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

Academic Article
Publication Date:
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.
Iris type:
01.01 Articolo in rivista
Keywords:
DNA methylation; DNMT inhibitors; docking; epigenetics; structure-activity relationships
List of contributors:
Cencioni, Chiara; Spallotta, Francesco
Authors of the University:
CENCIONI CHIARA
SPALLOTTA FRANCESCO
Handle:
https://iris.cnr.it/handle/20.500.14243/358540
Published in:
CHEMICAL BIOLOGY & DRUG DESIGN (PRINT)
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-84990181134&origin=inward
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