<HashMap><database>GNPS</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://massive-ftp.ucsd.edu/v06/MSV000093497/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Metabolomics</omics_type><submitter>Wilton Ricardo Sala-Carvalho</submitter><instrument_platform>HPLC-MS ESI low resolution (Thermo-Fischer)</instrument_platform><species>Brittonodoxa Subpinnata</species><full_dataset_link>https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=fa46caae090741f2b7b48fe508005e1e</full_dataset_link><submitter_email>wiltonsala@hotmail.com</submitter_email><submitter_affiliation>Universidade de Sao Paulo</submitter_affiliation><sample_protocol></sample_protocol><repository>GNPS</repository><file_size>77</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 - Brittonodoxa subpinnata soluble extract</name><description>For HPLC-MS2 analysis, 50 mg of plant material was extracted with 5 mL of 80% methanol. The supernatant was collected and submitted to a cleanup process through a C18 SPE by activating the column with methanol and equilibrating it with ultrapure water. The extract was loaded into the column and eluted with 5 mL of the following solvents: ultrapure water, followed by 25% methanol, 50% methanol, and washed with methanol. The fractions were joined, transferred to a tube, and vacuum dried.</description><dates><publication>Sat Nov 25 14:04:00 GMT 2023</publication></dates><accession>MSV000093497</accession><cross_references><TAXONOMY>663595</TAXONOMY></cross_references></HashMap>