Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_0031



Chemical Information
Antiviral agent IDDrugRepV_0031
Antiviral agent nameNitazoxanide Drug Bank
IUPAC Name[2-[(5-nitro-1,3-thiazol-2-yl)carbamoyl]phenyl] acetate PubChem
SMILES (canonical)CC(=O)OC1=CC=CC=C1C(=O)NC2=NC=C(S2)[N+](=O)[O-] PubChem
Molecular FormulaC12H9N3O5S PubChem
Molecular Weight (g/mol)307.28 PubChem
InChlInChI=1S/C12H9N3O5S/c1-7(16)20-9-5-3-2-4-8(9)11(17)14-12-13-6-10(21-12)15(18)19/h2-6H,1H3,(H,13,14,17) PubChem
Common NameNitazoxanide Drug Bank
SynonymsNitaxozanid | Nitaxozanide | Nitazoxanida | Nitazoxanidum
Structural Information
  
Clinical Information
CategoryAntiparasitic products, Insectisides and Repellents
Primary Indication (Clinical trial phases)Approved, Investigational, Vet approved Drug Bank
Secondary Indication (Clinical trial phases)Phase III
Biological Information
Primary Indication (Disease Category) Infectious Disease
Primary Indication (Disease)Diarrhea
Secondary Indication Influenza virus (IAV) NA B (Yamagata lineage)World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Potential drug target)ERp57
Secondary Indication (Model system) [cell lines/ animal models]MDCK-SIAT
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)1000 FFU
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Time of drug delivery) After adsorption
Secondary Indication (Duration of drug delivery)24 hours
Secondary Indication (Drug concentration)0.6 μM
Secondary Indication (Cell based assay)Focus forming reduction assay
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) EC50 [ 50 % ]
Secondary Indication (Cytotoxicity)61.2± 15.1 μM
ReferenceTilmanis D, van Baalen C, Oh DY, Rossignol JF, Hurt AC..The susceptibility of circulating human influenza viruses to tizoxanide, the active metabolite of ni.Antiviral Res. 2017 Nov;147:142-148. doi: 10.1016/j.antiviral.2017.10.002. Epub 2017 Oct 3. PMID:28986103 PubMed
CommentActive circulating metabolite of nitazoxanide. This is the first report on the susceptibility of circulating viruses to tizoxanide. The focus reduction assay format described is sensitive, robust, and less laborious than traditional cell based antiviral assays, making it highly suitable for the surveillance of tizoxanide susceptibility in circulating seasonal influenza viruses