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MK-8527

🥰Excellent
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

🥰Excellent
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%
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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
ColorWhite
AppearanceSolid
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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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% Saline/PBS/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 μLSaline/PBS/ddH2OTargetMol | 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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