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(1R,2R)-MK-8189
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Catalog No. T73462LCas No. 1424378-99-3
Alias (1R,2R)MK-8189, (1R,2R)MK8189
(1R,2R)-MK-8189 is an isomer of MK-8189 and can be used for biochemistry experoments. MK-8189 is a potent and selective pyrimidine PDE10A inhibitor.
(1R,2R)-MK-8189
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Catalog No. T73462LAlias (1R,2R)MK-8189, (1R,2R)MK8189Cas No. 1424378-99-3
(1R,2R)-MK-8189 is an isomer of MK-8189 and can be used for biochemistry experoments. MK-8189 is a potent and selective pyrimidine PDE10A inhibitor.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $195 | - | In Stock | |
| 5 mg | $483 | - | In Stock | |
| 10 mg | $692 | - | In Stock | |
| 25 mg | $1,080 | - | In Stock | |
| 50 mg | $1,490 | - | In Stock | |
| 100 mg | $1,970 | - | In Stock | |
| 200 mg | $2,690 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Batch Information
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Purity:>99.99%
ee:97.98%
Appearance:Solid
Color:Yellow
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | (1R,2R)-MK-8189 is an isomer of MK-8189 and can be used for biochemistry experoments. MK-8189 is a potent and selective pyrimidine PDE10A inhibitor. |
| Targets&IC50 | PDE10A:1.6 nM |
| In vitro | MK-8189 is a highly selective PDE10A inhibitor with an IC₅₀ of 1.6 nM and >500,000-fold selectivity over other PDE families. MK-8189 binds reversibly to human PDE10A with a dissociation half-life of 6.7 minutes at 25 °C[1]. |
| In vivo | In rats, oral MK-8189 (0.25–0.75 mg/kg) reversed MK-801–induced hyperactivity and improved novel object recognition, indicating antipsychotic and pro-cognitive effects. Efficacy correlated with brain PDE10A occupancy[1]. |
| Synonyms | (1R,2R)MK-8189, (1R,2R)MK8189 |
| Molecular Weight | 382.48 |
| Formula | C19H22N6OS |
| Cas No. | 1424378-99-3 |
| Smiles | C(OC=1C=C(NCC2=NN=C(C)S2)N=C(C)N1)[C@H]3[C@@H](C3)C4=CC=C(C)C=N4 |
| Relative Density. | no data available |
| Storage | store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Calculator
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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
Dose Conversion
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Tech Support
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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