目錄:MedChemExpress LLC>>生化試劑>> JNJ-42153605 | MCE
CAS | 1254977-87-1 | 純度 | 99.24% |
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分子量 | 400.44 | 分子式 | C??H??F?N? |
供貨周期 | 現貨 | 規格 | 100 mg |
貨號 | HY-18162 | 應用領域 | 醫療衛生,化工,生物產業,制藥 |
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CAS No. : 1254977-87-1
產品活性:JNJ-42153605 is a positive allosteric modulator of the metabotropic glutamate 2 (mGlu2) receptor with an EC50 of 17 nM.
研究領域:GPCR/G Protein | Neuronal Signaling
作用靶點:mGluR
In Vitro: JNJ-42153605 is assessed for its selectivity for the mGlu2 receptor and is found to not have agonist or antagonist activity toward other mGlu receptor subtypes up to 30 μM. JNJ-42153605 shows high permeability with no indication for P-glycoprotein efflux.
In Vivo: JNJ-42153605 shows a central in vivo efficacy by inhibition of REM sleep state at a dose of 3 mg/kg po in the rat sleep-wake EEG paradigm, a phenomenon shown to be mGlu2 mediated. In mice, JNJ-42153605 shows reversed PCP-induced hyperlocomotion with an ED50 of 5.4 mg/kg sc, indicative of antipsychotic activity. JNJ-42153605 shows a rapid rate of absorption from the gastrointestinal tract, reaching the maximal concentration after 0.5 h. Clearance in vivo is moderate to high in both rat and dog (35 and 29 mL/min/kg, respectively). Elimination halflives are on the shorter side across the species, being 2.7 h in rat and 0.8-1.1 h in dog.
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