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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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[381]
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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[382]
展鹏 , 康东伟 and 刘新泳.
Design, synthesis, and antiviral evaluation of novel hydrazone substituted thiophene[3,2-d]pyrimidin.
Chem Biol Drug Des,
2018.
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[383]
展鹏 and 刘新泳.
Design, synthesis and biological evaluation of novel ligustrazine-chalcone hybrids as anti-ischemic .
2018.
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[384]
展鹏 , 康东伟 and 刘新泳.
新型乙酰胺取代的多拉韦林衍生物及其前药的设计、合成和活性评价.
2018.
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[385]
展鹏 and 刘新泳.
Privileged structure-derived design, synthesis and biological evaluation of novel DAPY analogues as .
2018.
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[386]
展鹏 , 康东伟 and 刘新泳.
基于靶标结构的新型噻吩并嘧啶类HIV-1 NNRTIs抗艾滋病候选药物的发现.
2018.
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[387]
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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[388]
展鹏 , 康东伟 and 刘新泳.
Discovery of a propionamide prodrug of K-5a2 with improved aqueous solubility and oral bioavailabili.
2018.
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[389]
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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[390]
展鹏 , 康东伟 and 刘新泳.
药学专业无机化学教学方法的改良.
《药学教育》,
2018.
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[391]
展鹏 , 康东伟 and 刘新泳.
Discovery of bioactive molecular via a privileged scaffold repositioning approach..
2018.
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[392]
展鹏 , 康东伟 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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[393]
展鹏 , 康东伟 and 刘新泳.
新型HIV-1 RNase H抑制剂的设计、合成与活性评价.
2018.
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[394]
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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[395]
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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[396]
刘新泳 and 展鹏.
抗艾滋病药物设计新策略：多靶点及多价态结合配体.
《中国药物化学杂志》,
23,
406,
2013.
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[397]
刘新泳 and 展鹏.
Heterocycle-thioacetic Acid Motif: A Privileged Molecular Scaffold with Potent, Broad-Ranging Pharma.
Current Pharmaceutical Design,
2013.
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[398]
刘新泳 and 展鹏.
Design, synthesis and acetylcholinesterase (AChE) inhibition assay of novel 9-(1-(substituted-benzy.
E-JOURNAL OF CHEMISTRY,
2013.
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[399]
刘新泳 and 展鹏.
The HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors (Part V): Capravirine and Its Analogues.
Curr Med Chem. 2012;19(36):6138-49.,
2012.
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[400]
刘新泳 and 展鹏.
Discovery of novel pyridazinylthioacetamides as potent HIV-1 NNRTIs using a structure-based bioisost.
Med. Chem. Commun., 2013,4, 810-816.,
2013.
