<HashMap><database>GNPS</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://massive-ftp.ucsd.edu/v05/MSV000091455/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Metabolomics</omics_type><submitter>Daniela B. B. Trivella</submitter><submitter>Rafael de Felicio</submitter><instrument_platform>ESI-qQTOF Impact II</instrument_platform><species>Annulohypoxylon Moriforme Ma9</species><full_dataset_link>https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=5519c33713c543e4b1e95363b4562e71</full_dataset_link><submitter_affiliation>Brazilian Center for Research in Energy and Materials</submitter_affiliation><submitter_email>daniela.trivella@lnbio.cnpem.br</submitter_email><submitter_email>rafael.felicio@lnbio.cnpem.br</submitter_email><sample_protocol></sample_protocol><repository>GNPS</repository><file_size>19</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 Annulohypoxylon moriforme MA9: NP3_MS_Workflow case validation: proteasome inhibitor candidates</name><description>Ethyl acetate extract of Annukihypoxylon moriforme MA9 strain (endophytic fungi) showed potent proteasome inhibition. It was performed chromatographic steps to generated two sets of bioactive enriched fractions. Extract and fractions were submitted to UPLC-MS/MS analysis and MS data was evaluated by NP3_MS_Workflow to predict most probable m/z candidate responsable for proteasome inhibition.   </description><dates><publication>Thu Mar 09 09:12:00 GMT 2023</publication></dates><accession>MSV000091455</accession><cross_references/></HashMap>