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162 related items for PubMed ID: 3278814

  • 1. Bacterial cysteine conjugate beta-lyase and the metabolism of cysteine S-conjugates: structural requirements for the cleavage of S-conjugates and the formation of reactive intermediates.
    Vamvakas S, Berthold K, Dekant W, Henschler D.
    Chem Biol Interact; 1988; 65(1):59-71. PubMed ID: 3278814
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  • 5. Enzymatic transformation of mercapturic acids derived from halogenated alkenes to reactive and mutagenic intermediates.
    Vamvakas S, Dekant W, Berthold K, Schmidt S, Wild D, Henschler D.
    Biochem Pharmacol; 1987 Sep 01; 36(17):2741-8. PubMed ID: 3307787
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  • 6. Cysteine conjugate beta-lyase-catalyzed bioactivation of bromine-containing cysteine S-conjugates: stoichiometry and formation of 2,2-difluoro-3-halothiiranes.
    Finkelstein MB, Dekant W, Anders MW.
    Chem Res Toxicol; 1996 Sep 01; 9(1):227-31. PubMed ID: 8924595
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  • 8. Bioactivation of cysteine conjugates of 1-nitropyrene oxides by cysteine conjugate beta-lyase purified from Peptostreptococcus magnus.
    Kataoka K, Kinouchi T, Akimoto S, Ohnishi Y.
    Appl Environ Microbiol; 1995 Nov 01; 61(11):3781-7. PubMed ID: 8526486
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  • 9. Mutagenicity of the cysteine S-conjugate sulfoxides of trichloroethylene and tetrachloroethylene in the Ames test.
    Irving RM, Elfarra AA.
    Toxicology; 2013 Apr 05; 306():157-61. PubMed ID: 23416178
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  • 11. Roles of cysteine conjugate beta-lyase and S-oxidase in nephrotoxicity: studies with S-(1,2-dichlorovinyl)-L-cysteine and S-(1,2-dichlorovinyl)-L-cysteine sulfoxide.
    Lash LH, Sausen PJ, Duescher RJ, Cooley AJ, Elfarra AA.
    J Pharmacol Exp Ther; 1994 Apr 05; 269(1):374-83. PubMed ID: 8169843
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  • 12. Cysteine conjugate beta-lyase-dependent biotransformation of the cysteine S-conjugates of the sevoflurane degradation product compound A in human, nonhuman primate, and rat kidney cytosol and mitochondria.
    Iyer RA, Anders MW.
    Anesthesiology; 1996 Dec 05; 85(6):1454-61. PubMed ID: 8968194
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  • 13. Cysteine conjugate beta-lyase-dependent biotransformation of the cysteine S-conjugates of the sevoflurane degradation product 2-(fluoromethoxy)-1,1,3,3,3-pentafluoro-1-propene (compound A).
    Iyer RA, Anders MW.
    Chem Res Toxicol; 1997 Jul 05; 10(7):811-9. PubMed ID: 9250416
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  • 14. Bioactivation of S-(2,2-dihalo-1,1-difluoroethyl)-L-cysteines and S-(trihalovinyl)-L-cysteines by cysteine S-conjugate beta-lyase: indications for formation of both thionoacylating species and thiiranes as reactive intermediates.
    Commandeur JN, King LJ, Koymans L, Vermeulen NP.
    Chem Res Toxicol; 1996 Jul 05; 9(7):1092-102. PubMed ID: 8902263
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  • 15. Quantitation of multiple pathways for the metabolism of nephrotoxic cysteine conjugates using selective inhibitors of L-alpha-hydroxy acid oxidase (L-amino acid oxidase) and cysteine conjugate beta-lyase.
    Stevens JL, Hatzinger PB, Hayden PJ.
    Drug Metab Dispos; 1989 Jul 05; 17(3):297-303. PubMed ID: 2568912
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  • 16. Structure-mutagenicity and structure-cytotoxicity studies on bromine-containing cysteine S-conjugates and related compounds.
    Finkelstein MB, Vamvakas S, Bittner D, Anders MW.
    Chem Res Toxicol; 1994 Jul 05; 7(2):157-63. PubMed ID: 8199303
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  • 18. Assessment of unscheduled DNA synthesis in a cultured line of renal epithelial cells exposed to cysteine S-conjugates of haloalkenes and haloalkanes.
    Vamvakas S, Dekant W, Henschler D.
    Mutat Res; 1989 Apr 05; 222(4):329-35. PubMed ID: 2704384
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  • 19. Renal cysteine conjugate beta-lyase. Bioactivation of nephrotoxic cysteine S-conjugates in mitochondrial outer membrane.
    Lash LH, Elfarra AA, Anders MW.
    J Biol Chem; 1986 May 05; 261(13):5930-5. PubMed ID: 3700378
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  • 20. Thioacylating agents as ultimate intermediates in the beta-lyase catalysed metabolism of S-(pentachloro-butadienyl)-L-cysteine.
    Dekant W, Berthold K, Vamvakas S, Henschler D.
    Chem Biol Interact; 1988 May 05; 67(1-2):139-48. PubMed ID: 3168080
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