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Human serum attenuates the activity of protease inhibitors toward wild-type and mutant human immunodeficiency virus.

J. Leonard, A. Molla, S. Vasavanonda, 1998, Virology.

Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir

A. D. Rodrigues, J. Leonard, A. Hsu, 1997, Antimicrobial agents and chemotherapy.

Discovery of ritonavir, a potent inhibitor of HIV protease with high oral bioavailability and clinical efficacy.

A. Molla, S. Vasavanonda, D. Norbeck, 1998, Journal of medicinal chemistry.

Cyclobut-A and cyclobut-G, carbocyclic oxetanocin analogs that inhibit the replication of human immunodeficiency virus in T cells and monocytes and macrophages in vitro

D. Norbeck, H. Mitsuya, S. Broder, 1990, Antimicrobial Agents and Chemotherapy.

New inhibitors of renin that contain novel phosphostatine Leu-Val replacements.

R. Maki, K. Marsh, J. Plattner, 1990, Journal of medicinal chemistry.