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Atazanavir sulfate
Cat No.
CEI-0218
Description
Atazanavir sulfate
Alias
BMS-232632, BMS-232632-05, Reyataz
CAS No.
229975-97-7
Molecular Weight
802.93
Purity
>99%
Storage
2 years at -20centigrade Powder
Synonyms
BMS-232632, BMS-232632-05, Reyataz
Targets
HIV protease
Molecular Formula
C38H52N6O7.H2SO4
Solubility
DMSO 104 mg/mL, Water
In vitro
Atazanavir inhibits the proteolytic cleavage of the viral gag precursor p55 polyprotein with IC50 of ~47 nM in virus-infected H9 cells. Atazanavir exhibits potent antiviral activity with EC50 of 3.89 nM in RF/MT-2 strains. Atazanavir is shown to be an inhibitor of bilirubin glucuronidation with IC50 of 2.4 uM. Atazanavir inhibits recombinant UGT1A1 with Ki of 1.9 uM. Atazanavir inhibits cell growth in U251, T98G, and LN229 glioblastoma cell lines, with strikingly increased GRP78 and CHOP protein levels. Atazanavir causes a prominent increase of polyubiquitinated proteins of various different sizes in U251 glioblastoma cells. Atazanavir also inhibits human 20S proteasome with IC50 of 26 uM. Atazanavir (30 uM) changes the magnitudes of ER stress and UPR gene expression in HepG2 cells. Atazanavir (30 mM) causes a 2.5-fold increase in immunoreactive P-gp expression with decreased intracellular Rh123 in LS180V cells.
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