ABSTRACT
A series of symmetry-based HIV protease inhibitors was designed and synthesized. Modification of the core regiochemistry and stereochemistry significantly affected the potency, metabolic stability, and oral bioavailability of the inhibitors, as did the variation of a pendent arylmethyl P3 group. Optimization led to the selection of two compounds, 10c (A-790742) and 9d (A-792611), for advancement to preclinical studies. Both compounds displayed low nanomolar potency against wild type HIV in the presence of human serum, low rates of metabolism in human liver microsomes, and high oral bioavailability in animal models. The compounds were examined in a preclinical model for the hyperbilirubinemia observed with some HIV PIs, and both exhibited less bilirubin elevation than comparator compounds. X-ray crystallographic analyses of the new cores were used to examine differences in their binding modes. The antiviral activity of the compounds against protease inhibitor resistant strains of HIV was also determined.
Subject(s)
Carbamates/chemical synthesis , Dipeptides/chemical synthesis , HIV Protease Inhibitors/chemical synthesis , Putrescine/analogs & derivatives , Pyridines/chemical synthesis , Animals , Binding Sites , Biological Availability , Caco-2 Cells , Carbamates/metabolism , Carbamates/pharmacology , Cell Membrane Permeability , Crystallography, X-Ray , Dipeptides/adverse effects , Dipeptides/pharmacology , Dogs , Drug Resistance, Viral , HIV Protease/genetics , HIV Protease Inhibitors/adverse effects , HIV Protease Inhibitors/pharmacology , HIV-1/drug effects , HIV-1/enzymology , HIV-1/genetics , Humans , Hyperbilirubinemia/chemically induced , Hyperlipidemias/chemically induced , Hyperlipidemias/metabolism , In Vitro Techniques , Microsomes, Liver/metabolism , Models, Molecular , Mutation , Putrescine/chemical synthesis , Putrescine/metabolism , Putrescine/pharmacology , Pyridines/adverse effects , Pyridines/pharmacology , Rats , Rats, Gunn , Stereoisomerism , Structure-Activity RelationshipABSTRACT
A practical preclinical model for the hyperbilirubinemia produced by human immunodeficiency virus protease inhibitors has been developed. Indinavir and atazanavir produced significant hyperbilirubinemia, whereas amprenavir, the negative control, was indistinguishable from the ritonavir booster dose. This model was used to disqualify an exploratory protease inhibitor from development.