Battaglia Arturo, Bernacki Ralph J, Bertucci Carlo, Bombardelli Ezio, Cimitan Samanta, Ferlini Cristiano, Fontana Gabriele, Guerrini Andrea, Riva Antonella
Istituto CNR per La Sintesi Organica e Fotoreattività "I.S.O.F.", via Gobetti 101, 40129 Bologna, Italy.
J Med Chem. 2003 Nov 6;46(23):4822-5. doi: 10.1021/jm034146v.
A series of 2'-methyl taxoids were synthesized and essayed for growth inhibition experiments conducted in human ovarian cancer cell line A2780wt and its counterparts A2780cis, A2780tax, and A2780adr, resistant to cisplatin, paclitaxel, and doxorubicin, respectively, to test the effect of this substituent on the antitumor activity. Additional experiments were performed on MCF-7 human breast cancer cell line and MCF7-R resistant to doxorubicin. In several cases these taxoids were more active than paclitaxel showing subnanomolar IC(50) values.