National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Jiangsu Key Laboratory for High Technology Research of TCM Formulae, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Department of Organic Chemistry, China Pharmaceutical University, Nanjing 211198, China.
J Med Chem. 2020 Nov 12;63(21):12403-12428. doi: 10.1021/acs.jmedchem.0c00696. Epub 2020 Jul 21.
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.
Fms 样酪氨酸激酶 3(FLT3)是 III 类受体酪氨酸激酶(RTK)家族的重要成员,参与造血细胞和淋巴细胞的增殖。近年来,越来越多的证据表明,FLT3 的激活和突变与急性髓系白血病(AML)的发生和发展密切相关。针对 FLT3 的小分子抑制剂的探索引起了药物化学家的广泛关注,有望为 AML 治疗带来新的希望。在这篇综述中,我们特别强调了 FLT3 介导的 JAK/STAT、RAS/MAPK 和 PI3K/AKT/mTOR 信号通路。还总结了 2014 年以来报道的具有代表性的 FLT3 抑制剂的结构特性和生物学活性。此外,还进一步分析了新型 FLT3 抑制剂当前进展中存在的主要挑战,旨在为未来的药物发现提供指导。