<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14</volume><submitter>Yang R</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Xiao-Er-An-Shen decoction (XEASD), a TCM formula composed of sixteen Chinese medicinal herbs, has been used to alleviate tic disorders (TD) in clinical practice for many years. However, the chemical basis underlying the therapeutic effects of XEASD in the treatment of TD remains unknown. &lt;b>Purpose:&lt;/b> The present study aimed to determine the major chemical components of XEASD and its prototype compounds and metabolites in mice biological samples. &lt;b>Methods:&lt;/b> The chemical constituents in XEASD were identified using ultra-high Performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS/MS). Following this, XEASD was orally administered to mice, and samples of plasma, urine, feces, bile, and tissue were collected in</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>1219866</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10652787</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chemical characterization and metabolic profiling of Xiao-Er-An-Shen Decoction by UPLC-QTOF/MS.</pubmed_title><pmcid>PMC10652787</pmcid><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Mo P</pubmed_authors><pubmed_authors>Yang R</pubmed_authors><pubmed_authors>Zheng P</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Wei L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemical characterization and metabolic profiling of Xiao-Er-An-Shen Decoction by UPLC-QTOF/MS.</name><description>&lt;b>Background:&lt;/b> Xiao-Er-An-Shen decoction (XEASD), a TCM formula composed of sixteen Chinese medicinal herbs, has been used to alleviate tic disorders (TD) in clinical practice for many years. However, the chemical basis underlying the therapeutic effects of XEASD in the treatment of TD remains unknown. &lt;b>Purpose:&lt;/b> The present study aimed to determine the major chemical components of XEASD and its prototype compounds and metabolites in mice biological samples. &lt;b>Methods:&lt;/b> The chemical constituents in XEASD were identified using ultra-high Performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS/MS). Following this, XEASD was orally administered to mice, and samples of plasma, urine, feces, bile, and tissue were collected in</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T13:15:45.707Z</modification><creation>2025-04-04T13:15:45.707Z</creation></dates><accession>S-EPMC10652787</accession><cross_references><pubmed>38027020</pubmed><doi>10.3389/fphar.2023.1219866</doi></cross_references></HashMap>