首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Novel chiral derivatization reagents possessing a pyridylthiourea structure for enantiospecific determination of amines and carboxylic acids in high-throughput liquid chromatography and electrospray-ionization mass spectrometry for chiral metabolomics identification
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Novel chiral derivatization reagents possessing a pyridylthiourea structure for enantiospecific determination of amines and carboxylic acids in high-throughput liquid chromatography and electrospray-ionization mass spectrometry for chiral metabolomics identification

机译:具有吡啶硫基脲结构的新型手性衍生试剂,用于高通量液相色谱和电喷雾电离质谱中对映体特异性测定胺和羧酸,用于手性代谢组学鉴定

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This paper reports the synthesis and the application of novel derivatization reagents possessing a pyridylthiourea structure for the enantiospecific determination of chiral amines and carboxylic acids in high-throughput LC-ESI-MS/MS. The novel reagents, i.e., (R)-. N-(3-pyridylthiocarbamoyl)pyrrolidine-2-carboxylic acid (PyT-C) and (S)-3-amino-1-(3-pyridylthiocarbamoyl)pyrrolidine (PyT-N), were evaluated as chiral derivatization reagents for the enantiomeric determination of chiral amines and carboxylic acids, respectively, in terms of separation efficiency by reversed-phase chromatography and detection sensitivity by ESI-MS/MS. The chiral amines and carboxylic acids were easily labeled with PyT-C and PyT-N, respectively, at 60. °C in 60. min in the presence of 2,2'-dipyridyl disulfide (DPDS) and triphenylphosphine (TPP) as the activation reagents. The resulting diastereomers were completely separated by reversed-phase chromatography using a small particle (1.7. μm) ODS column (Rs. =. 3.54-6.00 for carboxylic acids and Rs. =. 3.07-4.75 for amines). A highly sensitive detection at the sub-fmol level was also obtained from the SRM chromatograms at a single monitoring ion, m/. z 137.0 (0.72-1.46. fmol for carboxylic acids and 0.55-1.89. fmol for amines). The proposed procedure using PyT-C and PyT-N was applied to the determination of chiral amines and carboxylic acids spiked into human saliva, as a model study of chiral metabonomics identification. dl-Amino acid methyl esters and N-acetyl dl-amino acids, which are the representatives as the chiral amines and carboxylic acids, in the saliva were clearly identified by the present method. Because the same product ion at m/. z 137.0 was obtained from collision-induced dissociation (CID) of protonated molecular ions of all the derivatives, the proposed procedure using both reagents (i.e., PyT-C and PyT-N) seems to be useful for chiral metabolomics identification having selected functional groups (i.e., amines and carboxylic acids).
机译:本文报道了具有吡啶基硫脲结构的新型衍生化试剂的合成和应用,用于高通量LC-ESI-MS / MS中手性胺和羧酸的对映体测定。新型试剂,即(R)-。 N-(3-吡啶基硫代氨基甲酰基)吡咯烷-2-羧酸(PyT-C)和(S)-3-氨基-1-(3-吡啶基硫代氨基甲酰基)吡咯烷(PyT-N)被评估为对映体的手性衍生试剂反相色谱分离效率和ESI-MS / MS的检测灵敏度分别测定了手性胺和羧酸。在2,2'-联吡啶二硫醚(DPDS)和三苯基膦(TPP)存在下,在60.分钟,60。°C下,分别用PyT-C和PyT-N容易地标记手性胺和羧酸。活化剂。使用小颗粒(1.7.μm)ODS色谱柱(对于羧酸,Rs。=。3.54-6.00,对于胺,Rs。=。3.07-4.75)通过反相色谱法完全分离得到的非对映异构体。还可以通过单监测离子m /的SRM色谱图获得亚fmol水平的高灵敏度检测结果。 z 137.0(对于羧酸为0.72-1.46fmol,对于胺为0.55-1.89.fmol)。拟议的使用PyT-C和PyT-N的方法被用于测定掺入人唾液中的手性胺和羧酸,作为手性代谢组学鉴定的模型研究。通过本方法清楚地鉴定了唾液中代表手性胺和羧酸的dl-氨基酸甲基酯和N-乙酰基dl-氨基酸。因为相同的产物离子为m /。 z 137.0是从所有衍生物的质子化分子离子的碰撞诱导解离(CID)中获得的,使用这两种试剂(即PyT-C和PyT-N)的拟议程序似乎对鉴定具有选定官能团的手性代谢组学很有用(即胺和羧酸)。

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