Journal of Natural Products · 2011 · 30 citations · 22 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsHeterocyclic ChemistryHeterocyclic CompoundsNatural Product Drug DiscoveryOncology PharmacologyQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisAnticancer Compound ScreeningChemical Structure-activity RelationshipsSingle-crystal DiffractionSingle-crystal X-ray DiffractionX-ray Diffraction Analysis
Eight new halogenated C(15) acetogenins, 1-8, were isolated from the organic extract of the red alga Laurencia marilzae. The structure elucidation and the assignments of the relative configurations were established by extensive use of spectroscopic studies, particularly 1D and 2D NMR data, while the absolute configurations of compounds 1 and 5 were determined by single-crystal X-ray diffraction analysis. Compounds 1, 2, 4, 5, and 7, along with the previously reported related cyclic ether obtusallene IV (9), were evaluated against six human solid tumor cell lines. All compounds were found to be essentially inactive (GI(50) > 10 μg/mL).
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On enantiomorph-polarity estimation
H. D. Flack · Acta Crystallographica Section A Foundations of Crystallography · 1983 · 10.4K citations
Natural Sciences, Chemistry, Physics +10
Nobuaki Matsumori, Daisuke Kaneno, Michio Murata et al. · The Journal of Organic Chemistry · 1999 · 769 citations
John W. Blunt, Brent R. Copp, Murray H. G. Munro et al. · Natural Product Reports · 2010 · 407 citations · Full text