澳门新葡亰平台官网师资

卫涛

药学系副主任,化学教研室主任(兼任)
姓名 卫涛 性别
学历 博士 职称 副教授
职务 药学系副主任,化学教研室主任(兼任) 电子邮件 weitao55@163.com




教育经历


1998.09–2002.7   吉林化工学院,获学士学位,环境工程专业                                              

2002.09–2005.05 东南大学,获硕士学位,材料物理与化学专业

2010.09-2015.05  南京理工大学,获博士学位,物理化学专业



工作经历


1.2005.08-至今,澳门新葡新京化学教研室,副教授

 


承担科研项目情况


1.浙江省自然基金:新型螺杂环异构体FGFR1抑制剂的设计、反应机理、合成及抗肿瘤活性研究,项目承担人,2012.1~2014.12,项目编号:LY12H30005,已结题

2.温州市科技局资助项目:异黄酮类药物分子设计的理论研究。项目承担人,起止时间:2009.3-2011.12,项目编号:Y20090101,已结题

3.温州医学院科研发展基金项目(N0.XNK07040,2007/01-2008/12,参与)

4.Sandwich教学法在《无机化学与分析化学》课程教学中的应用,校级教改课题,主持,已结题

5.参与国家自然基金:非ATP竞争性的IKK-β抑制剂的设计发现及其药理活性研究,2014.1-2014.12,已结题6.参与浙江省医药卫生科技计划项目(2010QNA015),项目名称:rh-bFGF对帕金森实验动物神经递质通路的调节及分子机制研究,起止年月:2010年06月-2012年07月,排名第二,已结题7..参与国家自然基金:萘甲酸盐类离子液体对β-双酮类抗生素配合物的强荧光增敏机理与分析应用,项目编号:21377100,已结题

6.参与浙江省医药卫生科技计划项目(2010QNA015),项目名称:rh-bFGF对帕金森实验动物神经递质通路的调节及分子机制研究,起止年月:2010年06月-2012年07月,排名第二,已结题

7.参与国家自然基金:萘甲酸盐类离子液体对β-双酮类抗生素配合物的强荧光增敏机理与分析应用,项目编号:21377100,已结题



研究方向


1.抗肿瘤药物设计、合成、药理活性研究



代表性论著


1.Yuqiao Wang*, Wei Wang, Shasha Wang, Wenjing Chu, Tao Wei*, Haijun Tao,Chuanxiang Zhang, Yueming Sun. Enhanced photoelectrochemical detection of L-ysteine based on the ultrathin polythiophene layer sensitized anatase TiO2 on F-doped tin oxide substrates[J]. Sensors and Actuators B: Chemical, 232 (2016) 448–453. 一区,IF=4.758

2.Tao Wei, Weihua Zhu, Jingjing Zhang and Heming Xiao. DFT study on energetic tetrazolo-[1,5-b]-1,2,4,5-tetrazine and 1,2,4-triazolo-[4,3-b]-1,2,4,5-tetrazine derivatives,J. of Hazardous Materials,2010, 179 (1-3):581-590.(IF=4.144,一区)

3.Jianzhang Wu*,Jiansong Ji*,Bixia Weng,Peihong Qiu,Karvannan Kanchana,Tao Wei,Yi Wang,Yuepiao Cai,Xiaokun Li,Guang Liang. Discovery of novel non-ATP competitive FGFR1 inhibitors and evaluation of their anti-tumor activity in non-small cell lung cancer in vitro and in vivo. Oncotarget 2014, 5(12):4543-4553. (SCI, IF=6.627)

4.Yi Wang,Yuepiao Cai,Jiansong Ji,Zhiguo Liu,Chengguang Zhao,Yunjie Zhao,Tao Wei,Xueqian Shen,Xiuhua Zhang,Xiaokun Li*,Guang Liang*,Discovery and identification of new non-ATP competitive FGFR1 inhibitors with therapeutic potential on non-small-cell lung cancer. Cancer Letters 2014, 344: 82-89. (SCI, IF=5.621)

5.Wang Yi,Jie Hu,Yuepiao Cai,Shanmei Xu,Bixia Weng,Kesong Peng,Xiaoyan Wei,Tao Wei,Huiping Zhou,Xiaokun Li,Guang Liang*. An Oxygen-Chelate Complex, Palladium Bis-acetylacetonate, Induces Apoptosis in H460 Cells via Endoplasmic Reticulum Stress Pathway Rather than Interacting with DNA. Journal of Medicinal Chemistry 2013, 56: 9601-9611. (SCI, IF=5.447)

6.Tao Wei, Weihua Zhu, Xiaowen Zhang,Yu-Fang Li, and Heming Xiao,Molecular Design of 1,2,4,5-Tetrazine-Based High-Energy Density Materials. J. Phys. Chem. A 2009, 113(33), 9404-9412. (IF=2.918,它引:122).
7.Tao Wei, Jianzhang Wu, Weihua Zhu, Chenchen Zhang, Heming Xiao, Characterization of nitrogen-bridged 1,2,4,5-tetrazine-, furazan-, and 1H-tetrazole-based polyheterocyclic compounds: heats of formation, thermal stability, and detonation properties. J. Mol. Model. 2012, 18(8), 3467-3479(SCI,IF=1.871)
8.张婧婧,高洪伟,卫涛*,王朝杰. 高能量密度材料3,3′-偶氮-1,2,4,5-四嗪衍生物的分子设计. 物理化学学报,2010,26(12):3337-3344. (SCI,IF=0.718)
9.刘永芹,高洪伟,卫涛*,张婧婧,韩佳伟,王朝杰,吴建章. 酚羟基取代异黄酮类化合物的抗氧化活性理论筛选[J]. 计算机与应用化学,2013,30(5):531-536.
10.Jianzhang Wu*,Jiansong Ji*,Bixia Weng,Peihong Qiu,Karvannan Kanchana,Tao Wei,Yi Wang,Yuepiao Cai,Xiaokun Li,Guang Liang. Discovery of novel non-ATP competitive FGFR1 inhibitors and evaluation of their anti-tumor activity in non-small cell lung cancer in vitro and in vivo. Oncotarget 2014, 5(12):4543-4553. (SCI, IF=6.627)
11.Yi Wang,Yuepiao Cai,Jiansong Ji,Zhiguo Liu,Chengguang Zhao,Yunjie Zhao,Tao Wei,Xueqian Shen,Xiuhua Zhang,Xiaokun Li*,Guang Liang*,Discovery and identification of new non-ATP competitive FGFR1 inhibitors with therapeutic potential on non-small-cell lung cancer. Cancer Letters 2014, 344: 82-89. (SCI, IF=5.621)
12.Wang Yi,Jie Hu,Yuepiao Cai,Shanmei Xu,Bixia Weng,Kesong Peng,Xiaoyan Wei,Tao Wei,Huiping Zhou,Xiaokun Li,Guang Liang*.An Oxygen-Chelate Complex, Palladium Bis-acetylacetonate, Induces Apoptosis in H460 Cells via Endoplasmic Reticulum Stress Pathway Rather than Interacting with DNA. Journal of Medicinal Chemistry 2013, 56: 9601-9611. (SCI, IF=5.447)

                                       

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