Synthesis and Antileukemic Activity of Novel 2-(4-(2,4-dimethoxybenzoyl)phenoxy)-1-(4-(3-(piperidin-4-yl)propyl)piperidin-1-yl)ethanone Derivatives
作者:Kambappa Vinaya、Chandagirikoppal V. Kavitha、Doddakunche S. Prasanna、Siddappa Chandrappa、Somasagara R. Ranganatha、Sathees C. Raghavan、Kanchugarakoppal S. Rangappa
DOI:10.1111/j.1747-0285.2011.01307.x
日期:2012.3
A series of novel 2‐(4‐(2,4‐dimethoxybenzoyl)phenoxy)‐1‐(4‐(3‐(piperidin‐4‐yl)propyl) piperidin‐1‐yl)ethanone derivatives 9(a–e) and 10(a–g) were synthesized and characterized by 1H NMR, IR, mass spectral, and elemental analysis. These novel compounds were evaluated for their antileukemic activity against two human leukemic cell lines (K562 and CEM) by using the 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐di
一系列新颖的2-(4-(2,4-二甲氧基苯甲酰基)苯氧基)-1-(4-(3-(哌啶-4-基)丙基)哌啶-1-基)乙酮衍生物9(a - e)和10(一-克)被合成和表征通过1 H NMR,IR,质谱和元素分析。通过使用3-(4,5-二甲基噻唑-2-基)-2-,5-二苯基四唑溴化物测定法评估了这些新型化合物对两种人类白血病细胞系(K562和CEM)的抗白血病活性。一些测试化合物显示出良好的抗增殖活性与IC 50个值范围为1.6至8.0μ米。化合物9c,9e,以及在苯环对位上具有吸电子卤素取代基的10f,对测试的人类白血病细胞(K562和CEM)显示出优异的体外效能。