Synthesis and In Vitro Anti-Breast Cancer Activity of Trametenolic Acid B Derivatives

Article Preview

Abstract:

Six compounds were synthesized from the lanostane-type tetracyclic triterpenoid of trametenolic acid B with the aim of obtaining more active compounds, which were characterized by NMR, IR, ESI-MS and elemental analysis. Their cytotoxic activities were evaluated against the breast cancer cell line MD-AMB-231. The compound 3b exhibited the best anti-proliferative effect than trametenolic acid B and other derivatives with the IC50 of 17.78 µM.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 634-638)

Pages:

1135-1138

Citation:

Online since:

January 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] T. Henkel, R. M. Brumne, H. Muller and F. Reichel. Angew. Chem. Int. Ed. 38 (1999), p.643.

Google Scholar

[2] Y. Kashiwada, H. -K. Wang, T. Nagao, S. Kitanaka, I. Yasuda, T. Fujioka, T. Yamagishi, L. M. Cosentino, M. Kozuka, H. Okabe, Y. Ikeshiro, C. -Q. Hu, E. Yeh and K. -H. Lee. J. Nat. Prod. 61 (1998), p.1090.

DOI: 10.1021/np9800710

Google Scholar

[3] T. Honda, B. V. Rounds, L. Bore, H. J. Finlay, F. G. Favaloro, Jr., N. Suh, Y. Wang, M. B. Sporn, and G. W. Gribble. J. Med. Chem. 43 (2000), p.4233.

Google Scholar

[4] W. -L. Xiao, R. -T. Li, S. -X. Huang, J. -X. Pu and H. -D. Sun. Nat. Prod. Rep. 25 (2008), p.871.

Google Scholar

[5] K. L. Lang, I. T. Silva, L. A. Zimmermann, V. R. Machado, M. R. Teixeira, M. I. Lapuh, M. A. Galetti, J. A. Palermo, G. M. Cabrera, L. S. C. Bernardes, C. M. O. Simões, E. P. Schenkel, M. S. B. Caro and F. J. Durán. Bioorg. Med. Chem. 20 (2012).

DOI: 10.1016/j.bmc.2012.03.001

Google Scholar

[6] T. Tai, A. Akahori and T. Shingu. Phytochem. 32 (1993), p.1239.

Google Scholar

[7] H. -J. Su, Y. -F. Fann, M. -I. Chung, S. -J. Won and C. -N. Lin, J. Nat. Prod. 63 (2000), p.514.

Google Scholar

[8] R. Tanaka, M. Toyoshima and T. Yamada. Phytochem. Lett. 4 (2011), p.328.

Google Scholar

[9] T. Nakata, T. Yamada, S. Taji, H. Ohishi, S. Wada, H. Tokuda, K. Sakuma and R. Tanaka. Bioorg. Med. Chem. 15 (2007), p.257.

Google Scholar

[10] F. Cateni, P. Martinuzzi, M. Zacchigna, V. Lucchini, M. Anderluh, A. Piltaver, O. Doljak. Lett. Drug Des. Discov. 7 (2010), p.521.

DOI: 10.2174/157018010791526340

Google Scholar