Callophycoic acids and callophycols from the Fijian red alga Callophycus serratus

Callophycoic acids A−H (1−8) and callophycols A and B (9 and 10) were isolated from extracts of the Fijian red alga Callophycus serratus, and identified by NMR, X-ray, and mass spectral analyses. These natural products represent four novel carbon skeletons, providing the first examples of diterpene−benzoic acids and diterpene−phenols in macroalgae. Compounds 1−10 exhibited antibacterial, antimalarial, and anticancer activity, although they are less bioactive than diterpene-benzoate macrolides previously isolated from this red alga

Bromophycolides C-I from the Fijian red alga Callophycus serratu

Bromophycolides C-I (1-7) were isolated from extracts of the Fijian red alga Callophycus serratus and identified by NMR and mass spectral techniques. These novel natural products share a carbon skeleton and biosynthetic origin with previously identified bromophycolides A (8) and B (9), which form a rare group of diterpene-benzoate macrolides. Bromophycolides C-I (1-7) displayed modest antineoplastic activity against a range of human tumor cell lines

Antineoplastic diterpene-benzoate macrolides from the Fijian red alga Callophycus serratus

Three diterpene-benzoate natural products, with novel carbon skeletons and an unusual proposed biosynthesis, were isolated from extracts of the Fijian red alga Callophycus serratus and identified by a combination of X-ray crystallographic, NMR, and mass spectral analyses. Bromophycolide A (1) displayed cytotoxicity against several human tumor cell lines via specific apoptotic cell death. This represents the first discovery of natural products incorporating a diterpene and benzoate skeleton into a macrolide system

Novel antineoplastic diterpene-benzoates from the Fijian red alga Callophycus serratus

Red macroalgae are well-known for the production of brominated metabolites, including terpenoids and phenols, yet some taxa within the Rhodophyta remain relatively unstudied. Herein, we report the discovery of unusual diterpene-benzoate natural products representing three novel carbon skeletons, from the red alga Callophycus serratus collected in Fiji. Included among the new compounds were 15- and 16-membered macrolides as well as non-macrocyclic diterpene-benzoic acid structural motifs, all apparently sharing the same 27-carbon biosynthetic precursor. Biological activities of these compounds included moderate antibacterial, antiviral, and antineoplastic effects via specific apoptotic cell death