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Discovery of TAK-659 an orally available investigational inhibitor of Spleen Tyrosine Kinase (SYK)

机译:TAK-659的口服酪氨酸激酶(SYK)研究抑制剂的发现

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Spleen Tyrosine Kinase (SYK) is a non-receptor cytoplasmic tyrosine kinase that is primarily expressed in hematopoietic cells. SYK is a key mediator for a variety of inflammatory cells, including B cells, mast cells, macrophages and neutrophils and therefore, an attractive approach for treatment of both inflammatory diseases and oncology indications. Using in house co-crystal structure information, and structure-based drug design, we designed and optimized a novel series of heteroaromatic pyrrolidinone SYK inhibitors resulting in the selection of the development candidate TAK-659. TAIL-659 is currently undergoing Phase I clinical trials for advanced solid tumor and lymphoma malignancies, a Phase Ib study in advanced solid tumors in combination with nivolumab, and PhIb/II trials for relapsed/refractory AML (C) 2016 Elsevier Ltd. All rights reserved.
机译:脾酪氨酸激酶(SYK)是一种非受体胞质酪氨酸激酶,主要在造血细胞中表达。 SYK是包括B细胞,肥大细胞,巨噬细胞和嗜中性粒细胞在内的多种炎性细胞的关键介体,因此是治疗炎性疾病和肿瘤适应症的一种有吸引力的方法。利用内部共晶体结构信息和基于结构的药物设计,我们设计和优化了一系列新的杂芳族吡咯烷酮SYK抑制剂,从而选择了开发候选TAK-659。 TAIL-659目前正在接受针对晚期实体瘤和淋巴瘤恶性肿瘤的I期临床试验,针对结合nivolumab的晚期实体瘤的Ib期研究以及针对复发/难治性AML(C)的PhIb / II试验2016 Elsevier Ltd.版权所有保留。

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