Abstract
TYK2 (tyrosine-protein kinase 2) is a non-receptor protein kinase belonging to the JAK family and is closely associated with various diseases, such as psoriasis, inflammatory bowel disease, systemic lupus erythematosus. TYK2 activates the downstream proteins STAT1-5 by participating in the signal transduction of immune factors such as IL-12, IL-23, and IL-10, resulting in immune expression. The activity of the inhibitor TYK2 can effectively block the transduction of excessive immune signals and treat diseases. TYK2 inhibitors are divided into two types of inhibitors according to the different binding sites. One is a TYK2 inhibitor that binds to JH2 and inhibits its activity through an allosteric mechanism. The representative inhibitor is BMS-986165, developed by Bristol-Myers Squibb. The other class binds to the JH1 adenosine triphosphate (ATP) site and prevents the catalytic activity of the kinase by blocking ATP and downstream phosphorylation. This paper mainly introduces the protein structure, signaling pathway, synthesis, structure-activity relationship and clinical research of TYK2 inhibitors.
Keywords: Tyrosine-protein kinase 2 (TYK2), signal path, TYK2 inhibitors, synthesis, structure-activity relationship, human disease.
Current Medicinal Chemistry
Title:Targeting TYK2 for Fighting Diseases: Recent Advance of TYK2 Inhibitors
Volume: 31 Issue: 20
Author(s): Si-Shi Du, Yu-Qing Fang, Wen Zhang and Guo-Wu Rao*
Affiliation:
- College of Pharmaceutical Science, Institute of Drug Development & Chemical Biology, Zhejiang University of Technology, Hangzhou, 310014, P. R. China
Keywords: Tyrosine-protein kinase 2 (TYK2), signal path, TYK2 inhibitors, synthesis, structure-activity relationship, human disease.
Abstract: TYK2 (tyrosine-protein kinase 2) is a non-receptor protein kinase belonging to the JAK family and is closely associated with various diseases, such as psoriasis, inflammatory bowel disease, systemic lupus erythematosus. TYK2 activates the downstream proteins STAT1-5 by participating in the signal transduction of immune factors such as IL-12, IL-23, and IL-10, resulting in immune expression. The activity of the inhibitor TYK2 can effectively block the transduction of excessive immune signals and treat diseases. TYK2 inhibitors are divided into two types of inhibitors according to the different binding sites. One is a TYK2 inhibitor that binds to JH2 and inhibits its activity through an allosteric mechanism. The representative inhibitor is BMS-986165, developed by Bristol-Myers Squibb. The other class binds to the JH1 adenosine triphosphate (ATP) site and prevents the catalytic activity of the kinase by blocking ATP and downstream phosphorylation. This paper mainly introduces the protein structure, signaling pathway, synthesis, structure-activity relationship and clinical research of TYK2 inhibitors.
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Cite this article as:
Du Si-Shi, Fang Yu-Qing, Zhang Wen and Rao Guo-Wu*, Targeting TYK2 for Fighting Diseases: Recent Advance of TYK2 Inhibitors, Current Medicinal Chemistry 2024; 31 (20) . https://dx.doi.org/10.2174/0929867330666230324163414
DOI https://dx.doi.org/10.2174/0929867330666230324163414 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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