Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_1947



Chemical Information
Antiviral agent IDDrugRepV_1947
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
Structural Information
  
Clinical Information
CategoryAntiparasitic products, Insectisides and Repellents
Primary Indication (Clinical trial phases)Approved, Investigational, Vet approved Drug Bank
Biological Information
Primary Indication (Disease Category) Infectious Disease
Primary Indication (Disease)Diarrhea
Secondary Indication Zika virus (ZIKV) NA SZ-WIV01World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Potential drug target)Host Factor- depleting intracellular Ca2+ stores
Secondary Indication (Model system) [cell lines/ animal models]Vero
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)48 hours
Secondary Indication (Drug concentration)10 μM
Secondary Indication (Cell based assay)Real-time PCR
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) Relative intracellular RNA level [ 20 NA ]
ReferenceCao RY, Xu YF, Zhang TH, Yang JJ, Yuan Y, Hao P, Shi Y, Zhong J, Zhong W..Pediatric Drug Nitazoxanide: A Potential Choice for Control of Zika..Open Forum Infect Dis. 2017 Feb 3;4(1):ofx009. doi: 10.1093/ofid/ofx009. eCollection 2017 Winter. PMID:28480282 PubMed
CommentNitazoxanide and its bioactive metabolite, tizoxanide have anti-ZIKV potential in vitro and exerts antiviral effect possibly by targeting the viral postattachment step.