Literature DB >> 25676805

Targeting Influenza A Virus RNA Promoter.

Angel Bottini1,2, Surya K De1, Bainan Wu1, Changyan Tang3, Gabriele Varani3, Maurizio Pellecchia1.   

Abstract

The emergence of drug-resistant strains of influenza virus makes exploring new classes of inhibitors that target universally conserved viral targets a highly important goal. The influenza A viral genome is made up of eight single-stranded RNA-negative segments. The RNA promoter, consisting of the conserved sequences at the 3' and 5' end of each RNA genomic segment, is universally conserved among influenza A virus strains and in all segments. Previously, we reported on the identification and NMR structure of DPQ (6,7-dimethoxy-2-(1-piperazinyl)-4-quinazolinamine) (compound 1) in complex with the RNA promoter. Here, we report on additional screening and SAR studies with compound 1, including ex vivo anti-influenza activity assays, resulted in improved cellular activity against influenza A virus in the micromolar range.
© 2015 John Wiley & Sons A/S.

Entities:  

Keywords:  chemical biology; drug design; drug discovery

Mesh:

Substances:

Year:  2015        PMID: 25676805      PMCID: PMC4531110          DOI: 10.1111/cbdd.12534

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  23 in total

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Authors:  S González; J Ortín
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Review 3.  Protein families and RNA recognition.

Authors:  Yu Chen; Gabriele Varani
Journal:  FEBS J       Date:  2005-05       Impact factor: 5.542

4.  Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery.

Authors:  R A Houghten; C Pinilla; S E Blondelle; J R Appel; C T Dooley; J H Cuervo
Journal:  Nature       Date:  1991-11-07       Impact factor: 49.962

5.  The use of positional scanning synthetic peptide combinatorial libraries for the rapid determination of opioid receptor ligands.

Authors:  C T Dooley; R A Houghten
Journal:  Life Sci       Date:  1993       Impact factor: 5.037

Review 6.  Drugs in development for influenza.

Authors:  David A Boltz; Jerry R Aldridge; Robert G Webster; Elena A Govorkova
Journal:  Drugs       Date:  2010-07-30       Impact factor: 9.546

Review 7.  Drug sensitivity, drug-resistant mutations, and structures of three conductance domains of viral porins.

Authors:  Mukesh Sharma; Conggang Li; David D Busath; Huan-Xiang Zhou; Timothy A Cross
Journal:  Biochim Biophys Acta       Date:  2010-07-23

8.  Identification of small molecules that interfere with H1N1 influenza A viral replication.

Authors:  Angel Bottini; Surya K De; Bas J G Baaten; Bainan Wu; Elisa Barile; Stephen Soonthornvacharin; John L Stebbins; Linda M Bradley; Sumit K Chanda; Maurizio Pellecchia
Journal:  ChemMedChem       Date:  2012-11-08       Impact factor: 3.466

9.  Small molecule inhibitors of influenza A and B viruses that act by disrupting subunit interactions of the viral polymerase.

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Review 10.  Antiviral agents active against influenza A viruses.

Authors:  Erik De Clercq
Journal:  Nat Rev Drug Discov       Date:  2006-12       Impact factor: 84.694

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3.  SILCS-RNA: Toward a Structure-Based Drug Design Approach for Targeting RNAs with Small Molecules.

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7.  Subsite Ligand Recognition and Cooperativity in the TPP Riboswitch: Implications for Fragment-Linking in RNA Ligand Discovery.

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Journal:  ACS Chem Biol       Date:  2022-01-21       Impact factor: 5.100

Review 8.  The Emerging Role of RNA as a Therapeutic Target for Small Molecules.

Authors:  Colleen M Connelly; Michelle H Moon; John S Schneekloth
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Review 9.  Recent Advances in Developing Small Molecules Targeting Nucleic Acid.

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Review 10.  Structural and Functional Motifs in Influenza Virus RNAs.

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Journal:  Front Microbiol       Date:  2018-03-29       Impact factor: 5.640

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