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方浩
-
教授
博士生导师
硕士生导师
- 主要任职：山东大学药学院药物化学研究所教授、博士生导师
- 性别：男
- 毕业院校：中国药科大学
- 学历：博士研究生毕业
- 学位：博士生
- 在职信息：在职
- 所在单位：药学院
- 入职时间： 2004-12-23
- 学科：药物化学
- 电子邮箱：phenopro@163.com
访问量：
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[41]
侯旭奔.
Inhibition of striatal-enriched protein tyrosine phosphatase by targeting computationally revealed c.
European Journal of Medicinal Chemistry,
190,
2020.
-
[42]
梁啸.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
BIOORGANIC CHEMISTRY,
103,
2020.
-
[43]
梁涛.
HDAC-Bax Multiple Ligands Enhance Bax-Dependent Apoptosis in HeLa Cells.
《Journal of Medicinal Chemistry》,
63,
12083,
2020.
-
[44]
肖鹏 and 侯旭奔.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
Bioorg Chem.,
2020.
-
[45]
孙金鹏 and 侯旭奔.
Inhibition of striatal-enriched protein tyrosine phosphatase by targeting computationally revealed c.
EUR J MED CHEM,
190,
2020.
-
[46]
侯旭奔
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
Bioorganic&MedicinalChemistry,
28,
2020.
-
[47]
杨新颖 and 侯旭奔.
Design, synthesis and biological evaluation of tyrosine derivatives as Mcl-1 inhibitors.
EUR J MED CHEM,
191,
2020.
-
[48]
杨新颖 , 方浩 , 侯旭奔 and 陈晨.
Design, synthesis and preliminary bioactivity evaluations of 8-hydroxyquinoline derivatives as matri.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
2019.
-
[49]
孙金鹏 , 方浩 and 于晓.
Fast identification of novel lymphoid tyrosine phosphatase inhibitors using target-ligand interactio.
J Med Chem,
57,
9309,
2014.
-
[50]
杨新颖 , 方浩 and 徐玉良.
Additive- and Photocatalyst-Free Borylation of Arylazo Sulfones under Visible Light.
journal of organic chemistry,
83,
12831,
2018.
-
[51]
杨新颖 , 方浩 and 刘仁帅.
Discovery and development of substituted tyrosine derivatives as Bcl-2/Mcl-1 inhibitors.
Bioorganic & medicinal chemistry,
26,
4907,
2018.
-
[52]
侯旭奔 , 杨新颖 , 方浩 and 陈晨.
Design, synthesis and biological evaluation of quinoline derivatives as HDAC class I inhibitors.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
133,
11,
2017.
-
[53]
李敏勇 , 方浩 and 刘婷婷.
Design, synthesis and preliminary biological evaluation of indole-3-carboxylic acid-based skeleton o.
Bioorganic & medicinal chemistry,
25,
1939,
2017.
-
[54]
方浩 and 万义超.
Improved binding affinities of pyrrolidine derivatives as Mcl-1 inhibitors by modifying amino acid s.
Bioorganic & medicinal chemistry,
25,
138,
2017.
-
[55]
方浩 and 孙金鹏.
Fast Identification of Novel Lymphoid Tyrosine Phosphatase Inhibitors Using Target？Ligand Interacti.
Journal of Medicinal Chemistry,
57,
9309,
2014.
-
[56]
方浩 and 徐文方.
Development of Tetrahydroisoquinoline-Based Hydroxamic Acid Derivatives: Potent Histone Deacetylase .
Journal of Medicinal Chemistry,
54,
2823,
2011.
-
[57]
方浩.
Enhancing the Sensitivity of Pharmacophore-Based Virtual Screening by Incorporating Customized ZBG F.
Jounal of chemical information modeling,
55,
861,
2015.
-
[58]
杨新颖 , 方浩 and 徐玉良.
Additive- and Photocatalyst-Free Borylation of Arylazo Sulfones under Visible Light.
journal of organic chemistry,
83,
12831,
2018.
-
[59]
方浩.
Protein Flexibility in Docking-Based Virtual Screening: Discovery of Novel Lymphoid-Specific Tyrosin.
Jounal of chemical information modeling,
55(9):1973-1983,
1973,
2015.
-
[60]
方浩.
Enhancing the Sensitivity of Pharmacophore-Based Virtual Screening by Incorporating Customized ZBG F.
Jounal of chemical information modeling,
55,
861,
2015.
