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Development of peptoid-based heteroaryl-decorated histone deacetylase (HDAC) inhibitors with dual-stage antiplasmodial activity.

Authors :
Stopper D
de Carvalho LP
de Souza ML
Kponomaizoun CE
Winzeler EA
Held J
Hansen FK
Source :
European journal of medicinal chemistry [Eur J Med Chem] 2024 Nov 05; Vol. 277, pp. 116782. Date of Electronic Publication: 2024 Aug 16.
Publication Year :
2024

Abstract

Dynamics of epigenetic modifications such as acetylation and deacetylation of histone proteins have been shown to be crucial for the life cycle development and survival of Plasmodium falciparum, the deadliest malaria parasite. In this study, we present a novel series of peptoid-based histone deacetylase (HDAC) inhibitors incorporating nitrogen-containing bicyclic heteroaryl residues as a new generation of antiplasmodial peptoid-based HDAC inhibitors. We synthesized the HDAC inhibitors by an efficient multicomponent protocol based on the Ugi four-component reaction. The subsequent screening of 16 compounds from our mini-library identified 6i as the most promising candidate, demonstrating potent activity against asexual blood-stage parasites (IC <subscript>50</subscript> Pf3D7 = 30 nM; IC <subscript>50</subscript> PfDd2 = 98 nM), low submicromolar activity against liver-stage parasites (IC <subscript>50</subscript> PbEEF = 0.25 μM), excellent microsomal stability (t <subscript>1/2</subscript>  > 60 min), and low cytotoxicity to HEK293 cells (IC <subscript>50</subscript>  = 136 μM).<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.)

Details

Language :
English
ISSN :
1768-3254
Volume :
277
Database :
MEDLINE
Journal :
European journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
39208744
Full Text :
https://doi.org/10.1016/j.ejmech.2024.116782