ACS Medicinal Chemistry Letters · 2010 · 200 citations · 20 references
MedicineMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyAntiretroviral TherapyAntiviral PharmacologyCytochrome P450 EnzymesCytochrome P450 InteractionsCytochrome P450-mediated MetabolismEnzyme InhibitionAqueous Solubility ImprovementCyp3a4 InteractionsCyp450-mediated InteractionsCytochrome P450 Enzyme InhibitionCytochrome P450 Structure-function Relationships
Cobicistat (3, GS-9350) is a newly discovered, potent, and selective inhibitor of human cytochrome P450 3A (CYP3A) enzymes. In contrast to ritonavir, 3 is devoid of anti-HIV activity and is thus more suitable for use in boosting anti-HIV drugs without risking selection of potential drug-resistant HIV variants. Compound 3 shows reduced liability for drug interactions and may have potential improvements in tolerability over ritonavir. In addition, 3 has high aqueous solubility and can be readily coformulated with other agents.
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Antiretroviral Treatment of Adult HIV Infection
Scott M. Hammer, Joseph J. Eron, Peter Reiss et al. · JAMA · 2008 · 1K citations
Thorir D. Bjornsson, John T. Callaghan, Heidi J. Einolf et al. · Drug Metabolism and Disposition · 2003 · 784 citations