CAS NO: | 219832-49-2 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | MP-A08 is a highly selective ATP competitive sphingosine kinase (SPHK1) inhibitor that targets bothSphK1andSphK2with Ki values of 6.9 ± 0.8 μM and 27 ± 3 μM, respectively. | ||||||||||||||||
体外研究 (In Vitro) | MP-A08 blocks pro-proliferative signalling pathways, induces mitochondrial-associated apoptosis in a SK-dependent manner, and reduces the growth of human lung adenocarcinoma tumours in a mouse xenograft model by both inducing tumour cell apoptosis and inhibiting tumour angiogenesis. MP-A08 inhibit SphK2, cause a decrease in EC barrier integrity in vitro in both cell type.[2] | ||||||||||||||||
体内研究 (In Vivo) | MP-A08 suppresses the growth of human lung tumor xenografts in mice. | ||||||||||||||||
分子量 | 519.64 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C27H25N3O4S2 | ||||||||||||||||
CAS 号 | 219832-49-2 | ||||||||||||||||
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 : ≥ 50 mg/mL(96.22 mM) *"≥" means soluble, but saturation unknown. 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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