cris.boxmetadata.label.title
Chemical constituents and antileukemic activity of Eugenia dysenterica
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.january 2017
cris.boxmetadata.label.accesslevel
open access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Vitek R.
de Novais L.M.R.
Torquato H.F.V.
de Carvalho M.G.
de Sousa P.T.
Jacinto M.J.
da Silva V.C.
Universidade Federal de São Paulo
cris.boxmetadata.label.publisher
Taylor and Francis Ltd.
cris.boxmetadata.label.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.
cris.boxmetadata.label.citationstartpage
1930
cris.boxmetadata.label.citationendpage
1934
cris.boxmetadata.label.volume
31
cris.boxmetadata.label.issue
16
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Bioquímica, Biología molecular
cris.boxmetadata.label.subjects
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-85006860849
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Natural Product Research
cris.boxmetadata.label.containerissn
14786419
peru-layout.shadow-copies
Directorio de Producción Científica
Scopus