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RO-9187

Catalog No. T16774Cas No. 876708-03-1

RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).

RO-9187

RO-9187

Catalog No. T16774Cas No. 876708-03-1
RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).
Pack SizePriceAvailabilityQuantity
2 mg$1135 days
5 mg$2365 days
50 mg$7216-8 weeks
100 mg$9976-8 weeks
1 mL x 10 mM (in DMSO)$2185 days
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Product Introduction

Bioactivity
Description
RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).
Targets&IC50
HCV:171 nM
In vitro
RO-9187 suppresses RNA synthesis by HCV polymerases from either HCV genotypes 1a and 1b or containing S96T or S282T point mutations with similar potencies, suggesting no cross-resistance with either R1479 or 2′-C-methyl nucleosides. RO-9187 is excellent substrates for deoxycytidine kinase and is phosphorylated with efficiencies up to 3-fold higher than deoxycytidine. The formation of RO-9187-TP increased in a time- and dose-dependent manner [1].
In vivo
Plasma exposures of RO-9187 in rats increase dose-dependently from 10 to 2000 mg/kg after oral administration. Plasma concentrations of RO-9187 (1.4 and 26 μM) are achieved in rats and dogs at the 10 mg/kg dose, respectively, with concentrations reaching up to 57 μM in rats at 2000 mg/kg/day[1].
Chemical Properties
Molecular Weight284.23
FormulaC9H12N6O5
Cas No.876708-03-1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 7.14 mg/mL (25.12 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM3.5183 mL17.5914 mL35.1828 mL175.9139 mL
5 mM0.7037 mL3.5183 mL7.0366 mL35.1828 mL
10 mM0.3518 mL1.7591 mL3.5183 mL17.5914 mL
20 mM0.1759 mL0.8796 mL1.7591 mL8.7957 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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