Suppr超能文献

3-N-[3-[3-(1-哌啶甲基)苯氧基]丙基]氨基-4-氨基-1,2,5-噻二唑-1-氧化物(L-643,441)作为离体胃腺H2受体拮抗剂的性质研究

Studies on the properties of 3-N-[3-[3-(1-piperidinomethyl)phenoxy]-propyl]amino-4-amino-1,2, 5-thiadiazole-1-oxide (L-643,441) as an H2-receptor antagonist in isolated gastric glands.

作者信息

Shepherd-Rose A J, Pendleton R G

出版信息

Eur J Pharmacol. 1984 Oct 1;105(1-2):57-63. doi: 10.1016/0014-2999(84)90648-4.

Abstract

The H2-receptor blocking properties of L-643,441 were compared with ranitidine in isolated rabbit gastric glands. [14C]Aminopyrine uptake was used as the indicator of gastric acid secretion. Unlike ranitidine, inhibition by L-643,441 was time-dependent, only partially reversible, and was not surmounted by increasing doses of histamine. These and other findings are similar to those found previously in guinea pig atria, providing further evidence that at the receptor level, the mechanism of action of L-643, 441 is different from standard H2-receptor antagonists such as ranitidine.

摘要

在分离的兔胃腺中,比较了L-643,441与雷尼替丁的H2受体阻断特性。使用[14C]氨基比林摄取作为胃酸分泌的指标。与雷尼替丁不同,L-643,441的抑制作用是时间依赖性的,仅部分可逆,并且不会因组胺剂量增加而被克服。这些以及其他发现与先前在豚鼠心房中发现的结果相似,进一步证明在受体水平上,L-643,441的作用机制与雷尼替丁等标准H2受体拮抗剂不同。

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