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- W2232615845 abstract "Injection of [3H]aflatoxin B1 into rats yielded covalently bound derivatives in hepatic DNA, rRNA, and protein. Mild acid hydrolysis of the DNA and rRNA adducts formed a derivative indistinguishable from 2,3-dihydro-2,3-dihydroxy-aflatoxin B1. The data indicate that approximately 60% of the nucleic acid adducts were derived from reactions in vivo with aflatoxin B1-2,3-oxide. Acid hydrolysis of rRNA-[3Haflatoxin B1 adduct formed by human liver microsomes in vitro also liberated the dihydrodiol in significant amount. The 2,3-oxide of aflatoxin B1 is a probable ultimate carcinogenic metabolite." @default.
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- W2232615845 date "1974-10-01" @default.
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- W2232615845 title "Aflatoxin B1-2,3-oxide: Evidence for its formation in rat liver in vivo and by human liver microsomes in vitro" @default.
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- W2232615845 doi "https://doi.org/10.1016/0006-291x(74)90417-3" @default.
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