Literature DB >> 8875147

Reactivity parameters in structure-activity relationship-based risk assessment of chemicals.

J D McKinney1.   

Abstract

New approaches to the risk assessment process are needed that might be more definitive and satisfying to the scientific community, interest groups, and the public at large. This commentary examines an alternative approach that is based on understanding the relationships of chemical structure and reactivity properties to the toxicokinetic behavior of chemicals in biological systems. This approach is based on the likelihood that there is a limited number of triggering (reactivity) mechanisms by which chemicals can express their toxicity at the molecular level. The fundamental importance of electrophilic character of chemicals as a determinant of their critical molecular reactivities and interactions with biological material in the expression of toxicity is supported. Such an approach also takes advantage of the maturing field of theoretical/computational chemistry in understanding important molecular recognition and reactivity processes (both qualitatively and quantitatively) for chemicals that can underlie their biological/toxicological activity. A process that permits assessment of reaction equivalents delivered to biological systems may hold promise for grouping chemicals by common triggering mechanisms with clearly delineated toxicological endpoints.

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Year:  1996        PMID: 8875147      PMCID: PMC1469427          DOI: 10.1289/ehp.96104810

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  29 in total

Review 1.  Risk assessment of environmental chemicals.

Authors:  A Fan; R Howd; B Davis
Journal:  Annu Rev Pharmacol Toxicol       Date:  1995       Impact factor: 13.820

2.  A physico-chemical screening test for chemical carcinogens: the ke test.

Authors:  G Bakale; R D McCreary
Journal:  Carcinogenesis       Date:  1987-02       Impact factor: 4.944

Review 3.  Chemical mechanisms of halocarbon metabolism.

Authors:  T L Macdonald
Journal:  Crit Rev Toxicol       Date:  1983       Impact factor: 5.635

Review 4.  Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and related compounds: environmental and mechanistic considerations which support the development of toxic equivalency factors (TEFs).

Authors:  S Safe
Journal:  Crit Rev Toxicol       Date:  1990       Impact factor: 5.635

5.  Structure-activity relationships in halogenated biphenyls: unifying hypothesis for structural specificity.

Authors:  J D McKinney; P Singh
Journal:  Chem Biol Interact       Date:  1981-01       Impact factor: 5.192

6.  Complexation of arsenic species in rabbit erythrocytes.

Authors:  M Delnomdedieu; M M Basti; M Styblo; J D Otvos; D J Thomas
Journal:  Chem Res Toxicol       Date:  1994 Sep-Oct       Impact factor: 3.739

7.  Three-dimensional quantitative structure-activity relationships of dioxins and dioxin-like compounds: model validation and Ah receptor characterization.

Authors:  C L Waller; J D McKinney
Journal:  Chem Res Toxicol       Date:  1995-09       Impact factor: 3.739

8.  Assessment of the propensity for covalent binding of electrophiles to biological substrates.

Authors:  R M Carlson
Journal:  Environ Health Perspect       Date:  1990-07       Impact factor: 9.031

Review 9.  Mechanisms of general anesthesia.

Authors:  N P Franks; W R Lieb
Journal:  Environ Health Perspect       Date:  1990-07       Impact factor: 9.031

10.  Structure-induction versus structure-toxicity relationships for polychlorinated biphenyls and related aromatic hydrocarbons.

Authors:  J D McKinney; K Chae; E E McConnell; L S Birnbaum
Journal:  Environ Health Perspect       Date:  1985-05       Impact factor: 9.031

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