Current application status and structure–activity relationship of selective and non-selective JAK inhibitors in diseases

贾纳斯激酶 JAK-STAT信号通路 酪氨酸激酶2 斯达 Janus激酶1 癌症研究 医学 鲁索利替尼 信号转导 酪氨酸激酶 药理学 生物 细胞因子 受体 免疫学 车站3 内科学 遗传学 血小板源性生长因子受体 生长因子 骨髓 骨髓纤维化
作者
Tong Li,Xianjing Yang,Juan Zhu,Ying Liu,Xiaobao Jin,Gong Chen,Lianbao Ye
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:122: 110660-110660 被引量:14
标识
DOI:10.1016/j.intimp.2023.110660
摘要

JAK kinase includes four family members: JAK1, JAK2, JAK3, and TYK2. It forms the JAK-STAT pathway with signal transmitters and activators of subscription (STAT). This pathway is one of the main mechanisms by which many cytokine receptors transduce intracellular signals, it is associated with the occurrence of various immune, inflammatory, and tumor diseases. JAK inhibitors block the signal transduction of the JAK-STAT pathway by targeting JAK kinase. Based on whether they target multiple subtypes of JAK kinase, JAK inhibitors are categorized into pan-JAK inhibitors and selective JAK inhibitors. Compared with pan JAK inhibitors, selective JAK inhibitors are associated with a specific member, thus more targeted in therapy, with improved efficacy and reduced side effects. Currently, a number of JAK inhibitors have been approval for disease treatment. This review summarized the current application status of JAK inhibitors that have been marketed, advances of JAK inhibitors currently in phase Ш clinical trials, and the structure-activity relationship of them, with an intention to provide references for the development of novel JAK inhibitors.
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