Scherrer Robert A, Leo Albert J
BIOpKa, 3416 Ebba Street, White Bear Lake, MN 55110, USA fax: 651-770-7831.
BioByte Corp. 201 W. 4thStreet, #204, Claremont, CA 91711, USA.
Mol Inform. 2010 Oct 11;29(10):687-93. doi: 10.1002/minf.201000093. Epub 2010 Oct 8.
Classical Hansch analysis for most series of ionizable compounds cannot identify the active species as being neutral or ionized. The log P(N) and log P(I) of these series are too highly correlated. We have found a simple solution to this problem by just combining data obtained at more than one pH (multi-pH QSAR). A bonus is that the statistical power of a series is increased one fold for each pH level added. Datasets of simple homologous series serve as proofs of concept. Two of these reveal hidden correlations involving both the neutral and ionized species. These "true" correlations would be impossible to find at a single pH. An example is the inhibition of monoamine oxidase by a series of primary n-alkylamines. Multi-pH QSAR indicates that the protonated amine enhances inhibition and the neutral species diminishes it. This paper illustrates the first substantial use in QSAR of the species-specific terms, log D(N) (neutral) and log D(I) (ionized). Multi-pH QSAR can give direction to lead development and facilitate the In-Silico modeling of ADMET processes by associating rate-limiting steps with the correct ionization state.
对于大多数可电离化合物系列,经典的Hansch分析无法确定活性物种是中性还是离子化形式。这些系列的log P(N)和log P(I)相关性过高。我们通过合并在多个pH值下获得的数据(多pH值QSAR)找到了解决这个问题的简单方法。一个额外的好处是,每增加一个pH值水平,系列的统计效力就会提高一倍。简单同系物系列的数据集可作为概念验证。其中两个揭示了涉及中性和离子化物种的隐藏相关性。这些“真实”的相关性在单一pH值下是不可能找到的。一个例子是一系列伯正烷基胺对单胺氧化酶的抑制作用。多pH值QSAR表明,质子化胺增强抑制作用,而中性物种则减弱抑制作用。本文阐述了物种特异性术语log D(N)(中性)和log D(I)(离子化)在QSAR中的首次实质性应用。多pH值QSAR可以为先导化合物开发提供方向,并通过将限速步骤与正确的电离状态相关联,促进ADMET过程的计算机模拟。