0000000000873663

AUTHOR

Michael L. Gross

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Structure elucidation of the adducts formed by fjord region Dibenzo[a,l]pyrene-11,12-dihydrodiol 13,14-epoxides with deoxyguanosine.

1999

Model adducts to be used in the identification of biologically formed adducts were synthesized by reaction of fjord-region dibenzo[a,l]pyrene 11,12-dihydrodiol 13,14-epoxides (DB[a,l]PDE) and deoxyadenosine (dA). The (+/-)-anti-DB[a,l]PDE was reacted with dA in dimethylformamide at 100 degrees C for 30 min to give four DB[a, l]PDE-14-N(6)dA adducts: (-)-anti-trans (26%), (+)-anti-trans (26%), (-)-anti-cis (17%), and (+)-anti-cis (17%). The (+/-)-syn-DB[a,l]PDE was reacted with dA under the same conditions to yield four DB[a, l]PDE-14-N(6)dA adducts and one N7Ade adduct: (+)-syn-cis (19%), (+)-syn-trans (13%), (-)-syn-cis (19%), (-)-syn-trans (13%), and (+/-)-syn-DB[a,l]PDE-14-N7Ade (22%). T…

Steric effectsCircular dichroismMagnetic Resonance SpectroscopyMolecular StructureStereochemistryDeoxyguanosineGeneral MedicineDNAFast atom bombardmentToxicologyMass SpectrometryAdductDihydroxydihydrobenzopyreneschemistry.chemical_compoundDNA AdductsStructure-Activity RelationshipSpectrometry FluorescenceDeoxyadenosinechemistryDimethylformamidePyreneStereoselectivityChromatography High Pressure LiquidChemical research in toxicology
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