Literature DB >> 2114277

Relationships of quantitative structure-activity for normal aliphatic alcohols.

T W Schultz1, L M Arnold, T S Wilke, M P Moulton.   

Abstract

The relative toxicity of 14 normal aliphatic alcohols has been determined as 48-hr 50% population growth inhibition (log BR, biological response) of Tetrahymena pyriformis. A linear relationship was observed between log BR and the 1-octanol/water partition coefficient (log Kow). Comparison of log BR with 96-hr 50% mortality data for Pimephales promelas revealed excellent agreement between the two test systems. A relatively constant steady-state biophase toxicant concentration is calculated for each alcohol. Calculated chemical activity increased with an increase in hydrocarbon chain length. In addition, there was good agreement between chemical activity and the activity coefficient for narcosis.

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Year:  1990        PMID: 2114277     DOI: 10.1016/0147-6513(90)90026-2

Source DB:  PubMed          Journal:  Ecotoxicol Environ Saf        ISSN: 0147-6513            Impact factor:   6.291


  3 in total

1.  Structure-toxicity relationships for unsaturated alcohols to Tetrahymena pyriformis: C5 and C6 analogs and primary propargylic alcohols.

Authors:  T W Schultz; M Tichy
Journal:  Bull Environ Contam Toxicol       Date:  1993-11       Impact factor: 2.151

2.  Structure-toxicity relationships for Tetrahymena: aliphatic aldehydes.

Authors:  T W Schultz; S E Bryant; D T Lin
Journal:  Bull Environ Contam Toxicol       Date:  1994-02       Impact factor: 2.151

3.  From data point timelines to a well curated data set, data mining of experimental data and chemical structure data from scientific articles, problems and possible solutions.

Authors:  Villu Ruusmann; Uko Maran
Journal:  J Comput Aided Mol Des       Date:  2013-07-25       Impact factor: 3.686

  3 in total

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