<HashMap><database>GNPS</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://massive-ftp.ucsd.edu/v07/MSV000094717/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Metabolomics</omics_type><submitter>Jason Crawford</submitter><instrument_platform>6550 iFunnel Q-TOF LC/MS</instrument_platform><species>Homo Sapiens (ncbitaxon:9606)</species><full_dataset_link>https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=7ac407b98d854632a04bae7025827e80</full_dataset_link><submitter_email>jason.crawford@yale.edu</submitter_email><submitter_affiliation>Yale University</submitter_affiliation><sample_protocol></sample_protocol><repository>GNPS</repository><file_size>23</file_size><ptm_modification>MS:1002864 - No post-translational-modifications are included in the identified peptides of this dataset</ptm_modification><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>GNPS Human AKR1C3 Binds Agonists of GPR84 and Participates in an Expanded Polyamine Pathway</name><description>In vitro metabolomics with AKR1C3 and HEPG2 Metabolome 

Files and corresponding conditions: 

C3only: Enzyme (AKR1C3) only condition with NADPH co-factor added 

WTmed: this is medium only control containing HEPG2 extract and NADPH. 

WTmed+C3:  this is a no-cofactor control containing enzyme and HEPG2 extract. 

WTmed+C3+PH:  this is all components together with enzyme, HEPG2 extract and NADPH co-factor. 

Reversed-phase chromatography was performed with a Kinetex (Cat. # 00G-4601-E0) 5 um C18 100 A column (250 by 4.6 mm), using a water:acetonitrile gradient containing 0.1% formic acid at 0.7 mL/min flow rate: 0-30 min, 10% to 100% acetonitrile. 
Positive mode (qTOF)</description><dates><publication>Wed May 08 12:19:00 BST 2024</publication></dates><accession>MSV000094717</accession><cross_references/></HashMap>