A review of the animal pharmacology of roxatidine acetate
1. 请及时下载文件确认是否正确, 系统将在 2026-10-19 16:10:15 删除文件
2. 如若文件有误请驳回应助文件, 求助状态即回到求助中
3. 如若文件正确请及时点击确认, 若超过时后系统自动默认为已完结
注: 所有应助的资源仅供学习交流使用, 不得违反相关法律法规
DOI:
文献链接:
其他信息:
J Scholtholt, M Bickel, AW Herling
Drugs, 1988
Springer
Summary Roxatidine acetate (TZU 0460/HOE 760)[N-(3-[3-(1-piperidinylmethyl)-phenoxy]-propyl) acetoxyacetamide hydrochloride] is a specific and competitive H2-receptor antagonist with a chemical structure different from those of cimetidine, ranitidine and famotidine. Roxatidine acetate and its main metabolite roxatidine inhibit histamine-induced gastric acid secretion in vitro with a potency greater than that of cimetidine, and in the range of that produced by ranitidine. Gastric acid secretion following stimulation with dibutyryl …

