Syntheses of 7-Substituted α-Cyperone Derivatives for Selective Sigma-1 Receptor over Cannabinoid-1 Receptor Binding Affinities

Ju-Young Park; Kee-Won Kim; Sung-Hwa Yoon; Young-Bae Kwon; Young-Gyun Shin

首页> 外文期刊>Bulletin of the Korean Chemical Society >Syntheses of 7-Substituted α-Cyperone Derivatives for Selective Sigma-1 Receptor over Cannabinoid-1 Receptor Binding Affinities

【24h】

Syntheses of 7-Substituted α-Cyperone Derivatives for Selective Sigma-1 Receptor over Cannabinoid-1 Receptor Binding Affinities

机译：选择性Sigma-1受体的7-取代α-Cyperone衍生物的合成优于大麻素1受体的结合亲和力

获取原文

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Bulletin of the Korean Chemical Society》 |2013年第11期|共页
作者
Ju-Young Park; Kee-Won Kim; Sung-Hwa Yoon; Young-Bae Kwon; Young-Gyun Shin;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种
中图分类化学;
关键词

相似文献

外文文献
中文文献
专利

1. Syntheses of 7-Substituted α-Cyperone Derivatives for Selective Sigma-1 Receptor over Cannabinoid-1 Receptor Binding Affinities [J] . Ju-Young Park, Young-Gyun Shin, Kee-Won Kim Bulletin of the Korean Chemical Society . 2013,第11期

机译：选择性的Sigma-1受体的7-取代的α-Cyperone衍生物的合成优于大麻素1受体的结合亲和力
2. Novel 2-phenylimidazo(1,2-a)pyridine derivatives as potent and selective ligands for peripheral benzodiazepine receptors: synthesis, binding affinity, and in vivo studies. [J] . Trapani G, Franco M, Latrofa A, Journal of Medicinal Chemistry . 1999,第19期

机译：新型2-苯基咪唑并（1,2-a）吡啶衍生物作为外围苯并二氮杂receptor受体的有效和选择性配体：合成，结合亲和力和体内研究。
3. Inter-residue coupling contributes to high-affinity subtype-selective binding of alpha-bungarotoxin to nicotinic receptors [J] . Sine Steven M., Huang Sun, Li Shu-Xing, The Biochemical Journal . 2013,第Pta2期

机译：残基间偶联有助于α-邦加毒素与烟碱样受体的高亲和力亚型选择性结合
4. Proteolytic stability of neuropeptide Y analogues with high binding affinity for Y_1 and Y_2 receptors [C] . Irfan U.Khan, Regina Reppich, Annette G.Beck-Sickinger International Peptide Symposium;European Peptide Symposium . 2005

机译：γ1和Y_2受体具有高结合亲和力的神经肽Y类似物的蛋白水解稳定性
5. Synthesis and evaluation of novel N-alkylamine derivatives as high affinity sigma-1 receptor ligands. [D] . Chu, Uyen B. 2011

机译：合成和评估新型N-烷基胺衍生物作为高亲和力sigma-1受体配体。
6. Design Syntheses and Biological Evaluation of 14-Heteroaromatic Substituted Naltrexone Derivatives: Pharmacological Profile Switch from Mu Opioid Receptor Selectivity to Mu/Kappa Opioid Receptor Dual Selectivity [O] . Yunyun Yuan, Saheem A. Zaidi, Orgil Elbegdorj, -1

机译：设计合成和生物学评估的14-Heroaromatic取代纳曲酮衍生物：从Mu阿片类药物受体选择性向Mu / Kappa阿片类药物受体双重选择性的药理学概况转换
7. Novel 17 Substituted Pregnadiene Derivatives as 5.ALPHA.-Reductase Inhibitors and Their Binding Affinity for the Androgen Receptor [O] . Marisa Cabeza, Eugenio Flores, Ivonne Heuze, 2004

机译：新的17个取代的妊娠衍生物为5.Alpha.-还原酶抑制剂及其对雄激素受体的结合亲和力
8. Short-Term Desensitization of Muscarinic Cholinergic Receptors in Mouse Neuroblastoma Cells: Selective Loss of Agonist Low-Affinity and Pirenzepine High-Affinity Binding Sites [R] . Cioffi, C. L., El-Fakahany, E. E. 1986

机译：小鼠神经母细胞瘤细胞中毒蕈碱胆碱能受体的短期脱敏：激动剂低亲和力和哌仑西平高亲和力结合位点的选择性丧失

Syntheses of 7-Substituted α-Cyperone Derivatives for Selective Sigma-1 Receptor over Cannabinoid-1 Receptor Binding Affinities

著录项

相似文献

相关主题

期刊订阅