<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(23)</volume><submitter>Đulovic A</submitter><pubmed_abstract>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.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>8431</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9736730</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Glucosinolates of Sisymbrium officinale and S. orientale.</pubmed_title><pmcid>PMC9736730</pmcid><pubmed_authors>Marijan S</pubmed_authors><pubmed_authors>Ruscic M</pubmed_authors><pubmed_authors>Đulovic A</pubmed_authors><pubmed_authors>Popovic M</pubmed_authors><pubmed_authors>Blazevic I</pubmed_authors><pubmed_authors>Burcul F</pubmed_authors><pubmed_authors>Cikes Culic V</pubmed_authors><pubmed_authors>Anđelkovic N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glucosinolates of Sisymbrium officinale and S. orientale.</name><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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-20T03:36:19.273Z</modification><creation>2025-04-20T03:36:19.273Z</creation></dates><accession>S-EPMC9736730</accession><cross_references><pubmed>36500524</pubmed><doi>10.3390/molecules27238431</doi></cross_references></HashMap>