Telik, Inc., 700 Hansen Way, Palo Alto, California 94304, United States.
J Med Chem. 2011 Mar 24;54(6):1667-81. doi: 10.1021/jm1012903. Epub 2011 Feb 22.
Through the application of TRAP (target-related affinity profiling), we identified a novel class of heteroaroylphenylureas that inhibit human CCL2-induced chemotaxis of monocytes/macrophages both in vitro and in vivo. This inhibition was concentration-dependent and selective with regard to other chemokines. The compounds, however, did not antagonize the binding of (125)I-labeled CCL2 to the CCR2 receptor nor did they block CCR2-mediated signal transduction responses such as calcium mobilization. Optimization of early leads for potency and pharmacokinetic parameters resulted in the identification of 17, a potent inhibitor of chemotaxis (IC(50) = 80 nM) with excellent oral bioavailability in rats (F = 60%). Compound 17 reduced swelling and joint destruction in two rat models of rheumatoid arthritis and delayed disease onset and produced near complete resolution of symptoms in a mouse model of multiple sclerosis.
通过应用 TRAP(与靶标相关的亲和分析),我们鉴定了一类新型的杂芳基苯脲类化合物,它们能够在体外和体内抑制人 CCL2 诱导的单核细胞/巨噬细胞趋化作用。这种抑制作用呈浓度依赖性,并且对其他趋化因子具有选择性。然而,这些化合物既不拮抗(125)I 标记的 CCL2 与 CCR2 受体的结合,也不阻断 CCR2 介导的信号转导反应,如钙动员。对早期先导化合物的效力和药代动力学参数进行优化,鉴定出了 17,它是一种有效的趋化作用抑制剂(IC50 = 80 nM),在大鼠中具有优异的口服生物利用度(F = 60%)。化合物 17 减少了两种类风湿关节炎大鼠模型中的肿胀和关节破坏,并延迟了疾病发作,并在多发性硬化症的小鼠模型中产生了几乎完全的症状缓解。