Prediction of the genotoxicity of aromatic and heteroaromatic amines using electrotopological state indices

Author:

Cash Gordon G.

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference18 articles.

1. A QSAR investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test;Debnath;Environ. Mol. Mutagen.,1992

2. S.C. Basak, G.D. Grunwald, G.J. Niemi. Use of graph-theoretic and geometrical molecular descriptors in structure-activity relationships, in: A.T. Balaban (Ed.), From Chemical Topology to Three-Dimensional Geometry, Plenum Press, New York, 1997 (Chapter 4).

3. A comprehensive QSAR treatment of the genotoxicity of heteroaromatic and aromatic amines;Maran;Quant. Struct. Act. Relat.,1999

4. Predicting mutagenicity of chemicals using topological and quantum chemical parameters: a similarity based study;Basak;Chemosphere,1995

5. S.C. Basak, D.R. Mills, A.T. Balaban, B.D. Gute, Prediction of mutagenicity of aromatic and heteroaromatic amines from structure: a hierarchical QSAR approach, J. Chem. Inf. Comput. Sci. 40 (2000), in press.

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