CE-245677 is a potent reversible inhibitor of Tie2 and TrkA/B kinases with a cellular IC50s of 4.7 and 1 nM.
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产品名称 | Tie-2 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Tie2 kinase inhibitor 1 |
++
Tie-2, IC50: 0.25 μM |
99%+ | |||||||||||||||||
MGCD-265 analog |
+++
Tie-2, IC50: 7 nM |
99%+ | |||||||||||||||||
Pexmetinib | ✔ | p38 MAPK | 99%+ | ||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | The Tie receptor tyrosine kinases play an important role in the development of endothelial tissues. The Tie receptors (Tie1 and Tie2) and their ligands (angiopoietins) are highly involved in the survival and functional integrity of the vasculature. CE-245677 is a potent reversible inhibitor of Tie2 and TrkA/B kinases with IC50 values of 4.7 and 1nM, respectively. It showed over 1000-fold selectivity against other angiogenic receptor tyrosine kinases, including kinase insert domain receptor, platelet-derived growth factor receptor, and fibroblast growth factor receptors, and gene family panels. CE-245677 also exhibited good oral bioavailability (F=80%) in rat pharmacokinetic study[1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.95mL 0.39mL 0.19mL |
9.74mL 1.95mL 0.97mL |
19.48mL 3.90mL 1.95mL |
CAS号 | 717899-97-3 |
分子式 | C24H22Cl2N6O3 |
分子量 | 513.376 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
溶解度 |
DMSO: 120 mg/mL(233.75 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |