8-(N-2-fluorenylacetamido)guanosine, an arylamidation reaction product of guanosine and the carcinogen N-acetoxy-N-2-fluorenylacetamide in neutral solution.
about
Carcinogens as frameshift mutagens: metabolites and derivatives of 2-acetylaminofluorene and other aromatic amine carcinogensSite-specific incorporation of N-(deoxyguanosin-8-yl)-2-acetylaminofluorene (dG-AAF) into oligonucleotides using modified 'ultra-mild' DNA synthesisLesion bypass in yeast cells: Pol eta participates in a multi-DNA polymerase process.Acylation of carcinogenic hydroxamic acids by carbamoyl phosphate to form reactive estersGenetic and epigenetic changes in rat preneoplastic liver tissue induced by 2-acetylaminofluoreneRequirement of Rad5 for DNA polymerase zeta-dependent translesion synthesis in Saccharomyces cerevisiaeCoding and conformational properties of oligonucleotides modified with the carcinogen N-2-acetylaminofluorene.Single adduct mutagenesis: strong effect of the position of a single acetylaminofluorene adduct within a mutation hot spot.UvrAB activity at a damaged DNA site: is unpaired DNA present?Purification and characterization of pol kappa, a DNA polymerase encoded by the human DINB1 gene.Recognition of chemically damaged DNA by the gene 32 protein from bacteriophage T4.Kinetics of DNA Repair in Ultraviolet-Irradiated and N-acetoxy-2-acetylaminofluorene-Treated Mammalian Cells.Circular dichroism of poly(dG-dC) modified by the carcinogens N-methyl-4-aminoazobenzene or 4-aminobiphenyl.Differences in removal of acetylaminofluorene and pyrimidine dimers from the DNA of cultured mammalian cellsSynthetic and oxidative studies on 8-(arylamino)-2'-deoxyguanosine and -guanosine derivatives.Activity of carcinogens that bind to the C8 position of guanine residues in an assay specific for the detection of -2 frameshift mutations in a defined hot spot.Some historical aspects of N-aryl carcinogens and their metabolic activationConformation of oligonucleotides and nucleic acids modified with 2-aminofluorene or 2-acetylaminofluorene.Studies on the conformation and dynamics of the C8-substituted guanine adduct of the carcinogen acetylaminofluorene; model for a possible Z-DNA modified structure.N-acetoxy-2-acetylaminofluorene modification of a deoxyoligonucleotide duplex.Infectivity and reconstitution of TMV RNA modified with N-acetoxy-2-acetylaminofluorene or benzol [a] pyrene 7,8-dihydrodiol 9,10 oxide.Termination of vitro DNA synthesis at AAF adducts in the DNAMutagenic replication in human cell extracts of DNA containing site-specific N-2-acetylaminofluorene adducts.Site-specific modification of the lactose operator with acetylaminofluoreneDifferent levels of induction of RecA protein in E. coli (PQ 10) after treatment with two related carcinogensEquilibrium binding of carcinogens and antitumor antibiotics to DNA: site selectivity, cooperativity, allosterism.Reactivity of antibodies to guanosine modified by the carcinogen N-acetoxy-N-2-acetylaminofluorene.Evidence for a new Z-type left-handed DNA helix: properties of Z(WC)-DNA.Effect of carcinogenic adducts on transcription by T7 RNA polymerase.Chemically modified nucleic acids as immunodetectable probes in hybridization experiments.Repair and mutagenesis of plasmid DNA modified by ultraviolet irradiation or N-acetoxy-N-2-acetylaminofluoreneAminofluorene-DNA adduct formation in Salmonella typhimurium exposed to the carcinogen N-hydroxy-2-acetylaminofluorene.Temporal distinction between repair and mutagenesis of benzopyrene adducts after SOS induction in Escherichia coli.DNA adduct-induced stabilization of slipped frameshift intermediates within repetitive sequences: implications for mutagenesis.Recognition of chemical carcinogen-modified DNA by a DNA-binding protein.DNA repair and mutagenesis in mammalian cells.Mechanism of aromatic amine carcinogen bypass by the Y-family polymerase, Dpo4.Carcinogen-induced frameshift mutagenesis in repetitive sequences.Carcinogenic adducts induce distinct DNA polymerase binding orientations.Cellular strategies for accommodating replication-hindering adducts in DNA: control by the SOS response in Escherichia coli.
P2860
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P2860
8-(N-2-fluorenylacetamido)guanosine, an arylamidation reaction product of guanosine and the carcinogen N-acetoxy-N-2-fluorenylacetamide in neutral solution.
description
1967 nî lūn-bûn
@nan
1967年の論文
@ja
1967年学术文章
@wuu
1967年学术文章
@zh-cn
1967年学术文章
@zh-hans
1967年学术文章
@zh-my
1967年学术文章
@zh-sg
1967年學術文章
@yue
1967年學術文章
@zh
1967年學術文章
@zh-hant
name
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@en
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@nl
type
label
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@en
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@nl
prefLabel
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@en
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@nl
P2093
P356
P1433
P1476
8-(N-2-fluorenylacetamido)guan ...... acetamide in neutral solution.
@en
P2093
P304
P356
10.1021/BI00853A029
P407
P577
1967-01-01T00:00:00Z