The Discovery and Development of the N-Substituted trans-3,4-Dimethyl-4-(3′-hydroxyphenyl)piperidine Class of Pure Opioid Receptor Antagonists

被引:17
|
作者
Carroll, F. Ivy [1 ]
Dolle, Roland E. [2 ]
机构
[1] Res Triangle Inst, Ctr Organ & Med Chem, Res Triangle Pk, NC 27709 USA
[2] Cubist Pharmaceut, Lexington, MA 02421 USA
关键词
alvimopan; drug design; JDTic; medicinal chemistry; opioid antagonists; CARBOXAMIDO-BIARYL ETHERS; SELECTIVE ANTAGONISTS; INVERSE AGONISTS; COCAINE ABUSERS; KAPPA; RATS; POTENT; IDENTIFICATION; SEEKING; CONFORMATION;
D O I
10.1002/cmdc.201402142
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
N-Substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidines are a class of pure opioid receptor antagonists with a novel pharmacophore. This opioid receptor antagonist pharmacophore was used as a lead structure to design and develop several interesting and useful opioid receptor antagonists. In this review we describe: 1) early SAR studies that led to the discovery of LY255582 and analogues that are nonselective opioid receptor antagonists developed for the treatment of obesity; 2) the discovery and commercialization of LY246736 (alvimopan; ENTEREG (R)), a peripherally selective opioid receptor antagonist that accelerates the time to upper and lower GI recovery following surgeries that include partial bowel resection with primary anastomosis; and 3) the discovery and development of the potent and selective kappa opioid receptor antagonist JDTic and analogues as potential pharmacotherapies for treating depression, anxiety, and substance abuse (nicotine, alcohol, and cocaine). In addition, the use of JDTic for obtaining the X-ray structure of the human kappa opioid receptor is discussed.
引用
收藏
页码:1638 / 1654
页数:17
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