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J Med Chem. 2012 Mar 22;55(6):2623-40. doi: 10.1021/jm201454n. Epub 2012 Mar 6.
Herein, we describe the synthesis and SAR of a series of small molecule macrocycles that selectively inhibit JAK2 kinase within the JAK family and FLT3 kinase. Following a multiparameter optimization of a key aryl ring of the previously described SB1518 (pacritinib), the highly soluble 14l was selected as the optimal compound. Oral efficacy in the murine collagen-induced arthritis (CIA) model for rheumatoid arthritis (RA) supported 14l as a potential treatment for autoimmune diseases and inflammatory disorders such as psoriasis and RA. Compound 14l (SB1578) was progressed into development and is currently undergoing phase 1 clinical trials in healthy volunteers.
在这里,我们描述了一系列小分子大环化合物的合成和 SAR 研究,这些化合物能够选择性地抑制 JAK 家族和 FLT3 激酶中的 JAK2 激酶。在对之前描述的 SB1518(帕克里替尼)的关键芳基环进行多参数优化后,选择高水溶性的 14l 作为最佳化合物。在治疗类风湿关节炎(RA)的鼠胶原诱导关节炎(CIA)模型中的口服疗效表明,14l 可能是一种治疗自身免疫性疾病和炎症性疾病的潜在药物,如银屑病和 RA。化合物 14l(SB1578)已进入开发阶段,目前正在健康志愿者中进行 1 期临床试验。