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Isolation, Characterization and Antiproliferative Activity of New Metabolites from the South African Endemic Red Algal Species Laurencia alfredensis.
Dziwornu, Godwin A; Caira, Mino R; Mare, Jo-Anne de la; Edkins, Adrienne L; Bolton, John J; Beukes, Denzil R; Sunassee, Suthananda N.
Afiliação
  • Dziwornu GA; Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa. dzwgod001@myuct.ac.za.
  • Caira MR; Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa. mino.caira@uct.ac.za.
  • Mare JA; Biomedical Biotechnology Research Unit, Department of Biochemistry and Microbiology, Rhodes University, Grahamstown 6140, South Africa. j.delamare@ru.ac.za.
  • Edkins AL; Biomedical Biotechnology Research Unit, Department of Biochemistry and Microbiology, Rhodes University, Grahamstown 6140, South Africa. a.edkins@ru.ac.za.
  • Bolton JJ; Department of Biological Sciences, University of Cape Town, Rondebosch 7701, South Africa. john.bolton@uct.ac.za.
  • Beukes DR; Marine Research (Ma-Re) Institute, University of Cape Town, Rondebosch 7701, South Africa. john.bolton@uct.ac.za.
  • Sunassee SN; School of Pharmacy Department of Pharmaceutical Chemistry, University of the Western Cape, Bellville 7535, South Africa. dbeukes@uwc.ac.za.
Molecules ; 22(4)2017 Mar 23.
Article em En | MEDLINE | ID: mdl-28333106
ABSTRACT
The marine red algae of the genus Laurencia have been widely studied for their structurally diverse and biologically active secondary metabolites. We report here the natural product investigation of the organic extract of a newly identified South African endemic species, Laurencia alfredensis. A sequence of column chromatography, preparative TLC and normal phase HPLC resulted in the isolation of eleven compounds comprising three labdane-type diterpenes (1-3), four polyether triterpenes (4-7), three cholestane-type ecdysteroids (8-10) and a glycolipid (11). Compounds 1-3, 5-8 and 10 have not previously been reported, while compound 9 is reported here for the first time from a natural source and the known compound 11 isolated for the first time from the genus Laurencia. The structural elucidation and the relative configuration assignments of the compounds were accomplished by extensive use of 1D- and 2D-NMR, HR-ESI-MS, UV and IR spectroscopic techniques, while the absolute configuration of compound 1 was determined by single-crystal X-ray diffraction analysis. All compounds were evaluated against the MDA-MB-231 breast and HeLa cervical cancer cell lines. Compound 2 exhibited low micromolar antiproliferative activity (IC50 = 9.3 µM) against the triple negative breast carcinoma and compound 7 was similarly active (IC50 = 8.8 µM) against the cervical cancer cell line.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Glicolipídeos / Ecdisteroides / Laurencia Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Glicolipídeos / Ecdisteroides / Laurencia Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article