Title : Inhibition of human cytochromes P450 in vitro by ritonavir and cobicistat.

Pub. Date : 2017 Dec

PMID : 28960344






4 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 OBJECTIVES: Ritonavir and cobicistat are strong inhibitors of human cytochrome P450-3A (CYP3A) isoforms, and are used clinically as pharmacokinetic boosting agents for other antiretroviral drugs. Ritonavir cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 OBJECTIVES: Ritonavir and cobicistat are strong inhibitors of human cytochrome P450-3A (CYP3A) isoforms, and are used clinically as pharmacokinetic boosting agents for other antiretroviral drugs. Ritonavir cytochrome P450 family 3 subfamily A member 4 Homo sapiens
3 KEY FINDINGS: Ritonavir and cobicistat both were strong inhibitors of CYP3A4, with IC50 values of 0.014 and 0.032 mum, respectively. Ritonavir cytochrome P450 family 3 subfamily A member 4 Homo sapiens
4 CONCLUSIONS: Consistent with previous reports, both ritonavir and cobicistat were highly potent inhibitors of CYP3A. Ritonavir cytochrome P450 family 3 subfamily A member 4 Homo sapiens