• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

将一些二氢吡啶类似物作为二氢吡啶受体探针的放射性配体结合研究。

Radioligand binding studies on some dihydropyridine analogues as probes of the dihydropyridine receptor.

作者信息

Kettmann V, Drímal J, Svétlík J

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Comenius University, Bratislava, Slovak Republik.

出版信息

Pharmazie. 1996 Oct;51(10):747-50.

PMID:8941943
Abstract

The affinity of two compounds, closely related to 1,4-dihydropyridines, was determined in competition binding experiments using canine cerebral cortex membranes and [3H]nitrendipine as a radioligand. Some aspects of structure-affinity relationships are discussed in relation to existing models of the dihydropyridine binding site.

摘要

在使用犬大脑皮层膜和[3H]尼群地平作为放射性配体的竞争结合实验中,测定了两种与1,4 - 二氢吡啶密切相关的化合物的亲和力。结合二氢吡啶结合位点的现有模型,讨论了结构 - 亲和力关系的一些方面。

相似文献

1
Radioligand binding studies on some dihydropyridine analogues as probes of the dihydropyridine receptor.将一些二氢吡啶类似物作为二氢吡啶受体探针的放射性配体结合研究。
Pharmazie. 1996 Oct;51(10):747-50.
2
Competitive binding experiments reveal differential interactions for dihydropyridine calcium channel activators and antagonists at dihydropyridine receptors on mouse brain membranes.竞争性结合实验揭示了二氢吡啶类钙通道激活剂和拮抗剂在小鼠脑膜二氢吡啶受体上的不同相互作用。
Can J Physiol Pharmacol. 1994 Jul;72(7):738-45. doi: 10.1139/y94-105.
3
The 1,4-dihydropyridine receptor: a regulatory component of the Ca2+ channel.1,4-二氢吡啶受体:钙通道的一种调节成分。
J Cardiovasc Pharmacol. 1984;6 Suppl 7:S949-55.
4
[Photoactivated radioactive analogs of calcium antagonists of 1,4-dihydropyridine series: synthesis and covalent labeling of the receptor in rabbit skeletal muscle].
Biokhimiia. 1988 Aug;53(8):1247-55.
5
New 1,4-dihydropyridines conjugated to furoxanyl moieties, endowed with both nitric oxide-like and calcium channel antagonist vasodilator activities.与呋咱基部分共轭的新型1,4 - 二氢吡啶,兼具一氧化氮样和钙通道拮抗剂血管舒张活性。
J Med Chem. 1998 Dec 31;41(27):5393-401. doi: 10.1021/jm9803267.
6
Combinatorial synthesis and screening of a chemical library of 1,4-dihydropyridine calcium channel blockers.
Bioorg Med Chem. 1998 Jul;6(7):883-9. doi: 10.1016/s0968-0896(98)00048-0.
7
Binding characteristics of the calcium channel antagonist [3H]-nitrendipine in tissues from ethanol-dependent rats.乙醇依赖大鼠组织中钙通道拮抗剂[3H]-尼群地平的结合特性
Alcohol Alcohol. 1994 May;29(3):283-93.
8
Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain.重组高亲和力二氢吡啶结合域的保守钙离子拮抗剂结合特性及推测的折叠结构
Biochem J. 2000 May 1;347 Pt 3(Pt 3):829-36.
9
The time course of up-regulation and down-regulation of dihydropyridine binding sites during the development of physical dependence on ethanol.乙醇身体依赖发展过程中,二氢吡啶结合位点上调和下调的时间进程。
Proc West Pharmacol Soc. 1994;37:77-80.
10
Ligand based approach to L-type calcium channel by imidazo[2,1-b]thiazole-1,4-dihydropyridines: from heart activity to brain affinity.基于配体的咪唑并[2,1-b]噻唑-1,4-二氢吡啶类化合物对 L 型钙通道的作用:从心脏活性到脑亲和力。
J Med Chem. 2013 May 23;56(10):3866-77. doi: 10.1021/jm301839q. Epub 2013 May 9.

引用本文的文献

1
rac-2-Methyl-3,4,5,6-tetra-hydro-2H-2,6-methano-1,3-benzoxazocin-4-one.消旋-2-甲基-3,4,5,6-四氢-2H-2,6-亚甲基-1,3-苯并恶唑啉-4-酮
Acta Crystallogr Sect E Struct Rep Online. 2010 May 22;66(Pt 6):o1402. doi: 10.1107/S1600536810017848.