The hydrophobic fragmental constant approach for calculating log P in octanol/water and aliphatic hydrocarbon/water systems

被引:72
作者
Mannhold, R
Rekker, RF
机构
[1] Univ Dusseldorf, Dept Laser Med, Mol Drug Res Grp, D-40225 Dusseldorf, Germany
[2] Vrije Univ Amsterdam, Fac Chem, Dept Pharmacochem, Leiden Amsterdam Ctr Drug Res, NL-1081 HV Amsterdam, Netherlands
关键词
aliphatic hydrocarbon/water partitioning; calculation procedures; fragmental methods; lipophilicity; octanol/water partitioning;
D O I
10.1023/A:1008782809845
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Lipophilicity is a prime physicochemical parameter in describing both pharmacodynamic and pharmacokinetic aspects of drug action. Its quantitative descriptor (log P) is measured in or calculated for different model solvent systems depending on the respective scientific interest. The first part of this article focuses on the hydrophobic fragmental constant approach (Sigma f system) for octanol/water partitioning. The original approach and its revisions are presented, followed by recipes for the practical procedure of Sigma f calculations and a detailed description of how to apply the correction factor C-M. A Sigma f system for application in the study of aliphatic hydrocarbon/water (ahc/w) partitioning is described in the second part of the article. The current version is based on an optimized coupling of the ahc/w system with f constants for octanol/water partitioning. A total of 70 f(ahc) values are now available.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 21 条
[1]   HYDROGEN-BONDING .33. FACTORS THAT INFLUENCE THE DISTRIBUTION OF SOLUTES BETWEEN BLOOD AND BRAIN [J].
ABRAHAM, MH ;
CHADHA, HS ;
MITCHELL, RC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (09) :1257-1268
[2]  
DARVAS F, 1987, QSAR DRUG DESIGN TOX, P70
[3]  
HANSCH C, 1983, POMONA COLL MED CHEM
[4]  
Hansch C., 1995, Exploring QSAR-Fundamentals and Applications in Chemistry and Biology
[5]  
Mannhold R, 1998, QUANT STRUCT-ACT REL, V17, P517, DOI 10.1002/(SICI)1521-3838(199812)17:06<517::AID-QSAR517>3.3.CO
[6]  
2-C
[7]   Calculation procedures for molecular lipophilicity: A comparative study [J].
Mannhold, R ;
Dross, K .
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 1996, 15 (05) :403-409
[8]   COMPARATIVE-EVALUATION OF THE PREDICTIVE POWER OF CALCULATION PROCEDURES FOR MOLECULAR LIPOPHILICITY [J].
MANNHOLD, R ;
REKKER, RF ;
SONNTAG, C ;
TERLAAK, AM ;
DROSS, K ;
POLYMEROPOULOS, EE .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (12) :1410-1419
[9]  
NYS GG, 1973, CHIM THER, V8, P521
[10]  
NYS GG, 1974, EUR J MED CHEM, V9, P361