化学
马普替林
立体化学
细胞培养
三环
体外
药理学
细胞凋亡
活力测定
P-糖蛋白
作用机理
外周血单个核细胞
去甲肾上腺素转运体
抗抑郁药
生物化学
运输机
多重耐药
内分泌学
生物
海马体
抗生素
基因
遗传学
作者
Y.M. McNamara,Sandra A. Bright,Andrew J. Byrne,Suzanne M. Cloonan,Thomas McCabe,D. Clive Williams,Mary J. Meegan
标识
DOI:10.1016/j.ejmech.2013.10.076
摘要
The synthesis of a diverse library of compounds structurally related to maprotiline, a norepinephrine reuptake transporter (NET) selective antidepressant which has recently been identified as a novel in vitro antiproliferative agent against Burkitt's lymphoma (BL) cell lines is reported. A series of 9,10-dihydro-9,10-ethanoanthracenes were synthesised with modifications to the bridge of the dihydroethanoanthracene structure and with alterations to the basic side chain. A number of compounds were found to reduce cell viability to a greater extent than maprotiline in BL cell lines. In addition a related series of novel 9-substituted anthracene compounds were investigated as intermediates in the synthesis of 9,10-dihydro-9,10-ethanoanthracenes. These compounds proved the most active from the screen and were found to exert a potent caspase-dependant apoptotic effect in the BL cell lines, while having minimal effect on the viability of peripheral blood mononuclear cells (PBMCs). Compounds also displayed activity in multi-drug resistant (MDR) cells.
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