Literature DB >> 28549734

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

Mariateresa Badolato1, Gabriele Carullo1, Biagio Armentano1, Salvatore Panza1, Rocco Malivindi1, Francesca Aiello2.   

Abstract

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]oxazin-5-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.
Copyright © 2017 Elsevier Ltd. All rights reserved.

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Keywords:  Anti-proliferative activity; Benzoxazin-5-one; Cancer cell lines; Cell cycle analysis; Suzuki-Miyaura cross coupling

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Year:  2017        PMID: 28549734     DOI: 10.1016/j.bmcl.2017.05.046

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Synthesis and Fungicidal Activity of 1-(Carbamoylmethyl)-2-aryl-3,1-benzoxazines.

Authors:  Zi-Long Tang; Lian Wang; Jing-Zhao Tan; Yi-Chao Wan; Yin-Chun Jiao
Journal:  Molecules       Date:  2017-07-06       Impact factor: 4.411

  1 in total

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