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κ 型阿片肽受体配体及其在药物研发中的潜力。

Peptide Kappa Opioid Receptor Ligands and Their Potential for Drug Development.

机构信息

Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, USA.

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, USA.

出版信息

Handb Exp Pharmacol. 2022;271:197-220. doi: 10.1007/164_2021_519.

Abstract

Ligands for kappa opioid receptors (KOR) have potential uses as non-addictive analgesics and for the treatment of pruritus, mood disorders, and substance abuse. These areas continue to have major unmet medical needs. Significant advances have been made in recent years in the preclinical development of novel opioid peptides, notably ones with structural features that inherently impart stability to proteases. Following a brief discussion of the potential therapeutic applications of KOR agonists and antagonists, this review focuses on two series of novel opioid peptides, all-D-amino acid tetrapeptides as peripherally selective KOR agonists for the treatment of pain and pruritus without centrally mediated side effects, and macrocyclic tetrapeptides based on CJ-15,208 that can exhibit different opioid profiles with potential applications such as analgesics and treatments for substance abuse.

摘要

κ 型阿片受体(KOR)配体有望成为非成瘾性镇痛药,用于治疗瘙痒、情绪障碍和物质滥用。这些领域仍然存在着重大的未满足的医疗需求。近年来,新型阿片肽的临床前开发取得了重大进展,特别是那些具有固有稳定性的结构特征的阿片肽。在简要讨论了 KOR 激动剂和拮抗剂的潜在治疗应用后,本综述重点介绍了两类新型阿片肽,全 D-氨基酸四肽作为外周选择性 KOR 激动剂,用于治疗疼痛和瘙痒,而无中枢介导的副作用,以及基于 CJ-15,208 的大环四肽,可表现出不同的阿片样特性,具有作为镇痛药和治疗物质滥用等潜在应用。

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