AZD-8529 is a potent, highly selective and orally bioavailable positive allosteric modulator of mGluR2 , with an EC 50 of 285 nM, and shows no positive allosteric modulator responses at 20-25 M on the mGluR1 , 3, 4, 5, 6, 7, and 8 subtypes. In Vitro AZD-8529 potentiates the effects of glutamate at mGluR2 with an EC 50 of 195 nM. AZD-8529 does not elicit antagonist responses on mGluRs at 25 μM. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo AZD-8529 (0.3-mg/kg, i.m.) reduces nicotine priming-induced and cue-induced reinstatement in squirrel monkeys . AZD-8529 (30 mg/kg; i.p.) decreases the increased extracellular dopamine induced by nicotine in accumbens shell of freely-moving rats . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Sprague-Dawley rats Dosage: 10 mg/kg, 30 mg/kg Administration: Intraperitoneal injection; 2 hours before nicotine injections Result: Decreased the increased extracellular dopamine induced by nicotine (0.4 mg/kg, s.c.) in accumbens shell of freely-moving rats. Form:Oil IC50& Target:mGluR2 285 nM (EC 50 )
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AZD-8529
CAS number：1092453-15-0 molecular formula：C24H24F3N5O3
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| Chinese alias | - | ||
| English alias | MS-29057 | UNII-6H81G454I7 | AZD-8529 free base | EX-A7769 | 7-Methyl-5-(3-(piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl)-2-(4-(trifluoromethoxy)benzyl)isoindolin-1-one | 6H81G454I7 | SCHEMBL2124540 | AZD 8529 [WHO-DD] | Q27074805 | 1092453-15-0 (free base) | ||
| CAS number | 1092453-15-0 | molecular formula | C24H24F3N5O3 |
| molecular weight | 487.47 g/mol | Exact mass | ≥98% |
| PSA | 83.700 Ų | logp | 3.100 |
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