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Epoxidation of (+/-)-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene during (bi)sulfite autoxidation: activation of a procarcinogen by a cocarcinogen.

The (bi)sulfite ion undergoes extensive autoxidation in neutral aqueous media with the formation of sulfur trioxide radical anion that is detected by ESR. The radical anion subsequently reacts with molecular oxygen to form a peroxyl radical. We find that when (+/-)-trans-7,8-dihydroxy-7,8-dihydroben...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Reed, G A, Curtis, J F, Mottley, C, Eling, T E, Mason, R P
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1986
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC386746/
https://ncbi.nlm.nih.gov/pubmed/3463979
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