HPK1-IN-32 is a potent and selective HPK1 inhibitor with an IC 50 of 65 nM. HPK1-IN-32 can be used for the research of HPK1 related disorders or diseases.
性状
Solid
IC50 & Target[1][2]
HPK1
体外研究(In Vitro)
HPK1-IN-32 (Example A34, 0-2 μM, 2 h) 抑制 Jurkat 细胞内 pSLP76 活性,IC50 为 65 nM。 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
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Sanjia XU, et al. 3-[(1h-pyrazol-4-yl)oxy]pyrazin-2-amine compounds as hpk1 inhibitor and use thereof. Patent. WO2022068848.
溶解度数据
In Vitro: DMSO : 50 mg/mL (93.17 mM; Need ultrasonic)配制储备液