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Characterization of Nucleoside and DNA Adducts Formed by S-(1-Acetoxymethyl)glutathione and Implications for Dihalomethane−Glutathione Conjugates

Autor: M K Hartman, F. P. Guengerich, R G Mundkowski, B J Morris, Glenn A. Marsch, M L Manier

Publikováno v: Chemical Research in Toxicology. 14:600-608

S-(1-Acetoxymethyl)glutathione (GSCH(2)OAc) was synthesized and used as a model for the reaction of glutathione (GSH)-dihaloalkane conjugates with nucleosides and DNA. Previously, S-[1-(N(2)-deoxyguanosinyl)methyl]GSH had been identified as the major

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6c33b766e676b14f1304ea014ab60d
https://doi.org/10.1021/tx010006h

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A derivatization and validation strategy for determining the spatial localization of endogenous amine metabolites in tissues using MALDI imaging mass spectrometry

Autor: M. L. Manier, J. M. Spraggins, M. L. Reyzer, J. L. Norris, R. M. Caprioli

Publikováno v: Journal of Mass Spectrometry. 49:ii-ii

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::97b15ba156cf1a3787fd65da671ba16f
https://doi.org/10.1002/jms.3273

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