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MK-8527

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Catalog No. T86907Cas No. 1810869-23-8
Alias MK8527

MK-8527 is an orally active HIV-1 inhibitor and nucleoside reverse transcriptase translocation inhibitor with an IC₅₀ of 0.21 nM. It is phosphorylated intracellularly to its active triphosphate form, exhibiting antiviral activity.

MK-8527

MK-8527

😃Good
Purity: 99.15%
Catalog No. T86907Alias MK8527Cas No. 1810869-23-8
MK-8527 is an orally active HIV-1 inhibitor and nucleoside reverse transcriptase translocation inhibitor with an IC₅₀ of 0.21 nM. It is phosphorylated intracellularly to its active triphosphate form, exhibiting antiviral activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$118-In Stock
2 mg$176-In Stock
5 mg$297-In Stock
10 mg$476-In Stock
25 mg$953-In Stock
50 mg$1,480-In Stock
1 mL x 10 mM (in DMSO)$327-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.15%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
MK-8527 is an orally active HIV-1 inhibitor and nucleoside reverse transcriptase translocation inhibitor with an IC₅₀ of 0.21 nM. It is phosphorylated intracellularly to its active triphosphate form, exhibiting antiviral activity.
In vitro
MK-8527 inhibits viral replication in human peripheral blood mononuclear cells (PBMCs), with a half maximal inhibitory concentration (IC50) of 0.21 nM [5].
In vivo
The pharmacokinetic (PK) profile of MK-8527 in rats and rhesus monkeys was characterized by low-to-moderate clearance and volume of distribution, with good oral absorption (57% and 100% in rats and monkeys, respectively). Following oral administration of MK-8527 to monkeys, MK-8527-TP exhibited an intracellular half-life of approximately 48 h in PBMCs, significantly longer than the apparent plasma half-life of the parent compound (approximately 7 h) [5].
SynonymsMK8527
Chemical Properties
Molecular Weight308.72
FormulaC13H13ClN4O3
Cas No.1810869-23-8
SmilesNC1=C2C(N(C=C2)[C@@H]3O[C@](C#C)(CO)[C@@H](O)C3)=NC(Cl)=N1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 90 mg/mL (291.53 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.2392 mL16.1959 mL32.3918 mL161.9591 mL
5 mM0.6478 mL3.2392 mL6.4784 mL32.3918 mL
10 mM0.3239 mL1.6196 mL3.2392 mL16.1959 mL
20 mM0.1620 mL0.8098 mL1.6196 mL8.0980 mL
50 mM0.0648 mL0.3239 mL0.6478 mL3.2392 mL
100 mM0.0324 mL0.1620 mL0.3239 mL1.6196 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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