<HashMap><database>MetaboLights</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/m_MTBLS14174_LC-MS_positive_reverse-phase_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/m_MTBLS14174_LC-MS_negative_reverse-phase_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/a_MTBLS14174_LC-MS_positive_reverse-phase.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/s_MTBLS14174.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/a_MTBLS14174_LC-MS_negative_reverse-phase.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174/i_Investigation.txt</Txt></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><ftp_download_link>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14174</ftp_download_link><metabolite_identification_protocol>Metabolites were identified by matching accurate mass (&lt;20 ppm) and MS/MS spectra against HMDB, MassBank, and an in-house library.</metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - negative - reverse-phase</instrument_platform><instrument_platform>Liquid Chromatography MS - positive - reverse-phase</instrument_platform><chromatography_protocol>Chromatography was performed on a Shimadzu Nexera UHPLC system using an ACQUITY UPLC HSS T3 column (2.1 × 100 mm, 1.8 µm). Mobile phase: 0.1% formic acid in water (A) and acetonitrile (B). Gradient: 0-15 min, 0-100% B. Flow rate: 0.3 mL/min, column temperature: 40°C, injection volume: 6 µL.</chromatography_protocol><publication>Deciphering early weaning stress cross-talk between gut microbiota with host gene expression and metabolic adaptation insights from lambs.</publication><submitter_name>Tao Zhong</submitter_name><submitter_affiliation>Sichuan Agricultural University</submitter_affiliation><organism_part>serum</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>For metabolite extraction, 100 μL of serum sample was mixed with 300 μL of pre-chilled methanol/acetonitrile/water (2:2:1, v/v/v). The mixture was vortexed for 30 seconds, sonicated in an ice bath for 1 hour, then incubated at -20°C for 1 hour to precipitate proteins. After centrifugation at 16,000 × g for 20 minutes at 4°C, the supernatant was collected and dried in a vacuum concentrator. For LC-MS analysis, the dried extract was reconstituted in 100 μL of methanol/water (1:1, v/v), centrifuged at 20,000 × g for 20 minutes at 4°C, and the supernatant was used for analysis. A pooled quality control (QC) sample was prepared by mixing equal volumes of all samples and was used to monitor system stability throughout the analysis.</extraction_protocol><organism>Ovis aries</organism><data_transformation_protocol>Raw data were processed using MS-DIAL for peak alignment and feature extraction. Features with >50% missing values were removed. Total peak area normalization was applied, and data were UV-scaled using R software.</data_transformation_protocol><study_factor>Weaning status</study_factor><study_factor>Weaning protocol</study_factor><submitter_email>zhongtao@sicau.edu.cn</submitter_email><metabolights_link>https://www.ebi.ac.uk/metabolights/MTBLS14174</metabolights_link><sample_collection_protocol>Serum samples were collected from Hu sheep at 30 days of age before and after weaning. Blood samples were collected from the jugular vein into vacuum tubes without anticoagulant, allowed to clot at room temperature for 30 minutes, and then centrifuged at 3,000 × g for 10 minutes. The serum was separated and immediately frozen in liquid nitrogen, then stored at -80°C until analysis.</sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Metabolomics</study_design><study_design>Ovis aries</study_design><study_design>Biological specimen</study_design><study_design>Weaning</study_design><study_design>untargeted analysis</study_design><study_design>Serum</study_design><study_design>Shimadzu Nexera UHPLC system</study_design><study_design>Thermo Scientific Q Exactive Plus</study_design><study_design>untargeted metabolite profiling</study_design><curator_keywords>Metabolomics</curator_keywords><curator_keywords>Ovis aries</curator_keywords><curator_keywords>Biological specimen</curator_keywords><curator_keywords>Weaning</curator_keywords><curator_keywords>untargeted analysis</curator_keywords><curator_keywords>Serum</curator_keywords><curator_keywords>Shimadzu Nexera UHPLC system</curator_keywords><curator_keywords>Thermo Scientific Q Exactive Plus</curator_keywords><curator_keywords>untargeted metabolite profiling</curator_keywords><mass_spectrometry_protocol>Mass spectrometry was performed on a Thermo Scientific Q Exactive Plus with HESI source. Scan range: 70-1050 m/z, resolution: 70,000. Data were acquired in positive and negative ion modes. MS/MS was triggered for the top 10 precursors with NCE of 20, 30, and 40 eV.</mass_spectrometry_protocol><metabolite_name>Taurine</metabolite_name><metabolite_name>Aminohippuric acid</metabolite_name><metabolite_name>Ascorbic acid</metabolite_name><metabolite_name>D-Leucine</metabolite_name><metabolite_name>Phenylacetylglutamine</metabolite_name><metabolite_name>2H-Pyrido[1,2-a][1,4,7,10]tetraazacyclododecine-1,4,7,10(3H,12H)-tetrone, 3-(7,8-dihydroxy-6-oxooctyl)octahydro-9-(1-methylpropyl)-6-(phenylmethyl)-</metabolite_name><metabolite_name>Cholic acid</metabolite_name><metabolite_name>PC(16:0/18:2)</metabolite_name><metabolite_name>6-Benzyl-3-butan-2-yl-9-(7-hydroxy-6-oxooctyl)-1,4,7,10-tetrazabicyclo[10.4.0]hexadecane-2,5,8,11-tetrone</metabolite_name><metabolite_name>Histidine</metabolite_name><metabolite_name>Succinoadenosine</metabolite_name><metabolite_name>PC(16:0/16:0)</metabolite_name><metabolite_name>N-Caproylglycine</metabolite_name><metabolite_name>Tropic acid</metabolite_name><metabolite_name>LPC(15:0)</metabolite_name><metabolite_name>Kajiichigoside F1</metabolite_name><metabolite_name>3-Methylhistidine</metabolite_name><metabolite_name>Phosphoric acid</metabolite_name><metabolite_name>Threonine</metabolite_name><metabolite_name>6-Hydroxy-2,6,10,10-tetramethyl-1-oxaspiro[4.5]dec-8-yl 6-O-[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)tetrahydro-2-furanyl]-beta-D-glucopyranoside</metabolite_name><metabolite_name>(2E,6E,12E)-19-(2-Amino-2-oxoethyl)-9,11-dihydroxy-8-methoxy-10,12,14-trimethyl-15-oxohenicosa-2,6,12-trienedioic acid</metabolite_name><metabolite_name>[9-[(E)-3-acetyloxy-4-methylhex-4-en-2-yl]-12-hydroxy-3-(2-hydroxypropan-2-yl)-10-methoxy-6a,12b-dimethyl-8,11-dioxo-1,2,3,4a,5,6,12,12a-octahydropyrano[3,2-a]xanthen-1-yl] acetate</metabolite_name><metabolite_name>4-Hydroxyhippuric acid</metabolite_name><metabolite_name>16,17-Dihydroxykauran-18-oic acid</metabolite_name><metabolite_name>4-Hydroxybenzoic acid</metabolite_name><metabolite_name>Bonactin</metabolite_name><metabolite_name>Avocadyne 1-acetate</metabolite_name><metabolite_name>Citrulline</metabolite_name><metabolite_name>Corylifol A</metabolite_name><metabolite_name>Propionylcarnitine</metabolite_name><metabolite_name>1,10-Epoxygermacrone</metabolite_name><metabolite_name>Sebacic acid</metabolite_name><metabolite_name>Phenol</metabolite_name><metabolite_name>Salicin</metabolite_name><metabolite_name>Carnequinazoline A</metabolite_name><metabolite_name>Acetaminophen</metabolite_name><metabolite_name>Sphinganine 1-phosphate</metabolite_name><metabolite_name>3',4'-Dimethoxyflavonol</metabolite_name><metabolite_name>6,8-Dihydroxy-2-methylmercaptopurine</metabolite_name><metabolite_name>cyclo[DL-Nle(Unk)-D-Phe-xiIle-Pip]</metabolite_name><metabolite_name>LPG(17:0)</metabolite_name><metabolite_name>Ergothioneine</metabolite_name><metabolite_name>2-[5,7-dihydroxy-3-oxo-6-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-1H-isoindol-2-yl]pentanedioic acid</metabolite_name><metabolite_name>Glutamic acid</metabolite_name><metabolite_name>Suberic