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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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[41]
康东伟.
Exploring the hydrophobic channel of NNIBP leads to the discovery of novel piperidine-substituted th.
ACTA PHARMACEUTICA SINICA B,
10,
878,
2020.
-
[42]
康东伟.
2,4,5-Trisubstituted Pyrimidines as Potent HIV-1 NNRTIs: Rational Design, Synthesis, Activity Evalua.
《Journal of Medicinal Chemistry》,
64,
4239,
2021.
-
[43]
封达.
Design, synthesis, and evaluation of "dual-site"-binding diarylpyrimidines targeting both NNIBP and .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
211,
2021.
-
[44]
汪昭.
Targeting dual tolerant regions of binding pocket: Discovery of novel morpholine-substituted diarylp.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
206,
2020.
-
[45]
康东伟.
Structure-Activity Relationship Exploration of NNIBP Tolerant Region I Leads to Potent HIV-1 NNRTIs.
ACS INFECTIOUS DISEASES,
6,
2225,
2020.
-
[46]
康东伟.
Further Exploring Solvent-Exposed Tolerant Regions of Allosteric Binding Pocket for Novel HIV-1 NNRT.
ACS Medicinal Chemistry Letters,
9,
370,
2018.
-
[47]
Yang, Yang.
Structural basis for potent and broad inhibition of HIV-1 RT by thiophene[3,2-d] pyrimidine non-nucl.
Elife,
7,
2018.
-
[48]
展鹏 , 王德凤 , 刘新泳 and 李忠.
Design, synthesis and biological evaluation of “Multi-Site”-binding influenza virus neuraminidase .
EUR J MED CHEM,
2019.
-
[49]
展鹏 , 康东伟 and 刘新泳.
Novel urate transporter 1 (URAT1) inhibitors: a review of recent patent literature (2016-2019).
Expert Opin Ther Pat.,
2019.
-
[50]
展鹏 , 刘新泳 and 康东伟.
Exploring the hydrophobic channel of NNIBP leads to the discovery of novel piperidinesubstituted thi.
ACTA PHARMACEUTICA SINICA B,
2019.
-
[51]
展鹏 , 刘新泳 and 康东伟.
Discovery of novel 1,4-disubstituted 1,2,3-triazole phenylalanine derivatives as HIV-1 capsid inhibi.
RSC Adv.,
2019.
-
[52]
展鹏 , 刘新泳 and 刘涛.
法匹拉韦合成路线图解.
中国药物化学杂志,
2018.
-
[53]
展鹏 , 刘新泳 and 霍志鹏.
抗艾滋病药物新靶标及其小分子抑制剂的研究进展.
药学学报,
2018.
-
[54]
刘新泳 and 展鹏.
Recent Advances in the Structure-based Rational Design of TNKSIs..
Mol. BioSyst.,,
2014.
-
[55]
刘新泳 and 展鹏.
Discovery of novel indolylarylsulfones as potent HIV-1 NNRTIs via structure-guided scaffold morphing.
EUR J MED CHEM,
2019.
-
[56]
刘新泳 , 展鹏
Overview of Recent Strategic Advances in Medicinal Chemistry.
J Med Chem,
2019.
-
[57]
刘新泳 , 展鹏 and 梁晓红.
Design, Synthesis and Evaluation of Novel Heteroaryldihydropyrimidines Derivatives as Non-nucleoside.
Chem Biol Drug Des,
2019.
-
[58]
展鹏 , 刘新泳 and 贾海永.
Design, synthesis and primary biological evaluation of the novel 2-pyridone derivatives as potent no.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
136,
144,
2017.
-
[59]
刘新泳 , 展鹏 , 张硕
Efficient drug discovery by rational lead hybridization based on crystallographic overlay.
Drug Discovery Today,
24,
805,
2019.
-
[60]
展鹏 , 刘新泳 and 黄伯世.
Discovery of novel DAPY-IAS hybrid derivatives as potential HIV-1 inhibitors using molecular hybridi.
Bioorganic & medicinal chemistry,
25,
4397,
2017.
