Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
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The Influenza Virus Polymerase Complex: An Update on Its Structure, Functions, and Significance for Antiviral Drug DesignIn vitro and in vivo efficacy of fluorodeoxycytidine analogs against highly pathogenic avian influenza H5N1, seasonal, and pandemic H1N1 virus infections.Approaches and strategies for the treatment of influenza virus infections.Efficiency of incorporation and chain termination determines the inhibition potency of 2'-modified nucleotide analogs against hepatitis C virus polymeraseThe fight against the influenza A virus H1N1: synthesis, molecular modeling, and biological evaluation of benzofurazan derivatives as viral RNA polymerase inhibitors.Development of antivirals against influenza.Anti-influenza virus agents: synthesis and mode of action.Antimicrobial strategies: inhibition of viral polymerases by 3'-hydroxyl nucleosides.Yet another ten stories on antiviral drug discovery (part D): paradigms, paradoxes, and paraductions.Biochemical characterization of recombinant influenza A polymerase heterotrimer complex: Endonuclease activity and evaluation of inhibitors.Mutagenic analysis of the 5' arm of the influenza A virus virion RNA promoter defines the sequence requirements for endonuclease activity.Hairpin loop structure in the 3' arm of the influenza A virus virion RNA promoter is required for endonuclease activity.An in vitro fluorescence based study of initiation of RNA synthesis by influenza B polymerase.Distinct Effects of T-705 (Favipiravir) and Ribavirin on Influenza Virus Replication and Viral RNA Synthesis.Biochemical characterization of recombinant influenza A polymerase heterotrimer complex: Polymerase activity and mechanisms of action of nucleotide analogs.Mechanism of action of T-705 ribosyl triphosphate against influenza virus RNA polymerase.2'-deoxy-4'-azido nucleoside analogs are highly potent inhibitors of hepatitis C virus replication despite the lack of 2'-alpha-hydroxyl groups.Synthesis and biological evaluation of purine 2'-fluoro-2'-deoxyriboside ProTides as anti-influenza virus agents.RNA and DNA hydrolysis are catalyzed by the influenza virus endonuclease.Nucleosides for the treatment of respiratory RNA virus infections.
P2860
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P2860
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@en
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@nl
type
label
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@en
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@nl
prefLabel
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@en
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@nl
P2093
P2860
P356
P1476
Inhibition of influenza virus transcription by 2'-deoxy-2'-fluoroguanosine.
@en
P2093
P2860
P304
P356
10.1128/AAC.39.11.2454
P407
P577
1995-11-01T00:00:00Z