98% Min GS9350 Cobicistat Cyp17 Inhibitor Cas 1004316-88-4
98% Min GS9350 Cobicistat Cyp17 Inhibitor Cas 1004316-88-4
| Product name:Cobicistat | Purity:98% min |
| CAS NO:1004316-88-4 | Solubility:DMSO : 100 mg/mL (128.86 mM) |
| Molecular Formula:C40H53N7O5S2 | Package:Package according to customer requirements |
| Molecular Weight:776.023 | Storage:Store at -20℃ |
Cobicistat, also known as GS9350, is an approved drug for use in the treatment of infection with the human immunodeficiency virus (HIV). Like ritonavir (Norvir), cobicistat is of interest not for its anti-HIV properties, but rather its ability to inhibit liver enzymes that metabolize other medications used to treat HIV, notably elvitegravir, an HIV integrase inhibitor currently under investigation itself. By combining cobicistat with elvitegravir, higher concentrations of elvitgravir are achieved in the body with lower dosing, theoretically enhancing elvitgravir's viral suppression while diminishing its adverse side-effects. In contrast with ritonavir, the only currently approved booster, cobicistat has no anti-HIV activity of its own. Cobicistat is a component of the four-drug, fixed-dose combination HIV treatment elvitegravir/cobicistat/emtricitabine/tenofovir (known as the "Quad Pill"). The Quad Pill was approved by the FDA in August 2012 for use in the United States and is owned by Gilead Sciences.
P450 (e.g. CYP17) inhibitor Related Products:
Abiraterone; Abiraterone acetate; Ketoconazole; Orteronel(racemic); Orteronel; Galeterone; Ozagrel; Ritonavir; Posaconazole; Voriconazole; Fluconazole; Clarithromycin
[1]. Lianhong Xu, et al. Cobicistat (GS-9350): A Potent and Selective Inhibitor of Human CYP3A as a Novel Pharmacoenhancer. ACS Med. Chem. Lett., 2010, 1 (5), pp 209–213
[2]. Temesgen Z. Cobicistat, a pharmacoenhancer for HIV treatments. Drugs Today (Barc). 2013 Apr;49(4):233-7.
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