| Literature DB >> 26034338 |
Yixi Liu1, Emily Cheng1, L Harinantenaina Rakotondraibe1, Peggy J Brodie1, Wendy Applequist2, Richard Randrianaivo3, Andriamalala Rakotondrafara3, Michel Ratsimbason4, Vincent E Rasamison4, David G I Kingston1.
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.Entities:
Keywords: Antiproliferative activity; Butanolide; Lauraceae; Ocotea macrocarpa
Year: 2015 PMID: 26034338 PMCID: PMC4448737 DOI: 10.1016/j.tetlet.2015.01.172
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415