生物活性 | |||
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描述 | L-798106 is a potent and highly selective prostanoid EP3 receptor antagonist (Ki values are 0.3, 916, > 5000 and > 5000 nM at EP3, EP4, EP1 and EP2, respectively), and it can attenuate sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.86mL 0.37mL 0.19mL |
9.32mL 1.86mL 0.93mL |
18.64mL 3.73mL 1.86mL |
参考文献 |
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