Journal of Natural Products · 2016 · 49 citations · 21 references
Natural SciencesBiochemistryChemistryBioorganic ChemistryDrug DiscoveryOrganic ChemistryAmino Acid ChemistryAntimicrobial PeptidesMarine Drug DiscoveryPeptide AnalysisPeptide ChemistryPeptide Drug DiscoveryAbsolute Configuration AssignmentAbsolute Configuration DeterminationAntitrypanosomal TherapyBioactive Marine PeptidesCyclic PeptidesDegradationHydrolysisMarine Polyketides
Janadolide, a new cyclic polyketide-peptide hybrid possessing a tert-butyl group, was isolated from an Okeania sp. marine cyanobacterium. The gross structure was elucidated by spectroscopic analyses, and the absolute configurations of the amino acid moieties were determined by acid hydrolysis and chiral-phase HPLC analyses. The absolute configuration of the two stereogenic centers in the polyketide moiety was elucidated based on a combination of degradation reactions and spectroscopic analyses including the phenyl-glycine methyl ester method. Janadolide showed potent antitrypanosomal activity with an IC50 value of 47 nM without cytotoxicity against human cells at 10 μM.
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Hendrik Luesch, Wesley Y. Yoshida, Richard E. Moore et al. · Journal of the American Chemical Society · 2001 · 372 citations
Marcelino Gutiérrez, Takashi Suyama, Niclas Engene et al. · Journal of Natural Products · 2008 · 154 citations