| 药物分子设计与定量构效关系研究进展 |
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| 引用本文： | 周卫红,苗志伟,文欣,刘小兰,缪方明. 药物分子设计与定量构效关系研究进展[J]. 天津师范大学学报(自然科学版), 1999, 0(1) |
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| 作者姓名： | 周卫红 苗志伟 文欣 刘小兰 缪方明 |
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| 作者单位： | 天津师范大学晶体化学研究所 |
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| 摘 要： | 介绍了药物分子设计与定量构效关系的发展概况与研究进展（２Ｄ－ＱＳＡＲ,３Ｄ－ＱＳＡＲ,ＭＤ－ＱＳＡＲ）,为开发新药及化工、医药的发展提供了信息．
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| 关 键 词： | 药物分子设计 定量构效关系 配体 受体 |
The Developments of Drug Molecular Design and QSAR Study |
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| Zhou Wei hong Miao Zhi wei Wen Xin Liu Xiao lan Miao Fang ming. The Developments of Drug Molecular Design and QSAR Study[J]. Journal of Tianjin Normal University(Natural Science Edition), 1999, 0(1) |
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| Authors: | Zhou Wei hong Miao Zhi wei Wen Xin Liu Xiao lan Miao Fang ming |
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| Abstract: | This paper introduces the developments of quantitative structure activity relationships (QSAR, 2D QSAR, 3D QSAR, MD QSAR) and computer aided drug design (CADD), which will be very useful for development of novel pharmaceuticals, chemical and pharmaceutical industries in our country. |
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| Keywords: | molecular drug design quantitative structure activity relationships ligand substrate |
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