表皮生长因子受体酪氨酸激酶抑制剂的药效团研究 |
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引用本文: | 彭涛,裴剑锋,周家驹. 表皮生长因子受体酪氨酸激酶抑制剂的药效团研究[J]. 化学学报, 2003, 61(3): 430-434 |
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作者姓名: | 彭涛 裴剑锋 周家驹 |
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作者单位: | 中国科学院过程工程研究所,北京,100080 |
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基金项目: | 国家基础研究发展规划基金 (No .G1 9980 51 1 1 5)资助项目 |
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摘 要: | 根据一系列表皮生长因子受体酪氨酸激酶抑制剂的三维定量构效关系研究,得 到了该类抑制剂的药效团,研究结果与Novartis的药效团模型相当类似.药效团包 括一个氢键受体,一个氢键给体,一个疏水区和一个带有氯或溴原子药效团对于研 究表皮生长因子受体酪氨酸激酶抑制剂结构与活性的关系具有重要的意义.通过三 维数据库搜索可能会得到新的先导化合物.
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关 键 词: | 酪氨酸酶 抑制剂 定量构效关系 |
修稿时间: | 2002-07-09 |
Pharmacophore Analysis of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors |
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Affiliation: | Institute of Process Engineering,Chinese Academy of Sciences |
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Abstract: | A three-dimensional pharmacophore of epidermal growth factor receptor tyrosine kinase inhibitors was obtained based upon 3D-QSAR of a series of these inhibitors. The result was accordant with the pharmacophore model given by the scientists at Novartis. The pharmacophore included a hydrogen bond receptor, a hydrogen bond donor, a hydrophobic area and a phenyl ring with a chlorine or a bromine atom. This pharmacophore is very useful for clarifying the structure-activity relationships of EGFR tyrosine kinase inhibitors. Some lead compounds may be acquired through three-dimensional database searching. |
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Keywords: | pharmacophore EGFR tyrosine kinase inhibitor active site |
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