Metcalf Matthew D, Coop Andrew
Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 Penn Street, Baltimore, MD 21201, USA.
AAPS J. 2005 Oct 27;7(3):E704-22. doi: 10.1208/aapsj070371.
Antagonists of the kappa opioid receptor were initially investigated as pharmacological tools that would reverse the effects of kappa opioid receptor agonists. In the years following the discovery of the first selective kappa opioid antagonists, much information about their chemistry and pharmacology has been elicited and their potential therapeutic uses have been investigated. The review presents the current chemistry, ligand-based structure activity relationships, and pharmacology of the known nonpeptidic selective kappa opioid receptor antagonists. This manuscript endeavors to provide the reader with a useful reference of the investigations made to define the structure-activity relationships and pharmacology of selective kappa opioid receptor antagonists and their potential uses as pharmacological tools and as therapeutic agents in the treatment of disease states.
κ-阿片受体拮抗剂最初作为药理学工具进行研究,用于逆转κ-阿片受体激动剂的作用。在首个选择性κ-阿片受体拮抗剂被发现后的数年里,已获得了许多关于其化学和药理学的信息,并对其潜在治疗用途进行了研究。本综述介绍了已知非肽类选择性κ-阿片受体拮抗剂的当前化学、基于配体的构效关系及药理学。本手稿旨在为读者提供一份有用的参考资料,内容涉及为确定选择性κ-阿片受体拮抗剂的构效关系和药理学及其作为药理学工具和治疗疾病状态的治疗剂的潜在用途所开展的研究。