Guengerich et al., 1999 - Google Patents
Formation and reactions of N 7-aminoguanosine and derivativesGuengerich 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 …
- 238000006243 chemical reaction 0 title abstract description 118
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic 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
- C07D239/28—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-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 |