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顺式-(+/-)-甲基(1R,2S/1S,2R)-2-[(4-羟基-4-苯基哌啶-1-基)甲基]-1-(4-甲基苯基)环丙烷羧酸酯[(+/-)-PPCC)]的合成与拆分:具有神经保护作用的新型 sigma 受体配体。

Synthesis and resolution of cis-(+/-)-methyl (1R,2S/1S,2R)-2-[(4-hydroxy-4-phenylpiperidin-1-yl)methyl]-1-(4-methylphenyl)cyclopropanecarboxylate [(+/-)-PPCC)]: new sigma receptor ligands with neuroprotective effect.

机构信息

Department of Pharmaceutical Sciences, Medicinal Chemistry Section, University of Catania, Catania, Italy.

出版信息

J Med Chem. 2010 Aug 12;53(15):5881-5. doi: 10.1021/jm100116p.

Abstract

The enantiomers of cis-(+/-)-methyl (1R,2S/1S,2R)-2-[(4-hydroxy-4-phenylpiperidin-1-yl)methyl]-1-(4-methylphenyl)cyclopropanecarboxylate [1, (+/-)-PPCC], a selective sigma ligand, were synthesized. The (+)- and (-)-enantiomers bind predominantly to sigma(1) receptors and have a reduced sigma(2) affinity. Both individually restore the astroglial oxidative status modified by glutamate, counteracting also transglutaminase-2 overexpression. They exhibited in vivo anti-opioid effects on kappa opioid (KOP) receptor-mediated analgesia. Our findings demonstrate that the enantiomers display mainly sigma(1) agonist activity and that they have neuroprotective effects.

摘要

顺式-(+/-)-甲基(1R,2S/1S,2R)-2-[(4-羟基-4-苯基哌啶-1-基)甲基]-1-(4-甲基苯基)环丙烷羧酸酯[1,(+/-)-PPCC],一种选择性的西格玛配体,被合成出来。(+)-和(-)-对映异构体主要与西格玛(1)受体结合,并且对西格玛(2)的亲和力降低。两者都可以单独恢复谷氨酸引起的星形胶质细胞氧化状态,也可以对抗转谷氨酰胺酶-2的过度表达。它们在体内表现出对κ阿片受体(KOP)介导的镇痛的抗阿片作用。我们的研究结果表明,对映异构体主要显示西格玛(1)激动剂活性,并且具有神经保护作用。

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