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A new pyrrole alkaloid isolated from Arum palaestinum Boiss. and its biological activities.
El-Desouky, S K; Kim, Ki Hun; Ryu, Shi Young; Eweas, Ahmad Farouk; Gamal-Eldeen, Amira M; Kim, Young-Kyoon.
Afiliação
  • El-Desouky SK; College of Forest Science, Kookmin University, Seoul, Korea.
Arch Pharm Res ; 30(8): 927-31, 2007 Aug.
Article em En | MEDLINE | ID: mdl-17879743
ABSTRACT
The phytochemical analysis of the ethyl acetate fraction of Arum palaestinum Boiss. (Araceae) led to the isolation and identification of a new polyhydroxy alkaloid compound; (S)-3,4,5-trihydroxy-1 H-pyrrol-2(5H)-one (1), and other five known compounds; caffeic acid (2), isoorientin (3), luteolin (4) and vicenin 11 (5), as well as the rare compound 3,6,8-trimethoxy, 5,7,3',4'-tetrahydroxy flavone (6). The structural elucidations of all the compounds were based on spectroscopic data (1H- and 13C-NMR, DEPT, HSQC, HMBC and NOE difference techniques) and comparison with literature data. Investigation of the antioxidant activity of the ethyl acetate fraction indicated its strong scavenging capacity for 1,1 -diphenyl-2-picrylhydrazyl (DPPH) radicals (SC50 3.1+/-0.82 microg/mL). Moreover, the treatment of different human cancer cell lines with the ethyl acetate fraction led to dose-dependant suppression in the proliferation of both breast carcinoma cells (MCF-7; IC50 59.09+/-4.1 microg/mL) and lymphoblastic leukemia cells (1301; IC50 53.1+/-2.9 microg/mL); however, it was found to have no effect on the growth of hepatocellular carcinoma cells (Hep G2).
Assuntos
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Base de dados: MEDLINE Assunto principal: Pirróis / Sequestradores de Radicais Livres / Arum / Alcaloides / Antineoplásicos Fitogênicos Idioma: En Revista: Arch Pharm Res Ano de publicação: 2007 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Pirróis / Sequestradores de Radicais Livres / Arum / Alcaloides / Antineoplásicos Fitogênicos Idioma: En Revista: Arch Pharm Res Ano de publicação: 2007 Tipo de documento: Article