化学
异羟肟酸
连接器
癌症研究
药理学
癌细胞
细胞生长
药品
药物发现
毒性
血管内皮生长因子受体
自由能微扰
癌症
细胞毒性
肿瘤微环境
细胞
细胞培养
酶
结构-活动关系
组合化学
分子动力学
铅化合物
生物化学
癌症治疗
酶抑制剂
组蛋白脱乙酰基酶
肿瘤细胞
作者
Yaxin Li,Sisi Liu,Sha Hu,R. H. Zhang,Xiaoli Wang,Jiamin Xu,Keke Yao,Chenxuan Lu,G. -Y. Li,Zhigang Wu,Guo Cy,Leifu Yang,Liming Hu
标识
DOI:10.1021/acs.jmedchem.5c01650
摘要
The development of dual-targeted inhibitors represents a promising strategy to address the challenges of drug resistance and limited efficacy in cancer therapy. This study describes the design, synthesis, and evaluation of novel inhibitors targeting VEGFR2 and HDAC through a structure-based pharmacophore-merging strategy. We integrated the hydroxamic acid zinc-binding group and the linker into the back pocket of VEGFR2. Molecular dynamics (MD) simulations and free energy perturbation (FEP) calculations facilitated the optimization of the inhibitors, ultimately leading to the discovery of compound 10i, which demonstrated significant dual-inhibitory activity. In vitro assays demonstrated its potent antiproliferative effects against cancer cell lines, particularly HT-29, while maintaining a favorable safety profile for normal cells. In vivo evaluation using HT-29 and HCCLM3/Sorafenib xenograft models confirmed robust tumor growth inhibition (TGI = 64.40% and 89.72%), with no significant toxicity observed. These findings underscore the therapeutic potential of compound 10i as a VEGFR2/HDAC dual inhibitor.
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