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描述 | MF-766 is a potent, selective, and orally active EP4 antagonist with a Ki value of 0.23 nM. In functional testing, MF-766 is a full antagonist with an IC50 value of 1.4 nM[1][2].Cells were pretreated with MF-766 for 1 hour at a concentration of less than 10 μM and then stimulated with IL-2 (50 ng/mL). After 18 hours of action, MF-766 reversed PGE2-inhibited IFN-γ secretion in human NK cells. In addition, the viability of NK cells was not affected by MF-766[2]. |
Animal study | At a dose of 30 mg/kg, administered orally once daily for 21 days, MF-766 exhibited 89% tumour growth inhibition in the CT26 tumour model. However, there was no significant difference in the EMT6 and 4T1 tumour models, with TGIs of 66% and 40%, respectively[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.09mL 0.42mL 0.21mL |
10.45mL 2.09mL 1.05mL |
20.90mL 4.18mL 2.09mL |
CAS号 | 1050656-06-8 |
分子式 | C27H21F3N2O3 |
分子量 | 478.462 |
别名 | Compound 9a |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 50 mg/mL(104.5 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |