Three new butenolides, caulerpalide A and a pair of enantiomers, (+)-caulerpalide B and (À )-caulerpalide B, together with seven known compounds, have been isolated from the green alga Caulerpa racemosa var. turbinata. All these structures were determined by spectroscopic techniques. The absolute configurations of caulerpalide A, (+)-caulerpalide B and (À )-caulerpalide B were elucidated by the method of ECD calculation. This is the first separation of butenolides from the algae of genus Caulerpa. Additionally, the antibacterial activities of the nine isolated compounds were also evaluated.[a][b] Data can be exchanged freely.

In this paper, eight new galaxamide analogues (Z-1~Z-8) were synthesized and evaluated for their cytotoxic activities against five cancer cell lines, MCF-7, MD-MBA-231, HepG2, Hela, and A549, using MTT assays. The modified analogue Z-6 displayed broad spectrum cytotoxic activity toward each tested cell line with IC50 values of 1.65 ± 0.30 (MCF-7), 2.91 ± 0.17 (HepG2), 4.59 ± 0.27 (MD-MBA-231), 5.69 ± 0.37 (Hela), and 5.96 ± 0.41 (A549) μg/mL, respectively. The galaxamides Z-3 and Z-6 induced concentration-dependent apoptosis of the MCF-7 cells after 72 h as evaluated by the flow cytometry experiment. The results showed that these compounds could induce MCF-7 cell apoptosis by arresting the G0/G1 phase of the cell cycle and finally achieving the effect of inhibiting the proliferation of MCF-7 cells.

A new pyrrolidine alkaloid, acanthophoraine A (1), along with six known alkaloids (2-7), had been isolated from the red alga Acanthophora spicifera. The structures of these compounds were identified by spectroscopic analyses. The absolute configuration of 1 was established by ECD calculation.Compound 1 represents the first example of N-isobutyl pyrrolidone with an urea arm. The antimicrobial activity of 1 was also evaluated.

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Caulerspiros A (1) and B (2), a new pair of α-tocopheroid isomers, with five known compounds (3-7) were isolated from the green alga Caulerpa racemosa var. turbinata. Their structures were elucidated by the method of comprehensive spectroscopy. The absolute configurations of 1 and 2 were established by the methods of ECD calculation and comparing with the previously reported literatures.Compounds 1 and 2 represented the rare examples of α-tocopherol derivatives possessing a core unit of 1-oxaspiro[4.4]non 7-en-6-one. Additionally, the antibacterial activities of these seven compounds were also evaluated. However, the MIC value of all compounds exceed 128 μg/ml, none of them showed antibacterial activities.