本文重点介绍了哌嗪稠合三唑类药物发展中的挑战和机遇。阐述了基于[1,2,4]三唑并[4,3- a ]吡嗪平台的药物化学相关构建模块的方法。该方法可以从市售的廉价试剂开始快速、多克地获得目标衍生物。这些方法用于创建一个小型的三唑并吡嗪文库,其中 3 位具有多种取代基。显示了文库成员进一步合成应用用于药物合成的潜力。
The present invention features compounds that are HIV integrase inhibitors and therefore are useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.
The present invention features compounds that are HIV integrase inhibitors and therefore are useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.