Hydrophobic moments as physicochemical descriptors in structure-activity relationship studies of P-glycoprotein inhibitors

被引:6
作者
Koenig, Gerhard [1 ]
Chiba, Peter [2 ]
Ecker, Gerhard F. [1 ]
机构
[1] Univ Vienna, Dept Med Chem, Emerging Field Pharmacoinformat, A-1090 Vienna, Austria
[2] Med Univ Vienna, Inst Med Chem, Vienna, Austria
来源
MONATSHEFTE FUR CHEMIE | 2008年 / 139卷 / 04期
基金
奥地利科学基金会;
关键词
computer chemistry; propafenone; multidrug resistance; molecular modeling; antitumor agents;
D O I
10.1007/s00706-007-0819-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipophilicity is one of the major determining physicochemical descriptors for P- glycoprotein ( P- gp) inhibitory activity. In order to consider lipo-philicity as a space directed property, we apply the concept of hydrophobic moments on a set of propafenone-type inhibitors of P- glycoprotein and use them as descriptors in QSAR analyses. While the 0(th) moment is the sum of the atomic hydrophobicity coefficients, which is a measure for the total hydrophobicity of the molecule, the 1(st) moment ( or hydrophobic dipole) is a measure for the asymmetry of the distribution of hydrophobicities and therefore is analogous to the electrostatic dipole. The use of these hydrophobic dipole moments as independent variables remarkably improved the predictive power of QSAR models obtained.
引用
收藏
页码:401 / 405
页数:5
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