包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | HPK1-IN-3 is a potent and selective ATP-competitivehematopoietic progenitor kinase 1 (HPK1; MAP4K1)inhibitor with anIC50of 0.25 nM. HPK1-IN-3 hasIL-2cellular potency with an EC50of 108 nM in human peripheral blood mononuclear cells (PBMCs)[1]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | HPK1-IN-3 (compound 27; 0.25-4 μM; 24-h) treatment shows a statistically significant elevation of proinflammatory cytokines IL-6 and TNF-α was observed in a concentration-dependent manner in human monocyte-derived dendritic cells[1]. | ||||||||||||||||
分子量 | 490.45 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H22F4N6O2 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 83.33 mg/mL(169.91 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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