Natural Product Communications · 2014 · 10 citations · 12 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsCytotoxicity AssessmentCytotoxicity EvaluationStructure-activity Relationship AnalysisAnticancer ActivityChemical Structure-activity RelationshipsFruit PhytochemicalsMultidimensional Nmr SpectroscopyPharmacological ScreeningPlant Alkaloids
A new ent-kaurane glycoside, annoglabasin H (1), and three known ent-kauranes, annoglabasin E (2), annoglabasin B (3), and 19-nor-ent-kaurent-4-ol-17-oic acid (4) were isolated from the fruits of Annona glabra. Their structures were determined by the combination of spectroscopic and chemical methods, including 1D- and 2D-NMR spectroscopy, as well as by comparison with the NMR data reported in the literature. The cytotoxic activities of these compounds were evaluated on four human cancer cell lines, LU-1, MCF-7, SK-Mel2, and KB. Compound 1 exhibited significant cytotoxic activity on all tested human cancer cell lines with IC50 values ranging from 3.7 to 4.6 μM.
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Anticancer effects of Annona glabra plant extracts in human leukemia cell lines.
Curtis Bruce Cochrane, Priyanka Nair, Steven J. Melnick et al. · PubMed · 2008 · 71 citations
Medicine, Oncology, Pharmacology +16
Bioactive Kaurane Diterpenoids from <i>Annona glabra</i>
Fang‐Rong Chang, Pey-Yuh Yang, Jung‐Yaw Lin et al. · Journal of Natural Products · 1998 · 61 citations