Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_1594



Chemical Information
Antiviral agent IDDrugRepV_1594
Antiviral agent nameRibavirin Drug Bank
IUPAC Name1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide PubChem
SMILES (canonical)C1=NC(=NN1C2C(C(C(O2)CO)O)O)C(=O)N PubChem
SMILES (isomeric)C1=NC(=NN1[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)C(=O)N PubChem
Molecular FormulaC8H12N4O5 PubChem
Molecular Weight (g/mol)244.207 PubChem
InChlInChI=1S/C8H12N4O5/c9-6(16)7-10-2-12(11-7)8-5(15)4(14)3(1-13)17-8/h2-5,8,13-15H,1H2,(H2,9,16)/t3-,4-,5-,8-/m1/s1 PubChem
Common NameRibavirin Drug Bank
Synonyms1-beta-D-Ribofuranosyl-1,2,4-triazole-3-carboxamide | 1-beta-D-Ribofuranosyl-1H-1,2,4-triazole-3-carboxamide | RBV | Ribavirin | Ribavirina | Ribavirine | Ribavirinum | Tribavirin
Structural Information
  
Clinical Information
CategoryAntiinfectives For Systemic Use
Primary Indication (Clinical trial phases)Approved Drug Bank
Biological Information
Primary Indication (Disease Category) Infectious Disease
Primary Indication (Disease)Hepatitis C virus
Primary Indication (Drug target/Mode of Action) Potential E3 ubiquitin-protein ligase ariadne-2
Secondary Indication Rift Valley fever virus (RVFV) NA rMP12World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Potential drug target)Late stage in virus infection and caused a buildup of virions within cells
Secondary Indication (Model system) [cell lines/ animal models]HSAEC
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)0.1 MOI
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Time of drug delivery) Post infection
Secondary Indication (Duration of drug delivery)24 hours
Secondary Indication (Drug concentration)82 μM
Secondary Indication (Cell based assay)Plaque assay
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) Log Reduction [ 4.5 Logs reduction ]
ReferenceBenedict A, Bansal N, Senina S, Hooper I, Lundberg L, de la Fuente C, Narayanan A, Gutting B, Kehn-H.Repurposing FDA-approved drugs as therapeutics to treat Rift Valley fever virus infection..Front Microbiol. 2015 Jul 8;6:676. doi: 10.3389/fmicb.2015.00676. eCollection 2015. PMID:26217313 PubMed
CommentDisplayed intracellular infectivity. siRNA knockdown of Raf proteins indicated that non-classical targets of sorafenib are likely important for the replication of RVFV.