anti-Nipah_176
anti-Nipah_ID | anti-Nipah_176 |
anti-Nipah Drug | 4-Amino-1-[(2R,4R,5R)-5-azido-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2(1H)-pyrimidinone |
Nipah virus strain | NiV (Rec. M-GFP2AM ) |
Approaches used to test anti-Nipah activity | Experimental |
Methods used to test anti-Nipah activity | in-vitro |
Models used to test anti-Nipah activity | NCI-H358 cells or SAECs |
Mode of infection to test anti-Nipah activity | Adsorption |
Viral titer to test anti-Nipah activity | 0.25-0.5 TCID50 |
Mode of Drug delivery for anti-Nipah activity | Culture |
Time of Drug delivery for anti-Nipah activity | Pre infection 1 hour |
Duration of Drug delivery for anti-Nipah activity | 48-168 hours |
Drug concentration used to test anti-Nipah activity | 0.37 ? 0.11 μM |
Assays used to test anti-Nipah activity | Fluorescence |
anti-Nipah activity | Decrease [Effective concentration (50 %)] |
References | Lo MK, Jordan PC, Stevens S, Tam Y, Deval J, Nichol ST, Spiropoulou CF. Susceptibility of paramyxoviruses and filoviruses to inhibition by 2'-monofluoro- and 2'-difluoro-4'-azidocytidine analogs. Antiviral Res. 2018 May;153:101-113. doi: 10.1016/j.antiviral.2018.03.009 |
Comments | The enhanced antiviral activity was observed against paramyxoviruses with both 2'diF-4'N3-C and 2'F-4'N3-C compared to R1479. The activity of these compounds against negative-strand RNA viruses endorses the development of 4'-modified nucleoside analogs as broad-spectrum therapeutics against zoonotic viruses of public health importance. |