生物活性 | |||
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描述 | DDR1-IN-1 exhibits potent and selective inhibition of the DDR1 receptor tyrosine kinase, with an IC50 of 105 nM. It is approximately four times less potent for DDR2, with an IC50 of 413 nM[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.81mL 0.36mL 0.18mL |
9.05mL 1.81mL 0.90mL |
18.10mL 3.62mL 1.81mL |
参考文献 |
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