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Daclatasvir: a team player rather than a prima donna in the treatment of hepatitis C.

AuthorsAlessio Aghemo, Raffaele De Francesco
JournalGut (Gut) Vol. 64 Issue 6 Pg. 860-2 (Jun 2015) ISSN: 1468-3288 [Electronic] England
PMID25193803 (Publication Type: Journal Article)
Chemical References
  • 8-cyclohexyl-N-((dimethylamino)sulfonyl)-1,1a,2,12b-tetrahydro-11-methoxy-1a-((3-methyl-3,8-diazabicyclo(3.2.1)oct-8-yl)carbonyl)cycloprop(d)indolo(2,1-a)(2)benzazepine-5-carboxamide
  • Antiviral Agents
  • Benzazepines
  • Carbamates
  • Heterocyclic Compounds, 3-Ring
  • Imidazoles
  • Indoles
  • NS3 protein, hepatitis C virus
  • Protease Inhibitors
  • Pyrrolidines
  • Sulfonamides
  • Viral Nonstructural Proteins
  • Simeprevir
  • Uridine Monophosphate
  • Valine
  • daclatasvir
  • Sofosbuvir
Topics
  • Antiviral Agents (administration & dosage)
  • Benzazepines (administration & dosage)
  • Carbamates
  • Drug Resistance, Viral
  • Drug Therapy, Combination
  • Genotype
  • Hepacivirus (drug effects)
  • Hepatitis C, Chronic (drug therapy, genetics, virology)
  • Heterocyclic Compounds, 3-Ring (administration & dosage)
  • Humans
  • Imidazoles (administration & dosage)
  • Indoles (administration & dosage)
  • Protease Inhibitors (administration & dosage)
  • Pyrrolidines
  • Simeprevir
  • Sofosbuvir
  • Sulfonamides (administration & dosage)
  • Uridine Monophosphate (administration & dosage, analogs & derivatives)
  • Valine (analogs & derivatives)
  • Viral Nonstructural Proteins (antagonists & inhibitors)

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