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1015073-42-3

中文名称 1015073-42-3
英文名称 PSI7409
CAS 1015073-42-3
分子式 C10H16FN2O14P3
分子量 500.16
MOL 文件 1015073-42-3.mol
更新日期 2024/05/20 09:54:47
1015073-42-3 结构式 1015073-42-3 结构式

基本信息

中文别名
化合物 T12572
英文别名
PSI7409
PSI-7409
PSI 7409
Uridine 5'-(tetrahydrogen triphosphate), 2'-deoxy-2'-fluoro-2'-methyl-, (2'R)-
(2R,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

物理化学性质

储存条件-20°C储存
溶解度少许溶于甲醇和水
形态固体
颜色白色至灰白色
稳定性吸湿性

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335
1015073-42-3价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2023/03/20HY-157451015073-42-3
PSI-7409
1015073-42-31mg2600元
2023/03/20HY-157451015073-42-3
PSI-7409
1015073-42-35mg7800元

常见问题列表

生物活性
PSI-7409是 Sofosbuvir (PSI-7977) 的5'-三磷酸活性代谢物。Sofosbuvir (PSI-7977) 是选择性和高活性的 HCV 核苷酸类似物抑制剂。
体外研究

PSI-7409 inhibits the enzymatic activities of these NS5BΔ21 polymerases in a dose-dependent manner. The IC 50 s for PSI-7409 against GT 1b, 2a, 3a, and 4a NS5B polymerases are 1.6 μM, 2.8 μM, 0.7 μM, and 2.6 μM, respectively. PSI-7409 is a weak inhibitor of DNA Pol α (IC 50 =550 μM). DNA Pol β and γ are not inhibited by 1 mM PSI-7409. A significant amount of RNA product is made in the presence of 500 μM PSI-7409, about 85%. In clone A cells, the levels of PSI-7409 gradually increases to a maximum concentration of about 25 μm over a period of 48 h. PSI-7409 forms at a much faster rate in primary human hepatocytes, achieving a maximum intracellular concentration of ∼100 μM at 4 h and remains at that concentration for 48 h.

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