Journal of Natural Products · 2013 · 24 citations · 12 references
Natural SciencesMarine BiologyPharmacologyCancer PharmacologyDrug DiscoveryMarine BiodiversityHeterocyclic ChemistryMarine Bioactive CompoundsMarine PharmacologyPeptide AnalysisPeptide ChemistryAbsolute Configuration AssignmentAbsolute Configuration DeterminationAmino AcidsBioactive Marine MetabolitesBioactive Marine PeptidesFragmentationHydrolysisMacrocyclic Peptides
A macrocylic dodecapeptide, cycloforskamide, was isolated from the sea slug Pleurobranchus forskalii, collected off Ishigaki Island, Japan. Its planar structure was deduced by extensive NMR analyses and was further confirmed by MS/MS fragmentation analyses. Finally, the absolute configuration was determined by total hydrolysis and chiral-phase gas chromatographic analysis. This novel dodecapeptide contains three d-amino acids and three thiazoline heterocycles and exhibits cytotoxicity against murine leukemia P388 cells, with an IC50 of 5.8 μM.
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Eric W. Schmidt, James T. Nelson, David A. Rasko et al. · Proceedings of the National Academy of Sciences · 2005 · 570 citations · Full text
Proline Cis−Trans Isomerization and Protein Folding
William J. Wedemeyer, Ervin Welker, Harold A. Scheraga · Biochemistry · 2002 · 448 citations
Cyril Portmann, Judith F. Blom, Karl Gademann et al. · Journal of Natural Products · 2008 · 132 citations · Full text