含哌嗪化合物作为受体配体的研究进展

被引:12
作者
甘淋玲 [1 ]
蔡佳利 [2 ]
周成合 [1 ,2 ]
机构
[1] 西南大学药学院
[2] 西南大学化学化工学院
关键词
哌嗪; 多巴胺受体; 5-羟色胺受体; α1肾上腺素受体; 抗精神病药; 抗抑郁;
D O I
暂无
中图分类号
R91 [药物基础科学];
学科分类号
1007 ;
摘要
目的综述了含哌嗪化合物作为受体配体的研究进展。方法综合国内外文献阐述了含哌嗪化合物作为多巴胺(DA)受体、5-羟色胺(5-HT)受体、α1肾上腺素受体(α1-AR)、黑皮质素-4受体(MC4R)以及σ受体配体等方面的最新研究概况。结果与结论含哌嗪化合物作为相应的受体配体具有广泛的生物活性,是目前研究开发的活跃领域之一,随着研究的不断深入,将有越来越多选择性高、药动学性质好的含哌嗪环药物应用于临床。
引用
收藏
页码:1361 / 1368
页数:8
相关论文
共 7 条
[1]   Pharmacological and pharmacokinetic characterization of 2-piperazine-α-isopropyl benzylamine derivatives as melanocortin-4 receptor antagonists [J].
Chen, Chen ;
Tucci, Fabio C. ;
Jiang, Wanlong ;
Tran, Joe A. ;
Fleck, Beth A. ;
Hoare, Sam R. ;
Wen, Jenny ;
Chen, Takung ;
Johns, Michael ;
Markison, Stacy ;
Foster, Alan C. ;
Marinkovic, Dragan ;
Chen, Caroline W. ;
Arellano, Melissa ;
Harman, John ;
Saunders, John ;
Bozigian, Haig ;
Marks, Daniel .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (10) :5606-5618
[2]   Synthesis and in vitro activity of N′-cyano-4-(2-phenylacetyl)-N-o-tolylpiperazine-1-carboximidamide P2X7 antagonists [J].
Morytko, Michael J. ;
Betschmann, Patrick ;
Woller, Kevin ;
Ericsson, Anna ;
Chen, Haipeng ;
Donnelly-Roberts, Diana L. ;
Namovic, Marian T. ;
Jarvis, Michael F. ;
Carroll, William A. ;
Rafferty, Paul .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (06) :2093-2096
[3]  
Structure–activity relationships of novel piperazines as antagonists for the melanocortin-4 receptor[J] . Dai Nozawa,Taketoshi Okubo,Takaaki Ishii,Hiroyuki Kakinuma,Shigeyuki Chaki,Shigeru Okuyama,Atsuro Nakazato.Bioorganic & Medicinal Chemistry . 2007 (5)
[4]  
Novel piperazines: Potent melanocortin-4 receptor antagonists with anxiolytic-like activity[J] . Dai Nozawa,Taketoshi Okubo,Takaaki Ishii,Kazuaki Takamori,Shigeyuki Chaki,Shigeru Okuyama,Atsuro Nakazato.Bioorganic & Medicinal Chemistry . 2007 (6)
[5]  
Novel potent neuropeptide Y Y5 receptor antagonists: Synthesis and structure–activity relationships of phenylpiperazine derivatives[J] . Toshiyuki Takahashi,Aya Sakuraba,Tomoko Hirohashi,Takunobu Shibata,Masaaki Hirose,Yuji Haga,Katsumasa Nonoshita,Tetsuya Kanno,Junko Ito,Hisashi Iwaasa,Akio Kanatani,Takehiro Fukami,Nagaaki Sato.Bioorganic & Medicinal Chemistry . 2006 (22)
[6]  
N ′,2-Diphenylquinoline-4-carbohydrazide based NK 3 receptor antagonists II[J] . Jason M. Elliott,Robert W. Carling,Gary G. Chicchi,James Crawforth,Peter H. Hutson,A. Brian Jones,Sarah Kelly,Rose Marwood,Georgina Meneses-Lorente,Elena Mezzogori,Fraser Murray,Michael Rigby,Inmaculada Royo,Michael G.N. Russell,Duncan Shaw,Bindi Sohal,Kwei Lan Tsao,Brian Williams.Bioorganic & Medicinal Chemistry Letters . 2006 (22)
[7]  
KKHA-761, a potent D 3 receptor antagonist with high 5-HT 1A receptor affinity, exhibits antipsychotic properties in animal models of schizophrenia[J] . Woo-Kyu Park,Daeyoung Jeong,Heeyeong Cho,Seong Jin Lee,Mi Young Cha,Ae Nim Pae,Kyung Il Choi,Hun Yeong Koh,Jae Yang Kong.Pharmacology, Biochemistry and Behavior . 2005 (2)