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Glucosinolates of Sisymbrium officinale and S. orientale
Glucosinolates (GSLs) from Sysimbrium officinale and S. orientale were analyzed qualitatively and quantitatively by their desulfo-counterparts using UHPLC-DAD-MS/MS. Eight GSLs were identified in S. officinale, including Val-derived (glucoputranjivin) and Trp-derived (4-hydroxyglucobrassicin, glucob...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9736730/ https://www.ncbi.nlm.nih.gov/pubmed/36500524 http://dx.doi.org/10.3390/molecules27238431 |
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author | Đulović, Azra Popović, Marijana Burčul, Franko Čikeš Čulić, Vedrana Marijan, Sandra Ruščić, Mirko Anđelković, Nikolina Blažević, Ivica |
author_facet | Đulović, Azra Popović, Marijana Burčul, Franko Čikeš Čulić, Vedrana Marijan, Sandra Ruščić, Mirko Anđelković, Nikolina Blažević, Ivica |
author_sort | Đulović, Azra |
collection | PubMed |
description | Glucosinolates (GSLs) from Sysimbrium officinale and S. orientale were analyzed qualitatively and quantitatively by their desulfo-counterparts using UHPLC-DAD-MS/MS. Eight GSLs were identified in S. officinale, including Val-derived (glucoputranjivin) and Trp-derived (4-hydroxyglucobrassicin, glucobrassicin, 4-methoxyglucobrassicin, and neoglucobrassicin) as the major ones followed by Leu-derived (Isobutyl GSL), Ile-derived (glucocochlearin) and Phe/Tyr-derived (glucosinalbin). Different S. orientale plant parts contained six GSLs, with Met-derived (progoitrin, epiprogoitrin, and gluconapin) and homoPhe-derived (gluconasturtiin) as the major ones, followed by glucosinalbin and neoglucobrassicin. GSL breakdown products obtained by hydrodistillation (HD) and microwave-assisted distillation from S. officinale, as well as isopropyl isothiocyanate, as the major volatile in both isolates, were tested for their cytotoxic activity using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Generally, all volatile isolates showed similar activity toward the three cancer cell lines. The best activity was shown by isopropyl isothiocyanate at a concentration of 100 µg/mL after 72 h of incubation, with 53.18% for MDA-MB-231, 56.61% for A549, and 60.02% for the T24 cell line. |
format | Online Article Text |
id | pubmed-9736730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97367302022-12-11 Glucosinolates of Sisymbrium officinale and S. orientale Đulović, Azra Popović, Marijana Burčul, Franko Čikeš Čulić, Vedrana Marijan, Sandra Ruščić, Mirko Anđelković, Nikolina Blažević, Ivica Molecules Article Glucosinolates (GSLs) from Sysimbrium officinale and S. orientale were analyzed qualitatively and quantitatively by their desulfo-counterparts using UHPLC-DAD-MS/MS. Eight GSLs were identified in S. officinale, including Val-derived (glucoputranjivin) and Trp-derived (4-hydroxyglucobrassicin, glucobrassicin, 4-methoxyglucobrassicin, and neoglucobrassicin) as the major ones followed by Leu-derived (Isobutyl GSL), Ile-derived (glucocochlearin) and Phe/Tyr-derived (glucosinalbin). Different S. orientale plant parts contained six GSLs, with Met-derived (progoitrin, epiprogoitrin, and gluconapin) and homoPhe-derived (gluconasturtiin) as the major ones, followed by glucosinalbin and neoglucobrassicin. GSL breakdown products obtained by hydrodistillation (HD) and microwave-assisted distillation from S. officinale, as well as isopropyl isothiocyanate, as the major volatile in both isolates, were tested for their cytotoxic activity using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Generally, all volatile isolates showed similar activity toward the three cancer cell lines. The best activity was shown by isopropyl isothiocyanate at a concentration of 100 µg/mL after 72 h of incubation, with 53.18% for MDA-MB-231, 56.61% for A549, and 60.02% for the T24 cell line. MDPI 2022-12-02 /pmc/articles/PMC9736730/ /pubmed/36500524 http://dx.doi.org/10.3390/molecules27238431 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Đulović, Azra Popović, Marijana Burčul, Franko Čikeš Čulić, Vedrana Marijan, Sandra Ruščić, Mirko Anđelković, Nikolina Blažević, Ivica Glucosinolates of Sisymbrium officinale and S. orientale |
title | Glucosinolates of Sisymbrium officinale and S. orientale |
title_full | Glucosinolates of Sisymbrium officinale and S. orientale |
title_fullStr | Glucosinolates of Sisymbrium officinale and S. orientale |
title_full_unstemmed | Glucosinolates of Sisymbrium officinale and S. orientale |
title_short | Glucosinolates of Sisymbrium officinale and S. orientale |
title_sort | glucosinolates of sisymbrium officinale and s. orientale |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9736730/ https://www.ncbi.nlm.nih.gov/pubmed/36500524 http://dx.doi.org/10.3390/molecules27238431 |
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