Journal of Natural Products · 2007 · 54 citations · 18 references
PharmacyBiochemistryMicrobiologyBioorganic ChemistryNatural Product BiosynthesisOrganic ChemistryAmino Acid ChemistryNonribosomal Peptide BiosynthesisPeptide AnalysisPeptide ChemistryPeptide IdentificationPhenylpropanoid BiosynthesisBioactive Marine PeptidesCyclic PeptidesDe Novo Structure ElucidationMarine Cyanobacterial Natural Product BiosynthesisMarine Nonribosomal Peptide BiosynthesisNonribosomal PeptidesPeptide Natural Products
The isolation and structure elucidation of two cyclic peptides, pahayokolides A (1) and B (2), is described. Structural features determined for these compounds include a pendent N-acetyl-N-methyl leucine, both E- and Z-dehydrobutyrines, a homophenylalanine, and an unusual polyhydroxy amino acid that is most likely of mixed polyketide synthase/nonribosomal peptide synthase origin. These peptides were purified from a new species of cyanobacteria of the genus Lyngbya, which was isolated from a periphyton mat from the Florida Everglades.
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1H, 13C and 15N chemical shift referencing in biomolecular NMR
David S. Wishart, Colin G. Bigam, Jian Yao et al. · Journal of Biomolecular NMR · 1995 · 2.4K citations