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BMS-929075

Katalog-Nr.GC70501

BMS-929075 ist ein potenter und oral aktiver HCV NS5B Replikat-allosterischer Inhibitor an der Palmenstelle.

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BMS-929075 Chemische Struktur

Cas No.: 1217338-97-0

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1 mg
204,00 $
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents
BMS-929075 is a potent and orally active HCV NS5B replicase palm site allosteric inhibitor. BMS-929075 shows high oral bioavailability. BMS-929075 shows cytotoxicity.

BMS-929075 (0-60 µM) shows cytotoxicity with CC50 values of 60, >12.5, >50 µM for Huh-7, HepG2, primary human hepatocytes, respectively[1].

BMS-929075 (compound 37) (2 mg/kg for i.v.; 6 mg/kg for p.o.) shows good pharmacokinetic parameters with oral bioavailability of 48% in rats[1].
Pharmacokinetic Parameters of BMS-929075 in Male Sprague-Dawley rats[1].

IVPO
speciesCl (mL/min/kg)IV t1/2(hr)Vss(L/kg)Cmax(µM)Tmax(hr)AUC (µM h)C6 liver (µM)C24 liver (µM)C24 liver/plasma (µM)F% (mL/min/kg)
rat1.74.70.77.5454.515.11.121.648
Rats, 2 mg/kg i.v.; 6 mg/kg p.o.[1].

References:
[1]. Yeung KS, et al. Discovery of a Hepatitis C Virus NS5B Replicase Palm Site Allosteric Inhibitor (BMS-929075) Advanced to Phase 1 Clinical Studies. J Med Chem. 2017 May 25;60(10):4369-4385.

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