• 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

14C-N-N'-二环丙基-甲基-哌嗪二盐酸盐的药代动力学。首次通讯:大鼠体内的消除平衡、血浆及血液动力学、代谢情况

Pharmacokinetics of 14C-N-N'-dicyclopropyl-methyl-piperazine-dichlorhydrate. 1st Communication: balance of elimination, plasma and blood kinetics, metabolism in rats.

作者信息

Tufenkji A E, Campistron G, Malbosc R, Declume C, Dormard Y, Atabakhsh F, Benard P, Houin G

机构信息

Laboratoire de Pharmacologie-Pharmacocinétique, Faculté des Sciences Pharmaceutiques, Toulouse, France.

出版信息

Arzneimittelforschung. 1993 Mar;43(3):323-6.

PMID:8489560
Abstract

N-N'-Dicyclopropyl-methyl-piperazine-dichlorhydrate (Ino 2628-CZ) is a novel inotropic compound. The absorption, distribution, excretion and metabolism of radiochemically labelled 14C-Ino 2628-CZ has been studied in male and female rats after intravenous and oral administration. The compound was mainly excreted during the first 24 h after both administrations, although traces of radioactivity were still measured at 7 days post-dose. About 20% of the drug is excreted in the urine unchanged. Nine metabolites were separated, four of them being characterized.

摘要

N-N'-二环丙基甲基哌嗪二盐酸盐(Ino 2628-CZ)是一种新型的强心化合物。对放射性化学标记的14C-Ino 2628-CZ在雄性和雌性大鼠静脉内和口服给药后的吸收、分布、排泄和代谢情况进行了研究。两种给药方式后,该化合物主要在最初24小时内排出,不过在给药后7天仍可检测到微量放射性。约20%的药物以原形经尿液排出。分离出了9种代谢物,其中4种已得到表征。

相似文献

1
Pharmacokinetics of 14C-N-N'-dicyclopropyl-methyl-piperazine-dichlorhydrate. 1st Communication: balance of elimination, plasma and blood kinetics, metabolism in rats.14C-N-N'-二环丙基-甲基-哌嗪二盐酸盐的药代动力学。首次通讯:大鼠体内的消除平衡、血浆及血液动力学、代谢情况
Arzneimittelforschung. 1993 Mar;43(3):323-6.
2
Pharmacokinetics of 14C-N-N'-dicyclopropyl-methyl-piperazine-dichlorhydrate. 2nd communication: tissue distribution in rats.14C-N-N'-二环丙基-甲基-哌嗪二盐酸盐的药代动力学。第二篇通讯:大鼠体内的组织分布
Arzneimittelforschung. 1993 Apr;43(4):436-40.
3
Pharmacokinetics of 14C-N-N'-dicyclopropyl-methyl-piperazine-dichlorhydrate. 3rd communication: whole-body autoradiographic study in Cynomolgus monkeys after oral administration.14C-N-N'-二环丙基-甲基-哌嗪二盐酸盐的药代动力学。第三次通讯:口服给药后食蟹猴的全身放射自显影研究。
Arzneimittelforschung. 1993 May;43(5):516-20.
4
Linear pharmacokinetics of a new inotropic agent.一种新型正性肌力药物的线性药代动力学。
Arzneimittelforschung. 1994 Apr;44(4):471-3.
5
Pharmacokinetics of prulifloxacin. 1st communication: absorption, distribution and excretion in rats, dogs and monkeys after a single administration.普卢利沙星的药代动力学。首次通信:单次给药后在大鼠、狗和猴子体内的吸收、分布及排泄情况
Arzneimittelforschung. 1997 Mar;47(3):276-84.
6
Pharmacokinetics of NS-49, a phenethylamine class alpha 1A-adrenoceptor agonist. 1st communication: absorption and excretion in rats after a single administration of 14C-NS-49.苯乙胺类α1A -肾上腺素能受体激动剂NS - 49的药代动力学。首次通讯:单次给予14C - NS - 49后在大鼠体内的吸收与排泄
Arzneimittelforschung. 1999 May;49(5):434-40. doi: 10.1055/s-0031-1300439.
7
Absorption, distribution, metabolism, and excretion of N,N-diethyl-M-toluamide in the rat.N,N-二乙基间甲苯酰胺在大鼠体内的吸收、分布、代谢及排泄
Drug Metab Dispos. 1996 Feb;24(2):156-63.
8
Metabolism and excretion of the novel antipsychotic drug ziprasidone in rats after oral administration of a mixture of 14C- and 3H-labeled ziprasidone.口服14C和3H标记的齐拉西酮混合物后,新型抗精神病药物齐拉西酮在大鼠体内的代谢和排泄。
Drug Metab Dispos. 1997 Feb;25(2):206-18.
9
Pharmacokinetics of (+/-)-4-diethylamino-1,1-dimethylbut-2-yn-1-yl 2-cyclohexyl-2-hydroxy-2-phenylacetate monohydrochloride monohydrate. 1st communication: absorption, distribution and excretion after single administration of 14C-labeled compound to rats and dogs.盐酸一水合(±)-4-二乙氨基-1,1-二甲基丁-2-炔-1-基 2-环己基-2-羟基-2-苯基乙酸酯的药代动力学。首次通讯:给大鼠和狗单次给予14C标记化合物后的吸收、分布和排泄。
Arzneimittelforschung. 1997 Feb;47(2):151-9.
10
Pharmacokinetics of the new thyrotropin releasing hormone analogue montirelin hydrate. 1st communication: plasma concentrations, metabolism and excretion after a single intravenous administration to rats, dogs and monkeys.新型促甲状腺素释放激素类似物水合蒙替瑞林的药代动力学。首次通讯:对大鼠、狗和猴子单次静脉给药后的血浆浓度、代谢及排泄情况
Arzneimittelforschung. 1996 Feb;46(2):106-13.