Synthesis and anti-proliferative activity of a small library of 7-substituted 5H-pyrrole [1,2-a][3,1]benzoxazin-5-one derivatives

被引:6
|
作者
Badolato, Mariateresa [1 ]
Carullo, Gabriele [1 ]
Armentano, Biagio [1 ]
Panza, Salvatore [1 ]
Malivindi, Rocco [1 ]
Aiello, Francesca [1 ]
机构
[1] Univ Calabria, Dipartimento Farm & Sci Salute & Nutr, Arcavacata Rende, Edificio Polifunz, I-87036 Arcavacata Di Rende, CS, Italy
关键词
Benzoxazin-5-one; Anti-proliferative activity; Suzuki-Miyaura cross coupling; Cell cycle analysis; Cancer cell lines; BREAST-CANCER CELLS; IDENTIFICATION; BENZOXAZINONE; ANTAGONISTS;
D O I
10.1016/j.bmcl.2017.05.046
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, we investigate the anti-proliferative activity of a small library of 7-substituted 5H-pyrrolo [1,2-a][3,1]benzoxazin-5-one derivatives, against a panel of human cancer cell lines. We reported the synthesis of these compounds in a previous work. 7-Bromo-5H-benzo[d]pyrrolo[2,1-b][1,3]oxazin-5-one showed a promising anti-proliferative effect. As starting material for Suzuki-Miyaura cross coupling reaction, it was selected for the design and the synthesis of six further derivatives, with the aim to better define structure-activity relationships. The anti-proliferative MTT assay revealed a dose-dependent reduction of cell viability, especially for 7-([1,1'-biphenyl]-4-yl)-5H-benzo[d]pyrrolo[2,1-b][1,3]oxazin5-one. Cell cycle and western blotting analysis suggested apoptosis as possible mechanism for its anti proliferative activity. These preliminary results encourage our interest for further optimizations. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3092 / 3095
页数:4
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