鲁索利替尼
激酶
托法替尼
重新调整用途
药物重新定位
贾纳斯激酶
伊布替尼
基诺美
药理学
医学
类风湿性关节炎
免疫学
生物
药品
白血病
细胞生物学
慢性淋巴细胞白血病
生态学
骨髓
骨髓纤维化
作者
Rinky Raghuvanshi,Sandip B. Bharate
标识
DOI:10.1021/acs.jmedchem.0c01467
摘要
Kinases are a group of therapeutic targets involved in the progression of numerous diseases, including cancer, rheumatoid arthritis, Alzheimer's disease, and viral infections. The majority of approved antiviral agents are inhibitors of virus-specific targets that are encoded by individual viruses. These inhibitors are narrow-spectrum agents that can cause resistance development. Viruses are dependent on host cellular proteins, including kinases, for progression of their life-cycle. Thus, targeting kinases is an important therapeutic approach to discovering broad-spectrum antiviral agents. As there are a large number of FDA approved kinase inhibitors for various indications, their repurposing for viral infections is an attractive and time-sparing strategy. Many kinase inhibitors, including baricitinib, ruxolitinib, imatinib, tofacitinib, pacritinib, zanubrutinib, and ibrutinib, are under clinical investigation for COVID-19. Herein, we discuss FDA approved kinase inhibitors, along with a repertoire of clinical/preclinical stage kinase inhibitors that possess antiviral activity or are useful in the management of viral infections.
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