Identification and development of the 1,4-benzodiazepin-2-one and quinazoline-2,4-dione scaffolds as submicromolar inhibitors of HAT
作者:Rachel L. Clark、Carol J. Clements、Michael P. Barrett、Simon P. Mackay、Rajendra P. Rathnam、George Owusu-Dapaah、John Spencer、Judith K. Huggan
DOI:10.1016/j.bmc.2012.08.049
日期:2012.10
A library of 1,4-benzodiazepines has been synthesised and evaluated for activity against Trypanosoma brucei, a causative parasite of Human African Trypanosomiasis (HAT). The most potent of these derivatives has an MIC value of 0.97 μM. Herein we report the design, synthesis and biological evaluation of the abovementioned compounds.
合成了一个1,4-苯并二氮杂卓的文库,并评估了其对布鲁氏锥虫(人类非洲锥虫病(HAT)的致病性寄生虫)的活性。这些衍生物中最有效的MIC值为0.97μM。本文中我们报告了上述化合物的设计,合成和生物学评估。