Revisiting Structure-activity Relationships: Unleashing the potential of selective Janus kinase 1 inhibitors

被引:0
|
作者
Shan, Mengyi [1 ]
Zhao, Xuan [1 ]
Sun, Peng [1 ]
Qu, Xinhao [1 ]
Cheng, Gang [1 ]
Qin, Lu-Ping [1 ]
机构
[1] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou 310053, Peoples R China
基金
中国国家自然科学基金;
关键词
Janus kinases; Structure-activity Relationship; Selectivity; Druggability; JAK-STAT PATHWAY; RHEUMATOID-ARTHRITIS; PRECLINICAL CHARACTERIZATION; PSEUDOKINASE DOMAIN; IDENTIFICATION; DISCOVERY; CYTOKINES; DESIGN; ACTIVATION; STRATEGIES;
D O I
10.1016/j.bioorg.2024.107506
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Janus kinases (JAKs), a kind of non-receptor tyrosine kinases, the function has been implicated in the regulation of cell proliferation, differentiation and apoptosis, immune, inflammatory response and malignancies. Among them, JAK1 represents an essential target for modulating cytokines involved in inflammation and immune function. Rheumatoid arthritis, atopic dermatitis, ulcerative colitis and psoriatic arthritis are areas where approved JAK1 drugs have been applied for the treatment. In the review, we provided a brief introduction to JAK1 inhibitors in market and clinical trials. The structures of high active JAK1 compounds (IC50 <= 0.1 nM) were highlighted, with primary focus on structure-activity relationship and selectivity. Moreover, the druggability processes of approved drugs and high active compounds were analyzed. In addition, the issues involved in JAK1 compounds clinical application as well as strategies to surmount these challenges, were discussed.
引用
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页数:21
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