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Isolation and Structure Elucidation of Enniatins L, M<sub>1</sub>, M<sub>2</sub>, and N: Novel Hydroxy Analogs
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Citations
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References
2004
Year
Natural Product SynthesisBioorganic ChemistryFirst Enniatin AnalogsBiochemistryNatural SciencesMedicineMedicinal FungiStructure ElucidationPeptide ScienceChemical BiologyPharmacologyEnniatins LPharmaceutical ChemistryDrug DiscoveryNovel Hydroxy AnalogsNew Cyclohexadepsipeptides
Abstract Four new cyclohexadepsipeptides, enniatins L ( 1 ), M 1 ( 2 ), M 2 ( 3 ), and N ( 4 ), have been isolated from an unidentified fungus (BCC 2629), together with the known enniatins B ( 5 ), H ( 6 ), and I ( 7 ), MK1688 ( 8 ), and enniatin B 4 ( 9 ). Compounds 1 – 4 are the first enniatin analogs with an OH group at the side chain of one of the 2‐hydroxycarboxylic acid residues. The structures of 1 – 4 were elucidated by spectroscopic means and by X‐ray crystallography.
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