Literature DB >> 929197

Polychlorobornane components of toxaphene: structure-toxicity relations and metabolic reductive dechlorination.

M A Saleh, W V Turner, J E Casida.   

Abstract

2,2,5-endo,6-exo,8,9,10-Heptachlorobornane and four derivatives of this heptachlorobornane, with an additional chlorine atom at position 3-exo,8,9, or 10, account for a major portion of the acute toxicity of toxaphene and for up to 23 percent of toxaphene composition as analyzed by open tubular column gas-liquid chromatography with an electron capture detector. Both in several organisms and model environmental systems and on photolysis, this heptachlorobornane undergoes facile reductive dechlorination at the geminal-dichloro group and sometimes dehydrochlorination.

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Year:  1977        PMID: 929197     DOI: 10.1126/science.929197

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  4 in total

1.  Metabolism of toxaphene by the isolated perfused bovine liver.

Authors:  R M Maiorino; F M Whiting; W H Brown; B L Reid; J W Stull
Journal:  Arch Environ Contam Toxicol       Date:  1984-09       Impact factor: 2.804

2.  Metabolism of toxaphene components in rats.

Authors:  P S Chandurkar; F Matsumura
Journal:  Arch Environ Contam Toxicol       Date:  1979       Impact factor: 2.804

3.  Toxicity of chlorinated bornane (toxaphene) residues isolated from Great Lakes lake trout (Salvelinus namaycush).

Authors:  J W Gooch; F Matsumura
Journal:  Arch Environ Contam Toxicol       Date:  1987-05       Impact factor: 2.804

4.  The greening of pesticide-environment interactions: some personal observations.

Authors:  John E Casida
Journal:  Environ Health Perspect       Date:  2012-01-18       Impact factor: 9.031

  4 in total

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