| In vitro: | | Nat Prod Commun. 2013 Mar;8(3):287-8. |  | New bioactive secondary metabolites from Bornean red alga, Laurencia similis (Ceramiales).[Pubmed:  23678792] |  | METHODS AND RESULTS:
 A Bomean red algal population of Laurencia similis Nam et Saito was analyzed for its secondary metabolite composition. Seven compounds were identified: ent-1(10)-aristolen-9beta-ol (1), (+)-aristolone (2), Axinysone B (3), 9-aristolen-1alpha-ol (4), 2,3,5,6-tetrabromoindole (5), 1-methyl-2,3,5,6-tetrabromoindole (6), and 1-methyl-2,3,5-tribromoindole (7). Compound 1 was identified as a new optical isomer of 1(10)-aristolen-9beta-ol.
 CONCLUSIONS:
 Compounds 1, 4 and 5 exhibited good antibacterial activity against antibiotic resistant clinical bacteria and cytotoxic effects against selected cancer cell lines.
 |  | Phytochemistry Letters, 2013, 6(3):345-349. |  | Novel spiro-sesquiterpene from the mushroom Anthracophyllum sp. BCC18695[Reference: WebLink] |  | METHODS AND RESULTS:
 A novel spiro-sesquiterpene, anthracophyllic acid (1), and a new aristolane sesquiterpene, anthracophyllone (2), were isolated from the mushroom Anthracophyllum sp. BCC18695, together with seven known compounds including aurisins A (3), G (4), K (5), nambinone A, nambinone C, axinysone A, and Axinysone B. The relative configuration of 1 and the hitherto unknown absolute stereochemistry of 3 were determined based on X-ray spectroscopic data.
 CONCLUSIONS:
 Biological activities including antimalarial activity against Plasmodium falciparum K1 strain, antibacterial property against Bacillus cereus, and cytotoxicity against MCF-7, KB, NCI-H187, and Vero cells of the isolated compounds were also evaluated.
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