Turner S R, Strohbach J W, Tommasi R A, Aristoff P A, Johnson P D, Skulnick H I, Dolak L A, Seest E P, Tomich P K, Bohanon M J, Horng M M, Lynn J C, Chong K T, Hinshaw R R, Watenpaugh K D, Janakiraman M N, Thaisrivongs S
Department of Structural, Analytical & Medicinal Chemistry, Pharmacia & Upjohn, Inc., 301 Henrietta Street, Kalamazoo, Michigan 49001, USA.
J Med Chem. 1998 Aug 27;41(18):3467-76. doi: 10.1021/jm9802158.
A broad screening program previously identified phenprocoumon (1) as a small molecule template for inhibition of HIV protease. Subsequent modification of this lead through iterative cycles of structure-based design led to the activity enhancements of pyrone and dihydropyrone ring systems (II and V) and amide-based substitution (III). Incorporation of sulfonamide substitution within the dihydropyrone template provided a series of highly potent HIV protease inhibitors, with structure-activity relationships described in this paper. Crystallographic studies provided further information on important binding interactions responsible for high enzymatic binding. These studies culminated in compound VI, which inhibits HIV protease with a Ki value of 8 pM and shows an IC90 value of 100 nM in antiviral cell culture. Clinical trials of this compound (PNU-140690, Tipranavir) for treatment of HIV infection are currently underway.
之前一个广泛的筛选项目确定苯丙香豆素(1)是一种用于抑制HIV蛋白酶的小分子模板。通过基于结构设计的迭代循环对该先导化合物进行后续修饰,提高了吡喃酮和二氢吡喃酮环系统(II和V)以及酰胺基取代(III)的活性。在二氢吡喃模板中引入磺酰胺取代得到了一系列高效的HIV蛋白酶抑制剂,本文描述了其构效关系。晶体学研究提供了有关负责高酶结合的重要结合相互作用的更多信息。这些研究最终得到了化合物VI,其抑制HIV蛋白酶的Ki值为8 pM,在抗病毒细胞培养中的IC90值为100 nM。该化合物(PNU-140690,替拉那韦)用于治疗HIV感染的临床试验目前正在进行。