Opportunities and challenges in the discovery of allosteric modulators of GPCRs for treating CNS disorders

被引:212
作者
Conn, P. Jeffrey [1 ]
Lindsley, Craig W. [1 ]
Meiler, Jens [2 ]
Niswender, Colleen M. [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Vanderbilt Ctr Neurosci Drug Discovery, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
METABOTROPIC GLUTAMATE RECEPTORS; PROTEIN-COUPLED RECEPTOR; METHYL-D-ASPARTATE; IN-VIVO VALIDATION; SUBTYPE; 5; STRUCTURAL INSIGHTS; MEDIATED MODULATION; SIGNALING PATHWAYS; MOLECULAR SWITCHES; ANTIPSYCHOTIC-LIKE;
D O I
10.1038/nrd4308
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Novel allosteric modulators of G protein-coupled receptors (GPCRs) are providing fundamental advances in the development of GPCR ligands with high subtype selectivity and novel modes of efficacy that have not been possible-with traditional approaches. As new allosteric modulators are advancing as drug candidates, we are developing an increased understanding of the major advantages and broad range of activities that can be achieved with these agents through selective modulation of specific signalling pathways, differential effects on GPCR honnodinners versus lieterodinners, and other properties. This understanding creates exciting opportunities, as well as unique challenges, in the optimization of novel therapeutic agents for disorders of the central nervous system.
引用
收藏
页码:692 / 708
页数:17
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