Literature DB >> 16279767

SAR by MS: discovery of a new class of RNA-binding small molecules for the hepatitis C virus: internal ribosome entry site IIA subdomain.

Punit P Seth1, Alycia Miyaji, Elizabeth A Jefferson, Kristin A Sannes-Lowery, Stephen A Osgood, Stephanie S Propp, Ray Ranken, Christian Massire, Rangarajan Sampath, David J Ecker, Eric E Swayze, Richard H Griffey.   

Abstract

A new class of small molecules that bind the HCV RNA IRES IIA subdomain with sub-micromolar affinity is reported. The benzimidazole 'hit' 1 with a KD approximately 100 microM to a 29-mer RNA model of Domain IIA was identified from a 180000-member library using mass spectrometry-based screening methods. Further MS-assisted SAR (structure-activity relationships) studies afforded benzimidazole derivatives with sub-micromolar binding affinity for the IIA RNA construct. The optimized benzimidazoles demonstrated activity in a cellular replicon assay at concentrations comparable to their KD for the RNA target.

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Year:  2005        PMID: 16279767     DOI: 10.1021/jm050815o

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  53 in total

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Review 5.  Functional RNA structures throughout the Hepatitis C Virus genome.

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Journal:  Curr Opin Virol       Date:  2017-05-13       Impact factor: 7.090

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8.  2-Aminobenzoxazole ligands of the hepatitis C virus internal ribosome entry site.

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Journal:  Bioorg Med Chem Lett       Date:  2014-06-04       Impact factor: 2.823

9.  Ligand-responsive RNA mechanical switches.

Authors:  Mark A Boerneke; Thomas Hermann
Journal:  RNA Biol       Date:  2015       Impact factor: 4.652

10.  Selection of cyclic peptide aptamers to HCV IRES RNA using mRNA display.

Authors:  Alexander Litovchick; Jack W Szostak
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-29       Impact factor: 11.205

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