Multivalent approaches and beyond: novel tools for the investigation of dopamine D2 receptor pharmacology

被引:8
作者
Kopinathan, Anitha [1 ,2 ]
Scammells, Peter J. [1 ]
Lane, J. Robert [2 ]
Capuano, Ben [1 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Med Chem, 381 Royal Parade, Parkville, Vic 3052, Australia
[2] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, 381 Royal Parade, Parkville, Vic 3052, Australia
关键词
allosteric; bitopic; bivalent; D2R; designed multiple ligands; dopamine D-2 receptor; multivalent; orthosteric; PROTEIN-COUPLED RECEPTORS; NEGATIVE ALLOSTERIC MODULATOR; POSITRON-EMISSION-TOMOGRAPHY; ANTAGONIST BIVALENT LIGANDS; ADENOSINE A(2A) RECEPTORS; PARKINSONS-DISEASE; FUNCTIONAL SELECTIVITY; BIASED AGONISM; D2; RECEPTOR; HOMOBIVALENT LIGANDS;
D O I
10.4155/fmc-2016-0010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The dopamine D-2 receptor (D2R) has been implicated in the symptomology of disorders such as schizophrenia and Parkinson's disease. Multivalent ligands provide useful tools to investigate emerging concepts of G protein-coupled receptor drug action such as allostery, bitopic binding and receptor dimerization. This review focuses on the approaches taken toward the development of multivalent ligands for the D2R recently and highlights the challenges associated with each approach, their utility in probing D2R function and approaches to develop new D2R-targeting drugs. Furthermore, we extend our discussion to the possibility of designing multitarget ligands. The insights gained from such studies may provide the basis for improved therapeutic targeting of the D2R.
引用
收藏
页码:1349 / 1372
页数:24
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