|
|
|
|
|
| SILVA,EWERTON A.S. DA; LÔBO,LÍVIA T.; SILVA,GEILSON A. DA; SOUZA FILHO,ANTONIO PEDRO DA S.; SILVA,MILTON N. DA; ARRUDA,ALBERTO C.; GUILHON,GISELLE M.S.P.; SANTOS,LOURIVALDO S.; ARRUDA,MARA S.P.. |
| In some previous studies, we described the isolation of nine compounds from leaves of Derris urucu, a species found widely in the Amazon rainforest, identified as five stilbenes and four dihydroflavonols. In this work, three of these dihydroflavonols [urucuol A (1), urucuol B (2) and isotirumalin (3)] were evaluated to identify their potential as allelochemicals, and we are also reporting the isolation and structural determination of a new flavonoid [5,3′-dihydroxy-4′-methoxy-(7,6:5″,6″)-2″,2″-dimethylpyranoflavanone (4)]. We investigated the effects of the dihydroflavonols 1-3 on seed germination and radicle and hypocotyl growth of the weed Mimosa pudica, using solutions at 150 mg.L–1. Urucuol B, alone, was the substance with the greatest potential to... |
| Tipo: Info:eu-repo/semantics/article |
Palavras-chave: Derris urucu; Flavonoids; Allelopathy; Development of weeds; Seed germination. |
| Ano: 2013 |
URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652013000300881 |
| |
|
|
| MARINHO,ANDREY M.R.; MARINHO,PATRÍCIA S.B.; SANTOS,LOURIVALDO S.; RODRIGUES FILHO,EDSON; FERREIRA,IZABEL C.P.. |
| In this work we are reporting the isolation by classical methods of chromatography of six polyketides from Penicillium herquei. The compounds citreorosein ( 1) , emodin ( 2) , janthinone ( 3) , citrinin ( 4) , citrinin H1 ( 5) and dicitrinol ( 6) were identified by spectral methods of 1D and 2D NMR and MS. Compounds 1, 2 and 3 were tested against promastigotes forms of Leishmania brasiliensis and 1 and 2 were also assayed against Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis and showed good activity. |
| Tipo: Info:eu-repo/semantics/article |
Palavras-chave: Polyketides; Biological assay; P. herquei. |
| Ano: 2013 |
URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652013000300909 |
| |
|
|
|
