Interaction of CYP3A4 with the inhibitor cobicistat: Structural and mechanistic insights and comparison with ritonavir-Reference-Cited by-同舟云学术

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Interaction of CYP3A4 with the inhibitor cobicistat: Structural and mechanistic insights and comparison with ritonavir

Published:2024-08 Issue: Volume:758 Page:110071
ISSN:0003-9861
Container-title:Archives of Biochemistry and Biophysics
language:en
Short-container-title:Archives of Biochemistry and Biophysics

Author:

Sevrioukova Irina F.^ORCID

Funder

Office of Science

National Institute of General Medical Sciences

National Institutes of Health

National Institute of Environmental Health Sciences

Publisher

Elsevier BV

Reference32 articles.

1. ABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humans;Kempf;Proc. Natl. Acad. Sci. U. S. A.,1995

2. Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir;Kempf;Antimicrob. Agents Chemother.,1997

3. Pharmacokinetic enhancers for HIV drugs;Xu;Curr. Opin. Invest. Drugs,2009

4. Cobicistat versus ritonavir: similar pharmacokinetic enhancers but some important differences;Tseng;Ann. Pharmacother.,2017

5. Cobicistat (GS-9350): a potent and selective inhibitor of human CYP3A as a novel pharmacoenhancer;Xu;ACS Med. Chem. Lett.,2010

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