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IDX184

Catalog No. T27586Cas No. 1036915-08-8
Alias IDX-184, IDX 184

IDX184 is a potent, orally active, targeted HCV polymerase inhibitor and nucleoside polymerase.IDX184 effectively inhibits HCV polymerase (IC50=0.31 μM, Ki=52.3 nM). IDX184 is a liver-targeted nucleotide prodrug with anti-HCV activity that inhibits HCV NS5B polymerase and can be used in combination with pegylated interferon-α2a and ribavirin for the primary treatment of chronic hepatitis C. It has been shown to inhibit HCV polymerase and nucleoside polymerase.

IDX184

IDX184

Purity: 99.29%
Catalog No. T27586Alias IDX-184, IDX 184Cas No. 1036915-08-8
IDX184 is a potent, orally active, targeted HCV polymerase inhibitor and nucleoside polymerase.IDX184 effectively inhibits HCV polymerase (IC50=0.31 μM, Ki=52.3 nM). IDX184 is a liver-targeted nucleotide prodrug with anti-HCV activity that inhibits HCV NS5B polymerase and can be used in combination with pegylated interferon-α2a and ribavirin for the primary treatment of chronic hepatitis C. It has been shown to inhibit HCV polymerase and nucleoside polymerase.
Pack SizePriceAvailabilityQuantity
1 mg$191In Stock
5 mg$480In Stock
10 mg$687In Stock
25 mg$1,080In Stock
50 mg$1,480In Stock
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Purity:99.29%
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Product Introduction

Bioactivity
Description
IDX184 is a potent, orally active, targeted HCV polymerase inhibitor and nucleoside polymerase.IDX184 effectively inhibits HCV polymerase (IC50=0.31 μM, Ki=52.3 nM). IDX184 is a liver-targeted nucleotide prodrug with anti-HCV activity that inhibits HCV NS5B polymerase and can be used in combination with pegylated interferon-α2a and ribavirin for the primary treatment of chronic hepatitis C. It has been shown to inhibit HCV polymerase and nucleoside polymerase.
Targets&IC50
HCV polymerase:0.31 μM (IC50), HCV polymerase:52.3 nM (Ki)
In vitro
IDX184, a liver-targeted prodrug of the nucleotide 2′-MeG-MP, serves as a hepatitis C virus polymerase inhibitor with liver-specific targeting.[1]
IDX184 is not toxic (CC50>100μM) in any tested cell line.[2]
IDX184 is a second-generation, orally bioavailable nucleotide prodrug designed to provide increased anti-HCV efficacy and safety versus the parent nucleoside. In HCV replicon testing, IDX184 is the most potent inhibitor (EC50=0.3-0.45 μM) compared to any of the 2’ or 4’ modified nucleosides (EC50=4-6 μM) and is also highly inhibitory in the JFH-1 infectious system (EC50=0.06-0.11 μM).[2]
AliasIDX-184, IDX 184
Chemical Properties
Molecular Weight626.62
FormulaC25H35N6O9PS
Cas No.1036915-08-8
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (79.79 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.5959 mL7.9793 mL15.9586 mL79.7932 mL
5 mM0.3192 mL1.5959 mL3.1917 mL15.9586 mL
10 mM0.1596 mL0.7979 mL1.5959 mL7.9793 mL
20 mM0.0798 mL0.3990 mL0.7979 mL3.9897 mL
50 mM0.0319 mL0.1596 mL0.3192 mL1.5959 mL

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