马俊杰

副教授 硕士生导师



个人信息
  • 性别:男
  • 学历:博士研究生
  • 学位:理学博士学位
  • 入职时间:2015-07-16
  • 所在单位:华侨大学医学院
  • 电子邮箱:
  • 在职信息:在岗

个人简介

主要研究方向:

      针对疾病的临床需求,基于致病靶点的结构和机制,通过合理设计、合成和评价,获得兼具良好成药性和生物活性的“候选药物分子”。




教育经历

2012.9 -- 2015.7

[1]沈阳药科大学 | 药物化学 | 博士研究生 | 博士学位

工作经历

2020.1 -- 至今 华侨大学 | 医学院 | 副教授

2015.7 -- 2019.12 华侨大学 | 医学院 | 讲师

科研项目
论文成果

[1]Design, synthesis, evaluation and molecular modeling of quinazoline derivatives bearing amino acids as small-molecule PD-L1 inhibitors.[J].Journal of Computer-Aided Molecular Design,2025,39:55.

[2]Discovery of novel biphenyl compounds bearing hydroxamic acid moiety as the first PD-L1/class I HDACs dual inhibitors.[J].Journal of Enzyme Inhibition and Medicinal Chemistry,2025,40(1):2461190.

[3]Design, Synthesis, and Evaluation of 8-(o-Tolyl)quinazoline Derivatives as Small-Molecule PD-1/PD-L1 Antagonists.ACS Medicinal Chemistry Letters,2024,15518-523.

[4]Advances in nonclassical phenyl bioisosteres for drug structural optimization.Future Medicinal Chemistry,2022,141681-1692.

[5]Advances in research on 3C-like protease (3CLpro) inhibitors against SARS-CoV-2 since 2020.RSC Med. Chem.,2022,149-21.

[6]Discovery of quinazoline derivatives as novel small-molecule inhibitors targeting the programmed cell death-1/programmed cell death-ligand 1 (PD-1/PD-L1) interaction.European Journal of Medicinal Chemistry,2022,229113998.

[7]Advances of biphenyl small-molecule inhibitors targeting PD-1/PD-L1 interaction in cancer immunotherapy.Future Med. Chem.,2021,1497-113.

[8]Design, Synthesis, Biological Activity and Molecular Docking Study of Coumarin Derivatives Bearing 2-Methyl-Biphenyl Moiety.Chem. Res. Chinese Universities,2019,35410-417.

[9]Semicarbazone derivatives bearing phenyl moiety: synthesis, anticancer activity, cell cycle, apoptosis-inducing and metabolic stability study.Chemical & Pharmaceutical Bulletin,2019,67351-360.

授课信息