Journal of Natural Products · 2006 · 121 citations · 20 references
PharmacyBiochemistryPharmacologyDrug DiscoveryMass Spectrometric AnalysisStructure-activity RelationshipsNatural Product Drug DiscoveryStructure-activity Relationship AnalysisAmino Acid AnalysisCytotoxicity AssaysMedicinal Chemistry ApplicationsPharmacological Screening
Two new cyclic depsipeptide derivatives, kahalalides R (1) and S (2), together with two known congeners, kahalalides F (3) and D (4), were isolated from the Indian sacoglossan mollusk Elysia grandifolia. The structures of the new compounds were unambiguously established on the basis of NMR spectroscopic (1H, 13C, COSY, HMBC) and mass spectrometric (FABMS, ESIMS, MALDI-TOF/PSD) data, which also included Marfey amino acid analyses. The new derivative kahalalide R was found to exert comparable or even higher cytotoxicity than the potential drug candidate kahalalide F toward the MCF7 human mammary carcinoma cell line.
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