首页> 外文期刊>Journal of Medicinal Chemistry >Discovery of the macrocycle (9 E)-15-(2-(Pyrrolidin-1-yl)ethoxy)-7,12,25- trioxa-19,21,24-triaza-tetracyclo[18.3.1.1(2,5).1(14,18)]hexacosa-1(24),2,4,9, 14(26),15,17,20,22-nonaene (SB1578), a potent inhibitor of Janus kinase 2/Fms-liketyrosine kinase-3 (JAK2/FLT3) for the treatment of rheumatoid arthritis
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Discovery of the macrocycle (9 E)-15-(2-(Pyrrolidin-1-yl)ethoxy)-7,12,25- trioxa-19,21,24-triaza-tetracyclo[18.3.1.1(2,5).1(14,18)]hexacosa-1(24),2,4,9, 14(26),15,17,20,22-nonaene (SB1578), a potent inhibitor of Janus kinase 2/Fms-liketyrosine kinase-3 (JAK2/FLT3) for the treatment of rheumatoid arthritis

机译:发现大环(9 E)-15-(2-(吡咯烷基-1-基)乙氧基)-7,12,25-三恶唑-19,21,24-三氮杂-四环[18.3.1.1(2,5) .1(14,18)] hexacosa-1(24),2,4,9,14(26),15,17,20,22-壬二烯(SB1578),Janus激酶2 / Fms-liketyrosine的有效抑制剂激酶3(JAK2 / FLT3)用于治疗类风湿关节炎

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摘要

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.
机译:本文中,我们描述了一系列小分子大环化合物的合成和SAR,这些小分子大环化合物选择性抑制JAK家族和FLT3激酶内的JAK2激酶。在对先前描述的SB1518(pacritinib)的关键芳基环进行多参数优化之后,选择了高度可溶的14l作为最佳化合物。类风湿性关节炎(RA)的鼠类胶原诱导的关节炎(CIA)模型中的口服疗效支持14l作为自身免疫性疾病和炎性疾病(如牛皮癣和RA)的潜在治疗方法。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。

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