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侯旭奔
-
副教授
博士生导师
硕士生导师
- 性别：男
- 出生日期：1990-03-22
- 毕业院校：山东大学
- 学历：研究生(博士后)
- 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： 2018-12-18
- 学科：药物化学
- 办公地点：趵突泉校区景蓝斋
大学科技园3号楼1514室
- 电子邮箱：houxuben@163.com
访问量：
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[41]
杜金童.
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
BIOORGANIC & MEDICINAL CHEMISTRY Journal,
28,
2020.
-
[42]
周易.
Discovery of Peptide Boronate Derivatives as Histone Deacetylase and Proteasome Dual Inhibitors for .
《Journal of Medicinal Chemistry》,
63,
4701,
2020.
-
[43]
侯旭奔.
Inhibition of striatal-enriched protein tyrosine phosphatase by targeting computationally revealed c.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,
190,
2020.
-
[44]
梁啸.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
BIOORGANIC CHEMISTRY,
103,
2020.
-
[45]
梁涛.
HDAC-Bax Multiple Ligands Enhance Bax-Dependent Apoptosis in HeLa Cells.
《Journal of Medicinal Chemistry》,
63,
12083,
2020.
-
[46]
肖鹏 , 方浩 and 侯旭奔.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one.
Bioorg Chem.,
2020.
-
[47]
方浩 , 侯旭奔
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
Bioorganic&MedicinalChemistry,
28,
2020.
-
[48]
杨新颖 , 方浩 and 侯旭奔.
Design, synthesis and biological evaluation of tyrosine derivatives as Mcl-1 inhibitors.
EUR J MED CHEM,
191,
2020.
-
[49]
李康帅.
Identification and structure-function analyses of an allosteric inhibitor of the tyrosine phosphatas.
294,
8653,
2019.
-
[50]
侯旭奔 , 杨新颖 , 方浩 and 梁涛.
Design, Synthesis, and Biological Evaluation of 2,4-Imidazolinedione Derivatives as HDAC6 Isoform-Se.
ACS Medicinal Chemistry Letters,
10,
1122,
2019.
-
[51]
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.
-
[52]
杨新颖 , 方浩 , 侯旭奔 and 陈晨.
Design, synthesis and preliminary bioactivity studies of indomethacin derivatives as Bcl-2/Mcl-1 dua.
Bioorganic and medicinal chemistry,
2019.
-
[53]
杨新颖 , 侯旭奔 and 方浩.
High-performance liquid chromatographic enantioseparation of 3,5-disubstituted hydantoins analogs an.
Journal of Chromatography A,
2014.
-
[54]
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.
-
[55]
田志刚 , 侯旭奔 , 韩秋菊 , 陆楠 , 张建 , 张彩 , 于馨
HBV inhibits LPS-induced NLRP3 inflammasome activation and IL-1 beta production via suppressing the .
Journal of Hepatology,
66,
693,
2017.
-
[56]
侯旭奔 , 方浩 and 朱鹏举.
淋巴特异性酪氨酸磷酸酶抑制剂的研究进展.
《药学学报》,
52,
699,
2017.
-
[57]
侯旭奔 , 孙金鹏 , 方浩 and 肖鹏.
Computational Strategy for Bound State Structure Prediction in Structure-Based Virtual Screening: A .
Journal of Chemical Information and Modeling,
58,
2331,
2018.
-
[58]
侯旭奔 , 方浩 and 杨新颖.
High-performance liquid chromatographic enantioseparation of 3,5-disubstituted hydantoins analogs an.
Journal of Chromatography A,
2014.
-
[59]
张建 , 张彩 and 于馨.
HBV inhibits LPS-induced NLRP3 inflammasome activation and IL-1 beta production via suppressing the .
Journal of Hepatology,
66,
693,
2017.
-
[60]
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.
