| Conţinutul numărului revistei |
| Articolul precedent |
| Articolul urmator |
 866 0 |
 SM ISO690:2012CARBONE, Marianna, CIAVATTA, Maria-Letizia, MATHIEU, Veronique, INGELS, Aude, KISS, Robert, PASCALE, Paola, MOLLO, Ernesto, UNGUR, Nikon, GUO, Yuewei, GAVAGNIN, M. Marine Terpenoid Diacylguanidines: Structure, Synthesis, and Biological Evaluation of Naturally Occurring Actinofide and Synthetic Analogues. In: Journal of Natural Products, 2017, nr. 5(80), pp. 1339-1346. ISSN 0163-3864. DOI: https://doi.org/10.1021/acs.jnatprod.6b00941 |
| EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
 Journal of Natural Products |
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| Numărul 5(80) / 2017 / ISSN 0163-3864 | |
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| DOI:https://doi.org/10.1021/acs.jnatprod.6b00941 | |
| Pag. 1339-1346 | |
| Rezumat | |
A new diacylguanidine, actinofide (1), has been isolated from the marine mollusk Actinocyclus papillatus. The structure, exhibiting a guanidine moiety acylated by two terpenoid acid units, has been established by spectroscopic methods and secured by synthesis. Following this, a series of structural analogues have been synthesized using the same procedure. All of the compounds have been evaluated in vitro for the growth inhibitory activity against a variety of cancer cell lines. |
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| Cuvinte-cheie animals, Cell Line, tumor, Drug Screening, Humans, molecular structure, Mollusca, Structure-Activity Relationship, Terpenes, Assays, guanidine, Antitumor |
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