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Direct Alkylation of Deoxyguanosine by Azaserine Leads to <i>O</i><sup>6</sup>-Carboxymethyldeoxyguanosine

Susanne M. Geisen, Claudia M. N. Aloisi, Sabrina M. Huber, Emma S. Sandell, Nora A. Escher, Shana J. Sturla

2021Chemical Research in Toxicology13 citationsDOIOpen Access PDF

Abstract

-MedG in a human cell line exposed to l-azaserine and found maximal adduct levels after 48 h. The findings of this work elucidate the chemical basis of how l-azaserine reacts with deoxyguanosine and support its use as a chemical probe for N-nitroso compound exposure in carcinogenesis research, particularly concerning the identification of pathways and factors that promote adduct formation.

Topics & Concepts

AzaserineDeoxyguanosineAdductChemistryDNA adductGuanosineBiochemistryStereochemistryOrganic chemistryAmino acidGlutamineDNA Repair MechanismsAmino Acid Enzymes and MetabolismFolate and B Vitamins Research