acid</metabolite_name><metabolite_name>[1-(7-Hydroxy-2,4b,8,8-Tetramethyl-4,4a,5,6,7,8a,9,10-Octahydro-3H-Phenanthren-2-Yl)-2-[3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl]Oxyethyl] Acetate</metabolite_name><metabolite_name>LPE(18:0)</metabolite_name><metabolite_name>Lincomycin</metabolite_name><metabolite_name>Arginine</metabolite_name><metabolite_name>Kynurenine</metabolite_name><metabolite_name>Taurohyocholate</metabolite_name><metabolite_name>Chenodeoxycholylaspartic acid</metabolite_name><metabolite_name>LPC(17:0)</metabolite_name><metabolite_name>N-Methylglutamic acid</metabolite_name><metabolite_name>Glucosamine 6-phosphate</metabolite_name><metabolite_name>Creatinine</metabolite_name><metabolite_name>N-Acetylglutamic acid</metabolite_name><metabolite_name>Taurolithocholic acid</metabolite_name><metabolite_name>Phenylalanine</metabolite_name><metabolite_name>Dodecanedioic acid</metabolite_name><metabolite_name>Tryptophan</metabolite_name><metabolite_name>Phenylacetylglycine</metabolite_name><metabolite_name>5-Hydroxylysine</metabolite_name><metabolite_name>(2E)-3-{3-[(2-cyclohexylphenoxy)methyl]-4-methoxyphenyl}-1-(4-hydroxyphenyl)pr op-2-en-1-one</metabolite_name><metabolite_name>Pyridoxine</metabolite_name><metabolite_name>N-Acetylisoleucine</metabolite_name><metabolite_name>Pseudouridine</metabolite_name><metabolite_name>Pimelic acid</metabolite_name><metabolite_name>Xanthine</metabolite_name><metabolite_name>Prolylhydroxyproline</metabolite_name><metabolite_name>Citric acid</metabolite_name><metabolite_name>LPE(18:1)</metabolite_name><metabolite_name>Emodin</metabolite_name><metabolite_name>Poricoic acid A</metabolite_name><metabolite_name>3h-Indole-3-propanoic acid,a-amino-</metabolite_name><metabolite_name>[6,10a-Dihydroxy-4-(hydroxymethyl)-4,7,11b-trimethyl-9-oxo-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-][1]benzouran-5-yl] acetate</metabolite_name><metabolite_name>Glycolithocholic acid</metabolite_name><metabolite_name>PC(16:0/18:1)</metabolite_name><metabolite_name>5-[5-Hydroxy-3-(hydroxymethyl)pentyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid</metabolite_name><metabolite_name>Asparagine</metabolite_name><metabolite_name>2-(3-phenylpropanamido)acetic acid</metabolite_name><metabolite_name>LPC(14:0)</metabolite_name><metabolite_name>[(2-indol-3-ylethyl)amino]-N-(2-methoxyphenyl)carboxamide</metabolite_name><metabolite_name>Uracil</metabolite_name><metabolite_name>N-Acetylneuraminic acid</metabolite_name><metabolite_name>Pantothenic acid</metabolite_name><metabolite_name>Capryloyl glycine</metabolite_name><metabolite_name>(2E)-3-(4-Acetoxy-2,3-dihydroxy-2,5,5,8a-tetramethyldecahydro-1-naphthalenyl)acrylic acid</metabolite_name><metabolite_name>Guanosine</metabolite_name><metabolite_name>Cortisol</metabolite_name><metabolite_name>Thymidine</metabolite_name><metabolite_name>Creatine</metabolite_name><metabolite_name>3-phenyl-2-pyrrolylpropanoic acid</metabolite_name><metabolite_name>(23R,24R)-3beta-(Beta-D-Xylopyranosyloxy)-9beta,19-Cyclo-16beta,23:16,24-Diepoxy-5alpha-Lanosta-7-Ene-15alpha,25-Diol</metabolite_name><metabolite_name>Efavirenz</metabolite_name><metabolite_name>Shikimic acid</metabolite_name><metabolite_name>4-Methyoxybenzoyl-N-glycine</metabolite_name><metabolite_name>Cytochalasin B</metabolite_name><metabolite_name>Glycocholate</metabolite_name><metabolite_name>Pyrrolo[1,2-d][1,4,7,10,13,16]oxapentaazacyclononadecine-1,4,7,10,14,17(11H,16H)-hexone, 16-(3-chloro-2-hydroxypropyl)dodecahydro-5,8,9-trimethyl-6-(1-methylethyl)-3-(1-methylpropyl)-</metabolite_name><metabolite_name>LPA(18:1)</metabolite_name><metabolite_name>Acetylglycine</metabolite_name><metabolite_name>LPC(16:1)</metabolite_name><metabolite_name>Methionine sulfone</metabolite_name><metabolite_name>Chartarlactam