1,3,4-恶二唑衍生物的合成任务书

 2022-08-06 09:00:32

1. 1. 毕业设计(论文)的内容、要求、设计方案、规划等

研究内容:通过Discovery studio 3.1中的3D-QSAR(定量构效关系)对4-氨基喹唑啉衍生物的活性经行评价,并通过docking筛选出一批具有潜在活性的小分子。

本课题需要具有

1. 较强的动手能力和不懈的毅力;

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2. 参考文献(不低于12篇)

1. Jia-Jia Liu, Hui Zhang, Juan Sun, Zhong-Chang Wang, Yu-Shun Yang, Dong-Dong Li, Fei Zhang, Hai-Bin Gong, Hai-Liang Zhu*, Synthesis, biological evaluation of novel 4,5-dihydro-2H-pyrazole 2-hydroxyphenyl derivatives as BRAF inhibitors, Bioorg. Med. Chem. 2012, 20, 6089-6096.

2. Yu-Shun Yang, Qing-Shan Li, Shuai Sun, Yan-Bin Zhang, Xiao-Liang Wang, Fei Zhang, Jian-Feng Tang, Hai-Liang Zhu*, Design, modification and 3D QSAR studies of novel 2,3-dihydrobenzo[b][1,4]dioxin-containing 4,5-dihydro-1H-pyrazole derivatives as inhibitors of B-Raf kinase, Bioorg. Med. Chem. 2012, 20, 6048-6058.

3. Yin Luo, Li-Rong Zhang, Yang Hu, Shuai Zhang, Jie Fu, Xiao-Ming Wang, Hai-Liang Zhu*, Synthesis and Antimicrobial Activities of Oximes Derived from O-Benzylhydroxylamine as FabH Inhibitors, ChemMedChem, 2012, 7, 1587-1593.

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