Journal of Natural Products · 2016 · 65 citations · 21 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntifungal AgentsAntifungal PharmacologyFungal Secondary MetabolitesStructure-activity Relationship AnalysisBioactive Fungal MetabolitesFungal Bioactive CompoundsLichen BiologyNew Antifungal AgentsSingle-crystal DiffractionSingle-crystal X-ray Diffraction
Eight usnic acid derivatives, that is, usenamines A-F (1-6), usone (7), and isousone (8), together with the known (+)-usnic acid (9), were isolated from the lichen Usnea longissima. Their structures were elucidated using 1D and 2D NMR and MS data, and the absolute configurations of compounds 1 and 2 were defined by single-crystal X-ray diffraction analyses. Compounds 1, 2, and 8 showed inhibitory effects on the growth of human hepatoma HepG2 cells with IC50 values of 6.0-53.3 μM compared with methotrexate as the positive control, which had an IC50 value of 15.8 μM. Furthermore, 1 induced apoptosis of HepG2 cells in a dose-dependent manner at concentrations of 0-15.0 μM. The isolated compounds were also evaluated for their antifungal and antibacterial activities, with 7 and 8 exhibiting weak inhibitory effects on fungal Trichophyton rubrum spp. with an MIC value of 41.0 μM.
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A short history of<i>SHELX</i>
George M. Sheldrick · Acta Crystallographica Section A Foundations of Crystallography · 2007 · 87.4K citations · Full text
On enantiomorph-polarity estimation
H. D. Flack · Acta Crystallographica Section A Foundations of Crystallography · 1983 · 10.4K citations
Natural Sciences, Chemistry, Physics +10