Journal of Natural Products · 2011 · 56 citations · 9 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsFungal Secondary MetabolitesMarine Bioactive CompoundsMarine Natural ProductsMedicinal PlantsMetabolite IdentificationStructure-activity Relationship AnalysisBioactive Compounds From Marine FungiBioactive ConstituentsBioactive Marine MetabolitesMarine Fungal Natural ProductsMarine Fungi As Drug SourcesMarine Sponge MetabolitesX-ray Diffraction Analysis
Three new diterpenes, myrocin D (1), libertellenone E (2), and libertellenone F (3), and a new isocoumarin, decarboxyhydroxycitrinone (4), were isolated from the marine fungus Arthrinium sacchari, together with three known compounds (5-7). The structures of 1-4 were elucidated from spectroscopic data (NMR, MS, IR), and the absolute configurations of 1-3 were determined by X-ray diffraction analysis. The antiangiogenic activity of these compounds was evaluated by measuring their antiproliferation effects on human umbilical vein endothelial cells (HUVECs) and human umbilical artery endothelial cells (HUAECs). Compounds 4-7 showed inhibitory activity.
9
On enantiomorph-polarity estimation
H. D. Flack · Acta Crystallographica Section A Foundations of Crystallography · 1983 · 10.4K citations
Natural Sciences, Chemistry, Physics +10
Kazuo Kubo, Toshiyuki Shimizu, Shin-ichi Ohyama et al. · Journal of Medicinal Chemistry · 2005 · 146 citations · Full text