|
发布时间:2019-05-20 访问次数:999 作者: |
director office of strategic planning and discipline construction contact information office: room 1223, researching building 18 email: office phone: 86 21 64252584 office fax: 86 21 64252584
education 09/2003-07/2006 ph.d. drug design, shanghai institute of materia medica (simm), chinese academy of science (cas), shanghai, china 09/2000-07/2003 m.s. medicinal chemistry, shenyang pharmaceutical university, shenyang, china 09/1996-07/2000 b.e. pharmaceutical chemistry, shenyang pharmaceutical university, shenyang, china
professional experience 05/2018-now professor, director of office of strategic planning and discipline construction, east china university of science & technology, shanghai, china 05/2017-05/2018 professor, secretary of the party committee of school of pharmacy, east china university of science & technology, shanghai, china 09/2015-07/2017 professor, vice dean of school of pharmacy, east china university of science & technology, shanghai, china 09/2011-09/2015 professor, director of department of pharmaceutical sciences, school of pharmacy, east china university of science & technology, shanghai, china 03/2011-09/2011 associate professor, director of department of pharmaceutical sciences, school of pharmacy, east china university of science & technology, shanghai, china 12/2006-03/2011 associate professor, school of pharmacy, east china university of science & technology, shanghai, china 07/2006-12/2006 lecturer, school of pharmacy, east china university of science & technology, shanghai, china
research interests the secondary development of approved drugs discovery of unknown targets and new derivatives of approved drug probe novel anti-mrsa therapeutic agents targetting on bacterial virulence
publication baoli li#; shuaishuai ni#; fei mao#; feifei chen; yifu liu; hanwen wei; wenhua chen; jin zhu; lefu lan*; jian li*, novel terminal bipheny-based diapophytoene desaturases (crtn) inhibitors as anti-mrsa/visr/lrsa agents with reduced herg activity, journal of medicinal chemistry, 2018, 61(1): 224~250. yifu liu#; zuoquan xie#; dan zhao; jin zhu; fei mao; shuai tang; hui xu; cheng luo; meiyu geng; min huang*; jian li*, development of the first generation of disulfide-based subtype-selective and potent covalent pyruvate dehydrogenase kinase 1 (pdk1) inhibitors, journal of medicinal chemistry, 2017, 60(6): 2227~2244. yanli lu#; fei mao#; xiaokang li; xinyu zheng; manjiong wang; qing xu; jin zhu; jian li*, discovery of potent, selective stem cell factor receptor/platelet derived growth factor receptor alpha (c-kit/pdgfrα) dual inhibitor for the treatment of imatinib-resistant gastrointestinal stromal tumors (gists), journal of medicinal chemistry, 2017, 60(12): 5099~5119. shuaishuai ni#; hanwen wei#; baoli li#; feifei chen; yifu liu; wenhua chen; yixiang xu; xiaoxia qiu; xiaokang li; yanli lu; wenwen liu; linhao hu; dazheng lin; manjiong wang; xinyu zheng; fei mao; jin zhu; lefu lan*; jian li*, novel inhibitors of staphyloxanthin virulence factor in comparison with linezolid and vancomycin versus methicillin-resistant, linezolid-resistant, and vancomycin-intermediate staphylococcus aureus infections in vivo, journal of medicinal chemistry, 2017, 60(19): 8145~8159. weiqiang lu#; feixiong cheng#; wenzhong yan#; xi li; xue yao; wenqiang song; mingyao liu; xu shen; hualiang jiang; jin chen; jian li*; jin huang*, selectivetargeting p53wt lung cancer cells harboring homozygous p53 arg72 byan inhibitor of cypa, oncogene, 2017, 36(33): 4719~4731. feifei chen#; hongxia di#; youxin wang#; qiao cao; bin xu; xue zhang; nana yang; guijie liu; cai-guang yang; yong xu; hualiang jiang; fulin lian; naixia zhang; jian li*; lefu lan*, small-molecule targeting of a diapophytoene desaturase inhibits s. aureus virulence, nature chemical biology, 2016, 12(3): 174~179. youxin wang#; feifei chen#; hongxia di; yong xu; qiang xiao; xuehai wang; hanwen wei; yanli lu; lingling zhang; jin zhu; chunquan sheng; lefu lan*; jian li*, discovery of potent benzofuran-derived diapophytoene desaturase (crtn) inhibitors with enhanced oral bioavailability for the treatment of methicillin-resistant staphylococcus aureus (mrsa) infections, journal of medicinal chemistry, 2016, 59(7): 3215~3230. youxin wang#; hongxia di#; feifei chen; yong xu; qiang xiao; xuehai wang; hanwen wei; yanli lu; lingling zhang; jin zhu; lefu lan*; jian li*, discovery of benzocycloalkane derivatives efficiently blocking bacterial virulence for the treatment of methicillin-resistant s. aureus (mrsa) infections by targeting diapophytoene desaturase (crtn), journal of medicinal chemistry, 2016, 59(10): 4831~4848. wenyi sun#; zuoquan xie#; yifu liu#; dan zhao#; zhixiang wu; dadong zhang; hao lv; shuai tang; nan jin; hualiang jiang; minjia tan; jian ding; cheng luo*; jian li*; min huang*; meiyu geng*, jx06 selectively inhibits pyruvate dehydrogenase kinase pdk1 by a covalent cysteine modification, cancer research, 2015, 75(22): 4923~4936. huang huang; wenhua chen; yong xu; jian li*, i−/tbhp catalyzed csp3–n/csp2–n bond formation via oxidative coupling with benzophenone imine in water, green chemistry, 2015, 17(10): 4715~4719.
|
|
|
|