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A3AR modulator 1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
A3AR modulator 1图片
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
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
生物活性

A3AR modulator 1 (MRS8054) is an orally activeA3adenosine receptor(A3AR)(Adenosine Receptor) positive allosteric modulator (PAM). A3AR modulator 1 greatly enhances Cl-IB-MECA-stimulated [35S]GTPγS binding Emax[1].

IC50& Target[1]

Adenosine A3receptor

 

体外研究
(In Vitro)

A3AR modulator 1 (compound 39) shows a few weak off-target interactions, with Kivalues of 0.123 μM, 0.891 μM, and 2.6 μM for translocator protein (TSPO), opioid receptor σ2, and 5HT2B receptor, respectively[1].

体内研究
(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[1].

分子量

484.38

Formula

C23H25IN4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.