产品描述: | SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM. |
靶点: |
VEGFR |
体内研究: |
SKLB1002通过抑制VEGF诱导的VEGFR2激酶磷酸化和下游蛋白激酶,包括ERK,FAK和Src,明显抑制人脐静脉内皮细胞增殖,迁移,侵袭和管腔形成。SKLB1002对正常人细胞L-02细胞毒性显著降低 |
细胞实验: |
Cell proliferation is measured using MTT assay. Various cells including HUVECs, L-02, B16-F10, HepG2, and SW620 are treated with indicated concentrations of SKLB1002 for 24 hours. Vandetanib and sunitinib serve as positive controls. Each assay is replicated 3 times.(Only for Reference) |
参考文献: |
1.Zhang S, et al. Clin Cancer Res. 2011, 17(13), 4439-4450. 2.Nie W, et al. 2012. Doi 10.1007/s10238-012-0225-2. |
溶解性: |
DMSO:7 mg/mL (21.84 mM) Ethanol:<1 mg/mL H2O:<1 mg/mL |
保存条件: |
-20℃ |
配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
1 mM |
3.121 ml |
15.606 ml |
31.212 ml |
5 mM |
0.624 ml |
3.121 ml |
6.242 ml |
10 mM |
0.312 ml |
1.561 ml |
3.121 ml |
50 mM |
0.062 ml |
0.312 ml |
0.624 ml |
|
注意: |
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