Changelian Paul S, Moshinsky Deborah, Kuhn Cyrille F, Flanagan Mark E, Munchhof Michael J, Harris Thomas M, Whipple David A, Doty Jonathan L, Sun Jianmin, Kent Craig R, Magnuson Kelly S, Perregaux David G, Sawyer Perry S, Kudlacz Elizabeth M
Pfizer Global Research and Development, Groton, CT, USA.
Blood. 2008 Feb 15;111(4):2155-7. doi: 10.1182/blood-2007-09-115030. Epub 2007 Dec 19.
PF-956980 is a selective inhibitor of JAK3, related in structure to CP-690550, a compound being evaluated in clinical trials for rheumatoid arthritis and prevention of allograft rejection. PF-956980 has been evaluated against a panel of 30 kinases, and found to have nanomolar potency against only JAK3. Cellular and whole blood activity of this compound parallels its potency and selectivity in enzyme assays. It was effective in vivo at inhibiting the delayed type hypersensivity reaction in mice. We compared 2 commercially available JAK3 inhibitors (WHI-P131 and WHI-P154) in the same panel of biochemical and cellular assays and found them to be neither potent nor selective for JAK3. Both were found to be nanomolar inhibitors of the EGF receptor family of kinases. As these compounds have been used in numerous publications in the transplant and autoimmune disease literature, their specificity should be considered when interpreting these results.
PF-956980是JAK3的选择性抑制剂,其结构与CP-690550相关,CP-690550是一种正在进行类风湿性关节炎和预防同种异体移植排斥反应临床试验评估的化合物。PF-956980已针对一组30种激酶进行了评估,发现其仅对JAK3具有纳摩尔效力。该化合物的细胞和全血活性与其在酶分析中的效力和选择性相当。它在体内对抑制小鼠迟发型超敏反应有效。我们在同一组生化和细胞分析中比较了2种市售的JAK3抑制剂(WHI-P131和WHI-P154),发现它们对JAK3既无强效也无选择性。两者均被发现是表皮生长因子受体激酶家族的纳摩尔抑制剂。由于这些化合物已在移植和自身免疫性疾病文献的众多出版物中使用,在解释这些结果时应考虑它们的特异性。