1、教育经历
(1) 2005/09-2010/06, 南京大学, 生命科学学院,博士
(2) 2001/09-2005/06, 南京大学, 生命科学学院,学士
2、工作经历
(1) 2017/07 至今, 中国药科大学, 药学院, 副教授
(2) 2010/07-2017/06, 中国药科大学, 药学院, 讲师
(3) 2015/07-2016/07, University of Colorado Boulder, Department of Chemistry and Biochemistry,BioFrontiers Institute 访问学者
(1) 靶向性抗肿瘤小分子药物发现
(2) 体外诊断试剂研究
1、科研项目
(1)中国药科大学-三联生物联合实验室合作项目, 2022-07 至 2026-07,125万元,在研,主持;
(2)中国药科大学,中央高校基本科研业务费重点项目,2017-01至2018-12,15万元,2632018ZD09,已结题,主持;
(3)江苏省科技厅,江苏省自然科学基金面上项目,2012-07至2015-07,具有VEGFR-2和c-Met双重抑制作用的抗肿瘤化合物的设计、合成及生物活性研究,BK2012760,已结题,主持;
(4)国家自然科学基金委员会,青年基金项目,21102182,靶向VEGFR-2和HDAC的多靶点抗肿瘤化合物的设计、合成及生物活性评价,2012-01-01 至 2014-12-31,24万元,已结题,主持;
(5)教育部,博士点新教师基金项目,20110096120008,具有VEGFR-2和HDAC双重抑制活性的抗肿瘤化合物的设计、合成及生物活性研究,2012-01-01 至 2014-12-31,4万元,已结题,主持。
2、学术获奖
(1)2018-08江苏省教育教学与研究成果奖一等奖,排名第五;
(2)2009-01 教育部自然科学奖二等奖,排名第三。
1.Tsuboyama N, Wang R, Szczepanski AP, Chen H, Zhao Z, Shi L*, Wang L*. Therapeutic targeting of BAP1/ASXL3 sub-complex in ASCL1-dependent small cell lung cancer. Oncogene. 2022;41(15):2152-2162. (IF = 8.756)
2.Wang R, Liu H, You YY, Wang XY, Lv BB, Cao LQ, Xue JY, Xu YG*, Shi L*. Discovery of novel VEGFR-2 inhibitors embedding 6,7-dimethoxyquinazoline and diarylamide fragments. Bioorg Med Chem Lett. 2021;36:127788. (IF = 2.572)
3.Zhang QW, Ye ZD, Shi L*. c-Met kinase inhibitors: an update patent review (2014-2017). Expert Opin. Ther. Pat. 2019;29(1):25-41. (IF = 5.611)
4.Zhang QW, Ye ZD, Shen C, Tie HX, Wang L, Shi L*. Synthesis of novel 6,7-dimethoxy-4-anilinoquinolines as potent c-Met inhibitors. J Enzyme Inhib Med Chem. 2019;34(1):124-133. (IF = 4.673)
5.Zhang L, Shi L (co-first author), Soars SM, Kamps J, Yin H*. Discovery of Novel Small-Molecule Inhibitors of NF-κB Signaling with Antiinflammatory and Anticancer Properties. J Med Chem. 2018;61(14):5881-5899. (IF = 6.054)
6.Peng FW, Liu DK, Zhang QW, Xu YG*, Shi L*. VEGFR-2 inhibitors and the therapeutic applications thereof: a patent review (2012-2016). Expert Opin Ther Pat. 2017;27(9):987-1004. (IF = 2.867)
7.Peng FW, Xuan J, Wu TT, Xue JY, Ren ZW, Liu DK, Wang XQ, Chen XH, Zhang JW, Xu YG*, Shi L*. Design, synthesis and biological evaluation of N-phenylquinazolin-4-amine hybrids as dual inhibitors of VEGFR-2 and HDAC. Eur J Med Chem. 2016;109:1-12. (IF = 4.519)
8.Peng FW, Wu TT, Ren ZW, Xue JY, Shi L*. Hybrids from 4-anilinoquinazoline and hydroxamic acid as dual inhibitors of vascular endothelial growth factor receptor-2 and histone deacetylase. Bioorg Med Chem Lett. 2015;25(22):5137-41. (IF = 2.42)
9.Shi L*, Wu TT, Wang Z, Xue JY, Xu YG*. Discovery of N-(2-phenyl-1H-benzo[d]imidazol-5-yl)quinolin-4-amine derivatives as novel VEGFR-2 kinase inhibitors. Eur J Med Chem. 2014;84:698-707. (IF = 3.432)
10.Shi L*, Wu TT, Wang Z, Xue JY, Xu YG*. Discovery of quinazolin-4-amines bearing benzimidazole fragments as dual inhibitors of c-Met and VEGFR-2. Bioorg Med Chem. 2014;22(17):4735-44. (IF = 2.951)