间变性淋巴瘤激酶
克里唑蒂尼
铈替尼
阿列克替尼
癌症研究
间变性大细胞淋巴瘤
碱性抑制剂
化学
酪氨酸激酶
淋巴瘤
药理学
医学
肺癌
受体
免疫学
内科学
生物化学
恶性胸腔积液
作者
Xiaotian Kong,Peichen Pan,Huiyong Sun,Hongguang Xia,Xuwen Wang,Youyong Li,Tingjun Hou
标识
DOI:10.1021/acs.jmedchem.9b00446
摘要
and type-II ALK inhibitors with improved kinase selectivity and enhanced capability to combat drug resistance have also been reported. Moreover, the "proteolysis targeting chimera" (PROTAC) technique has been successfully applied in developing ALK degraders, which opened a new avenue for targeted ALK therapies. This review provides an overview of the physiological and biological functions of ALK, the discovery and development of drugs targeting ALK by focusing on their chemotypes, activity, selectivity, and resistance as well as potential therapeutic strategies to overcome drug resistance.
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