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AzddMeC

🥰Excellent
TargetMol
Catalog No. T26726Cas No. 87190-79-2
Alias CS-92, Azidodideoxymethylcytidine, Az-Dcme

AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.

AzddMeC

AzddMeC

🥰Excellent
TargetMol
Purity: 99.62%
Catalog No. T26726Alias CS-92, Azidodideoxymethylcytidine, Az-DcmeCas No. 87190-79-2
AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.
Pack SizePriceAvailabilityQuantity
1 mg$71In Stock
5 mg$172In Stock
10 mg$278In Stock
25 mg$562In Stock
50 mg$892In Stock
100 mg$1,490In Stock
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Purity:99.62%
ee:100%
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Product Introduction

Bioactivity
Description
AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.
Targets&IC50
HIV-1:9 nM (EC50, Human PBM cells), HIV-1:6 nM (EC50, Human macrophages)
In vitro
AzddMeC emerged as the most potent inhibitor of hepatitis B virus DNA polymerase (50% inhibitor dose, 0.03-0.35 μM). In contrast, cellular DNA polymerase was shown to be resistant to or partially (β) affected by AzddMeC. [4]
In vivo
Following intravenously and orally administered 60 mg/kg AzddMeC to male rhesus monkeys, 3'-azido-3'-deoxythymidine (AZT) was found to be the major metabolite of AzddMeC in monkeys. Serum concentrations of AzddMeC decreased rapidly in a biexponential manner with terminal half-lives ranging from 0.5 to 1.3 h. Total clearance of AzddMeC was 2.00 +/- 0.41 l/h/kg (mean +/- standard deviation) and the fraction of AzddMeC metabolized to AZT was 0.32 +/- 0.05. The total clearance was 2.00 +/- 0.41 l/h/kg (mean +/- standard deviation).[2]
AliasCS-92, Azidodideoxymethylcytidine, Az-Dcme
Chemical Properties
Molecular Weight266.26
FormulaC10H14N6O3
Cas No.87190-79-2
SmilesCc1cn([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)c(=O)nc1N
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 100 mg/mL (375.57 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.7557 mL18.7786 mL37.5573 mL187.7864 mL
5 mM0.7511 mL3.7557 mL7.5115 mL37.5573 mL
10 mM0.3756 mL1.8779 mL3.7557 mL18.7786 mL
20 mM0.1878 mL0.9389 mL1.8779 mL9.3893 mL
50 mM0.0751 mL0.3756 mL0.7511 mL3.7557 mL
100 mM0.0376 mL0.1878 mL0.3756 mL1.8779 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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