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Multimatrix Variation Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen Atoms in Alkaloids
[Image: see text] The reactivity of alkaloids in dehydrogenation was investigated using multimatrix variation matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) of over 20 different alkaloids with six matrices. The dehydrogenated molecular ions [M – H](+) generated by in-source...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732872/ https://www.ncbi.nlm.nih.gov/pubmed/36379021 http://dx.doi.org/10.1021/jasms.2c00221 |
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author | Yamagaki, Tohru Osawa, Tsukiho Fujikawa, Kohki Watanabe, Takehiro Sugahara, Kohtaro |
author_facet | Yamagaki, Tohru Osawa, Tsukiho Fujikawa, Kohki Watanabe, Takehiro Sugahara, Kohtaro |
author_sort | Yamagaki, Tohru |
collection | PubMed |
description | [Image: see text] The reactivity of alkaloids in dehydrogenation was investigated using multimatrix variation matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) of over 20 different alkaloids with six matrices. The dehydrogenated molecular ions [M – H](+) generated by in-source decay were detected in the MALDI mass spectra of some types of alkaloids such as reserpine. The dehydrogenation proceeded at the cyclic tertiary amine rather than double-bonded nitrogen atoms and indole rings involved in the electron-delocalized systems. The stable protonated primary amines hindered dehydrogenation. The laser-induced dehydrogenation correlated with the chemical properties and structures of alkaloids. Alkaloids were classified into three types by the ratio of dehydrogenation by comparing the relative abundances of [M – H](+), [M](•+), and [M + H](+) ions in α-cyano-4-hydroxycinnamic acid and 5-formylsalicylic acid matrices. Structural isomers were also discriminated by this method of analyzing the three molecular ions’ ratio using multimatrix variation MALDI-MS. |
format | Online Article Text |
id | pubmed-9732872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97328722022-12-10 Multimatrix Variation Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen Atoms in Alkaloids Yamagaki, Tohru Osawa, Tsukiho Fujikawa, Kohki Watanabe, Takehiro Sugahara, Kohtaro J Am Soc Mass Spectrom [Image: see text] The reactivity of alkaloids in dehydrogenation was investigated using multimatrix variation matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) of over 20 different alkaloids with six matrices. The dehydrogenated molecular ions [M – H](+) generated by in-source decay were detected in the MALDI mass spectra of some types of alkaloids such as reserpine. The dehydrogenation proceeded at the cyclic tertiary amine rather than double-bonded nitrogen atoms and indole rings involved in the electron-delocalized systems. The stable protonated primary amines hindered dehydrogenation. The laser-induced dehydrogenation correlated with the chemical properties and structures of alkaloids. Alkaloids were classified into three types by the ratio of dehydrogenation by comparing the relative abundances of [M – H](+), [M](•+), and [M + H](+) ions in α-cyano-4-hydroxycinnamic acid and 5-formylsalicylic acid matrices. Structural isomers were also discriminated by this method of analyzing the three molecular ions’ ratio using multimatrix variation MALDI-MS. American Chemical Society 2022-11-15 2022-12-07 /pmc/articles/PMC9732872/ /pubmed/36379021 http://dx.doi.org/10.1021/jasms.2c00221 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Yamagaki, Tohru Osawa, Tsukiho Fujikawa, Kohki Watanabe, Takehiro Sugahara, Kohtaro Multimatrix Variation Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen Atoms in Alkaloids |
title | Multimatrix Variation
Matrix-Assisted Laser Desorption/Ionization
Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen
Atoms in Alkaloids |
title_full | Multimatrix Variation
Matrix-Assisted Laser Desorption/Ionization
Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen
Atoms in Alkaloids |
title_fullStr | Multimatrix Variation
Matrix-Assisted Laser Desorption/Ionization
Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen
Atoms in Alkaloids |
title_full_unstemmed | Multimatrix Variation
Matrix-Assisted Laser Desorption/Ionization
Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen
Atoms in Alkaloids |
title_short | Multimatrix Variation
Matrix-Assisted Laser Desorption/Ionization
Mass Spectrometry as a Tool for Determining the Bonding of Nitrogen
Atoms in Alkaloids |
title_sort | multimatrix variation
matrix-assisted laser desorption/ionization
mass spectrometry as a tool for determining the bonding of nitrogen
atoms in alkaloids |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732872/ https://www.ncbi.nlm.nih.gov/pubmed/36379021 http://dx.doi.org/10.1021/jasms.2c00221 |
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