华侨大学马俊杰--华侨大学医学院马俊杰-- Design, synthesis and biological evaluation of VEGFR-2/HDAC dual inhibitors as multitargeted antitumor agents based on fruquintinib and vorinostat

马俊杰

访问量：

开通时间：..

最后更新时间：..

当前位置：华侨大学医学院马俊杰 >> 科学研究 >> 论文成果

Design, synthesis and biological evaluation of VEGFR-2/HDAC dual inhibitors as multitargeted antitumor agents based on fruquintinib and vorinostat

点击次数：

发表刊物：RSC Adv.

卷号：13

页面范围：28462-28480

是否译文：否

发表时间：2023-09-27

收录刊物：SCI

DOI码：10.1039/D3RA05542F

影响因子：3.9

上一条：Design, Synthesis, and Evaluation of 8-(o-Tolyl)quinazoline Derivatives as Small-Molecule PD-1/PD-L1 Antagonists

下一条：Advances in nonclassical phenyl bioisosteres for drug structural optimization