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[401] liuxinyong and 展鹏. Privileged Scaffolds or Promiscuous Binders: A Glance of Pyrrolo[2,1-f][1,2,4]triazines and Relat.... Curr Pharm Des. 2013;19(8):1528-48., 2013.
[402] liuxinyong and 展鹏. Arylazolyl(azinyl)thioacetanilides. Part 10: Design, synthesis and biological evaluation of novel.... 《Bioorg Med Chem.》, 20, 5527, 2012.
[403] liuxinyong and 李潇. Arylazolyl(azinyl) thioacetanilides. Part 10: Design, synthesis and biological evaluation of nove.... Bioorg. Med. Chem., 20, 5527, 2012.
[404] liuxinyong and guoxiuli. 内质网应激介导的细胞凋亡途径及新靶点药物. 《中国药学杂志》, 43, 1361, 2008.
[405] liuxinyong , chengyanna and guoxiuli. Reversal effect of ligustrazine derivate on multi-drug resistance in adriamycin-resistant cell li.... Toxicology in vitro 2011,25(4):937-943, 25, 937, 2011.
[406] liuxinyong , chengyanna and guoxiuli. Mechanism of Tetramethylpyrazine analogue CXC195 inhibition of hydrogen peroxide-induced apoptosi.... Biol Pharm Bull, 33, 432, 2010.
[407] liuxinyong and 展鹏. 抗艾滋病药物设计新策略：多靶点及多价态结合配体. 《中国药物化学杂志》, 23, 406, 2013.
[408] liuxinyong and 展鹏. Heterocycle-thioacetic Acid Motif: A Privileged Molecular Scaffold with Potent, Broad-Ranging Pha.... Current Pharmaceutical Design, 2013.
[409] liuxinyong and 展鹏. Rationally designed multitarget anti-HIV agents. Curr Med Chem, 20, 1743, 2013.
[410] liuxinyong and 展鹏. 以黄嘌呤氧化酶为靶点的新型非嘌呤类抗痛风及高尿酸血症药物研究进展. 《中国药物化学杂志》, 22, 403, 2012.

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