I</metabolite_name><metabolite_name>8-[2-(3,4-dihydroxy-2,5-dimethoxyoxolan-3-yl)ethyl]-4a,7,8-trimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-2,3-diol</metabolite_name><metabolite_name>Metacetamol</metabolite_name><metabolite_name>Glutamylleucine</metabolite_name><metabolite_name>Tyrosine</metabolite_name><metabolite_name>Prunin</metabolite_name><metabolite_name>Conglobatin</metabolite_name><metabolite_name>Gallic acid</metabolite_name><metabolite_name>3-Phenyllactic acid</metabolite_name><metabolite_name>Cinnamoylglycine</metabolite_name><metabolite_name>2,3,4-Trihydroxy-4'-ethoxybenzophenone</metabolite_name><metabolite_name>Tetradecanoylphorbol acetate</metabolite_name><metabolite_name>Vitamin K2</metabolite_name><metabolite_name>7,8-Dihydroxyflavone</metabolite_name><metabolite_name>cis-Aconitate</metabolite_name><metabolite_name>(4-oxido-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-4-ium-1-yl)methyl 2,3-dihydroxy-3-methylpentanoate</metabolite_name><metabolite_name>Hypoxanthine</metabolite_name><metabolite_name>Chenodeoxycholic acid</metabolite_name><metabolite_name>1-Carboxyethylphenylalanine</metabolite_name><metabolite_name>Ornithine</metabolite_name><metabolite_name>LPC(18:2)</metabolite_name><metabolite_name>(E)-4-[(1R,2S,3S,4R,8aS)-2,3,4-trihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one</metabolite_name><metabolite_name>Hippuric acid</metabolite_name><metabolite_name>5-Hydroxymethylcytosine</metabolite_name><metabolite_name>Enterolactone</metabolite_name><metabolite_name>Fusidic acid</metabolite_name><metabolite_name>Taurodeoxycholic acid</metabolite_name><metabolite_name>[1-(3,5-Dihydroxyphenyl)-12-hydroxytridecan-2-yl] acetate</metabolite_name><metabolite_name>N-(4-methylphenyl)-2-(1-methyl-3-phenylthioindol-2-yl)acetamide</metabolite_name><metabolite_name>Glutaminylarginine</metabolite_name><metabolite_name>Indole-3-Lactic Acid</metabolite_name><metabolite_name>LPC(18:1)</metabolite_name><metabolite_name>2-[(2,5-dimethyl(1,3-oxazolino[4,5-e]pyrimidin-7-yl))amino]-4-methylpentanoic acid</metabolite_name><metabolite_name>5-O-Methyllicoricidin</metabolite_name><metabolite_name>Indole-3-acetic acid</metabolite_name><metabolite_name>7-Benzofurancarboxylic acid, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-4-methoxy-6-(2-phenylethyl)-</metabolite_name><metabolite_name>3Beta-Hydroxy-23,24-Bisnorchol-5-Enic Acid</metabolite_name><metabolite_name>Suberylglycine</metabolite_name><metabolite_name>5-Hydroxyindoleacetate</metabolite_name><metabolite_name>Uric acid</metabolite_name><metabolite_name>Phosphocholine</metabolite_name><metabolite_name>Deoxycholic acid</metabolite_name><metabolite_name>3-Hydroxyflavone</metabolite_name><metabolite_name>15,16-DiHODE</metabolite_name><metabolite_name>Deoxycytidine</metabolite_name><metabolite_name>TMP</metabolite_name><metabolite_name>Cholylalanine</metabolite_name><metabolite_name>Glycodeoxycholic acid</metabolite_name><metabolite_name>PC(18:0/20:4)</metabolite_name><metabolite_name>8,11,14-Anacardic Acid</metabolite_name><metabolite_name>3,15-dibenzyl-1,4,12-trimethyl-1,4,7,10,13-pentazacyclopentadecane-2,5,8,11,14-pentone</metabolite_name><metabolite_name>Vanillin</metabolite_name><metabolite_name>Ncgc00385436-01!</metabolite_name><metabolite_name>Glutamine</metabolite_name></additional><is_claimable>false</is_claimable><name>Metabolome sequencing data of Hu Lambs</name><description>&lt;p>Serum metabolomic data of Hu sheep collected before and after weaning at 30, 40, and 50 days of age under three weaning strategies: abrupt weaning, single intermittent separation, and two-stage intermittent separation.&lt;/p></description><dates><publication>2026-03-28</publication><submission>2026-03-28</submission></dates><accession>MTBLS14174</accession><cross_references><MetaboLights>MTBLC64575</MetaboLights><MetaboLights>MTBLC88811</MetaboLights><MetaboLights>MTBLC88465</MetaboLights><ChEBI>CHEBI:64575</ChEBI><ChEBI>CHEBI:88811</ChEBI><ChEBI>CHEBI:88465</ChEBI></cross_references></HashMap>