%0 Journal Article %1 RN3 %A Pereira, D.M. %A Cheel, J. %A Areche, C. %A San-Martin, A. %A Rovirosa, J. %A Silva, L.R. %A Valentao, P. %A Andrade, P.B. %D 2011 %J Marine Drugs %K activity, anti-proliferative, antimicrobial antimicrobial, assay dqcauchile epitaondiol, extracts, flabelliforme, marine-algae, meroditerpenoids, natural-products, stypopodium %N 5 %P 852-862 %R 10.3390/md9050852 %T Anti-Proliferative Activity of Meroditerpenoids Isolated from the Brown Alga Stypopodium Flabelliforme against Several Cancer Cell Lines %U /brokenurl#<Go to ISI>://WOS:000292632500013 %V 9 %X The sea constitutes one of the most promising sources of novel compounds with potential application in human therapeutics. In particular, algae have proved to be an interesting source of new bioactive compounds. In this work, six meroditerpenoids (epitaondiol, epitaondiol diacetate, epitaondiol monoacetate, stypotriol triacetate, 14-ketostypodiol diacetate and stypodiol) isolated from the brown alga Stypopodium flabelliforme were tested for their cell proliferation inhibitory activity in five cell lines. Cell lines tested included human colon adenocarcinoma (Caco-2), human neuroblastoma (SH-SY5Y), rat basophilic leukemia (RBL-2H3), murine macrophages (RAW. 267) and Chinese hamster fibroblasts (V79). Antimicrobial activity of the compounds was also evaluated against Staphylococcus aureus, Salmonella typhimurium, Proteus mirabilis, Bacillus cereus, Enterococcus faecalis and Micrococcus luteus. Overall, the compounds showed good activity against all cell lines, with SH-SY5Y and RAW. 267 being the most susceptible. Antimicrobial capacity was observed for epitaondiol monoacetate, stypotriol triacetate and stypodiol, with the first being the most active. The results suggest that these molecules deserve further studies in order to evaluate their potential as therapeutic agents.

@article{RN3, abstract = {The sea constitutes one of the most promising sources of novel compounds with potential application in human therapeutics. In particular, algae have proved to be an interesting source of new bioactive compounds. In this work, six meroditerpenoids (epitaondiol, epitaondiol diacetate, epitaondiol monoacetate, stypotriol triacetate, 14-ketostypodiol diacetate and stypodiol) isolated from the brown alga Stypopodium flabelliforme were tested for their cell proliferation inhibitory activity in five cell lines. Cell lines tested included human colon adenocarcinoma (Caco-2), human neuroblastoma (SH-SY5Y), rat basophilic leukemia (RBL-2H3), murine macrophages (RAW. 267) and Chinese hamster fibroblasts (V79). Antimicrobial activity of the compounds was also evaluated against Staphylococcus aureus, Salmonella typhimurium, Proteus mirabilis, Bacillus cereus, Enterococcus faecalis and Micrococcus luteus. Overall, the compounds showed good activity against all cell lines, with SH-SY5Y and RAW. 267 being the most susceptible. Antimicrobial capacity was observed for epitaondiol monoacetate, stypotriol triacetate and stypodiol, with the first being the most active. The results suggest that these molecules deserve further studies in order to evaluate their potential as therapeutic agents.}, added-at = {2019-12-04T03:57:35.000+0100}, author = {Pereira, D.M. and Cheel, J. and Areche, C. and San-Martin, A. and Rovirosa, J. and Silva, L.R. and Valentao, P. and Andrade, P.B.}, biburl = {https://www.bibsonomy.org/bibtex/23a0e850a8c803820f0709c6d21a8ceb7/dqcauchile}, doi = {10.3390/md9050852}, interhash = {7007376fbf713369fb8219d1a33ac574}, intrahash = {3a0e850a8c803820f0709c6d21a8ceb7}, issn = {1660-3397}, journal = {Marine Drugs}, keywords = {activity, anti-proliferative, antimicrobial antimicrobial, assay dqcauchile epitaondiol, extracts, flabelliforme, marine-algae, meroditerpenoids, natural-products, stypopodium}, number = 5, pages = {852-862}, timestamp = {2019-12-04T03:58:17.000+0100}, title = {Anti-Proliferative Activity of Meroditerpenoids Isolated from the Brown Alga Stypopodium Flabelliforme against Several Cancer Cell Lines}, type = {Journal Article}, url = {/brokenurl#<Go to ISI>://WOS:000292632500013}, volume = 9, year = 2011 }