CAS NO: | 2703752-81-0 |
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 | GSK-872 hydrochloride is aRIPK3inhibitor, which binds RIP3 kinase domain with anIC50of 1.8 nM, and inhibits kinase activity with anIC50of 1.3 nM. GSK-872 hydrochloride decreases the RIPK3-mediatednecroptosisand subsequent cytoplasmic translocation and expression of HMGB1, as well as ameliorates brain edema and neurological deficits in early brain injury[1][2][3]. | ||||||||||||||||
IC50& Target | IC50: 1.3 nM (RIPK3)[1] | ||||||||||||||||
体外研究 (In Vitro) | GSK-872 (GSK'872; 0.01-3 μM; 24 hours) blocks TNF-induced necroptosis in human HT-29 cells in a concentration-dependent manner[1]. Cell Viability Assay[1]
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体内研究 (In Vivo) | GSK-872 hydrochloride (25 mM; intracerebroventricular injection) can attenuate brain edema and improve neurological function following subarachnoid hemorrhage (SAH) and reduce the number of necrotic cells. GSK-872 hydrochloride can also decrease the protein levels of RIPK3 and MLKL, and cytoplasmic translocation and expression of HMGB1, an important pro-inflammatory protein[3].
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分子量 | 419.95 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H18ClN3O2S2 | ||||||||||||||||
CAS 号 | 2703752-81-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 10 mg/mL(23.81 mM;ultrasonic and warming and heat to 60℃) H2O : 2.5 mg/mL(5.95 mM;ultrasonic and warming and heat to 60℃) 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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