Literature DB >> 22425031

Structure-activity relationship of selected polyphenol derivatives as inhibitors of Bax/Bcl-xL interaction.

Duc Duy Vo1, Fabien Gautier, Philippe Juin, René Grée.   

Abstract

This paper describes the synthesis of nine selected diaryl/heteroaryl-containing phenol and polyphenol derivatives which have been evaluated against Bax/Bcl-xL interaction in comparison with ABT-737. Using a BRET assay, six of these derivatives exhibit activity comparable to ABT-737 to disrupt Bax/Bcl-xL interaction. These preliminary results demonstrate that such polyphenol-derived molecules are attractive compounds regarding anticancer activity and that the phenol at position 3 is important regarding disruption of Bax/Bcl-xL interaction.
Copyright © 2012 Elsevier Masson SAS. All rights reserved.

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Year:  2012        PMID: 22425031     DOI: 10.1016/j.ejmech.2012.02.036

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  2 in total

1.  Molecular diversity of phenothiazines: design and synthesis of phenothiazine-dithiocarbamate hybrids as potential cell cycle blockers.

Authors:  Dong-Jun Fu; Ruo-Han Zhao; Jia-Huan Li; Jia-Jia Yang; Ruo-Wang Mao; Bo-Wen Wu; Ping Li; Xiao-Lin Zi; Qing-Qing Zhang; Hui-Jie Cai; Sai-Yang Zhang; Yan-Bing Zhang; Hong-Min Liu
Journal:  Mol Divers       Date:  2017-08-07       Impact factor: 2.943

2.  Bcl-xL controls a switch between cell death modes during mitotic arrest.

Authors:  N Bah; L Maillet; J Ryan; S Dubreil; F Gautier; A Letai; P Juin; S Barillé-Nion
Journal:  Cell Death Dis       Date:  2014-06-12       Impact factor: 8.469

  2 in total

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