Journal of Natural Products · 2008 · 41 citations · 9 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryPlant BiochemistryStructure-activity RelationshipsChemical Library DesignHormone ReceptorsHormone StructurePlant HormonesHormone Binding AffinityMarine Compound ScreeningNatural Product Library ScreeningRelative Configuration DeterminationStructure Elucidation Of Marine Natural Products
High-throughput screening of a plant and marine invertebrate extract library to find natural products with rat thyrotropin-releasing hormone (TRH) receptor-2 binding affinity led to the isolation of four new, myrtucommulones F-I (3-6), and two known, myrtucommulones A (1) and D (2), active acylphloroglucinols from the seeds of the Queensland tree Corymbia scabrida. Their structures were assigned from interpretation of 2D NMR and high-resolution ESIMS data. The relative configuration of the stereogenic centers for all six compounds was deduced from ROESY correlations. This is the first time that myrtucommulone A (1) has been isolated as a single pure compound. The structure of myrtucommulone D (2) has been revised. Myrtucommulones A, D, and F-I showed rat TRH receptor-2 binding affinity with IC50 values of 39, 11, 16, 24, 31, and 16 microM, respectively.
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Sture Forsén, Ferenc Merényi, Martin Nilsson et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1964 · 73 citations · Full text