Download Biological Reactive Intermediates VI: Chemical and by John D. Robertson, Joya Chandra, Vladimir Gogvadze (auth.), PDF

By John D. Robertson, Joya Chandra, Vladimir Gogvadze (auth.), Patrick M. Dansette, Robert Snyder, Marcel Delaforge, G. Gordon Gibson, Helmut Greim, David J. Jollow, Terrence J. Monks, I. Glenn Sipes (eds.)

This quantity offers a dialogue of the organic results produced following the metabolism of xenobiotic chemical compounds to chemically reactive metabolites, i.e., poisonous and carcinogenic results, that have been the foundation of all 5 past volumes during this sequence. specifically, this quantity devotes sections to structure-activity relationships, fresh advances within the realizing of the chemistry of reactive metabolites, and the new release and job of reactive oxygen species with exact emphasis on nitric oxide. There also are segments on DNA harm by means of reactive metabolites and DNA fix, tissue particular responses to BRIs, and human health and wellbeing results of BRIs. The papers that contain this quantity have been submitted via international classification scientists who have been in attendance on the Symposium on organic Reactive Intermediates VI on the Université René Descartes, July 16-20, 2000.

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Extra resources for Biological Reactive Intermediates VI: Chemical and Biological Mechanisms in Susceptibility to and Prevention of Environmental Diseases

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0. 95 for 10g(A) vs. L'lE(MeS' conj) represents the most successful attempt to relate all 11 haloacids according to the same property metric. Another measure of success of this parameter correlation, however, is its ability to reproduce the correct relative orderings of activities within chemically meaningful subclasses of the data set. A comparison of experimental vs. 71, n=9 1• .......... 95, n=11 -2 • 0 ~ 0 0 C\J 0 v 0 co -L'lE(MeS' conj) Figure 2. Regression plot of log(GSTZ activity) vs. L'lE(MeS' conj) for 11 haloacids.

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DeAngelo, A. , Daniel, F. , Most, B. , and Olson, G. , 1996, The carcinogenicity of dichloroacetic acid in the male Fischer 344 rat, Toxicol. 114:207221. Fernandez-Can6n, J. M. and Pefialva, M. , 1998, Characterization of a fungal maleylacetoacetate isomerase gene and identification of its human homologue, 1. BioI. Chem. 273:329-337. Karickhoff, S. , McDaniel, V. , Vellino, A. , Nute, D. , and Carriera, L. , 1991, Predicting chemical reactivity by computer, Environ. Toxicol. l0:1405-1416. -Y. and Richard, A.

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