were compared in order to determine the preferred absolute and relative configuration required for optimal anti-HIV activity. Anti-HIV potency and pharmacokinetic properties of the newly synthesized tricyclic octahydrophenanthroline inhibitors are presented and comparisons are made to previously reported bicyclic (8S)-N-methyl-5,6,7,8-tetrahydro-8-quinolinamine analogs.
描述了新的1,2,
3,4,4a,5,6,10b-八氢-1,10-
菲咯啉环系统的立体异构和非对映选择性合成。制备了所有四种非对映异构体的衍
生物,并在> 98%ee中分离。比较纯对映异构体,以确定最佳抗HIV活性所需的优选绝对和相对构型。介绍了新合成的
三环八氢
菲咯啉
抑制剂的抗HIV效能和药代动力学特性,并与先前报道的双环(8 S)-N-甲基-5,6,7,8-四氢-8-
喹啉胺类似物进行了比较。