Chemical Information | |
Antiviral agent ID | DrugRepV_3745 | |
Antiviral agent name | Falnidamol | |
IUPAC Name | 4-N-(3-chloro-4-fluorophenyl)-6-N-(1-methylpiperidin-4-yl)pyrimido[5,4-d]pyrimidine-4,6-diamine | |
SMILES (canonical) | CN1CCC(CC1)NC2=NC=C3C(=N2)C(=NC=N3)NC4=CC(=C(C=C4)F)Cl | |
Molecular Formula | C18H19ClFN7 | |
Molecular Weight (g/mol) | 387.847 | |
InChl | InChI=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) | |
Common Name | Falnidamol | |
Structural Information | |
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Clinical Information | |
Primary Indication (Clinical trial phases) | Investigational
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Biological Information | |
Primary Indication (Disease Category) | Non Infectious Disease
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Primary Indication (Disease) | Solid Tumor
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Secondary Indication | Ebola virus (EBOV) NA 1976 | |
Secondary Indication (Approaches) | Experimental | |
Secondary Indication (Methods) | In-vitro | |
Secondary Indication (Model system) [cell lines/ animal models] | A549
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Secondary Indication (Mode of drug delivery) | Culture
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Secondary Indication (Time of drug delivery) | Post infection
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Secondary Indication (Duration of drug delivery) | 72 hours
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Secondary Indication (Drug concentration) | 1.2 ± 0.2 μM
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Secondary Indication (Cell based assay) | Firefly luciferase assay
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Secondary Indication (Change) | Decrease
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Secondary Indication (Type of Inhibition) | EC50 [ 50 % ] | |
Secondary Indication (Cytotoxicity) | 24.3 ± 3.9 μM | |
Reference | Mohr 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
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Comment | BIBX 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.
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