De Michelis C, Rocheblave L, Priem G, Chermann J C, Kraus J L
Laboratoire de Chimie Biomoléculaire, Faculté des Sciences de Luminy, Université de la Mediterranée, Marseille, France.
Bioorg Med Chem. 2000 Jun;8(6):1253-62. doi: 10.1016/s0968-0896(00)00055-9.
A small focused library of 18 compounds incorporating the motif 1,3-(N,N'-dibenzyl)diamino-2-propanol has been synthesized, using adapted synthetic methodologies. These series of compounds were evaluated for their in vitro anti-HIV activity on infected MT4 cells (syncytium formation observation). Some of the new synthesized compounds show potent anti-HIV activities. EC50 values for compounds (31, 40, 34, 37 and 46) range from 0.1 to 1 microM. In order to determine at which level these new derivatives interfere with the HIV replicative cycle, inhibition assays on recombinant HIV protease and HIV integrase have been performed. None of the compounds were found active on these two enzymatic targets. Experiments are in progress in order to identify their biological target within the HIV replicative cycle.
采用改良的合成方法,合成了一个包含1,3-(N,N'-二苄基)二氨基-2-丙醇基序的由18种化合物组成的小型聚焦文库。对这些系列化合物在感染的MT4细胞上的体外抗HIV活性进行了评估(观察合胞体形成)。一些新合成的化合物显示出强效的抗HIV活性。化合物(31、40、34、37和46)的EC50值范围为0.1至1微摩尔。为了确定这些新衍生物在哪个水平上干扰HIV复制周期,已对重组HIV蛋白酶和HIV整合酶进行了抑制试验。未发现这些化合物对这两个酶靶点有活性。为了确定它们在HIV复制周期中的生物学靶点,相关实验正在进行中。