S1RA

S1RA(E-52862)是高活性和选择性的sigma-1受体(σ1R)拮抗剂,Ki为17nM,而对σ2R的Ki则高于1000nM。

信号通路 >> G 蛋白偶联受体/G 蛋白 >> Sigma Receptor

研究领域 >> 神经疾病

[1]. Díaz JL, et al. Synthesis and biological evaluation of the 1-arylpyrazole class of σ(1) receptor antagonists: identification of 4-{2-[5-methyl-1-(naphthalen-2-yl)-1H-pyrazol-3-yloxy]ethyl}morpholine (S1RA, E-52862). J Med Chem. 2012 Oct 11;55(19):8211-24.

[2]. Romero L, et al. Pharmacological properties of S1RA, a new sigma-1 receptor antagonist that inhibits neuropathic pain and activity-induced spinal sensitization. Br J Pharmacol. 2012 Aug;166(8):2289-306.

[3]. Vidal-Torres A, et al. Effects of the selective sigma-1 receptor antagonist S1RA on formalin-induced pain behavior and neurotransmitter release in the spinal cord in rats. J Neurochem. 2014 Jan 3.

UNC0642 | 1-[2-(3,4-二甲氧基苯基)乙基]-4-(3-苯基丙基)哌嗪盐酸盐 | BD-1047 | PRE-084 | 那可丁 | BD1063 | 西拉美新盐酸盐 | Roluperidone | 4-IBP | AVex-73 hydrochloride | S1RA盐酸盐 | 磷酸二甲啡烷 | σ-配体-1