaniasis is a debilitating disease caused by protozoan parasites of the genus Leishmania, which affects an estimated 12 million people worldwide. The discovery of new lead compounds for leishmaniasis is therefore a pressing concern for global health programs. The organic extract of a Panamanian collection of the marine cyanobacterium Lyngbya majuscula showed strong in vitro activity in two complementary screens against the tropical parasite Leishmania donovani, the causative agent of visceral leishmaniasis. Chromatographic separation of this complex mixture led to the isolation of the highly N-methylated linear lipopeptides, almiramides A-C (1-3). Comparison with the biological activities of a number of related metabolites and semisynthetic derivatives revealed key features required for activity and afforded one new compound (11) with superior in vitro activity. Subsequent synthesis of a library of simplified analogues led to the discovery of several compounds with improved therapeutic indices to the natural products.
利什曼病是一种由利什曼原虫属原生动物寄生虫引起的使人虚弱的疾病,估计全世界有 1200 万人受到影响。因此,为全球卫生计划发现新的利什曼病先导化合物是当务之急。来自巴拿马的海洋蓝藻 Lyngbya majuscula 的有机提取物在针对热带寄生虫利什曼原虫的两种互补筛选中表现出很强的体外活性,利什曼原虫是内脏利什曼病的病原体。对这种复杂混合物的色谱分离导致了高度 N-甲基化的线性脂肽,almiramides A-C(1-3)的分离。与许多相关代谢物和半合成衍生物的生物活性比较揭示了活性所必需的关键特征,并提供了一种具有优异体外活性的新化合物(11)。随后合成了一系列简化类似物文库,发现了几种化合物,其治疗指数优于天然产物。