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3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine and deoxyguanosine

3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine has been researched along with deoxyguanosine in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Andersson, R; Dragsted, LO; Frandsen, H; Grivas, S; Larsen, JC; Turesky, RJ1
Frandsen, H1
Brooks, M; Hott, LL; Moslener, M; Novak, M; Rajagopal, S; Toth, K1

Other Studies

3 other study(ies) available for 3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine and deoxyguanosine

ArticleYear
Formation of DNA adducts by the food mutagen 2-amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline (4,8-DiMeIQx) in vitro and in vivo. Identification of a N2-(2'-deoxyguanosin-8-yl)-4,8-DiMeIQx adduct.
    Carcinogenesis, 1994, Volume: 15, Issue:11

    Topics: Acetylation; Animals; Biotransformation; Carcinogens; Deoxyguanosine; DNA; DNA Adducts; Male; Mutagens; Quinoxalines; Rats; Rats, Wistar

1994
Excretion of DNA adducts of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline, PhIP-dG, PhIP-DNA and DiMeIQx-DNA from the rat.
    Carcinogenesis, 1997, Volume: 18, Issue:8

    Topics: Animals; Biomarkers; Carcinogens; Chromatography, High Pressure Liquid; Deoxyguanosine; DNA Adducts; Feces; Imidazoles; Male; Quinoxalines; Rats; Rats, Wistar; Time Factors

1997
Reactivity and selectivity of the N-acetyl-Glu-P-1, N-acetyl-Glu-P-2, N-acetyl-MeIQx, and N-acetyl-IQx nitrenium ions: comparison to carbocyclic N-arylnitrenium ions.
    Journal of the American Chemical Society, 2002, Jul-10, Volume: 124, Issue:27

    Topics: Acetylation; Carcinogens; Deoxyguanosine; Imidazoles; Kinetics; Quinolines; Quinoxalines

2002