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MS48107
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。
MS48107图片
CAS NO:2375070-79-2
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议

产品介绍
MS48107 是一种有效的 G 蛋白偶联受体 68 (GPR68) 的选择性正变构调节剂。MS48107 对 GPR68 的选择性高于密切相关的质子 GPCR,神经递质转运蛋白和 hERG 离子通道。MS48107 可以轻松穿越小鼠的血脑屏障 (BBB)。
Cas No.2375070-79-2
分子式C23H20FN5O2
分子量417.44
溶解度DMSO : 100 mg/mL (239.56 mM; Need ultrasonic)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). MS48107 is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. MS48107 can readily cross the blood-brain barrier (BBB) in mice[1].

5-HT2B has moderate binding affinity to MS48107 (compound 71) with a Ki value of 219 nM. At 5-HT2B receptors, MS48107 shows no agonist activity but display weak antagonist activity with a Ki value of 310 nM, respectively[1].MS48107 (compound 71) has agonist activity only at the MT1 and MT2 receptors. MS48107 is a weak full agonist at the MT1 receptor (EC50 = 320 nM) and a weak partial agonist activity at the MT2 receptor (EC50 = 540 nM). MS48107 displays low binding affinities to MT1 (5900 nM) and MT2 (1100 nM) receptors[1].

For MS48107 (compound 71), a single intraperitoneal injection at the dose of 25 mg/kg leads to high exposure levels (above 10 μM) in both plasma and brain at 0.5 h in mice (Swiss Albino mice). The high compound exposure levels in both plasma and brain are maintained for 2 h[1].

[1]. Xufen Yu, et al. Design, Synthesis, and Characterization of Ogerin-Based Positive Allosteric Modulators for G Protein-Coupled Receptor 68 (GPR68). J Med Chem. 2019 Aug 22;62(16):7557-7574.