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Chrotacumines E and F, Two New Chromone‐Alkaloid Analogs from <i>Dysoxylum acutangulum</i> (Meliaceae) Leaves
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Citations
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References
2013
Year
Molecular PharmacologyBiosynthesisNew Chromone‐alkaloid AnalogsNatural Product SynthesisBiochemistryBotanyMedicineNatural SciencesAlkaloidal FractionSecondary MetabolitePhytochemicalChrotacumines EPharmacologyPharmaceutical ChemistryPhytochemistryDrug DiscoveryTyrosinase InhibitorsDrug Analysis
A chemical investigation of the alkaloidal fraction of Dysoxylum acutangulum leaves led to the isolation and characterization of two new chromone alkaloid analogs named chrotacumines E and F (1 and 2, resp.). Structure elucidation of 1 and 2 was achieved by spectroscopic analyses, including 2D-NMR. Both of these alkaloids exhibited modest activities as tyrosinase inhibitors with 29.2 and 25.8% inhibition at 100 μg/ml, respectively.
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