Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_3745



Chemical Information
Antiviral agent IDDrugRepV_3745
Antiviral agent nameFalnidamol Drug Bank
IUPAC Name4-N-(3-chloro-4-fluorophenyl)-6-N-(1-methylpiperidin-4-yl)pyrimido[5,4-d]pyrimidine-4,6-diamine PubChem
SMILES (canonical)CN1CCC(CC1)NC2=NC=C3C(=N2)C(=NC=N3)NC4=CC(=C(C=C4)F)Cl PubChem
Molecular FormulaC18H19ClFN7 PubChem
Molecular Weight (g/mol)387.847 PubChem
InChlInChI=1S/C18H19ClFN7/c1-27-6-4-11(5-7-27)25-18-21-9-15-16(26-18)17(23-10-22-15)24-12-2-3-14(20)13(19)8-12/h2-3,8-11H,4-7H2,1H3,(H,21,25,26)(H,22,23,24) PubChem
Common NameFalnidamol Drug Bank
Structural Information
  
Clinical Information
Primary Indication (Clinical trial phases)Investigational Drug Bank
Biological Information
Primary Indication (Disease Category) Non Infectious Disease
Primary Indication (Disease)Solid Tumor
Secondary Indication Ebola virus (EBOV) NA 1976World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Model system) [cell lines/ animal models]A549
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Time of drug delivery) Post infection
Secondary Indication (Duration of drug delivery)72 hours
Secondary Indication (Drug concentration)1.2 ± 0.2 μM
Secondary Indication (Cell based assay)Firefly luciferase assay
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) EC50 [ 50 % ]
Secondary Indication (Cytotoxicity)24.3 ± 3.9 μM
ReferenceMohr EL, McMullan LK, Lo MK, Spengler JR, Bergeron E, Albarino CG, Shrivastava-Ranjan P, Chiang CF, Nichol ST, Spiropoulou CF, Flint M..Inhibitors of cellular kinases with broad-spectrum antiviral activity for hemorrhagic fever viruses..Antiviral Res. 2015 Aug;120:40-7. doi: 10.1016/j.antiviral.2015.05.003. Epub 2015 May 16. PMID:25986249 PubMed
CommentBIBX 1382 is an inhibitor of LASV and EBOV entry. OSU-03012 reduces LASV and EBOV virus titers and RNA levels, but does not inhibit entry or LASV Z-protein mediated assembly.