• 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

某些3-取代-2-(4-甲基-1-哌嗪基)-4-苯基喹啉的合成及5-羟色胺受体结合研究

Synthesis and 5-HT receptors binding studies of some 3-substituted-2-(4-methyl-1-piperazinyl)-4-phenylquinolines.

作者信息

Anzini M, Cappelli A, Vomero S, Campiani G, Cagnotto A, Skorupska M

机构信息

Dipartimento Farmaco Chimico Tecnologico-Università, Siena, Italy.

出版信息

Farmaco. 1991 Dec;46(12):1435-47.

PMID:1668253
Abstract

The syntheses of some 3-substituted-2-(4-methyl-1-piperazinyl)-4-phenylquinolines are reported. The title compounds were tested for their potential activities on 5-HT receptor subtypes and 5-HT uptake site; compounds 4b-d showed micromolar affinity for 5-HT3 and 5-HT uptake site.

摘要

报道了一些3-取代-2-(4-甲基-1-哌嗪基)-4-苯基喹啉的合成。对标题化合物在5-羟色胺(5-HT)受体亚型和5-HT摄取位点上的潜在活性进行了测试;化合物4b-d对5-HT3和5-HT摄取位点显示出微摩尔级亲和力。

相似文献

1
Synthesis and 5-HT receptors binding studies of some 3-substituted-2-(4-methyl-1-piperazinyl)-4-phenylquinolines.某些3-取代-2-(4-甲基-1-哌嗪基)-4-苯基喹啉的合成及5-羟色胺受体结合研究
Farmaco. 1991 Dec;46(12):1435-47.
2
Synthesis and 5HT-receptors affinity of some 4-phenylquinoline derivatives.某些4-苯基喹啉衍生物的合成及其对5-羟色胺受体的亲和力
Farmaco. 1989 Jun;44(6):555-63.
3
Characterization of 5-hydroxytryptamine receptors in rat stomach fundus.大鼠胃底5-羟色胺受体的特性研究
J Pharmacol Exp Ther. 1985 Dec;235(3):696-708.
4
Synthesis by microwave irradiation and binding properties of novel 5-HT(1A) receptor ligands.新型5-羟色胺(1A)受体配体的微波辐射合成及其结合特性
Eur J Med Chem. 2001 Nov-Dec;36(11-12):873-86.
5
Novel potent and selective central 5-HT3 receptor ligands provided with different intrinsic efficacy. 2. Molecular basis of the intrinsic efficacy of arylpiperazine derivatives at the central 5-HT3 receptors.具有不同内在活性的新型强效选择性中枢5-HT3受体配体。2. 芳基哌嗪衍生物在中枢5-HT3受体上内在活性的分子基础。
J Med Chem. 1999 May 6;42(9):1556-75. doi: 10.1021/jm981112s.
6
Novel potent and selective central 5-HT3 receptor ligands provided with different intrinsic efficacy. 1. Mapping the central 5-HT3 receptor binding site by arylpiperazine derivatives.具有不同内在活性的新型强效且选择性的中枢5-羟色胺3(5-HT3)受体配体。1. 用芳基哌嗪衍生物绘制中枢5-HT3受体结合位点。
J Med Chem. 1998 Feb 26;41(5):728-41. doi: 10.1021/jm970645i.
7
Structure-affinity relationship studies on arylpiperazine derivatives related to quipazine as serotonin transporter ligands. Molecular basis of the selectivity SERT/5HT3 receptor.作为5-羟色胺转运体配体的与喹哌嗪相关的芳基哌嗪衍生物的结构-亲和力关系研究。5-羟色胺转运体/5-羟色胺3型受体选择性的分子基础。
Bioorg Med Chem. 2005 May 16;13(10):3455-60. doi: 10.1016/j.bmc.2005.03.008.
8
Design and synthesis of long-chain arylpiperazines with mixed affinity for serotonin transporter (SERT) and 5-HT(1A) receptor.对血清素转运体(SERT)和5-HT(1A)受体具有混合亲和力的长链芳基哌嗪的设计与合成。
J Pharm Pharmacol. 2005 Oct;57(10):1319-27. doi: 10.1211/jpp.57.10.0011.
9
Flesinoxan challenge suggests that chronic treatment with paroxetine in rats does not desensitize receptors controlling 5-HT synthesis.氟西汀激发试验表明,大鼠长期接受帕罗西汀治疗不会使控制5-羟色胺合成的受体脱敏。
Neurochem Int. 2008 Dec;53(6-8):236-43. doi: 10.1016/j.neuint.2008.04.005. Epub 2008 Apr 22.
10
Modification of the structure of 4, 6-disubstituted 2-(4-alkyl-1-piperazinyl)pyridines: synthesis and their 5-HT2A receptor activity.4,6-二取代-2-(4-烷基-1-哌嗪基)吡啶结构的修饰:合成及其5-HT2A受体活性
Arch Pharm (Weinheim). 2003 Apr;336(2):104-10. doi: 10.1002/ardp.200390006.

引用本文的文献

1
Ethyl 2,6-dichloro-4-phenyl-quinoline-3-carboxyl-ate.2,6-二氯-4-苯基喹啉-3-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2009 Nov 4;65(Pt 12):o2982. doi: 10.1107/S1600536809045334.