CAS NO: | 745833-23-2 |
生物活性 | VX-702 is a highly selective inhibitor ofp38αMAPK, 14-fold higher potency against thep38αversusp38β[1]. | ||||||||||||||||
IC50& Target | p38α MAPK[1] | ||||||||||||||||
体外研究 (In Vitro) | Pre-incubation of platelets with VX-702 (1 μM) completely or partially inhibits p38 activation (IC50 4 to 20 nM) induced by platelet agonists including thrombin, SFLLRN, AYPGKF, U46619 and collagen. VX-702 shows no effect on platelet aggregation induced by any of the p38 MAPK agonists in the presence or absence of anti-platelet therapies[1]. | ||||||||||||||||
体内研究 (In Vivo) | The half-life of VX-702 is 16 to 20 hours, with a median clearance of 3.75 L/h and a volume of distribution of 73 L/kg. Both AUC and Cmax values are dose proportional for VX-702, which is predominantly cleared renally[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 404.32 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H12F4N4O2 | ||||||||||||||||
CAS 号 | 745833-23-2 | ||||||||||||||||
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 : ≥ 42 mg/mL(103.88 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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