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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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[201]
展鹏 , 刘新泳 and 高萍.
Design, synthesis, and biologic evaluation of novel galloyl derivatives as HIV-1 RNase H inhibitors.
Chemical Biology & Drug Design,
93,
582,
2019.
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[202]
展鹏 and 刘新泳.
Privileged structure-derived design, synthesis and biological evaluation of novel DAPY analogues as .
2018.
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[203]
展鹏 and 刘新泳.
First discovery of 5-hydroxypyrido[2,3-b]pyrazin-6(5H)-ones as HIV-1 ribonuclease H and integrase du.
2018.
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[204]
展鹏 and 刘新泳.
Discovery of novel phenylalanine derivatives as potent HIV-1 capsid inhibitors from click chemistry-.
2018.
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[205]
展鹏 and 刘新泳.
Design, synthesis and biological evaluation of oseltamivir derivatives targeting 430-cavity of influ.
2018.
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[206]
康东伟 , 展鹏 and 刘新泳.
Identification of dihydrofuro[3,4-d]pyrimidine derivatives as novel HIV-1 NNRTIs with promising anti.
2018.
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[207]
康东伟 , 展鹏 and 刘新泳.
The discovery of novel diarylpyri(mi) dine derivatives with high level activity against a wide varie.
Bioorganic & Medicinal Chemistry,
2018.
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[208]
展鹏 and 刘新泳.
Design, synthesis and biological evaluation of tacrine-1,2,3-triazole derivatives as potent cholines.
Med Chem Commun.,
2018.
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[209]
展鹏 , 康东伟 and 刘新泳.
Optimization of N-Substituted Oseltamivir Derivatives as Potent Inhibitors of Group-1 and -2 Influen.
J Med Chem.,
2018.
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[210]
康东伟 , 展鹏 and 刘新泳.
First discovery of a potential carbonate prodrug of NNRTI drug candidate RDEA427 with submicromolar .
Bioorg Med Chem Lett.,
2018.
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[211]
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.
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[212]
展鹏 and 刘新泳.
Discovery of C-1 modified oseltamivir derivatives as potent influenza neuraminidase inhibitors..
European Journal of Medicinal Chemistry,
2018.
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[213]
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.
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[214]
展鹏 , 康东伟 and 刘新泳.
Targeting the entrance channel of NNIBP: Discovery of diarylnicotinamide 1,4-disubstituted 1,2,3-tri.
Eur J Med Chem.,
2018.
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[215]
展鹏 , 康东伟 and 刘新泳.
Further Exploring Solvent-Exposed Tolerant Regions of Allosteric Binding Pocket for Novel HIV-1 NNRT.
ACS Med Chem Lett,
2018.
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[216]
展鹏 and 刘新泳.
Influenza A virus polymerase: an attractive target for next-generation anti-influenza therapeutics..
Drug Discov Today.,
2018.
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[217]
展鹏 and 刘新泳.
Design, synthesis and biological evaluation of novel ligustrazine-chalcone hybrids as anti-ischemic .
2018.
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[218]
康东伟 , 展鹏 and 刘新泳.
Discovery of a propionamide prodrug of K-5a2 with improved aqueous solubility and oral bioavailabili.
2018.
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[219]
展鹏 and 刘新泳.
Design, Synthesis and Biological Evaluation of Novel Imidazopyridine Thioglycolic Acid Derivatives a.
2018.
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[220]
康东伟 , 展鹏 and 刘新泳.
Current insights into anti-HIV drug discovery and development: a review of recent patent literature.
Expert Opin Ther Pat.,
2018.
