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Ribavirin

Ribavirin
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Purity:99.83%
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Ribavirin

Catalog No. T0684Cas No. 36791-04-5
Ribavirin (Tribavirin) is a synthetic nucleoside analog of ribofuranose with activity against hepatitis C virus and other RNA viruses.
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Pack SizePrice/USDAvailabilityQuantity
50 mg$39In Stock
100 mg$48In Stock
200 mg$78In Stock
500 mg$163In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Product Introduction

Bioactivity
Description
Ribavirin (Tribavirin) is a synthetic nucleoside analog of ribofuranose with activity against hepatitis C virus and other RNA viruses.
In vivo
ALT, AST activities and bilirubin levels are significantly loared by administration of JAT in combination with interferon and ribavirin (p<0.01). JAT, interferon or ribavirin alone with CCl4, livers appear to exhibit some liver protection against CCl4 as evident by the presence of normal hepatic cords, absence of necrosis and lesser fatty infiltration. Groups treated with JAT, Peg-interferon and ribavirin separately or in combination shows reduction in the expression of TGF- β and Bax. In the group treated by triple combination of interferon, ribavirin, and JAT, the expression level of p53 is markedly reduced[6]. Ribavirin capsules (400 mg of ribavirin)-treated Wistar rats show a significant decrease in activin-A and significant increase in follistatin at the serum and liver levels. Ribavirin has strong antiviral activity only when ribavirin is combined with either IFN-α or Peg-IFN-α[7]. Ribavirin (40 mg/kg, p.o.) significantly improves the antiviral efficacy of CM-10-18 in mice. Ribavirin inhibits DENV virus infection in cultured cells, but it is ineffective in reducing viremia in monotherapy[8].
Cell Research
The effect of Ribavirin on microglial cell viability is evaluated by the sulforhodamine B (SRB) chemosensitivity assay. Briefly, LPS-stimulated microglial cells are incubated for 48 h in the presence or absence of Ribavirin. Afterward, the cells are fixed in 10% (w/v) trichloroacetic acid for 1 h at 4°C, rinsed in tap water and stained with 0.4% (w/v) SRB in 1% acetic acid (100 μL/well) for 30 min at room temperature (RT). The cells are then rinsed three times in 1% acetic acid to remove the unbound stain. The protein bound stain is extracted with 200 μL 10 mM Tris base (pH 10.5) per well. The optical density is read at 540 nm, with correction at 670 nm. The results are presented as percentage of the control (non-stimulated/untreated microglial cells), that is arbitrarily set to 100%.
AliasTribavirin, ICN-1229, NSC-163039, RTCA
Chemical Properties
Molecular Weight244.2
FormulaC8H12N4O5
Cas No.36791-04-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
H2O: 24.4 mg/mL (100 mM)
DMSO: 45 mg/mL (184.28 mM)
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM4.0950 mL20.4750 mL40.9500 mL204.7502 mL
5 mM0.8190 mL4.0950 mL8.1900 mL40.9500 mL
10 mM0.4095 mL2.0475 mL4.0950 mL20.4750 mL
20 mM0.2048 mL1.0238 mL2.0475 mL10.2375 mL
50 mM0.0819 mL0.4095 mL0.8190 mL4.0950 mL
100 mM0.0410 mL0.2048 mL0.4095 mL2.0475 mL

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