| Literature DB >> 28004585 |
Renan Vitek1, Leice M R de Novais1, Heron F V Torquato2, Edgar J Paredes-Gamero2,3, Mário G de Carvalho4, Paulo T de Sousa1, Marcos J Jacinto1, Virgínia C da Silva1.
Abstract
The study about Eugenia dysenterica led to the isolation of 3-acetyl-urs-12-en-28-oic (1), 3-acetyl-olean-12-en-28-oic acid (2) and isoquercetin (3) from the stem barks, and of 3-O-β-glucopyranosyl-β-sitosterol (4), methyl 3-hydroxy-4-methoxybenzoate (5), methyl 4-hydroxyphenyl propionate (6), E-methyl-4-hydroxycinnamate (7), quercetin-3-O-(6ꞌꞌ-O-galloyl)-β-d-glucopyranoside (8) and quercetin-3-O-β-d-galactopyranoside (9) from the leaves. The structures 1-9 were set through the analysis of their NMR spectroscopic data. Compounds 2, 3 and 5-8 were reported for the first time in the Eugenia genus. Compound 8 reduced cell viability and presented IC50 values 40.3 and 36.7 μM, for the CCRF-CEM and the Kasumi-1 cells, respectively.Entities:
Keywords: Eugenia dysenterica; cell cycle arrest; cell death; cell differentiation; galloyl flavonol; leukemia
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Year: 2016 PMID: 28004585 DOI: 10.1080/14786419.2016.1261343
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861