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个人简介

学习经历 1981年9月~1985年7月:山东医学院药学系,获医学学士学位 1987年9月~1990年7月:山东医科大学药学系,获理学硕士学位 1998年4月~2001年3月:(日本)富山医科药科大学药学部,获药学博士学位 工作经历 1985年7月~1987年9月:山东医科大学药学部,助教 1990年9月~1995年9月:山东医科大学药学部,助教、讲师其中 1994年4月~1995年3月:日中医学会笹川医学奖学金(帝京大学药化学研究室) 1995年9月~1998年3月:(日本)帝京大学药化学研究室,访问学者 2001年4月~2004年3月:(日本)中外制药公司富士御殿场化学研究所,研究员 2004年4月~2005年3月:名古屋大学理学部有机化学研究室,JST特别研究员 2005年4月~至今:山东大学药学院有机化学教研室,教授

研究领域

1. 分子靶向抗肿瘤药物的设计与合成研究 针对肿瘤信号转导通路、肿瘤相关表观遗传学、激酶、微管蛋白等,主要进行小分子靶向抗肿瘤药物的设计、合成与评价研究 2. 抗老年痴呆(AD)药物研究 基于老年痴呆(阿尔茨海默病;AD)的表观遗传学靶点、GSK-3激酶等相关环节,设计、合成、筛选新型抗老年痴呆(AD)药物 3. 基于天然产物的新药发现研究 以天然产物的结构为基础,进行合理的结构修饰与药物发现研究,包括活性维生素D类肿瘤细胞分化诱导剂、肿瘤细胞凋亡诱导剂、免疫抑制剂和骨质疏松治疗药物等

近期论文

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C.-C. Ma, Z.-P. Liu*: Design and synthesis of coumarin derivatives as novel PI3K inhibitors. Anti-Cancer Agents Med. Chem. 2017, 17(3), 395–403. S. Tan, F. He, T. Kong, J. Wu* and Z.-P Liu*. Design, synthesis and tumor cell growth inhibitory activity of 3-nitro-2H-cheromene derivatives as histone deacetylaes inhibitors. Bioorg. & Med. Chem., 2017, 25, 4123–4132. Y.-N. Liu, J.-J. Wang, Y.-T. Ji, G.-D. Zhao, L.-Q. Tang, C.-M. Zhang, X.-L. Guo*, Z.-P. Liu*: Design, synthesis, and biological evaluation of 1-methyl-1,4-dihydroindeno[1,2-c]pyrazole analogues as potential anticancer agents targeting tubulin colchicine binding site. J. Med. Chem. 2016, 59(11), 5341–5355. G.-D. Zhao, Z.-P. Liu*: Structural revisions of the reported A-ring phosphine oxide synthon for ED-71 (Eldecalcitol) and a new synthesis. Tetrahedron, 2015, 71(42), 8033–8040. Y.-L. Jiang, S.-X. Li, Y.-J. Liu, L.-P. Ge, X.-Z. Han*, Z.-P. Liu*: Synthesis and evaluation of trehalose-based compounds as novel inhibitors of cancer cell migration and invasion. Chem. Biol. Drug Des., 2015, 86(5), 1017–1029. C. Liu, F. Xie, G.-D, Zhao, D.-F. Wang, H.-X. Lou*, Z.-P. Liu*: Synthetic studies towards 1α-hydroxysolasodine from diosgenin and the unexpected tetrahydrofuran ring opening in the Birch reduction process. Steroids, 2015, 104, 214–219. C. Liu, G.-D. Zhao, X. Mao, T. Suenaga, T. Fujishima, C.-M. Zhang, Z.-P. Liu*: Synthesis and biological evaluation of 1α,25-dihydroxyvitamin D3 analogues with aromatic side chains attached at C-17. Eur. J. Med. Chem. 2014, 85, 569–575. X. Qiu, G.-D. Zhao, L.-Q. Tang, Z.-P. Liu*: Design and synthesis of highly potent HIV-1 protease inhibitors with novel isosorbide-derived P2 ligands. Bioorg. & Med. Chem. Lett. 2014, 24, 2465–2468. G.-D. Zhao, Z.-P. Liu*: Stereoselective reduction of C-20 ketone of vitamin D CD-ring and a new synthetic approach to maxacalcitol. Steroids 2014, 88, 72–76. K. Han, X. Xu, G. Chen, Y. Zeng, J. Zhu, X. Du, Z. Zhang, B. Cao, Z. Liu, X. Mao*: Identification of a promising PI3K inhibitor for the treatment of multiple myeloma through the structural optimization. J. Hematology & Oncology 2014, 7, 9. S.-Q. Yin, M. Shi, T.-T. Kong, C.-M. Zhang, K. Han, B. Cao, Z. Zhang, X. Du, L.-Q. Tang, X. Mao*, Z.-P. Liu*: Preparation of S14161 and its analogues and the discovery of 6-bromo-8-ethoxy-3-nitro-2H-chromene as a more potent antitumor agent in vitro. Bioorg. & Med. Chem. Lett. 2013, 23, 3314–3319. Y.-L. Jiang, S. Miyanaga, X.-Z. Han, L.-Q. Tang, Y. Igarashi, I. Saiki, Z.-P. Liu*: Synthesis and structure–activity relationships studies of brartemicin analogs as anti-invasive agents. J. Antibiotics, 2013, 66, 531–537.

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