产品描述: | K02288 is a potent bone morphogenetic protein (BMP) type I receptor inhibitor with IC50s of 1.8, 1.1, 6.4 nM for ALK1, ALK2 and ALK6, respectively. K02288 shows slightly weaker inhibition against ALK3 and ALK6 with IC50s of of 5-34 nM. |
靶点: |
IC50:1.8 nM (ALK1), 1.1 nM (ALK2), 34.4 nM (ALK3), 6.3 nM (ALK6), 302 nM (ALK4), 321 nM (ALK5);ALK;TGF-beta/Smad |
体内研究: |
K02288 (1 µM) induces dysfunctional angiogenesis in a chick embryo CAM model |
参考文献: |
1. Sanvitale CE, et al. A new class of small molecule inhibitor of BMP signaling. PLoS One. 2013 Apr 30;8(4):e62721. 2. Kerr G, et al. A small molecule targeting ALK1 prevents Notch cooperativity and inhibits functional angiogenesis. Angiogenesis. 2015 Apr;18(2):209-17. |
溶解性: |
DMSO : ≥ 58.6 mg/mL (166.30 mM) |
保存条件: |
-20℃ |
配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
1 mM |
2.838 ml |
14.189 ml |
28.378 ml |
5 mM |
0.568 ml |
2.838 ml |
5.676 ml |
10 mM |
0.284 ml |
1.419 ml |
2.838 ml |
50 mM |
0.057 ml |
0.284 ml |
0.568 ml |
|
注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |