<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(21)</volume><submitter>Zhang X</submitter><pubmed_abstract>Liquiritin (LQ), the main bioactive constituent of licorice, is a common flavoring and sweetening agent in food products and has a wide range of pharmacological properties, including antidepressant-like, neuroprotective, anti-cancer and anti-inflammatory properties. This study investigated the metabolic pathways of LQ &lt;i>in vitro&lt;/i> (rat liver microsomes) and &lt;i>in vivo&lt;/i> (rat model) using ultra high-performance liquid chromatography coupled with hybrid triple quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS/MS). Moreover, supplementary tools such as key product ions (KPIs) were employed to search for and identify compounds. As a result, 56 &lt;i>in vivo&lt;/i> metabolites and 15 &lt;i>in vitro&lt;/i> metabolites were structurally characterized. Oxidation, reduction, hydrolysis, methylat</pubmed_abstract><journal>RSC advances</journal><pagination>11813-11827</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9079117</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of metabolites of liquiritin in rats by UHPLC-Q-TOF-MS/MS: metabolic profiling and pathway comparison &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i>.</pubmed_title><pmcid>PMC9079117</pmcid><pubmed_authors>Liang C</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Yin J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of metabolites of liquiritin in rats by UHPLC-Q-TOF-MS/MS: metabolic profiling and pathway comparison &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i>.</name><description>Liquiritin (LQ), the main bioactive constituent of licorice, is a common flavoring and sweetening agent in food products and has a wide range of pharmacological properties, including antidepressant-like, neuroprotective, anti-cancer and anti-inflammatory properties. This study investigated the metabolic pathways of LQ &lt;i>in vitro&lt;/i> (rat liver microsomes) and &lt;i>in vivo&lt;/i> (rat model) using ultra high-performance liquid chromatography coupled with hybrid triple quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS/MS). Moreover, supplementary tools such as key product ions (KPIs) were employed to search for and identify compounds. As a result, 56 &lt;i>in vivo&lt;/i> metabolites and 15 &lt;i>in vitro&lt;/i> metabolites were structurally characterized. Oxidation, reduction, hydrolysis, methylat</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-04T21:32:27.015Z</modification><creation>2025-04-04T21:32:27.015Z</creation></dates><accession>S-EPMC9079117</accession><cross_references><pubmed>35542822</pubmed><doi>10.1039/c7ra13760e</doi></cross_references></HashMap>