Abstract
Four new lactone compounds, named feigrisolides A to D (1 to 4), have been isolated from Streptomyces griseus. The chemical structures were determined by detail analysis of their spectroscopic data and chemical transformations. Structurally, the feigrisolides A (1) and B (2) are hepta-lactones, feigrisolide C (3) and D (4) are 16-membered macrodiolides. Biological studies showed that feigrisolide B (2) exhibited strong antibacterial, as well as medium cyctotoxic, and antiviral activities. Feigrisolides A (1), C (3) and D (4) are medium inhibitors of 3 α-hydroxysteroid-dehydrogenase (3 α-HSD) inhibiting activity.
Cite
CITATION STYLE
Tang, Y. Q., Sattler, I., Thiericke, R., Grabley, S., & Feng, X. Z. (2000). Feigrisolides A, B, C and D, new lactones with antibacterial activities from Streptomyces griseus. Journal of Antibiotics, 53(9), 934–943. https://doi.org/10.7164/antibiotics.53.934
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.