Antimitotic activity of methoxyconidiol, a meroterpene isolated from an ascidian.

Methoxyconidiol is a meroterpene previously extracted from the ascidian Aplidium aff. densum [A. Simon-Levert, A.

Temporal variation in the production of four secondary metabolites in a colonial ascidian.

The ecological and applied importance of ascidian secondary metabolites is well reported, but little is known about temporal variation in the production of these compounds. Here, we examined seasonal variation in the production of the four main pyridoacridine alkaloids (shermilamine B, kuanoniamine D, and their deacetylated forms) of the purple morph of the ascidian Cystodytes sp. Five replicate samples were taken monthly from July 2004 to February 2006, and analyzed by high-performance liquid chromatography.

Meroterpenes from the ascidian Aplidium aff. densum.

Chemical investigation of the ascidian Aplidium aff. densum collected at Masirah Island, Oman, has resulted in the isolation of five meroterpenes: two new ones, methoxyconidiol (1) and didehydroconicol (2), and three related, known compounds, 3-5. The structures of 1 and 2 were determined by a combination of mass spectrometry and one- and two-dimensional high-field NMR techniques.

Synthesis and characterization of the antitumor activities of analogues of meridine, a marine pyridoacridine alkaloid.

Marine compounds with pyridoacridine skeletons are known to exhibit interesting antitumor activities. Among these compounds, meridine has already been reported as having significant antitumor activities in vitro. We synthesized 24 analogues of meridine substituted on ring A with the aim of obtaining compounds that display significantly higher in vitro antitumor activities than meridine.

Structure-activity relationship for bromoindole carbaldehydes: effects on the sea urchin embryo cell cycle.

Natural derivatives of indole-3-carbaldehyde were isolated from the tropical marine ascidian Stomoza murravi. A series of 13 derivatives, three natural and 10 synthetic (brominated and N-methylated), were examined for their effects on cell division of sea urchin eggs. These derivatives were shown to inhibit the first mitotic cycle in a concentration-dependent manner.