Tricyclic ureas: a new class of HIV-1 protease inhibitors

Bioorg Med Chem Lett. 1998 Dec 15;8(24):3615-20. doi: 10.1016/s0960-894x(98)00659-3.

Abstract

A new class of tricyclic ureas containing a conformationally constrained proline was designed with the aid of molecular modeling. Efficient stereoselective intermolecular pinacol coupling represented the highlight of the synthesis. These rigid cyclic ureas are active towards HIV-1 protease, with 9 being the most potent compound (Ki = 9 nM) despite interacting with only three side chain binding pockets of HIV protease.

MeSH terms

  • Anti-HIV Agents / chemistry
  • Anti-HIV Agents / pharmacology*
  • HIV Protease Inhibitors / chemistry
  • HIV Protease Inhibitors / pharmacology*
  • HIV-1 / drug effects
  • Molecular Structure
  • Urea / analogs & derivatives*
  • Urea / chemistry
  • Urea / pharmacology*

Substances

  • Anti-HIV Agents
  • HIV Protease Inhibitors
  • Urea