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描述 | The steroid sulfatase hydrolyses estrone sulfate and plays a key role in the regulation of estrogenic steroid formation. The inhibition of steroid sulfatase is an important therapeutic strategy for the treatment of postmenopausal women with breast cancer. Irosustat is a potent inhibitor of steroid sulfatase with an IC50 value of 8nM in a placental microsome assay. It is an orally active, irreversible, and nonsteroidal inhibitor. A single dose of irosustat (10mg/kg, p.o.) inhibited estrone sulfatase activity in rat liver by 93%. Administration of irosustat (2mg/kg, p.o.) for 5 days inhibited estrone sulfate-stimulated growth of uteri in ovariectomized rats. Irosustat (2 and 10mg/kg, p.o.) also suppressed estrone sulfate-stimulated tumor growth in a dose-dependent manner[3]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.23mL 0.65mL 0.32mL |
16.16mL 3.23mL 1.62mL |
32.33mL 6.47mL 3.23mL |
CAS号 | 288628-05-7 |
分子式 | C14H15NO5S |
分子量 | 309.338 |
别名 | STX64;BN83495;COUMATE. Irosustat.;ST-64667;STX 64667;667-Coumate |
运输 | 蓝冰 |
存储条件 |
粉末 Keep in dark place,Sealed in dry,2-8°C 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
DMSO: 105 mg/mL(339.43 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |