| 摘要 |
<p>Compounds useful as inhibitors of retroviral proteases characterized by structures (I) and (II) wherein the X?1 and X2¿ groups may consist of 0 to 2 α-amino acid groups terminally substituted by hydrogen or one of a number of end groups, and the R?1 and R2¿ group can be selected from a wide variety of hydrocarbon radicals.</p> |
