生物活性 | |||
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靶点 |
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描述 | AMD 3465 hexahydrobromide is a potent, selective CXCR4 antagonist and exhibits 8-fold higher affinity than AMD 3100 and inhibits SDF-1α-ligand binding (Ki = 41.7 nM). |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.12mL 0.22mL 0.11mL |
5.58mL 1.12mL 0.56mL |
11.16mL 2.23mL 1.12mL |
参考文献 |
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