Chemistry & Biodiversity · 2014 · 32 citations · 13 references
PharmacyChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsHeterocyclic ChemistryStructure-activity Relationship AnalysisChemical Structure-activity RelationshipsMedicinal Aromatic PlantsPharmacological Screening
Three (9βH)-pimaranes, 1, 2, and 3, and two (9βH)-17-norpimaranes, 4 and 5, belonging to a rare compound class in nature, were obtained from the tubers of Icacina trichantha for the first time. Compound 1 is a new natural product, and 2-5 have been previously reported. The structures were elucidated based on NMR and MS data, and optical rotation values. The absolute configurations of (9βH)-pimaranes were unambiguously established based on X-ray crystallographic analysis. Full NMR signal assignments for the known compounds 2, 4, and 5, which were not available in previous publications, are also reported. All five isolates displayed cytotoxic activities on MDA-MB-435 cells (IC50 0.66-6.44 μM), while 2, 3, and 4 also exhibited cytotoxicities on HT-29 cells (IC50 3.00-4.94 μM).
13
Momilactones, growth inhibitors from rice, oryza sativa L.
Tadahiro Kato, Chizuko Kabuto, Nobuki Sasaki et al. · Tetrahedron Letters · 1973 · 216 citations
Cytotoxic and Antitumor Activity of Momilactone B from Rice Hulls
Sun-Jung Kim, Hae-Ryong Park, Eunju Park et al. · Journal of Agricultural and Food Chemistry · 2007 · 83 citations
Medicine, Biochemistry, Pharmacology +12