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Amitivir

Amitivir
Amitivir (LY 217896) is an inosine monophosphate dehydrogenase inhibitor. Amitivir inhibits the replication of dividing MDCK cells. Amitivir was associated with asymptomatic rises in serum uric acid levels and was ineffective in modifying the virologic or clinical course of experimental influenza A (H1N1) virus infection.
Catalog No. T26619Cas No. 111393-84-1
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Purity:97.35%
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Amitivir

Catalog No. T26619Cas No. 111393-84-1
Amitivir (LY 217896) is an inosine monophosphate dehydrogenase inhibitor. Amitivir inhibits the replication of dividing MDCK cells. Amitivir was associated with asymptomatic rises in serum uric acid levels and was ineffective in modifying the virologic or clinical course of experimental influenza A (H1N1) virus infection.
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Pack SizePriceAvailabilityQuantity
1 mg$133In Stock
5 mg$302In Stock
10 mg$447In Stock
25 mg$738In Stock
50 mg$987In Stock
100 mg$1,380In Stock
500 mg$2,790In Stock
1 mL x 10 mM (in DMSO)$213In Stock
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Product Introduction

Bioactivity
Description
Amitivir (LY 217896) is an inosine monophosphate dehydrogenase inhibitor. Amitivir inhibits the replication of dividing MDCK cells. Amitivir was associated with asymptomatic rises in serum uric acid levels and was ineffective in modifying the virologic or clinical course of experimental influenza A (H1N1) virus infection.
AliasLY217896, LY 217896, LY-217896
Chemical Properties
Molecular Weight126.14
FormulaC3H2N4S
Cas No.111393-84-1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 75 mg/ml (594.58 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM7.9277 mL39.6385 mL79.2770 mL396.3850 mL
5 mM1.5855 mL7.9277 mL15.8554 mL79.2770 mL
10 mM0.7928 mL3.9638 mL7.9277 mL39.6385 mL
20 mM0.3964 mL1.9819 mL3.9638 mL19.8192 mL
50 mM0.1586 mL0.7928 mL1.5855 mL7.9277 mL
100 mM0.0793 mL0.3964 mL0.7928 mL3.9638 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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