Plasma pharmacokinetics and urinary and biliary excretion of a new potent tripeptide HIV-1 protease inhibitor, KNI-272, in rats after intravenous administration
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine
Reference11 articles.
1. Human immunodeficiency virus protease: A target for aids therapy
2. The HIV-1 Protease as a Therapeutic Target for AIDS
3. HIV protease: a novel chemotherapeutic target for AIDS
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1. Divergent and Scalable Synthesis of α-Hydroxy/Keto-β-amino Acid Analogues by the Catalytic Enantioselective Addition of Glyoxylate Cyanohydrin to Imines;ACS Catalysis;2019-10-02
2. Physiologically based pharmacokinetics of KNI-272, a tripeptide HIV-1 protease inhibitor;BIOPHARM DRUG DISPOS;1999
3. Physiologically based pharmacokinetics of KNI-272, a tripeptide HIV-1 protease inhibitor;Biopharmaceutics & Drug Disposition;1999-05
4. Metabolic Characterization of a Tripeptide Human Immunodeficiency Virus Type 1 Protease Inhibitor, KNI-272, in Rat Liver Microsomes;Antimicrobial Agents and Chemotherapy;1999-03
5. A phase I trial of the pharmacokinetics, toxicity, and activity of KNI-272, an inhibitor of HIV-1 protease, in patients with AIDS or symptomatic HIV infection;Antiviral Research;1999-02
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