Name | Taribavirin |
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Synonyms |
Ribamidine
1-((2S,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-tetrahydrofuran-2-yl)-1H-1,2,4-triazole-3-carboxamide Prodrug of ribavirin Icn 3142 |
Description | Taribavirin is an inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus[1].Taribavirin, is a ribavirin prodrug, is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells (RBCs) and the development of hemolytic anemia[2]. |
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Related Catalog | |
In Vitro | Taribavirin (0-2 μM; 24 hours) significantly induces MCF-7 cell death, recording half inhibitory effect (IC50) of 0.756 μM in MCF-7 cells[1]. Cell Viability Assay[1] Cell Line: MCF-7 cells Concentration: 0 μM, 0.1 μM, 1 μM, 2 μM Incubation Time: 24 hours Result: Decreased MCF-7 cell growth. |
References |
Density | 2.08g/cm3 |
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Boiling Point | 595.5ºC at 760mmHg |
Molecular Formula | C8H13N5O4 |
Molecular Weight | 243.22000 |
Flash Point | 313.9ºC |
Exact Mass | 243.09700 |
PSA | 150.50000 |
Vapour Pressure | 5.01E-15mmHg at 25°C |
Index of Refraction | 1.851 |