SKI-I is a potent and selective inhibitor of human sphingosine kinase (SK), with an IC 50 of 1.2 μM for ST-hSK. SKI-I also inhibits hERK2 (IC 50 =11 μM). SKI-I induces apoptosis in tumor cell lines.
性状
Solid
IC50 & Target[1][2]
IC50: 1.2 μM (ST-hSK); 11 μM (hERK2)
体外研究(In Vitro)
SKI-I (Compound I; 5 μg/mL) inhibits SK activity by 99%.SKI-I (10 μM; 24 h) induces the apoptosis of T24 cells. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. French KJ, et, al. Discovery and evaluation of inhibitors of human sphingosine kinase. Cancer Res. 2003 Sep 15;63(18):5962-9.[2]. Sharma AK, et, al. Synthesis and bioactivity of sphingosine kinase inhibitors and their novel aspirinyl conjugated analogs. Eur J Med Chem. 2010 Sep;45(9):4149-56.
溶解度数据
In Vitro: DMSO : 100 mg/mL (246.04 mM; Need ultrasonic)配制储备液