中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantiospecific synthesis of all four Stereoisomers of novel bicyclic arylacetamides as kappa-Opioid agonists

文献类型:期刊论文

作者Long, YQ; Mou, QY; Qiu, DP; Wu, RQ
刊名CHINESE JOURNAL OF CHEMISTRY
出版日期2002-10
卷号20期号:10页码:1073-1079
关键词kappa-Opioid receptor agonist bicyclic arylacetamide conformational restriction enantiospecific synthesis
ISSN号1001-604X
文献子类Article
英文摘要Conformationally constrained bicyclic derivatives of the potent and selective kappa-oploid receptor agonist 2-(3,4-dichlorophenyl)-N-methyl-N-[(1S) -1-phenyl-2-(1-pyrrolidinyl)-ethyl] acetamide (3, ICI-199, 441) were designed to explore the effect of the conformational restriction and stereochemistry of the pharmacophoric ethylenediamine incorporated into the pyrrolidine on the affinity and x-selectivity. A facile enantiospecific synthetic route was established to afford all four stereoisomers starting from readily available ammo acids through mild cyclization and amide formation.
WOS关键词HIGHLY POTENT ; RECEPTORS ; SELECTIVITY ; AFFINITY ; AMINES
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000178644700027
出版者SCIENCE CHINA PRESS
源URL[http://119.78.100.183/handle/2S10ELR8/274325]  
专题药物化学研究室
通讯作者Long, YQ
作者单位Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Inst Materia Medica, Shanghai 200031, Peoples R China
推荐引用方式
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Long, YQ,Mou, QY,Qiu, DP,et al. Enantiospecific synthesis of all four Stereoisomers of novel bicyclic arylacetamides as kappa-Opioid agonists[J]. CHINESE JOURNAL OF CHEMISTRY,2002,20(10):1073-1079.
APA Long, YQ,Mou, QY,Qiu, DP,&Wu, RQ.(2002).Enantiospecific synthesis of all four Stereoisomers of novel bicyclic arylacetamides as kappa-Opioid agonists.CHINESE JOURNAL OF CHEMISTRY,20(10),1073-1079.
MLA Long, YQ,et al."Enantiospecific synthesis of all four Stereoisomers of novel bicyclic arylacetamides as kappa-Opioid agonists".CHINESE JOURNAL OF CHEMISTRY 20.10(2002):1073-1079.

入库方式: OAI收割

来源:上海药物研究所

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