Literature DB >> 13215

Use of distribution coefficients in quantitative structure-activity relationships.

R A Scherrer, S M Howard.   

Abstract

The use of distribution coefficients (log D) for the analysis of structure-activity relationships of ionizable compounds is described. (D is the ratio of the equilibrium concentration of compound in an organic phase to the total concentration of un-ionized and ionized species in the aqueous phase at a given pH.) Simpler equations, often with improved correlations, have resulted. This method has the advantage that the influence of pKa or equivalent electronic factors on distribution can be distinguished from electronic effects related to mechanism of action. Several absorption studies are reanalyzed as well as studies on membrane conductance and uncoupling of oxidative phosphorylation.

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Year:  1977        PMID: 13215     DOI: 10.1021/jm00211a010

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  19 in total

Review 1.  Quantitative structure-activity relationships (QSAR) and molecular modelling in cancer research.

Authors:  H Kubinyi
Journal:  J Cancer Res Clin Oncol       Date:  1990       Impact factor: 4.553

2.  Hydrophobicity of complex organic mixtures.

Authors:  E M Verbruggen; W M van Loon; J L Hermens
Journal:  Environ Sci Pollut Res Int       Date:  1996-09       Impact factor: 4.223

3.  The affinity of D2-like dopamine receptor antagonists determines the time to maximal effect on cocaine self-administration.

Authors:  Andrew B Norman; Michael R Tabet; Mantana K Norman; Brittney K Fey; Vladimir L Tsibulsky; Ronald W Millard
Journal:  J Pharmacol Exp Ther       Date:  2011-05-23       Impact factor: 4.030

4.  Column bleed in the analysis of highly polar substances: an overlooked aspect in HRMS.

Authors:  Bastian Schulze; Tobias Bader; Wolfram Seitz; Rudi Winzenbacher
Journal:  Anal Bioanal Chem       Date:  2020-01-16       Impact factor: 4.142

5.  Model-based QSAR for ionizable compounds: toxicity of phenols against Tetrahymena pyriformis.

Authors:  K Pirselová; S Baláz; T W Schultz
Journal:  Arch Environ Contam Toxicol       Date:  1996-02       Impact factor: 2.804

6.  The kinetics of the enzymatic O-methylation of catechols and catecholamines.

Authors:  M T Schüsler-Van Hees; G M Beijersbergen Van Henegouwen
Journal:  Pharm Weekbl Sci       Date:  1983-12-16

7.  Dissociation constants and lipophilicity of catecholamines and related compounds.

Authors:  F Mack; H Bönisch
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1979-12       Impact factor: 3.000

8.  Removal of xenobiotics from effluent discharge by adsorption on zeolite and expanded clay: an alternative to activated carbon?

Authors:  A Tahar; J M Choubert; C Miège; M Esperanza; K Le Menach; H Budzinski; C Wisniewski; M Coquery
Journal:  Environ Sci Pollut Res Int       Date:  2014-01-16       Impact factor: 4.223

9.  Quantitative structure-activity relationship studies on nitrofuranyl anti-tubercular agents.

Authors:  Kirk E Hevener; David M Ball; John K Buolamwini; Richard E Lee
Journal:  Bioorg Med Chem       Date:  2008-07-29       Impact factor: 3.641

10.  The octanol/water distribution of mercury compounds.

Authors:  S Halbach
Journal:  Arch Toxicol       Date:  1985-06       Impact factor: 5.153

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