(2′R)-2′-脱氧-2′-氟-2′-甲基脲苷

EC90：>100 μM (HCV replicon)[1]

DMSO：100 mg / mL（384.29 mM;需要超声波）

体内：1。逐个添加每种溶剂：10％DMSO 90％（20％SBE-β-CD在盐水中）溶解度：≥2.5mg / mL（9.61 mM）;澄清溶液2.逐个添加每种溶剂：10％DMSO 90％玉米油溶解度：≥2.5mg / mL（9.61 mM）;澄清溶液3.逐个添加每种溶剂：10％DMSO 40％PEG300 5％吐温-80 45％盐水溶解度：≥2.5mg/ mL（9.61mM）;明确解决方案

[1]. Clark JL, et al. Design, Synthesis, and Antiviral Activity of 2′-Deoxy-2′-fluoro-2′-C-methyl-cytidine, a Potent Inhibitor of Hepatitis C Virus Replication. J Med Chem. 2005 Aug 25;48(17):5504-8.

[2]. Ma H, et al. Characterization of the metabolic activation of hepatitis C virus nucleoside inhibitor beta-D-2′-Deoxy-2′-fluoro-2′-C-methylcytidine (PSI-6130) and identification of a novel active 5′-triphosphate species. J Biol Chem. 2007 Oct 12;282(41):29

[3]. Wang P, et al. An efficient and diastereoselective synthesis of PSI-6130: a clinically efficacious inhibitor of HCV NS5B polymerase. J Org Chem. 2009 Sep 4;74(17):6819-24.