New pigments with all unprecedented skeleton, named keronopsamides A-C, were isolated from the marine ciliate Pseudokeronopsis riccii. The structure of the most abundant secondary metabolite, keronopsamide A, was established through extended Nuclear Magnetic Resonance (NMR) analysis and mass spectrometric (MS) data obtained by using electrospray (ESI) and matrix assisted laser desorption (MALDI) ionizations. Structures of the minor analogues (keronopsamide B and C) were inferred from H-1 NMR, chemical correlation, and LC-MS measurements The analysis of NOE dipolar Couplings and quantum chemical calculations, carried out by density functional theory (DFT) oil the preferred rotamers of keronopsamide A, suggested a fully planar structure with amide bond in anti stereochemistry capable to break down the extended conjugation of the whole pi electronic system. Although the presence of a 2-substituted 3,4-dibromo-pyrrole moiety is reminiscent of previously isolated metabolites isolated from a cell extract of Pseudokeronopsis rubra (keronopsins), keronopsamides show a new molecular skeleton formally derived from a peptide-like condensation of a 3-pyrrolepropenoic acid with all unsaturated bromotyramine
Keronopsamides, a New Class of Pigments from Marine Ciliates.
Guella G;
2010
Abstract
New pigments with all unprecedented skeleton, named keronopsamides A-C, were isolated from the marine ciliate Pseudokeronopsis riccii. The structure of the most abundant secondary metabolite, keronopsamide A, was established through extended Nuclear Magnetic Resonance (NMR) analysis and mass spectrometric (MS) data obtained by using electrospray (ESI) and matrix assisted laser desorption (MALDI) ionizations. Structures of the minor analogues (keronopsamide B and C) were inferred from H-1 NMR, chemical correlation, and LC-MS measurements The analysis of NOE dipolar Couplings and quantum chemical calculations, carried out by density functional theory (DFT) oil the preferred rotamers of keronopsamide A, suggested a fully planar structure with amide bond in anti stereochemistry capable to break down the extended conjugation of the whole pi electronic system. Although the presence of a 2-substituted 3,4-dibromo-pyrrole moiety is reminiscent of previously isolated metabolites isolated from a cell extract of Pseudokeronopsis rubra (keronopsins), keronopsamides show a new molecular skeleton formally derived from a peptide-like condensation of a 3-pyrrolepropenoic acid with all unsaturated bromotyramineI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
