Structure-based design of nonpeptidic HIV protease inhibitors: the sulfonamide-substituted cyclooctylpyramones

  • J Med Chem. 1997 Mar 28;40(7):1149-64. doi: 10.1021/jm960441m.
H I Skulnick  1 ,  P D Johnson ,  P A Aristoff ,  J K Morris ,  K D Lovasz ,  W J Howe ,  K D Watenpaugh ,  M N Janakiraman ,  D J Anderson ,  R J Reischer ,  T M Schwartz ,  L S Banitt ,  P K Tomich ,  J C Lynn ,  M M Horng ,  K T Chong ,  R R Hinshaw ,  L A Dolak ,  E P Seest ,  F J Schwende ,  B D Rush ,  G M Howard ,  L N Toth ,  K R Wilkinson ,  K R Romines
Affiliations
  • 1. Discovery Chemistry Research, Pharmacia and Upjohn, Kalamazoo, Michigan 49001, USA.
Abstract

Recently, cyclooctylpyranone derivatives with m-carboxamide substituents (e.g. 2c) were identified as potent, nonpeptidic HIV Protease Inhibitors, but these compounds lacked significant Antiviral activity in Cell Culture. Substitution of a sulfonamide group at the meta position, however, produces compounds with excellent HIV Protease binding affinity and Antiviral activity. Guided by an iterative structure-based drug design process, we have prepared and evaluated a number of these derivatives, which are readily available via a seven-step synthesis. A few of the most potent compounds were further evaluated for such characteristics as pharmacokinetics and toxicity in rats and dogs. From this work, the p-cyanophenyl sulfonamide derivative 35k emerged as a promising inhibitor, was selected for further development, and entered phase I clinical trials.