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展鹏
-
教授
博士生导师
硕士生导师
- 性别：男
- 毕业院校：山东大学
- 学历：博士研究生毕业
- 学位：医学博士学位
- 在职信息：在职
- 所在单位：药学院
- 入职时间： 2010-07-26
- 办公地点：山东大学国家大学生科技园（二环南路）3号楼14层1435房间
- 电子邮箱：zhanpeng1982@sdu.edu.cn
访问量：
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[401]
刘新泳 and 展鹏.
Multivalent agents: a novel concept and preliminary practice in anti-HIV drug discovery.
Curr Med Chem. 2013 Feb 1;20(6):815-32.,
2013.
-
[402]
刘新泳 and 展鹏.
Privileged Scaffolds or Promiscuous Binders: A Glance of Pyrrolo[2,1-f][1,2,4]triazines and Related .
Curr Pharm Des. 2013;19(8):1528-48.,
2013.
-
[403]
刘新泳 and 展鹏.
Arylazolyl(azinyl)thioacetanilides. Part 10: Design, synthesis and biological evaluation of novel su.
《Bioorg Med Chem.》,
20,
5527,
2012.
-
[404]
刘新泳 and 展鹏.
Rationally designed multitarget anti-HIV agents.
Curr Med Chem,
20,
1743,
2013.
-
[405]
刘新泳 and 展鹏.
以黄嘌呤氧化酶为靶点的新型非嘌呤类抗痛风及高尿酸血症药物研究进展.
《中国药物化学杂志》,
22,
403,
2012.
-
[406]
刘新泳 and 展鹏.
Benzimidazole Heterocycle as a Privileged Scaffold in Antiviral Agents..
Mini-Rev Org. Chem.,
9,
397,
2012.
-
[407]
刘新泳 and 展鹏.
Discovery of Novel 2-(3-(2-Chlorophenyl) pyrazin-2-ylthio)-N-arylacetamides As Potent HIV-1 Inhibito.
Bioorg. Med. Chem.,
20,
6795,
2012.
-
[408]
刘新泳 and 展鹏.
Structure-based Bioisosterism Design, Synthesis and Biological Evaluation of Novel 1,2,4-Triazin-6-y.
Bioorg. Med. Chem. Lett.,
22,
7155,
2012.
-
[409]
刘新泳 and 展鹏.
Arylazolyl(azinyl)thioacetanilide. Part 9: Synthesis and Biological Investigation of Thiazolylthioac.
Arch. Pharm. Res.,
35,
975,
2012.
-
[410]
刘新泳 and 展鹏.
HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design..
Med Res Rev.,
33,
E1,
2013.
-
[411]
田野 , 展鹏 , 刘新泳 and 康东伟.
Structure-Based Optimization of Thiophene[3,2-d]pyrimidine Derivatives as Potent HIV-1 Non-nucleosid.
Journal of Medicinal Chemistry,
60,
4424,
2017.
-
[412]
展鹏 , 康东伟 and 刘新泳.
Discovery of Novel Diarylpyrimidine Derivatives as Potent HIV-1 NNRTIs Targeting the "NNRTI Adjacent.
ACS MED CHEM LETT.,
2018.
-
[413]
展鹏 and 刘新泳.
5-Hydroxypyrido[2,3-b]pyrazin-6(5H)-one derivatives as novel dual inhibitors of HIV-1 reverse transc.
Eur J Med Chem.,
2018.
-
[414]
展鹏 , 刘新泳 , 田野 and 康东伟.
Discovery of Thiophene[3,2-d]pyrimidine Derivatives as Potent HIV-1 NNRTIs Targeting the Tolerant Re.
ACS Medicinal Chemistry Letters,
8,
1188,
2017.
-
[415]
展鹏 , 康东伟 and 刘新泳.
Discovery of phenylalanine derivatives as potent HIV-1 capsid inhibitors from click chemistry-based .
Eur J Med Chem.,
2018.
-
[416]
展鹏 , 康东伟 and 刘新泳.
Discovery of novel diarylpyrimidines as potent HIV-1 NNRTIs by investigating the chemical space of a.
Org Biomol Chem.,
2018.
-
[417]
刘新泳.
Novel fluorine-containing DAPY derivatives as potent HIV-1 NNRTIs: a patent evaluation of WO2014072.
Expert Opin Ther Pat.,
25,
2015.
