| Autor: |
José A. F. P. Villar, Gustavo H. R. Viana, Leandro A. Barbosa, Fernando P. Varotti, Sarah C. Simões, Andersson Barison, Estrela M. P. V. E. Souza, Marina G. da Silva, Graziele D. da Silva |
| Jazyk: |
angličtina |
| Rok vydání: |
2012 |
| Předmět: |
|
| Zdroj: |
Molecules, Vol 17, Iss 9, Pp 10331-10343 (2012) |
| Druh dokumentu: |
article |
| ISSN: |
1420-3049 |
| DOI: |
10.3390/molecules170910331 |
| Popis: |
A series of new chalcones substituted with azide/triazole groups were designed and synthesized, and their cytotoxic activity was evaluated in vitro against the HeLa cell line. O-Alkylation, Claisen-Schmidt condensation and Cu(I)-catalyzed cycloaddition of azides with terminal alkynes were applied in key steps. Fifteen compounds were tested against HeLa cells. Compound 8c was the most active molecule, with an IC50 value of 13.03 µM, similar to the value of cisplatin (7.37 µM). |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
|
