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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：haofangcn@sdu.edu.cn
访问量：
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[21]
李佳.
Synthesis and evaluation of a UMI-77-based fluorescent probe for selective detecting Mcl-1 protein a.
BIOORGANIC & MEDICINAL CHEMISTRY Journal,
29,
2021.
-
[22]
杨越.
Enantioseparation of lysine derivatives on amylose tris (3, 5-dimethylphenylcarbamate) as chiral sta.
Journal of Chromatography A,
1632,
2020.
-
[23]
范颖.
Recent Advances in the Development of Selective Mcl-1 Inhibitors for the Treatment of Cancer (2017-P.
Recent Patents on Anti-Cancer Drug Discovery,
15,
306,
2020.
-
[24]
梁翰之.
Recent progress in development of cyclin-dependent kinase 7 inhibitors for cancer therapy.
EXPERT OPINION ON INVESTIGATIONAL DRUGS,
30,
61,
2021.
-
[25]
杜金童.
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
BIOORGANIC & MEDICINAL CHEMISTRY Journal,
28,
2020.
-
[26]
刘璐璐.
Design, synthesis and biological evaluation of tyrosine derivatives as Mcl-1 inhibitors.
European Journal of Medicinal Chemistry,
191,
2020.
-
[27]
杜金童.
Structure-based virtual screening, biological evaluation and biophysical study of novel Mcl-1 inhibi.
Future Medicinal Chemistry,
12,
1293,
2020.
-
[28]
周易.
Discovery of Peptide Boronate Derivatives as Histone Deacetylase and Proteasome Dual Inhibitors for .
《Journal of Medicinal Chemistry》,
63,
4701,
2020.
-
[29]
侯旭奔.
Inhibition of striatal-enriched protein tyrosine phosphatase by targeting computationally revealed c.
European Journal of Medicinal Chemistry,
190,
2020.
-
[30]
梁啸.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
BIOORGANIC CHEMISTRY,
103,
2020.
-
[31]
梁涛.
HDAC-Bax Multiple Ligands Enhance Bax-Dependent Apoptosis in HeLa Cells.
《Journal of Medicinal Chemistry》,
63,
12083,
2020.
-
[32]
肖鹏 and 侯旭奔.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
Bioorg Chem.,
2020.
-
[33]
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.
-
[34]
侯旭奔
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
Bioorganic&MedicinalChemistry,
28,
2020.
-
[35]
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.
-
[36]
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.
-
[37]
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.
-
[38]
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.
-
[39]
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.
-
[40]
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.
