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MK-8768 is a potent, selective, and orally bioavailable negative allosteric modulator of the mGluR2 class, exhibiting an IC50 of 9.6 nM and characterized by excellent brain permeability.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | Inquiry | 8-10 weeks | |
50 mg | Inquiry | 8-10 weeks |
Description | MK-8768 is a potent, selective, and orally bioavailable negative allosteric modulator of the mGluR2 class, exhibiting an IC50 of 9.6 nM and characterized by excellent brain permeability. |
In vitro | MK-8768 (40 nM, 5 min) inhibits mGluR2 enzyme activity in CHOdhfr cell lines overexpressing mGluR2, with an IC50 value of 0.9 nM [1]. |
In vivo | MK-8768 is primarily administered via intramuscular injection [1]. When given at a dose of 3 mg/kg, intramuscularly twice weekly, MK-8768 markedly mitigates the effects of scopolamine-induced damage in the Old-World monkey ORD model, preserving robust executive functions and attention [1]. |
Molecular Weight | 433.43 |
Formula | C21H22F3N5O2 |
Cas No. | 1432729-22-0 |
Storage | Shipping with blue ice. |
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