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Design and synthesis of N-benzoyl amino acid derivatives as DNA methylation inhibitors.

Authors :
Garella, Davide
Atlante, Sandra
Borretto, Emily
Cocco, Mattia
Giorgis, Marta
Costale, Annalisa
Stevanato, Livio
Miglio, Gianluca
Cencioni, Chiara
Fernández ‐ de Gortari, Eli
Medina ‐ Franco, José L.
Spallotta, Francesco
Gaetano, Carlo
Bertinaria, Massimo
Source :
Chemical Biology & Drug Design. Nov2016, Vol. 88 Issue 5, p664-676. 13p.
Publication Year :
2016

Abstract

The inhibition of human DNA Methyl Transferases ( DNMT) is a novel promising approach to address the epigenetic dysregulation of gene expression in different diseases. Inspired by the validated virtual screening hit NSC137546, a series of N-benzoyl amino acid analogues was synthesized and obtained compounds were assessed for their ability to inhibit DNMT-dependent DNA methylation in vitro. The biological screening allowed the definition of a set of preliminary structure-activity relationships and the identification of compounds promising for further development. Among the synthesized compounds, L-glutamic acid derivatives 22, 23, and 24 showed the highest ability to prevent DNA methylation in a total cell lysate. Compound 22 inhibited DNMT1 and DNMT3A activity in a concentration-dependent manner in the micromolar range. In addition, compound 22 proved to be stable in human serum and it was thus selected as a starting point for further biological studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17470277
Volume :
88
Issue :
5
Database :
Academic Search Index
Journal :
Chemical Biology & Drug Design
Publication Type :
Academic Journal
Accession number :
118584254
Full Text :
https://doi.org/10.1111/cbdd.12794