Please use this identifier to cite or link to this item: http://repositorio.ufc.br/handle/riufc/8459
Type: Artigo de Periódico
Title: Solanidane and iminosolanidane alkaloids from solanum campaniforme
Authors: Torres, Maria Conceição M.
Jorge, Roberta Jeane B.
Ximenes, Rafael M.
Alves, Natacha Teresa Queiroz
Santos, João Victor de A.
Marinho, Aline D.
Monteiro, Helena S.A.
Toyama, Marcos H.
Braz-Filho, Raimundo
Silveira, Edilberto R.
Pessoa, Otília Deusdênia L.
Keywords: Alcaloides de Solanáceas;Solanaceae;Bothrops
Issue Date: 2013
Publisher: Phytochemistry
Citation: TORRES, M. C. M. et al. Solanidane and iminosolanidane alkaloids from Solanum campaniforme. Phytochemistry, New York, 96, p. 457-464, dez. 2013.
Abstract: From the leaves of Solanum campaniforme (Solanaceae), eight solanidane alkaloids were isolated, four of which contain a p-hydroxyphenylethylamine unit. Their structures were established as: 22b,23b-epoxysolanida- 1,4-dien-3-one; 22a,23a-epoxy-10-epi-solanida-1,4,9-trien-3-one; 22a,23a-epoxy-solanida-4- en-3-one; 22b,23b-epoxy-solanida-4-en-3-one; (E)-N-[80(4-hydroxyphenyl)ethyl]-22a,23a-epoxy-solanida-1, 4,9-trien-3-imine; (E)-N-[80(4-hydroxyphenyl)ethyl]-22a,23a-epoxy-solanida-1,4-dien-3-imine; (Z)-N- [80(4-hydroxyphenyl)ethyl]-22a,23a-epoxy-solanida-1,4,9-trien-3-imine and (Z)-N-[80(4-hydroxyphenyl) ethyl]-22a,23a-epoxy-solanida-1,4-dien-3-imine. All structures were determined using spectroscopic techniques, such as 1D and 2D NMR, and HRESIMS. The cytotoxicity and the antiophidic activities of the alkaloids were evaluated. The alkaloids did not show any cytotoxicity, but inhibited the main toxic actions of Bothrops pauloensis venom.
URI: http://www.repositorio.ufc.br/handle/riufc/8459
ISSN: 0031-9422
Appears in Collections:DFIFA - Artigos publicados em revista científica

Files in This Item:
File Description SizeFormat 
2013_art_ntqalves.pdf987,48 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.