[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Guengerich et al., 1999 - Google Patents

Formation and reactions of N 7-aminoguanosine and derivatives

Guengerich et al., 1999

View PDF
Document ID
13828402338437593711
Author
Guengerich F
Mundkowski R
Voehler M
Kadlubar F
Publication year
Publication venue
Chemical research in toxicology

External Links

Snippet

Arylamines are mutagens and carcinogens and are thought to initiate tumors by forming adducts with DNA. The major adducts are C 8-guanyl, and we have previously suggested a role for guanyl-N 7 intermediates in the formation process. N 7-Aminoguanosine (Guo) was …
Continue reading at www.academia.edu (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Similar Documents

Publication Publication Date Title
Luo et al. Characterization of hydantoin products from one-electron oxidation of 8-oxo-7, 8-dihydroguanosine in a nucleoside model
Kennedy et al. Reactions of ester derivatives of carcinogenic N-(4-biphenylyl) hydroxylamine and the corresponding hydroxamic acid with purine nucleosides
Blount et al. Conformational constraint as a means for understanding RNA-aminoglycoside specificity
Kamiński et al. A study on the activation of carboxylic acids by means of 2-chloro-4, 6-dimethoxy-1, 3, 5-triazine and 2-chloro-4, 6-diphenoxy-1, 3, 5-triazine
Nechev et al. Synthesis of nucleosides and oligonucleotides containing adducts of acrolein and vinyl chloride
Guengerich et al. Formation and reactions of N 7-aminoguanosine and derivatives
Catalano et al. Chemical structure and properties of interstrand cross-links formed by reaction of guanine residues with abasic sites in duplex DNA
Samson-Thibault et al. Profiling cytosine oxidation in DNA by LC-MS/MS
Enya et al. An unusual DNA adduct derived from the powerfully mutagenic environmental contaminant 3-nitrobenzanthrone
Bálint et al. Structure‐Based Design and Synthesis of Harmine Derivatives with Different Selectivity Profiles in Kinase versus Monoamine Oxidase Inhibition
Lim et al. Overcoming the genotoxicity of a pyrrolidine substituted arylindenopyrimidine as a potent dual adenosine A2A/A1 antagonist by minimizing bioactivation to an iminium ion reactive intermediate
Knörlein et al. Nucleotide-amino acid π-stacking interactions initiate photo cross-linking in RNA-protein complexes
Müller et al. Analysis of 1, N 2-ethenoguanine and 5, 6, 7, 9-tetrahydro-7-hydroxy-9-oxoimidazo [1, 2-a] purine in DNA treated with 2-chlorooxirane by high performance liquid chromatography/electrospray mass spectrometry and comparison of amounts to other DNA adducts
Kawasaki et al. Hybridization-promoted and cytidine-selective activation for cross-linking with the use of 2-amino-6-vinylpurine derivatives
Martı́nez-Montero et al. Design and divergent synthesis of aza nucleosides from a chiral imino sugar
Harburn et al. Efficient synthesis of tyrosine-derived marine sponge metabolites via acylation of amines with a coumarin
Shafirovich et al. Photochemically catalyzed generation of site-specific 8-nitroguanine adducts in DNA by the reaction of long-lived neutral guanine radicals with nitrogen dioxide
Munter et al. Identification of adducts derived from reactions of (1-chloroethenyl) oxirane with nucleosides and calf thymus DNA
Olsen et al. Reaction of Glyoxal with 2 ‘-Deoxyguanosine, 2 ‘-Deoxyadenosine, 2 ‘-Deoxycytidine, Cytidine, Thymidine, and Calf Thymus DNA: Identification of DNA Adducts
Lim et al. In situ analysis of 8-oxo-7, 8-dihydro-2′-deoxyguanosine oxidation reveals sequence-and agent-specific damage spectra
Cui et al. Identification of adducts formed by reaction of N-acetoxy-3, 5-dimethylaniline with DNA
Liu et al. The acidity and proton affinity of the damaged base 1, n 6-ethenoadenine in the gas phase versus in solution: Intrinsic reactivity and biological implications
Wang et al. Reactions of α-acetoxy-N-nitrosopyrrolidine with deoxyguanosine and DNA
Gonçalves et al. Synthesis, Characterization, and Comparative 32P-Postlabeling Efficiencies of 2, 6-Dimethylaniline− DNA Adducts
Chworos et al. Characterization of the dehydro-guanidinohydantoin oxidation product of guanine in a dinucleotide