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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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[21]
梁翰之.
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梁涛.
Design, synthesis and biological evaluation of 3, 4-disubstituted-imidazolidine-2, 5-dione derivativ.
European Journal of Medicinal Chemistry,
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梁涛.
Design, synthesis and biological evaluation of 3, 4-disubstituted-imidazolidine-2, 5-dione derivativ.
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李雯.
Photopharmacology-based small-molecule proteolysis targeting chimeras: optical control of protein de.
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A novel selective histone deacetylase I inhibitor CC-4a activates latent HIV-1 through NF-kappa B pa.
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郭永真.
Recent Applications of Benzimidazole as a Privileged Scaffold in Drug Discovery.
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[31]
李雯.
Recent Advances in Small Molecule PROTACs for the Treatment of Cancer.
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赵雲鹏.
Recent Development of Novel HDAC6 Isoform-selective Inhibitors.
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Potential applications of BPFP1 in Bcl-2 protein quantification, carcinoma cell visualization, cell .
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李佳.
Synthesis and evaluation of a UMI-77-based fluorescent probe for selective detecting Mcl-1 protein a.
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Enantioseparation of lysine derivatives on amylose tris (3, 5-dimethylphenylcarbamate) as chiral sta.
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Recent Advances in the Development of Selective Mcl-1 Inhibitors for the Treatment of Cancer (2017-P.
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[37]
梁翰之.
Recent progress in development of cyclin-dependent kinase 7 inhibitors for cancer therapy.
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[38]
杜金童.
An in silico mechanistic insight into HDAC8 activation facilitates the discovery of new small-molecu.
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[39]
刘璐璐.
Design, synthesis and biological evaluation of tyrosine derivatives as Mcl-1 inhibitors.
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Structure-based virtual screening, biological evaluation and biophysical study of novel Mcl-1 inhibi.
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