Secondary Metabolites with Anti-Inflammatory Activity from Laurencia majuscula Collected in the Red Sea.

The chemical investigation of the organic extract of the red alga collected from Hurghada reef in the Red Sea resulted in the isolation of five C acetogenins, including four tricyclic ones of the maneonene type (-) and a 5-membered one (), 15 sesquiterpenes, including seven lauranes (-), one cuparane (), one -laurane (), one snyderane (), two chamigranes (, ), two rearranged chamigranes (, ) and one aristolane (), as well as a tricyclic diterpene () and a chlorinated fatty acid derivative (). Among them, compounds -, , , , , and are new natural products. The structures and the relative configurations of the isolated natural products have been established based on extensive analysis of their NMR and MS data, while the absolute configuration of maneonenes F () and G () was determined on the basis of single-crystal X-ray diffraction analysis. The anti-inflammatory activity of compounds , , -, , -, and - was evaluated by measuring suppression of nitric oxide (NO) release in TLR4-activated RAW 264.7 macrophages in culture. All compounds, except , exhibited significant anti-inflammatory activity. Among them, metabolites , and did not exhibit any cytostatic activity at the tested concentrations. The most prominent anti-inflammatory activity, accompanied by absence of cytostatic activity at the same concentration, was exerted by compounds and with IC values of 3.69 μM and 3.55 μΜ, respectively.