Fast-atom bombardment mass spectrometry of brassinosteroid analogs
Positive ion fast-atom bombardment mass spectra of brassinosteroid analogs have been systematically obtained for the first time. The spectra of six brassinosteroid analogs and their corresponding 22S,23S isomers included the protonated molecule in medium to high relative intensity. The fragmentation...
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Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_10440305_v8_n3_p270_Caballero |
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todo:paper_10440305_v8_n3_p270_Caballero2023-10-03T15:58:17Z Fast-atom bombardment mass spectrometry of brassinosteroid analogs Caballero, G.M. Gros, E.G. Centurión, O.T. Galagovsky, L.R. brassinosteroid steroid unclassified drug article fast atom bombardment mass spectrometry isomerism plant growth reaction analysis stereochemistry steroid analysis steroid metabolism Positive ion fast-atom bombardment mass spectra of brassinosteroid analogs have been systematically obtained for the first time. The spectra of six brassinosteroid analogs and their corresponding 22S,23S isomers included the protonated molecule in medium to high relative intensity. The fragmentation pattern is dominated by side chain cleavage. There is a marked preferential loss of acetic acid from the [M + H]+ ion of 5α-hydrogen-3β- acetylated derivatives compared to the 5α-hydroxy-3β-acetylated analogs. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10440305_v8_n3_p270_Caballero |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
brassinosteroid steroid unclassified drug article fast atom bombardment mass spectrometry isomerism plant growth reaction analysis stereochemistry steroid analysis steroid metabolism |
spellingShingle |
brassinosteroid steroid unclassified drug article fast atom bombardment mass spectrometry isomerism plant growth reaction analysis stereochemistry steroid analysis steroid metabolism Caballero, G.M. Gros, E.G. Centurión, O.T. Galagovsky, L.R. Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
topic_facet |
brassinosteroid steroid unclassified drug article fast atom bombardment mass spectrometry isomerism plant growth reaction analysis stereochemistry steroid analysis steroid metabolism |
description |
Positive ion fast-atom bombardment mass spectra of brassinosteroid analogs have been systematically obtained for the first time. The spectra of six brassinosteroid analogs and their corresponding 22S,23S isomers included the protonated molecule in medium to high relative intensity. The fragmentation pattern is dominated by side chain cleavage. There is a marked preferential loss of acetic acid from the [M + H]+ ion of 5α-hydrogen-3β- acetylated derivatives compared to the 5α-hydroxy-3β-acetylated analogs. |
format |
JOUR |
author |
Caballero, G.M. Gros, E.G. Centurión, O.T. Galagovsky, L.R. |
author_facet |
Caballero, G.M. Gros, E.G. Centurión, O.T. Galagovsky, L.R. |
author_sort |
Caballero, G.M. |
title |
Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
title_short |
Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
title_full |
Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
title_fullStr |
Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
title_full_unstemmed |
Fast-atom bombardment mass spectrometry of brassinosteroid analogs |
title_sort |
fast-atom bombardment mass spectrometry of brassinosteroid analogs |
url |
http://hdl.handle.net/20.500.12110/paper_10440305_v8_n3_p270_Caballero |
work_keys_str_mv |
AT caballerogm fastatombombardmentmassspectrometryofbrassinosteroidanalogs AT groseg fastatombombardmentmassspectrometryofbrassinosteroidanalogs AT centurionot fastatombombardmentmassspectrometryofbrassinosteroidanalogs AT galagovskylr fastatombombardmentmassspectrometryofbrassinosteroidanalogs |
_version_ |
1782029133888356352 |