DESIGN, SYNTHESIS, AND CONFORMATIONAL-ANALYSIS OF A NOVEL MACROCYCLIC HIV-PROTEASE INHIBITOR

Design modifications to the lead HnT-PR inhibitor 1 (MDL 73,669, K-i = 5 nM) have been postulated based on a computational model of the 1/HIV-PR complex. A novel macrocyclic inhibitor 8 (MDL 104,168) wherein the P-1 and P-3 Side chains of the original acyclic inhibitor have been joined retains good biological activity (K-i = 20 nM). NMR analysis of the precursor alcohol (S)-7 shows the conformation of the cyclic region to be very similar to that observed in the enzyme-bound 8 as determined by the computational model. Consistency of the computational model with NMR data and in vacuo molecular dynamics simulations provide the basis for postulating further modifications of the cyclic inhibitor expected to optimize its interactions with HIV-PR.