MRS2365 

MRS2365 is a potent and selective P2Y1 receptor (EC₅₀=0.4 nM) /[³⁵S]GTPγS binding/β-arrestin 2 recruitment agonist with an EC₅₀ of 0.4 nM. MRS2365 relieves mechanical allodynia and increases mechanical sensitivity. MRS2365 shows little agonist or antagonist activity at the P2Y12 or P2Y13 receptors^[1][2][3][4].

MRS2365 (1 µM 或 3 µM；2 min) 弱化了腺苷二磷酸 (ADP) 诱导的血小板聚集^[2]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

MRS2365 (0.03-0.3 mg/kg；腹腔注射；单剂量) 以剂量依赖性方式显著减轻雄性 wistar 大鼠神经病变 (Seltzer) 模型中的机械异常性疼痛^[3]。
MRS2365 (0.1-2 mg/kg；腹腔注射；单剂量) 增加了患有神经性疼痛的雄性 wistar 大鼠模型的缩爪阈值 (PWT) ^[3]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

483.33

C₁₃H₁₉N₅O₉P₂S

436847-09-5

Room temperature in continental US; may vary elsewhere.

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

• [1]. Mariya Chhatriwala, et al. Induction of novel agonist selectivity for the ADP-activated P2Y1 receptor versus the ADP-activated P2Y12 and P2Y13 receptors by conformational constraint of an ADP analog. J Pharmacol Exp Ther. 2004 Dec;311(3):1038-43.  [Content Brief]

  [2]. D M Bourdon, et al. (N)-methanocarba-2MeSADP (MRS2365) is a subtype-specific agonist that induces rapid desensitization of the P2Y1 receptor of human platelets. J Thromb Haemost. 2006 Apr;4(4):861-8.  [Content Brief]

  [3]. Andó RD, et al. A comparative analysis of the activity of ligands acting at P2X and P2Y receptor subtypes in models of neuropathic, acute and inflammatory pain. Br J Pharmacol. 2010 Mar;159(5):1106-17.  [Content Brief]

  [4]. Gao ZG, et al. Distinct Signaling Patterns of Allosteric Antagonism at the P2Y1 Receptor. Mol Pharmacol. 2017 Nov;92(5):613-626.  [Content Brief]