Journal of Natural Products · 2013 · 37 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryMolecular PharmacologyStructure-activity RelationshipsFungal BiochemistryFungal Secondary MetabolitesLigand BindingOpioid AnalgesicsOpioid PharmacologyStructure-activity Relationship AnalysisBioactive Fungal MetabolitesCannabinoid Structure-activity RelationshipsFungal Bioactive CompoundsReceptors
Bioassay-guided fractionation of a fungus Neocosmospora sp. (UM-031509) resulted in the isolation of three new resorcylic acid lactones, neocosmosin A (2), neocosmosin B (3), and neocosmosin C (4). Three known resorcylic acid lactones, monocillin IV (1), monocillin II (5), and radicicol (6), were also isolated and identified. The structures of these compounds were established on the basis of extensive 1D and 2D NMR spectroscopic analysis, mass spectrometric (ESIMS) data, and X-ray crystallography. Compounds 4-6 show good binding affinity for the human opioid receptors. These findings have important implications for evaluating the potential psychoactive effects with this class of compounds.
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A Greedy Algorithm for Aligning DNA Sequences
Zheng Zhang, Scott Schwartz, Lukas Wagner et al. · Journal of Computational Biology · 2000 · 5.6K citations
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