| Literature DB >> 16038954 |
Helder Lopes Teles1, Geraldo Humberto Silva, Ian Castro-Gamboa, Vanderlan da Silva Bolzani, José Odair Pereira, Claudio Miguel Costa-Neto, Renato Haddad, Marcos Nogueira Eberlin, Maria Claudia Marx Young, Angela Regina Araújo.
Abstract
An isolate of Curvularia sp. was obtained from the leaves of Ocotea corymbosa, a native plant of the Brazilian Cerrado. The ethyl acetate extract from culture of this fungus afforded two benzopyran derivatives: (2'S)-2-(propan-2'-ol)-5-hydroxy-benzopyran-4-one (2) and 2,3-dihydro-2-methyl-benzopyran-4,5-diol (4); and two known benzopyrans: 2-methyl-5-methoxy-benzopyran-4-one (1) and (2R)-2,3-dihydro-2-methyl-5-methoxy-benzopyran-4-one (3). The structures of 2 and 4 were established on the basis of comprehensive spectroscopic analysis, mainly using 1D and 2D NMR experiments. The benzopyrans 1 and 2 showed weak in vitro antifungal activity against Cladosporium sphaerospermum and C. cladosporioides. Analyses of the biological activities were also carried out on HeLa (human cervix tumor) and CHO (Chinese hamster ovary) cells, aiming to evaluate their potential effects on mammalian cell line proliferation. Results from both cell lines indicated that compound 2 was able to induce cell proliferation: 70% on HeLa cells and 25% on CHO cells.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16038954 DOI: 10.1016/j.phytochem.2005.04.043
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072