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翟鑫 老师的资料

 

姓名:翟鑫

性别:女

籍贯:黑龙江省哈尔滨市

联系电话:13998205230

E-Mail:zhaixin_syphu@126.com

职称/职务:教授

通讯地址:

办公地点:制药工程学院203室

教育经历:

1997.09-2001.07沈阳药科大学,制药工程学院, 工学学士学位;

2001.09-2006.07沈阳药科大学,药物化学专业硕博连读,博士学位;

2009.04-2009.08北海道药科大学,访问学者。

工作经历:

2006.08 沈阳药科大学,聘为助教;

2006.12 沈阳药科大学,聘为讲师;

2009.12 沈阳药科大学,聘为副教授,硕士生导师;

2016.12沈阳药科大学,聘为教授,博士生导师。

兼职情况:无

学科/研究方向:

药物化学/针对肿瘤及炎症的靶向小分子抑制剂的设计合成及活性研究

科研/获奖情况:

2013.08  荣获“第16届中国药学会施维雅青年药物化学奖”;

2014.04  荣获“霍英东基金会第十四届高校青年教师奖”;

2014.05  入选“辽宁省高等学校优秀人才支持计划”;

2014.06  荣获“第十一届沈阳市优秀科技工作者”;

2016.09  入选“辽宁省“百千万人才工程百层次人选”;

2017.09  评为“沈阳药科大学优秀共产党员”

2018.02  2017年辽宁省优秀硕士学位论文指导教师

2018.09  评为沈阳药科大学2017-2018年“三育人”标兵

2018.12  推荐为辽宁省高校“校园先锋示范岗”先进个人;

教学/指导研究生情况:

主讲《药物合成反应》、《药物化学》;共指导硕士研究生34人,博士研究生2人。

发表论文/出版著作:

代表性著作:

1. 《药物化学》,上海科学技术出版社,副主编,2011年9月第一版

2. 《药物合成反应》,中国医药科技出版社,参编, 2012年7月第一版

3. 《药物合成反应》,人民卫生出版社,参编2014年6月第1版

4. 《药物化学》,人民卫生出版社,参编2014年11月第1版

代表性论文:

1) Wenfeng Gou, Xuejiao Zhou, Zi Liu, Lijing Wang, Jiwei Shen, Xiaobo Xu, Zengqiang Li, Xin Zhai*, Daiying Zuo*, Yingliang Wu*. CD74-ROS1 G2032R mutation transcriptionally up-regulates Twist1 in non-small cell lung cancer cells leading to increased migration, invasion, and resistance to crizotinib. Cancer Letters, 2018, 422:19-28. (IF:6.48)

2) Yu Wang, Guogang Zhang, Gang Hu, Yanxin Bu, Hongrui Lei, Daiying Zuo, Mengting Han, Xin Zhai*, Ping Gong*. Design, synthesis and biological evaluation of novel 4-arylaminopyrimidine derivatives possessing hydrazone moiety as dual inhibitors of L1196M ALK and ROS1. European Journal of Medicinal Chemistry, 2016, 123:80-89. (IF:4.81)

3) Yu Wang, Shaowei Chen, Jiao Wang, Gang Hu, Wenfeng Gou, Daiying Zuo, Yucheng Gu, Ping Gong*, Xin Zhai*. Discovery of novel 2,4-diarylaminopyrimidine analogues as ALK and ROS1 dual inhibitors to overcome crizotinib-resistant mutants including G1202R. European Journal of Medicinal Chemistry, 2018,143:123-136. (IF: 4.81)

4) Ming Guo#, Daiying Zuo#, Junlong Zhang, Lingyun Xing, Wenfeng Gou, Feng Jiang, Nan Jiang, Dajun Zhang*, Xin Zhai*. Dual potent ALK and ROS1 inhibitors combating drug-resistant mutants: synthesis and biological evaluation of aminopyridine-containing diarylaminopyrimidine derivatives European Journal of Medicinal Chemistry, 2018, 158:322-333. (IF:4.81)

5) Hongrui Lei#, Nan Jiang#, Xiuqi Miao, Lingyun Xing, Ming Guo, Yang Liu, Haowen Xu, Ping Gong, Daiying Zuo*, Xin Zhai*. Discovery of novel mutant-combating ALK and ROS1 dual inhibitors bearing imidazolidin-2-one moiety with reasonable PK properties. European Journal of Medicinal Chemistry, 2019, 171:297-309 (IF:4.81)

6) Sijia Zhao, Yu Zhang, Hongyang Zhou, Shuancheng Xi, Bin Zou, Guanglong Bao, Limei Wang, Jiao Wang, Tianfang Zeng, Ping Gong, Xin Zhai*. Synthesis and biological evaluation of 4-(2-fluorophenoxy)-3, 3'-bipyridine derivatives as potential c-met inhibitors. European Journal of Medicinal Chemistry, 2016, 120:37-50. (IF: 4.81)

7) Xin Zhai, Xiaoqiang Wang, Jiao Wang, Jin Liu, DaiyingZuo, Nan Jiang, Tianfang Zeng, Xiuxiu Yang, Tongfei Jing & Ping Gong*. Discovery and Optimization of Novel 5-Indolyl-7-arylimidazo[1,2-a]pyridine-8-carbonitrile Derivatives as Potent Antitubulin Agents Targeting Colchicine-binding Site. Scientific Report, 2017, 7, 43398-43409. (IF:4.12)

8) Lingyun Xing, Tongfei Jing, Junlong Zhang, Ming Guo, Xiuqi Miao, Feng Jiang, Xin Zhai*. Design, synthesis and biological evaluation of novel N2-(2-alkyoxy-6-aliphatic aminopyridin-3-yl)-2,4-diaminepyrimidine derivatives as potential ALK inhibitors. Bioorganic Chemistry, 2018, 81, 689-699. (IF: 3.93)

9) Nan Jiang, Yanxin Bu, Minhua Nie, Dajun Zhang*, Xin Zhai*. Design, Synthesis and Structure–activity Relationships of Novel Diaryl Urea Derivatives as Potential EGFR Inhibitors. Molecules, 2016, 21(11):1572-1584. (IF:3.10)

Tongfei Jing, Xiuqi Miao, Feng Jiang, Ming Guo, Lingyun Xing, Junlong Zhang, Daiying Zuo, Hongrui Lei, Xin Zhai*. Discovery and optimization of tetrahydropyrido[4,3-d]pyrimidine derivatives as novel ATX and EGFR dual inhibitors. Bioorganic & Medicinal Chemistry, 2018, 26:1784-1796. (IF:2.88)

 

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