作者:Eric B. Lindgren、Monique A. de Brito、Thatyana R.A. Vasconcelos、Manuel O. de Moraes、Raquel C. Montenegro、Julliane D. Yoneda、Kátia Z. Leal
DOI:10.1016/j.ejmech.2014.08.039
日期:2014.10
Benzothiazole hydrazones have been synthesized and evaluated for their in vitro antiproliferative activity against three human cancer cell lines: HL-60 (leukemia), MDAMB-435 (breast) and HCT-8 (colon). The good cytotoxicity for the three cancer cell lines and theoretical profile of compounds 3o and 3p pointed them as promising lead molecules for anticancer drug design. (c) 2014 Elsevier Masson SAS. All rights reserved.