Author(s):
Ribeiro, Erika M. de O. ; Lima, Luciano S. ; David, Jorge Mauricio ; Vale, Ademir Evangelista do ; Lopes, Lucia M. Xavier ; David, Juceni Pereira de Lima ; Ribeiro, Erika M. de O. ; Lima, Luciano S. ; David, Jorge Mauricio ; Vale, Ademir Evangelista do ; Lopes, Lucia M. Xavier ; David, Juceni Pereira de Lima
Date: 2014
Origin: Oasisbr
Subject(s): Erythroxylum rimosum; Erythroxylaceae; Tropane alkaloid; Triterpenes; Acetylcholinesterase inhibition
Description
Texto completo: acesso restrito. p. 232–235
Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-11-24T13:38:48Z No. of bitstreams: 1 Erika M. de O. Ribeiro.pdf: 389823 bytes, checksum: 19bb1c79d3ca89eca1416f9f917ac5f2 (MD5)
Made available in DSpace on 2014-11-24T13:38:48Z (GMT). No. of bitstreams: 1 Erika M. de O. Ribeiro.pdf: 389823 bytes, checksum: 19bb1c79d3ca89eca1416f9f917ac5f2 (MD5) Previous issue date: 2013
A new tropane alkaloid, named the 7β-acetoxy-3β,6β-dibenzoyloxytropane (1), was isolated from a methanol extract of Erythroxylum rimosum O.E. Schulz leaves. Other known compounds were detected, including quercetin, kaempferol-3-O-α-l-arabinofuranoside, (+)-catechin, epicatechin, quercetin-3-O-α-arabinofuranoside, quercetin-3-O-α-arabinopyranoside, quercetin-3-O-β-arabinopyranoside, quercetin-3-β-glucopyranoside, kaempferol, quercetin-3-O-β-galactopyranoside, β-sitosterol, α-amyrin, β-amyrin, and the ester derivatives of these two amyrins. Compound 1 exhibited weak inhibition of acetylcholinesterase. Structural identification was performed using IR, ESIHRMS and one- and two-dimensional NMR data analyses and confirmed by comparison with literature data.