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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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[181]
刘新泳 and 展鹏.
Design, synthesis and biological evaluation of 3-benzyloxy-linked pyrimidinylphenylamine derivatives.
Bioorganic & medicinal chemistry,
2013.
-
[182]
刘新泳 and 展鹏.
Synthesis and anti-HIV evaluation of novel 1,2,4-triazole derivatives as potential non-nucleoside HI.
Letters in Drug Design & Discovery,
2013.
-
[183]
刘新泳 and 展鹏.
Design, synthesis and biological evaluation of N2, N4-disubstituted- 1,1,3-trioxo-2H,4H-pyrrolo[1,2-.
Bioorganic & medicinal chemistry,
2013.
-
[184]
刘新泳 , 展鹏 and 刘慧青.
Design, synthesis and biological evaluation of novel 3,5-disubstituted-1,2,6-thiadiazine-1,1-dione d.
Chemical Biology & Drug Design,
2013.
-
[185]
展鹏 and 刘新泳.
Heterocycle-thioacetic Acid Motif: A Privileged Molecular Scaffold with Potent, Broad-Ranging Pharma.
Current Pharmaceutical Design,
2013.
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[186]
展鹏 and 刘新泳.
Discovery of Novel 2-(3-(2-Chlorophenyl) pyrazin-2-ylthio)-N-arylacetamides As Potent HIV-1 Inhibito.
Bioorg. Med. Chem.,
20,
6795,
2012.
-
[187]
展鹏 and 刘新泳.
Structure-based Bioisosterism Design, Synthesis and Biological Evaluation of Novel 1,2,4-Triazin-6-y.
Bioorg. Med. Chem. Lett.,
22,
7155,
2012.
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[188]
展鹏 and 刘新泳.
Arylazolyl(azinyl)thioacetanilide. Part 9: Synthesis and Biological Investigation of Thiazolylthioac.
Arch. Pharm. Res.,
35,
975,
2012.
-
[189]
展鹏 and 刘新泳.
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.
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[190]
展鹏 and 刘新泳.
Rationally designed multitarget anti-HIV agents.
Curr Med Chem,
20,
1743,
2013.
-
[191]
展鹏 and 刘新泳.
Design, synthesis and acetylcholinesterase (AChE) inhibition assay of novel 9-(1-(substituted-benzy.
E-JOURNAL OF CHEMISTRY,
2013.
-
[192]
展鹏 and 刘新泳.
The HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors (Part V): Capravirine and Its Analogues.
Curr Med Chem. 2012;19(36):6138-49.,
2012.
-
[193]
展鹏 and 刘新泳.
Discovery of novel pyridazinylthioacetamides as potent HIV-1 NNRTIs using a structure-based bioisost.
Med. Chem. Commun., 2013,4, 810-816.,
2013.
-
[194]
展鹏 and 刘新泳.
Multivalent agents: a novel concept and preliminary practice in anti-HIV drug discovery.
Curr Med Chem. 2013 Feb 1;20(6):815-32.,
2013.
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[195]
展鹏 and 刘新泳.
Arylazolyl(azinyl)thioacetanilides. Part 10: Design, synthesis and biological evaluation of novel su.
《Bioorg Med Chem.》,
20,
5527,
2012.
-
[196]
刘新泳 and 展鹏.
Discovery of potent HIV-1 non-nucleoside reverse transcriptase inhibitors from arylthioacetanilide s.
Eur J Med Chem.,
2015.
-
[197]
展鹏 , 梁晓红 and 刘新泳.
Design, Synthesis and Evaluation of Novel Heteroaryldihydropyrimidines Derivatives as Non-nucleoside.
Chem Biol Drug Des,
2019.
-
[198]
展鹏 and 刘新泳.
HIV-1非核苷类逆转录酶抑制剂的研究进展(2014-2015).
《中国科技论文在线》,
2015.
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[199]
展鹏 and 刘新泳.
CDC25 磷酸酶抑制剂研究进展( 2008 ~ 2014 年).
《中国药物化学杂志》,
2015.
-
[200]
刘新泳.
Molecular design opportunities presented by solvent-exposed regions of target proteins.
Med Res Rev.,
2019.