2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
生物活性
Description
In Vivo
In Vitro
化合物的使用
Kinase Assay
Cell Assay
Animal Administration
参考文献
Potent EP2 receptor antagonist (IC50 = 16 nM for human EP2 receptors). Displays over 2000-fold selectivity for EP2 receptors over EP1, EP3, EP4, DP1 amd CRTH2 receptors; exhibits <30% binding at a diverse panel of GPCRs and ion channels at a concentration of 10 μM. Inhibits PGE2-induced increases in intracellular cAMP; reverses PGE2-invoked relaxation of mouse trachea (IC50 = 2.7 nM). For the detailed information of PF-04418948, the solubility of PF-04418948 in water, the solubility of PF-04418948 in DMSO, the solubility of PF-04418948 in PBS buffer, the animal experiment (test) of PF-04418948, the cell expriment (test) of PF-04418948, the in vivo, in vitro and clinical trial test of PF-04418948, the EC50, IC50,and affinity,of PF-04418948, For the detailed information of PF-04418948, the solubility of PF-04418948 in water, the solubility of PF-04418948 in DMSO, the solubility of PF-04418948 in PBS buffer, the animal experiment (test) of PF-04418948, the cell expriment (test) of PF-04418948, the in vivo, in vitro and clinical trial test of PF-04418948, the EC50, IC50,and affinity,of PF-04418948, Please contact DC Chemicals.
