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大黄素衍生物对口腔底癌细胞活性的构效关系研究
引用本文:赵蔡斌,闵锁田,葛红光. 大黄素衍生物对口腔底癌细胞活性的构效关系研究[J]. 西北药学杂志, 2007, 22(4): 179-181
作者姓名:赵蔡斌  闵锁田  葛红光
作者单位:陕西理工学院化学与环境科学学院,陕西,汉中,723000
基金项目:陕西理工学院专项科研项目
摘    要:目的探索建立大黄素衍生物抗口腔底癌细胞活性的构效关系模型。方法采用量子化学的AM1半经验算法,计算10个大黄素衍生物分子结构参数,并用逐步回归分析方法,拟定大黄素衍生物抗口腔底癌细胞活性的构效关系模型。结果建立了大黄素衍生物抗口腔底癌细胞活性的构效关系模型。结论大黄素衍生物抗口腔底癌细胞活性与此类化合物分子的疏水性参数、A环上的负电荷及第二条最低空轨道能量有关。

关 键 词:大黄素衍生物  口腔底癌细胞  构效关系  AM1算法
文章编号:1004-2407(2007)04-0179-03
收稿时间:2006-09-14
修稿时间:2006-09-14

QSAR study of emodin derivatives against the cell line of KB
ZHAO Cai-bin,MIN Suo-tian,GE Hong-guang. QSAR study of emodin derivatives against the cell line of KB[J]. Northwest Pharmaceutical Journal, 2007, 22(4): 179-181
Authors:ZHAO Cai-bin  MIN Suo-tian  GE Hong-guang
Affiliation:College of Chemistry and Environment Science, Shaanxi University of technology, Hanzhong 723000, China
Abstract:Objective To study quantitative structure-activity relationship of emodin derivatives against the cell line of KB. Methods By AM1 method in quantum chemistry, molecular structural parameters of 10 emodin derivatives have been calculated, and the relationship has been established between the activity against the cell line of KB and the molecular parameters by stepwise regression analysis (SRA). Result The QSAR model was established successfully. Conclusion The activity of emodin derivatives against the cell line of KB is related to the hydrophobic parameter, negative charge of A circle and energy of the second low unoccupied molecular orbit. This results are helpful for developing new drug against the cell line of KB.
Keywords:emodin derivatives  cell line of KB  quantitative structure-activity relationship  AM1 method
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