化学
髓系白血病
CD135型
Fms样酪氨酸激酶3
PI3K/AKT/mTOR通路
酪氨酸激酶
受体酪氨酸激酶
造血
蛋白激酶B
髓样
MAPK/ERK通路
酪氨酸激酶抑制剂
小分子
白血病
癌症研究
药理学
生物化学
激酶
突变
细胞生物学
信号转导
医学
免疫学
内科学
干细胞
癌症
基因
生物
作者
Yue Zhong,Runze Qiu,Shan‐Liang Sun,Chao Zhao,Tian‐Yuan Fan,Min Chen,Nian‐Guang Li,Zhi‐Hao Shi
标识
DOI:10.1021/acs.jmedchem.0c00696
摘要
Fms-like tyrosine kinase 3 (FLT3) is an important member of the class III receptor tyrosine kinase (RTK) family, which is involved in the proliferation of hematopoietic cells and lymphocytes. In recent years, increasing evidence have demonstrated that the activation and mutation of FLT3 is closely implicated in the occurrence and development of acute myeloid leukemia (AML). The exploration of small-molecule inhibitors targeting FLT3 has aroused wide interest of pharmaceutical chemists and is expected to bring new hope for AML therapy. In this review, we specifically highlighted FLT3 mediated JAK/STAT, RAS/MAPK, and PI3K/AKT/mTOR signaling. The structural properties and biological activities of representative FLT3 inhibitors reported from 2014 to the present were also summarized. In addition, the major challenges in the current advance of novel FLT3 inhibitors were further analyzed, with the aim to guide future drug discovery.
科研通智能强力驱动
Strongly Powered by AbleSci AI