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Antiproliferative Compounds from Ocotea macrocarpa from the Madagascar Dry Forest1.
Liu, Yixi; Cheng, Emily; Rakotondraibe, L Harinantenaina; Brodie, Peggy J; Applequist, Wendy; Randrianaivo, Richard; Rakotondrafara, Andriamalala; Ratsimbason, Michel; Rasamison, Vincent E; Kingston, David G I.
Afiliação
  • Liu Y; Department of Chemistry and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061.
  • Cheng E; Department of Chemistry and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061.
  • Rakotondraibe LH; Department of Chemistry and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061.
  • Brodie PJ; Department of Chemistry and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061.
  • Applequist W; Missouri Botanical Garden, P.O. Box 299, St. Louis Missouri 63166.
  • Randrianaivo R; Missouri Botanical Garden, Lot VP 31 Ankadibevava, Anjohy Antananarivo 101, Madagascar.
  • Rakotondrafara A; Missouri Botanical Garden, Lot VP 31 Ankadibevava, Anjohy Antananarivo 101, Madagascar.
  • Ratsimbason M; Centre National d'Application des Recherches Pharmaceutiques, B.P. 702, Antananarivo 101, Madagascar.
  • Rasamison VE; Centre National d'Application des Recherches Pharmaceutiques, B.P. 702, Antananarivo 101, Madagascar.
  • Kingston DG; Department of Chemistry and the Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061.
Tetrahedron Lett ; 56(23): 3630-3632, 2015 Jun 03.
Article em En | MEDLINE | ID: mdl-26034338
ABSTRACT
Bioassay-directed fractionation of an antiproliferative ethanol extract of the roots of Ocotea macrocarpa (Lauraceae) afforded the new butanolide macrocarpolide A (1), and the two new secobutanolides macrocarpolides B (2) and C (3), together with the known butanolides linderanolide B (4) and isolinderanolide (5). The structure elucidation of all compounds was carried out based on NMR and mass spectroscopic data analyses. The absolute configurations of all compounds isolated were determined by comparison of their optical rotation values with those found in literature. Compounds 1-5 showed good antiproliferative activities against the A2780 ovarian cell line, with IC50 values of 2.57 ± 0.12 (1), 1.98 ± 0.23 (2), 1.67 ± 0.05 (3), 2.43 ± 0.41 (4), and 1.65 ± 0.44 µM (5), respectively.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Tetrahedron Lett Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Tetrahedron Lett Ano de publicação: 2015 Tipo de documento: Article