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Design, synthesis and activity evaluation of novel FLT3 inhibitors
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You-li HOU1, 2, Peng-juan ZHAO1, 2, Ju LIU3, Wei-ke LIAO1, 2, Lei TANG1, 2, *
Acta Pharmaceutica Sinica | 2025, 60(6) : 1767 - 1777
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Acta Pharmaceutica Sinica | 2025, 60(6): 1767-1777
• Original Articles •
Design, synthesis and activity evaluation of novel FLT3 inhibitors
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You-li HOU1, 2, Peng-juan ZHAO1, 2, Ju LIU3, Wei-ke LIAO1, 2, Lei TANG1, 2, *
Affiliations
  • 1Guizhou Provincial Engineering Technology Research Center for Chemical Drug R & D, Guizhou Medical University, Guiyang 550004, China
  • 2School of Pharmacy, Guizhou Medical University, Guiyang 550004, China
  • 3School of Pharmaceutical Sciences, Liaoning University, Shenyang 110036, China
Published: 2025-06-12 doi: 10.16438/j.0513-4870.2025-0053
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In this study, a series of 4-phenoxypyridine derivatives containing imidazole-4-formamido and 1,2,4-triazole were designed and synthesized as novel inhibitors of Fms-like tyrosine kinase 3 (FLT3). The results showed that the series of compounds had good antiproliferative activity. Among them, the preferred compound 10c was in two cell lines containing FLT3-ITD (internal tandem duplication, ITD) mutations, namely human myeloid core solo leukemia cells (MV4-11) and human acute myeloid leukemia cells (Molm-13), with IC50 values of 1.90 and 5.78 μmol·L-1, respectively. Apoptosis and cycle results showed that compound 10c could promote apoptosis and prevent cells in S phase. Molecular docking results showed that compound 10c formed two π-π stacking effects with PHE691 and HIS809 of FLT3, and the pyridine parent nucleus and Linker part formed important hydrogen bonds with LYS644 and CYS694 of FLT3, respectively. In summary, compound 10c exhibited good anti-proliferation activity in vitro, which is of value for further in-depth research, and also lays the foundation for the development of more novel FLT3 inhibitors with novel structures.

Fms-like tyrosine kinase  /  proliferation activity  /  Fms-like tyrosine kinase 3 inhibitor  /  molecular docking  /  apoptosis  /  cell cycle
侯有丽, 赵鹏娟, 刘举, 廖伟科, 汤磊. 新型FLT3抑制剂的设计、合成及活性评价. 药学学报, 2025 , 60 (6) : 1767 -1777 . DOI: 10.16438/j.0513-4870.2025-0053
You-li HOU, Peng-juan ZHAO, Ju LIU, Wei-ke LIAO, Lei TANG. Design, synthesis and activity evaluation of novel FLT3 inhibitors[J]. Acta Pharmaceutica Sinica, 2025 , 60 (6) : 1767 -1777 . DOI: 10.16438/j.0513-4870.2025-0053
Year 2025 volume 60 Issue 6
286
138
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Article Info
doi: 10.16438/j.0513-4870.2025-0053
  • Receive Date:2025-01-16
  • Online Date:2026-09-20
  • Published:2025-06-12
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History
  • Received:2025-01-16
  • Revised:2025-03-21
Affiliations
    1Guizhou Provincial Engineering Technology Research Center for Chemical Drug R & D, Guizhou Medical University, Guiyang 550004, China
    2School of Pharmacy, Guizhou Medical University, Guiyang 550004, China
    3School of Pharmaceutical Sciences, Liaoning University, Shenyang 110036, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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