Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596796 | Bioorganic & Medicinal Chemistry Letters | 2010 | 5 Pages |
Abstract
A new aryl-hydrazide l-glutamic acid derivative, pygmeine (3), was isolated from a methanolic extract of Lichina pygmaea, a marine lichen. Synthetic derivatives obtained via a two-step coupling of l-glutamic acid with phenylhydrazine moieties were useful to elucidate the structure of 3 and to carry out biological assays. Thus, the cytotoxicity of the ortho-, meta-, and para-hydroxyl isomers along with their respective benzyl intermediates, and a natural methoxylated analog, were evaluated on murine and human melanoma cells (B16, A375). The para-hydroxyl isomer 6 was found to be the most active (IC50 = 1.6 μM) on B16 cells.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Catherine Roullier, Marylène Chollet-Krugler, Pierre van de Weghe, Françoise Lohézic-Le Devehat, Joël Boustie,