Solid-phase synthesis of oligonucleotides containing site-specific N-(2'-deoxyguanosin-8-yl)-2-(acetylamino)fluorene adducts using 9-fluorenylmethoxycarbonyl as the base-protecting group
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00213a038
Reference35 articles.
1. Strong sequence-dependent polymorphism in adduct-induced DNA structure: analysis of single N-2-acetylaminofluorene residues bound within the NarI mutation hot spot
2. DNA binding and mutation spectra of the carcinogen N-2-aminofluorene in Escherichia coli
3. The origin of human cancers
4. N-Hydroxylation: A New Metabolic Reaction Observed in the Rat with the Carcinogen 2-Acetylaminofluorene
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2. Conformational Preference and Fluorescence Response of a C-Linked C8-Biphenyl-Guanine Lesion in the NarI Mutational Hotspot: Evidence for Enhanced Syn Adduct Formation;Chemical Research in Toxicology;2017-12-14
3. Chemical Synthesis of Lesion-Containing Oligonucleotides for DNA Repair Studies;Modified Nucleic Acids in Biology and Medicine;2016
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5. Structural and biochemical impact of C8-aryl-guanine adducts within the NarI recognition DNA sequence: influence of aryl ring size on targeted and semi-targeted mutagenicity;Nucleic Acids Research;2014-10-31
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