SCYNEXIS, Inc., PO Box 12878, Research Triangle Park, NC 27709-2878, USA.
Future Med Chem. 2011 Aug;3(10):1259-78. doi: 10.4155/fmc.11.80.
Human African trypanosomiasis, caused by the kinetoplastid parasite Trypanosoma brucei, affects thousands of people across sub-Saharan Africa, and is fatal if left untreated. Treatment options for this disease, particularly stage 2 disease, which occurs after parasites have infected brain tissue, are limited due to inadequate efficacy, toxicity and the complexity of treatment regimens. We have discovered and optimized a series of benzoxaborole-6-carboxamides to provide trypanocidal compounds that are orally active in murine models of human African trypanosomiasis. A key feature of this series is the presence of a boron atom in the heterocyclic core structure, which is essential to the observed trypanocidal activity. We also report the in vivo pharmacokinetic properties of lead compounds from the series and selection of SCYX-7158 as a preclinical candidate.
人类非洲锥虫病由原生动物寄生虫布氏锥虫引起,影响撒哈拉以南非洲的数千人,如果不治疗,该病是致命的。由于疗效不足、毒性和治疗方案的复杂性,这种疾病的治疗选择,特别是在寄生虫感染脑组织后出现的 2 期疾病,受到限制。我们已经发现并优化了一系列苯并恶硼烷-6-羧酰胺,提供了在人类非洲锥虫病的鼠模型中具有口服活性的杀锥虫化合物。该系列的一个关键特征是杂环核心结构中存在硼原子,这对于观察到的杀锥虫活性是必不可少的。我们还报告了该系列的先导化合物的体内药代动力学特性,并选择 SCYX-7158 作为临床前候选药物。