代表性成果
1. Chen Shen, Hong Yue, Jianwen Pei, Xiaomin Guo, Tao Wang*, Junmin Quan* “Crystal structure of the death effector domains of caspase-8” BBRC, 2015, 463, 297–302.
2. Hong Yue, Feng Lu, Chen Shen, Junmin Quan* “Structure-based design of benzo[e]isoindole-1,3-dione derivatives as selective GSK-3β inhibitors to activate Wnt/β-catenin pathway” Bioorg. Chem. 2015, 61, 21–27.
3. Hongmei Shan, Yanxia Shi, Junmin Quan*. “Identification of Green Tea Catechins as Potent Inhibitors of the Polo-Box Domain of Polo-Like kinase 1” ChemMedChem. 2015, 10, 158-163.
4. Hongmei Shan, Tao Wang*, Junmin Quan*. “Crystal structure of the Polo-box Domains of Polo-like Kinase 2” BBRC, 2015, 456, 780–784.
5. Jun Xu, Chen Shen, Tao Wang*, Junmin Quan* “Structural basis for the inhibition of Polo-like kinase 1” Nat. Struct. Mol. Biol. 2013, 20, 1047-53. (Highlighted in cover and also by Nature China, 2 October 2013 | doi:10.1038/nchina.2013.92)
6. Dai L, Liu Y, Liu J, Wen X, Xu Z, Wang Z, Sun H, Tang S, Maguire AR, Quan J*, Zhang H*, Ye T*. “A novel CyclinE/CyclinA-CDK Inhibitor targets p27(Kip1) degradation, cell cycle progression and cell survival: Implications in cancer therapy.” Cancer Lett. 2013, 333, 103-112.
7. Jing Wang, Fei Lu, Qi Ren, Hong Sun, Zhengshuang Xu, Rongfeng Lan, Yuqing Liu, David Ward, Junmin Quan*, Tao Ye*, Hui Zhang*. “Novel Histone Demethylase LSD1 Inhibitors Selectively Target Cancer Cells with Pluripotent Stem Cell Properties” Cancer Res. 2011, 71, 7238-49. (Highlighted by Nature China, 4 January 2012 | doi:10.1038/nchina.2012.1)
8. Xiaolei Wang, Junmin Quan* “Intermediate-Assisted Multifunctional Catalysis in the Conversion of Flavin to 5,6-Dimethylbenzimidazole by BluB: A Density Functional Theory Study” J.Am. Chem. Soc. 2011, 133, 4079-4091.
9. Lintai Da, Junmin Quan*, YunDong Wu* “Understanding the binding mode and function of BMS-488043 against HIV-1 viral entry” Proteins: Struct., Funct., Bioinf. 2011, 79, 1810-1819.
10. Haixia Zou, Liyan Zhou, Yuanzhen Li, Hanbing Zhong, Zhengying Pan, Zhen Yang, Junmin Quan* “Benzo[e]isoindole-1,3-diones as Potential Inhibitors of Glycogen Synthase Kinase-3 (GSK-3). Synthesis, Kinase Inhibitory Activity, Zebrafish Phenotype” J. Med. Chem. 2010, 53, 994-1003.