CAS NO: | 1431985-92-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | K02288 is a potentbone morphogenetic protein(BMP) type I receptorinhibitor withIC50s of 1.8, 1.1, 6.4 nM forALK1,ALK2andALK6, respectively. K02288 shows slightly weaker inhibition againstALK3andALK6withIC50s of of 5-34 nM. | ||||||||||||||||
IC50& Target | IC50:1.8 nM (ALK1), 1.1 nM (ALK2), 34.4 nM (ALK3), 6.3 nM (ALK6), 302 nM (ALK4), 321 nM (ALK5)[1] | ||||||||||||||||
体外研究 (In Vitro) | K02288 reduces a robust phosphorylation of Smad1/5/8 induced by BMP4 stimulation, with an apparent IC50of 100 nM. K02288 causes near complete inhibition of Smad2 phosphorylation at 0.5 μM[1]. K02288 binds to ALK1 in an ATP-mimetic fashion with two hydrogen bonds to the kinase hinge. K02288 also inhibits BMP9-ALK1 signalling, and induces a hypersprouting phenotype in HUVECs[2]. | ||||||||||||||||
体内研究 (In Vivo) | K02288 (1 μM) induces dysfunctional angiogenesis in a chick embryo CAM model[2]. | ||||||||||||||||
分子量 | 352.38 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H20N2O4 | ||||||||||||||||
CAS 号 | 1431985-92-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
溶解性数据 | In Vitro: DMSO : ≥ 58.6 mg/mL(166.30 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
|