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Please store the product under the recommended conditions in the Certificate of Analysis.
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货期:电询
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MedChemExpress LLC
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电询
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A3AR modulator 1
MCE 国际站:A3AR modulator 1
产品活性:A3AR modulator 1 (MRS8054) 是一种具有口服活性的 A3 腺苷受体 (A3AR (Adenosine Receptor)) 正变构调节剂 (PAM)。A3AR modulator 1 极大地增强了 Cl-IB-MECA 刺激的 [35S]GTPγS 结合 Emax。
研究领域:GPCR/G Protein
作用靶点:Adenosine Receptor
In Vitro: A3AR modulator 1 (compound 39) shows a few weak off-target interactions, with Ki values of 0.123 μM, 0.891 μM, and 2.6 μM for translocator protein (TSPO), opioid receptor σ2, and 5HT2B receptor, respectively.
In Vivo: In fasted Wistar rats, A3AR modulator 1 (compound 39) has considerably longer in vivo half-life and improved oral bioavailability (3.44 h, 64.0%F at 3 mg/kg; 3.84 h, 61.5%F at 10 mg/kg), indicating substantial oral bioavailability.
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