New thiazole derivatives of the general formula I
and their salts with physiologically acceptable acids are described as well as a process for their manufacture. The new compounds exhibit histamine H-2 antagonist activity and may thus be used to inhibit gastric acid secretion and to treat gastric and peptic ulcers.
描述了通式 I 的新
噻唑衍
生物及其与生理上可接受的酸的盐类,以及它们的制造工艺。
的新
噻唑衍
生物及其与生理上可接受的酸的盐类,以及它们的制造工艺。这些新化合物具有
组胺 H-2 拮抗剂活性,因此可用于抑制胃酸分泌,治疗胃溃疡和消化性溃疡。