PeptideDB

MRS2365 trisodium

CAS: F: C13H16N5Na3O9P2S W: 549.28

MRS2365 trisodium is a potent and selective P2Y1 receptor (EC50=0.4 nM)/GTPγS binding/β-arrestin 2 recruitment agonist
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Bioactivity MRS2365 trisodium is a potent and selective P2Y1 receptor (EC50=0.4 nM)/[35S]GTPγS binding/β-arrestin 2 recruitment agonist. MRS2365 trisodium relieves mechanical allodynia and increases mechanical sensitivity[1][2][3][4].
Invitro MRS2365 trisodium (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]。
In Vivo MRS2365 trisodium (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 trisodium (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]。 Animal Model:
Name MRS2365 trisodium
Formula C13H16N5Na3O9P2S
Molar Mass 549.28
Appearance Liquid
Transport Room temperature in continental US; may vary elsewhere.
Storage

Solution, -20°C, 2 years

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