SC-52151, a novel inhibitor of the human immunodeficiency virus protease
| Autor: | Decrescenzo Gary A, J Marr, Mary Smidt, R Dillard, Heintz Robert M, Getman Daniel P, D Lansky, K Houseman, Michael Clare, Martin L. Bryant |
|---|---|
| Rok vydání: | 1995 |
| Předmět: |
medicine.medical_treatment
Molecular Sequence Data Biology Pharmacology Antiviral Agents Virus Nucleoside Reverse Transcriptase Inhibitor Rats Sprague-Dawley Zidovudine Dogs Pharmacokinetics medicine Animals Humans Urea HIV Protease Inhibitor Pharmacology (medical) Protease inhibitor (pharmacology) Amino Acid Sequence Protease HIV Drug Synergism HIV Protease Inhibitors Macaca mulatta Virology Rats Bioavailability Infectious Diseases Research Article Protein Binding medicine.drug |
| Zdroj: | Antimicrobial Agents and Chemotherapy. 39:2229-2234 |
| ISSN: | 1098-6596 0066-4804 |
| DOI: | 10.1128/aac.39.10.2229 |
| Popis: | SC-52151 is a potent, selective, tight-binding human immunodeficiency virus (HIV) protease inhibitor containing the novel (R)-(hydroxyethyl) urea isostere. The mean 50% effective concentration for lymphotropic, monocytotropic strains and field isolates of HIV type 1 (HIV-1), HIV-2, and simian immunodeficiency virus is 26 ng/ml (43 nM). The combination of SC-52151 and nucleoside reverse transcriptase inhibitors synergistically inhibited HIV-1 replication without additive toxicity. An extended postantiviral effect correlates with inhibition of gag and gag-pol polyprotein processing. SC-52151 is highly protein bound ( >90%) in human plasma, and the level of partitioning into erythrocytes is low. Physiological concentrations of alpha-1-acid glycoprotein, but not albumin, substantially affect the antiviral potency of SC-52151. The oral bioavailability of [14C]SC-52151 is 17% when it is administered as an elixir to the rat, dog, or monkey. Oxidation of the t-butyl moiety is the major route of biotransformation, and elimination is mainly by biliary excretion. No toxicologically significant effects have been observed in animals. Pharmacokinetic and metabolism studies in multiple animal species predict 20 to 30% systemic bioavailability, an elimination half-life of 1 to 2 h, and a volume of distribution of greater than 3 liters/kg in humans. |
| Databáze: | OpenAIRE |
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