Journal of Natural Products · 2010 · 55 citations · 27 references
PharmacyChemistryMedicinal ChemistryCancer PharmacologyDrug DiscoverySynthetic Medicinal ChemistryNatural Product Drug DiscoveryStructure-activity Relationship AnalysisAbsolute Configuration AssignmentAbsolute Configuration DeterminationAnticancer ActivityCircular DichroismCircular Dichroism AnalysisElectronic Circular DichroismSingle-crystal DiffractionSingle-crystal X-ray Diffraction
(-)-Gambogic acid (1), a biologically active "caged xanthone" from gamboge, the dried resin of Garcinia hanburyi, is of interest as a potential anticancer agent. The planar structure of (-)-gambogic acid has been determined previously by analysis of its detailed NMR data and confirmed by single-crystal X-ray diffraction, with the absolute configuration at C-13 deduced as R through a series of chemical degradations. Using (-)-morellic acid (2), an analogue of (-)-gambogic acid, as a model compound, the 5R, 7S, 10aS, 13R, 27S absolute configuration of (-)-gambogic acid was determined for the first time by comparison of physical and spectroscopic data, especially experimental and calculated electronic circular dichroism.
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Cytotoxic xanthones from Garcinia hanburyi
Jun Asano, Kazuhiro Chiba, Masahiro Tada et al. · Phytochemistry · 1996 · 193 citations
Zhao‐Qiu Wu, Qinglong Guo, Qidong You et al. · Biological and Pharmaceutical Bulletin · 2004 · 159 citations
Medicine, Oncology, Pharmacology +15