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Journal Abstract Search

161 related items for PubMed ID: 14680375

  • 1. Identification and characterization of a series of nucleoside adducts formed by the reaction of 2'-deoxyguanosine and 1,2,3,4-diepoxybutane under physiological conditions.
    Zhang XY, Elfarra AA.
    Chem Res Toxicol; 2003 Dec; 16(12):1606-15. PubMed ID: 14680375
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  • 2. Characterization of the reaction products of 2'-deoxyguanosine and 1,2,3,4-diepoxybutane after acid hydrolysis: formation of novel guanine and pyrimidine adducts.
    Zhang XY, Elfarra AA.
    Chem Res Toxicol; 2004 Apr; 17(4):521-8. PubMed ID: 15089094
    [Abstract] [Full Text] [Related]

  • 3. Reaction of 1,2,3,4-diepoxybutane with 2'-deoxyguanosine: initial products and their stabilities and decomposition patterns under physiological conditions.
    Zhang XY, Elfarra AA.
    Chem Res Toxicol; 2005 Aug; 18(8):1316-23. PubMed ID: 16097805
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  • 4. Characterization of 1,2,3,4-diepoxybutane-2'-deoxyguanosine cross-linking products formed at physiological and nonphysiological conditions.
    Zhang XY, Elfarra AA.
    Chem Res Toxicol; 2006 Apr; 19(4):547-55. PubMed ID: 16608166
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  • 5. Structural characterization of adducts formed in the reaction of 2,3-epoxy-4-hydroxynonanal with deoxyguanosine.
    Sodum RS, Chung FL.
    Chem Res Toxicol; 1989 Apr; 2(1):23-8. PubMed ID: 2519227
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  • 6. Kinetics and mechanism of the general-acid-catalyzed ring-closure of the malondialdehyde-DNA adduct, N2-(3-oxo-1-propenyl)deoxyguanosine (N2OPdG-), to 3-(2'-Deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-alpha]purin- 10(3H)-one (M1dG).
    Riggins JN, Pratt DA, Voehler M, Daniels JS, Marnett LJ.
    J Am Chem Soc; 2004 Sep 01; 126(34):10571-81. PubMed ID: 15327313
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  • 7. N6-(2-Deoxy-d- erythro-pentofuranosyl)-2,6-diamino-3,4-dihydro-4-oxo-5- N-(2-hydroxy-3-buten-1-yl)-formamidopyrimidine Adducts of 1,3-Butadiene: Synthesis, Structural Identification, and Detection in Human Cells.
    Groehler AS, Najjar D, Pujari SS, Sangaraju D, Tretyakova NY.
    Chem Res Toxicol; 2018 Sep 17; 31(9):885-897. PubMed ID: 30016111
    [Abstract] [Full Text] [Related]

  • 8. Synthesis, characterization, and in vitro quantitation of N-7-guanine adducts of diepoxybutane.
    Tretyakova NYu, Sangaiah R, Yen TY, Swenberg JA.
    Chem Res Toxicol; 1997 Jul 17; 10(7):779-85. PubMed ID: 9250412
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  • 14. Formation of adducts in the reaction of glyoxal with 2'-deoxyguanosine and with calf thymus DNA.
    Pluskota-Karwatka D, Pawłowicz AJ, Tomas M, Kronberg L.
    Bioorg Chem; 2008 Apr 17; 36(2):57-64. PubMed ID: 18078668
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  • 15. A novel DNA adduct, originating from 1,2-epoxy-3,4-butanediol, is the major DNA adduct after exposure to [2,3-(14)C]-1,3-butadiene,[4-(14)C]-1,2-epoxy-3-butane.
    Boogaard PJ, van Sittert NJ, Watson WP, de Kloe KP.
    Chem Biol Interact; 2001 Jun 01; 135-136():687-93. PubMed ID: 11397423
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  • 17. Mechanisms of formation of adducts from reactions of glycidaldehyde with 2'-deoxyguanosine and/or guanosine.
    Golding BT, Slaich PK, Kennedy G, Bleasdale C, Watson WP.
    Chem Res Toxicol; 1996 Jun 01; 9(1):147-57. PubMed ID: 8924584
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  • 19. trans,trans-2,4-decadienal-induced 1,N(2)-etheno-2'-deoxyguanosine adduct formation.
    Loureiro AP, Di Mascio P, Gomes OF, Medeiros MH.
    Chem Res Toxicol; 2000 Jul 01; 13(7):601-9. PubMed ID: 10898592
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