Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_3420



Chemical Information
Antiviral agent IDDrugRepV_3420
Antiviral agent nameDapivirine Drug Bank
IUPAC Name4-[[4-(2,4,6-trimethylanilino)pyrimidin-2-yl]amino]benzonitrile PubChem
SMILES (canonical)CC1=CC(=C(C(=C1)C)NC2=NC(=NC=C2)NC3=CC=C(C=C3)C#N)C PubChem
Molecular FormulaC20H19N5 PubChem
Molecular Weight (g/mol)329.407 PubChem
InChlInChI=1S/C20H19N5/c1-13-10-14(2)19(15(3)11-13)24-18-8-9-22-20(25-18)23-17-6-4-16(12-21)5-7-17/h4-11H,1-3H3,(H2,22,23,24,25) PubChem
Common NameDapivirine Drug Bank
Synonyms4-((4-(mesitylamino)pyrimidin-2-yl)amino)benzonitrile | Dapivirinum | DapivirineTMC-120 | Ring-004 | 4-[[4-(2,4,6-trimethylanilino)pyrimidin-2-yl]amino]benzonitrile
Structural Information
  
Clinical Information
Primary Indication (Clinical trial phases)Investigational Drug Bank
Biological Information
Primary Indication (Disease Category) Infectious Disease
Primary Indication (Disease)Acquired immunodeficiency syndrome
Secondary Indication Influenza virus (IAV) H1N1 A/WSN/1933 (H1N1)World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Model system) [cell lines/ animal models]A549
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)0.01 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)3 μM
Secondary Indication (Cell based assay)Plaque assay
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) Log reduction [ 1.7 Log ]
ReferenceHu Y, Zhang J, Musharrafieh RG, Ma C, Hau R, Wang J..Discovery of dapivirine, a nonnucleoside HIV-1 reverse transcriptase inhibitor, as a broad-spectrum.Antiviral Res. 2017 Sep;145:103-113. doi: 10.1016/j.antiviral.2017.07.016. Epub 2017 Aug 2. PMID:28778830 PubMed
CommentDapivirine inhibits the nuclear entry of viral ribonucleoproteins at the early stage of viral replication. As a result, viral RNA and protein synthesis were inhibited