<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(6)</volume><submitter>Crespo G</submitter><pubmed_abstract>An antifungal lipodepsipeptide was obtained from cultures of the fungus Foliophoma fallens CF-236885. Its structure, elucidated by HRMS and NMR spectroscopy, contained Gly, Thr, Asn, β-Ala, Orn, Ala, two Ser residues, and 3-hydroxy-4-methylhexadecanoic acid. The absolute configuration of its amino acid residues was determined using Marfey's analysis and J-based configuration analysis helped to establish the relative configuration of the 3-hydroxy-4-methylhexadecanoic acid moiety. A literature search retrieved a patent describing antibiotic TKR2999 (1), whose non-disclosed structure was confirmed to be identical to that found for our compound, according to its physicochemical properties and NMR spectra. Compound 1 displayed potent antifungal activity against Aspergillus fumigatus and a pane</pubmed_abstract><journal>Antibiotics (Basel, Switzerland)</journal><pagination>E278</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7345921</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Structural Elucidation of Antibiotic TKR2999, an Antifungal Lipodepsipeptide Isolated from the Fungus Foliophoma fallens.</pubmed_title><pmcid>PMC7345921</pmcid><pubmed_authors>Gonzalez-Menendez V</pubmed_authors><pubmed_authors>Sanchez P</pubmed_authors><pubmed_authors>Crespo G</pubmed_authors><pubmed_authors>Cautain B</pubmed_authors><pubmed_authors>de la Cruz M</pubmed_authors><pubmed_authors>Reyes F</pubmed_authors><pubmed_authors>Perez-Victoria I</pubmed_authors><pubmed_authors>Ortiz-Lopez FJ</pubmed_authors><pubmed_authors>Genilloud O</pubmed_authors><pubmed_authors>Vicente F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structural Elucidation of Antibiotic TKR2999, an Antifungal Lipodepsipeptide Isolated from the Fungus Foliophoma fallens.</name><description>An antifungal lipodepsipeptide was obtained from cultures of the fungus Foliophoma fallens CF-236885. Its structure, elucidated by HRMS and NMR spectroscopy, contained Gly, Thr, Asn, β-Ala, Orn, Ala, two Ser residues, and 3-hydroxy-4-methylhexadecanoic acid. The absolute configuration of its amino acid residues was determined using Marfey's analysis and J-based configuration analysis helped to establish the relative configuration of the 3-hydroxy-4-methylhexadecanoic acid moiety. A literature search retrieved a patent describing antibiotic TKR2999 (1), whose non-disclosed structure was confirmed to be identical to that found for our compound, according to its physicochemical properties and NMR spectra. Compound 1 displayed potent antifungal activity against Aspergillus fumigatus and a pane</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2025-04-22T19:38:00.26Z</modification><creation>2025-04-06T02:48:09.34Z</creation></dates><accession>S-EPMC7345921</accession><cross_references><pubmed>32466351</pubmed><doi>10.3390/antibiotics9060278</doi></cross_references></HashMap>