Applications of tandem mass spectrometry to the characterization of derivatized glutathione conjugates. Studies with S-(N-methylcarbamoyl)glutathione, a metabolite of the antineoplastic agent N-methylformamide.
Applications of tandem mass spectrometry to the characterization of derivatized glutathione conjugates. Studies with S-(N-methylcarbamoyl)glutathione, a metabolite of the antineoplastic agent N-methylformamide.
复制标题
串联质谱法在衍生化谷胱甘肽缀合物表征中的应用。
DOI:
10.1002/bms.1200160110
复制
发表时间:
1988
期刊:
影响因子:
--
通讯作者:
Baillie,TA
中科院分区:
文献类型:
--
作者:
Pearson,PG;Threadgill,MD;Howald,WN;Baillie,TA
Daughter ion spectra are reported for [M + H]+ions generated by fast atom bombardment mass spectrometry ofS‐(N‐methylcarbamoyl)glutathione (1) and a series of alkoxycarbonyl methyl ester derivatives thereof. Structurally informative, even‐electron fragment ions, which serve to define the nature of both the xenobiotic and peptide components of the conjugate, are observed in the collisionally activated dissociation (CAD) spectra of 1 and its ethoxy‐ and benzyloxycarbonyl methyl esters. Studies with thet‐butyloxycarbonyl (tBOC) methyl ester derivative, on the other hand, indicated that thetBOC group exerts a powerful directing influence on the CAD process, and that the major daughter ions in this case are associated with cleavage of thetBOC functionality itself and are of little diagnostic value. Of the derivatives examined, the benzyloxycarbonyl congener, which may be generated readily from 1 in aqueous media, is judged to be the most useful from the standpoints of ease of formation, desirable high‐performance liquid chromatographic properties, and informative mass spectral fragmentation characteristics under CAD conditions.