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Letermovir-d8

Catalog No. TMIH-0298

Letermovir-d8 is a deuterated compound of Letermovir. Letermovir has a CAS number of 917389-32-3. Letermovir (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.

Letermovir-d8
Other Forms of Letermovir-d8:
LetermovirT5396917389-32-3
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Letermovir-d8

Catalog No. TMIH-0298
Letermovir-d8 is a deuterated compound of Letermovir. Letermovir has a CAS number of 917389-32-3. Letermovir (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.
Pack SizePriceAvailabilityQuantity
1 mg$5147-10 days
5 mg$1,5407-10 days
10 mg$2,5707-10 days
25 mg$4,7507-10 days
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Product Introduction

Bioactivity
Description
Letermovir-d8 is a deuterated compound of Letermovir. Letermovir has a CAS number of 917389-32-3. Letermovir (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.
Chemical Properties
Molecular Weight580.6
FormulaC29H20D8F4N4O4
Storage & Solubility Information
StorageShipping with blue ice.

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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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