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Novel symmetrical phenylenediamines as potential anti-hepatitis C virus agents.


ABSTRACT: BACKGROUND:Despite the great progress made in the last 10 years, alternative strategies might help improving definitive treatment options against hepatitis C virus infection. METHODS:With the aim of identifying novel inhibitors of the hepatitis C virus-1b replication targeting the viral NS3 helicase, the structures of previously reported symmetrical inhibitors of this enzyme were rationally modified, and according to docking-based studies, four novel scaffolds were selected for synthesis and evaluation in the hepatitis C virus-1b subgenomic replicon assay. RESULTS:Among the newly designed compounds, one new structural family was found to inhibit the hepatitis C virus-1b replication in the micromolar range. This scaffold was chosen for further exploration and different novel analogues were synthesised and evaluated. CONCLUSIONS:Different new inhibitors of the hepatitis C virus genotype 1b replication were identified. Some of the new compounds show mild inhibition of the NS3 helicase enzyme.

SUBMITTER: Bassetto M 

PROVIDER: S-EPMC5890509 | biostudies-literature | 2015 Dec

REPOSITORIES: biostudies-literature

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Novel symmetrical phenylenediamines as potential anti-hepatitis C virus agents.

Bassetto Marcella M   Ferla Salvatore S   Leyssen Pieter P   Neyts Johan J   Yerukhimovich Mark M MM   Frick David N DN   O'Donnell Rachel R   Brancale Andrea A  

Antiviral chemistry & chemotherapy 20151201 5-6


<h4>Background</h4>Despite the great progress made in the last 10 years, alternative strategies might help improving definitive treatment options against hepatitis C virus infection.<h4>Methods</h4>With the aim of identifying novel inhibitors of the hepatitis C virus-1b replication targeting the viral NS3 helicase, the structures of previously reported symmetrical inhibitors of this enzyme were rationally modified, and according to docking-based studies, four novel scaffolds were selected for sy  ...[more]

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