生物活性 | |||
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描述 | PMX 53 is a potent C5a receptor antagonist (IC50 = 20 nM). Also MrgX2 agonist, it stimulates MrgX2-mediated mast cell degranulation, also inhibits C5a-induced hypernociception in rats, inhibits lung metastasis in a mouse breast cancer model and reduces atherosclerotic lesions in a mouse model of atherosclerosis. |
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 |