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Schultz, T.W.; Cajina-Quezada, M.; Dumont, J.N. Structure-toxicity Relationships of Selected Nitrogenous Heterocyclic Compounds. Arch. Environ. Contam. Toxicol. 1980, 9, 5, 591–598.

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Schultz, T.W.; Cajina-Quezada, M.; Dumont, J.N. Structure-toxicity Relationships of Selected Nitrogenous Heterocyclic Compounds. Arch. Environ. Contam. Toxicol. 1980, 9, 5, 591–598.

QDB archive DOI: 10.15152/QDB.58   DOWNLOAD

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Property logIGC50: 72-h Tetrahymena toxicity as log(IGC50) [log(mmol/L)]

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  • Ruusmann, V. Data for: Structure-toxicity Relationships of Selected Nitrogenous Heterocyclic Compounds. QsarDB repository, QDB.58. 2012. http://dx.doi.org/10.15152/QDB.58

  • Schultz, T. W.; Cajina-Quezada, M.; Dumont, J. N. Structure-toxicity Relationships of Selected Nitrogenous Heterocyclic Compounds. Arch. Environ. Contam. Toxicol. 1980, 9, 591–598. http://dx.doi.org/10.1007/BF01056938

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Title: Schultz, T.W.; Cajina-Quezada, M.; Dumont, J.N. Structure-toxicity Relationships of Selected Nitrogenous Heterocyclic Compounds. Arch. Environ. Contam. Toxicol. 1980, 9, 5, 591–598.
Abstract: A series of eleven nitrogen-containing heterocyclic compounds, which may be potentially associated with aqueous effluents from coal conversion technologies, were examined to determine the relationships between theirn-octanol/H2O partition coefficients, molecular weights, boiling points, and their toxicity monitored as reproduction impairment toTetrahymena pyriformis. Toxicity increases linearly with increased partition coefficient, molecular weight, and boiling point. All of these parameters increase with increased alkyl and ring addition.
URI: http://hdl.handle.net/10967/58
http://dx.doi.org/10.15152/QDB.58
Date: 2012-05-23


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