Cobicistat-d<sub>8</sub>

Cobicistat-d8

CAT N°: 26442
Price:

From 824.00 700.40

Cobicistat-d8 is intended for use as an internal standard for the quantification of cobicistat (Item No. 23433) by GC- or LC-MS. Cobicistat is an inhibitor of the cytochrome P450 (CYP) isomer CYP3A (IC50s = 30-285 nM for CYP3A metabolism of various HIV protease inhibitors).{41224} It is selective for CYP3A over other CYP isomers (IC50 = >25 ?M for CYP1A2, 2C8, 2C9, and 2C19). Cobicistat does not inhibit HIV-1 protease (IC50 = >30 ?M) or affect HIV replication in MT-2 cells (EC50 = >30 ?M). Formulations containing cobicistat have been used to slow the metabolism of concomitantly administered protease inhibitors in the treatment of HIV.{41225}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • thiazol-5-ylmethyl ((2R,5R)-5-((S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-4-(morpholino-d8)butanamido)-1,6-diphenylhexan-2-yl)carbamate
  • Correlated keywords
    • 2012598-79-5 1004316-88-4 deuterated deuterium GS-9350 GS9350 GCMS GC/MS LCMS LC/MS P-450 CYP-3A HIV1 MT2 CYP450 CYP2C8 CYP2C9 CYP2C19
  • Product Overview:
    Cobicistat-d8 is intended for use as an internal standard for the quantification of cobicistat (Item No. 23433) by GC- or LC-MS. Cobicistat is an inhibitor of the cytochrome P450 (CYP) isomer CYP3A (IC50s = 30-285 nM for CYP3A metabolism of various HIV protease inhibitors).{41224} It is selective for CYP3A over other CYP isomers (IC50 = >25 ?M for CYP1A2, 2C8, 2C9, and 2C19). Cobicistat does not inhibit HIV-1 protease (IC50 = >30 ?M) or affect HIV replication in MT-2 cells (EC50 = >30 ?M). Formulations containing cobicistat have been used to slow the metabolism of concomitantly administered protease inhibitors in the treatment of HIV.{41225}

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