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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Autores principales: Caballero, G.M., Gros, E.G., Centurión, O.T., Galagovsky, L.R.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_10440305_v8_n3_p270_Caballero
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spelling 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
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