中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Dual Ligands Targeting Dopamine D-2 and Serotonin 5-HT1A Receptors as New Antipsychotical or Anti-Parkinsonian Agents

文献类型:期刊论文

作者Ye, Na; Song, Zilan; Zhang, Ao1,2
刊名CURRENT MEDICINAL CHEMISTRY
出版日期2014-02
卷号21期号:4页码:437-457
关键词Atypical antipsychotics dopamine D-2 receptor dual ligands Parkinson's disease Schizophrenia Serotonin 5-HT1A receptor
ISSN号0929-8673
文献子类Article
英文摘要Psychiatric disorders like schizophrenia and neurode generative diseases like Parkinson's disease are associated with poly-factorial pathogenic mechanisms, with several neurotransmitter systems closely involved. In addition to the cerebral dopaminergic (DA) system, the serotoninergic (5-HT) system also plays a crucial role in regulating psycho-emotional, cognitive and motor functions in the central nervous system (CNS). Among the large 5-HT receptor family, accumulating data have revealed new insights into the therapeutic benefit of the 5-HT1A receptor in treating various CNS disorders, especially schizophrenia and Parkinson's disease. The present review discusses the advance of dual agents with mixed actions at the dopamine D-2 and serotonin 5-HT1A receptors in the treatment of these diseases. Aripiprazole was the only marketed drug with dual D-2 and 5-HT1A profile. It is a partial D-2 and 5-HT1A receptor agonist and has been prescribed as an atypical antipsychotical drug. Two other drugs Cariprazine and Pardoprunox are being investigated in clinic. Most of the other candidate compounds, including Bifeprunox, Sarizotan, Mazapertine succinate, PF-217830, and Adoprazine were discontinued due to either non-optimal pharmacokinetic properties or insufficient therapeutical efficacy. Although much effort has been done to highlight the advantages of the 5-HT1A and D-2 dual approach, it has to be pointed out that many of these drugs showed poly-pharmacological profile by targeting many other receptors and/or transporters besides the D-2 and 5-HT1A receptors. In this regard, 'pure' compounds exclusively acting on the D-2 and 5-HT1A receptors are highly needed to further validate this approach. Meanwhile, safety concerns and in vivo pharmacokinetic alerts should also be implanted to the drug design art early.
WOS关键词HALOPERIDOL-INDUCED CATALEPSY ; POTENTIAL ATYPICAL ANTIPSYCHOTICS ; RESTRICTED BENZAMIDE ANALOGS ; CENTRAL-NERVOUS-SYSTEM ; L-DOPA THERAPY ; AGONIST PROPERTIES ; IN-VIVO ; APORPHINE ENANTIOMERS ; NEUROCHEMICAL PROFILE ; BINDING-PROPERTIES
资助项目Chinese NSF[81125021] ; Chinese NSF[81373277] ; National Science & Technology Major Project on 'Key New Drug Creation and Manufacturing Program', China[2012ZX09103-101-035] ; National Science & Technology Major Project on 'Key New Drug Creation and Manufacturing Program', China[2012ZX 09301001-001] ; Interdisciplinary Cooperation Team" Program for Science and Technology Innovation (CAS)[00000000] ; National Program on Key Basic Research Project of China[2012CB910704] ; State Key Laboratory of Drug Research[SIMM1302KF-08] ; Shanghai Institute of Materia Medica[00000000]
WOS研究方向Biochemistry & Molecular Biology ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000331447700003
出版者BENTHAM SCIENCE PUBL LTD
源URL[http://119.78.100.183/handle/2S10ELR8/277203]  
专题药物化学研究室
通讯作者Zhang, Ao
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China;
2.Chinese Acad Sci, Shanghai Inst Mat Med, Synthet Organ & Med Chem Lab, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Ye, Na,Song, Zilan,Zhang, Ao. Dual Ligands Targeting Dopamine D-2 and Serotonin 5-HT1A Receptors as New Antipsychotical or Anti-Parkinsonian Agents[J]. CURRENT MEDICINAL CHEMISTRY,2014,21(4):437-457.
APA Ye, Na,Song, Zilan,&Zhang, Ao.(2014).Dual Ligands Targeting Dopamine D-2 and Serotonin 5-HT1A Receptors as New Antipsychotical or Anti-Parkinsonian Agents.CURRENT MEDICINAL CHEMISTRY,21(4),437-457.
MLA Ye, Na,et al."Dual Ligands Targeting Dopamine D-2 and Serotonin 5-HT1A Receptors as New Antipsychotical or Anti-Parkinsonian Agents".CURRENT MEDICINAL CHEMISTRY 21.4(2014):437-457.

入库方式: OAI收割

来源:上海药物研究所

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