| Literature DB >> 32659083 |
Yue Zhong1, Run-Ze Qiu1, Shan-Liang Sun1, Chao Zhao1, Tian-Yuan Fan1, Min Chen1, Nian-Guang Li1, Zhi-Hao Shi2.
Abstract
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.Entities:
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Year: 2020 PMID: 32659083 DOI: 10.1021/acs.jmedchem.0c00696
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446