• 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

[7TM receptors--from the olfactory system and new hormones against HIV infection].

作者信息

Schwartz T W

机构信息

Laboratoriecentret, laboratoriet for molekylaer farmakologi, Rigshospitalet, København.

出版信息

Ugeskr Laeger. 1997 Feb 24;159(9):1239-45.

PMID:9072867
Abstract

It has recently become evident that all types of chemical messengers, hormones and transmitters act through membrane receptors which constitute our largest superfamily of proteins, i.e. the G protein-coupled receptors. These proteins, which are characterized by having seven transmembrane segments (7TM), also act as, for example sensors for light and odor components in our sensory systems. Already today monoamine 7TM receptors are the target for many drugs; however, the development of non-peptide ligands for a variety of peptide receptors indicates that probably all 7TM receptors can become pharmacotherapeutic targets. The discovery that chemokine receptors function as the crucial cofactors for cell entry of HIV-1 suggests that antagonists or agonists for one or more chemokine 7TM receptor could be interesting agents against AIDS. The occurrence of a multitude of orphan 7TM receptors without known ligand indicates, that surprisingly large areas within endocrinology and neuroscience are still today waiting to be characterized.

摘要

相似文献

1
[7TM receptors--from the olfactory system and new hormones against HIV infection].
Ugeskr Laeger. 1997 Feb 24;159(9):1239-45.
2
Structure-based identification of binding sites, native ligands and potential inhibitors for G-protein coupled receptors.基于结构的G蛋白偶联受体结合位点、天然配体及潜在抑制剂的鉴定
Proteins. 2003 May 15;51(3):423-33. doi: 10.1002/prot.10362.
3
Use of constitutive G protein-coupled receptor activity for drug discovery.组成型G蛋白偶联受体活性在药物发现中的应用。
Mol Pharmacol. 2000 Jan;57(1):125-34.
4
[Chemokine receptors and its importance in the replication cycle of human immunodeficiency virus: clinical and therapeutic implications].[趋化因子受体及其在人类免疫缺陷病毒复制周期中的重要性:临床与治疗意义]
Acta Med Port. 2008 Sep-Oct;21(5):497-504. Epub 2009 Jan 16.
5
Dissecting G-protein-coupled receptors: structure, function, and ligand interaction.剖析G蛋白偶联受体:结构、功能及配体相互作用
Chembiochem. 2002 Oct 4;3(10):915-9. doi: 10.1002/1439-7633(20021004)3:10<915::AID-CBIC915>3.0.CO;2-L.
6
G-protein-coupled receptor oligomerization and its potential for drug discovery.G蛋白偶联受体寡聚化及其在药物发现中的潜力。
Nat Rev Drug Discov. 2002 Oct;1(10):808-20. doi: 10.1038/nrd913.
7
Summary of Wenner-Gren international symposium receptor-receptor interactions among heptaspanning membrane receptors: from structure to function.
J Mol Neurosci. 2005;26(2-3):293-4. doi: 10.1385/JMN:26:2-3:293.
8
Chapter 8. Activation mechanisms of chemokine receptors.第8章.趋化因子受体的激活机制。
Methods Enzymol. 2009;461:171-90. doi: 10.1016/S0076-6879(09)05408-1.
9
Orphan G-protein-coupled receptors: the next generation of drug targets?孤儿G蛋白偶联受体:下一代药物靶点?
Br J Pharmacol. 1998 Dec;125(7):1387-92. doi: 10.1038/sj.bjp.0702238.
10
Allosteric agonists of 7TM receptors: expanding the pharmacological toolbox.7跨膜受体的变构激动剂:拓展药理学工具箱
Trends Pharmacol Sci. 2006 Sep;27(9):475-81. doi: 10.1016/j.tips.2006.07.009. Epub 2006 Aug 4.