RESUMO
Two new pyrrolidine alkaloids, acanthophoraines B (1) and C (2), together with five known ones (3-7) were isolated from the red alga Acanthophora spicifera. Their structures were elucidated by extensive spectroscopic methods and single-crystal X-ray diffraction analysis. The absolute configuration of 2 was established by ECD calculation. The antibacterial activities of 1-7 were also evaluated.
Assuntos
Alcaloides , Anti-Infecciosos , Rodófitas , Alcaloides/farmacologia , Antibacterianos/farmacologia , Cristalografia por Raios X , Estrutura Molecular , Pirrolidinas/farmacologiaRESUMO
A new thiodiketopiperzaine, tedanizaine A (1), together with six known ones, were isolated from the marine sponge Tedania sp. Their structures were determined by spectroscopic analyses. The absolute configuration of 1 was established by ECD calculation. Compound 1 was the second example of thiodiketopiperazine bearing a thiazolidine unit. Cytotoxic activities of 1 were also evaluated.
