Novel tandem hydrogen migrations across five chemical bonds for 1,4-dihydropyridine using electrospray ionization FT-ICR mass spectrometry

被引:3
作者
Lin, Zhiwei [1 ]
Shi, Jinwen [2 ]
Gao, Xiang [2 ]
Zhao, Yufen [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Sch Pharmaceut Sci, Xiamen 361102, Peoples R China
基金
中国国家自然科学基金;
关键词
Tandem hydrogen migrations; 1,4-Dihydropyridine; Deuteriuth labeling; Fragmentation; ESI-FT-ICR MS; PERFORMANCE LIQUID-CHROMATOGRAPHY; HUMAN PLASMA; CALCIUM-CHANNEL; ADENINE-DINUCLEOTIDE; FRAGMENTATION; ANTAGONIST; NIMODIPINE; QUANTIFICATION; CHEMISTRY; ANALOGS;
D O I
10.1016/j.ijms.2016.05.024
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR MS) was applied to investigate the characteristic fragmentation patterns of 1, 4-dihydropyridines using collision-induced dissociation (CID) method in positive ion mode. The intra-molecular tandem hydrogen atom migrations were observed with gas phase Na+/H+ exchange by crossing five chemical bonds for 1,4-dihydropyridines. The possible rearrangement mechanisms were proposed for the first time, and the key structure of product ions were confirmed by high resolution tandem mass spectrometry and in solution hydrogen/deuterium labeling. The novel tandem hydrogen migration could be considered as a general fragmentation pattern for 1,4-dihydropyridine drugs because of their intrinsic chemical structures. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 34
页数:6
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