Suppr超能文献

新型H2拮抗剂HUK 978在大鼠、豚鼠和犬体内的抗分泌活性。

Anti-secretory activity of the novel H2-antagonist, HUK 978, in rat, guinea-pig and dog.

作者信息

Coombes J D, Norris D B, Rising T J, Ross B C, Steward A

出版信息

Life Sci. 1985 Nov 4;37(18):1719-26. doi: 10.1016/0024-3205(85)90300-5.

Abstract

The anti-secretory activity of the competitive H2-antagonist HUK 978 was determined in rat, guinea-pig and dog. In all systems examined, HUK 978 was more potent than cimetidine and ranitidine both intravenously and orally. In addition, the compound at approximately equipotent doses as these established H2-antagonists exhibited a significantly longer inhibitory profile following oral and systemic administration. Data from these pharmacological studies and the in vitro investigations previously reported, suggest that HUK 978 is a highly specific H2-antagonist and inhibits acid secretion for longer periods than other competitive compounds.

摘要

在大鼠、豚鼠和狗身上测定了竞争性H2拮抗剂HUK 978的抗分泌活性。在所有检测的系统中,HUK 978在静脉注射和口服时均比西咪替丁和雷尼替丁更有效。此外,该化合物在与这些已确立的H2拮抗剂剂量大致相当的情况下,口服和全身给药后显示出明显更长的抑制作用时间。这些药理学研究的数据以及先前报道的体外研究表明,HUK 978是一种高度特异性的H2拮抗剂,与其他竞争性化合物相比,其抑制胃酸分泌的时间更长。

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