专家意见
小分子
类风湿性关节炎
激酶
药物发现
医学
受体
药理学
计算生物学
生物信息学
癌症研究
免疫学
生物
重症监护医学
内科学
细胞生物学
遗传学
标识
DOI:10.1080/13543776.2016.1202926
摘要
There are currently many examples of highly potent and kinase selective IRAK4 inhibitors and some have been tested in various in vivo disease models, demonstrating robust pre-clinical efficacy. Several compounds appear to have the 'drug-like' properties to advance to the clinic, with Pfizer having already initiated several phase I studies.
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