Uchida M, Chihiro M, Morita S, Yamashita H, Yamasaki K, Kanbe T, Yabuuchi Y, Nakagawa K
Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd., Japan.
Chem Pharm Bull (Tokyo). 1990 Jun;38(6):1575-86. doi: 10.1248/cpb.38.1575.
A series of 4-substituted 8-[(2-benzimidazolyl)sulfinylmethyl]-1,2,3,4-tetrahydroquinolin es was synthesized and examined for their (H+ + K+)adenosine triphosphatase (ATPase)-inhibitory and antisecretory activities against histamine-induced gastric acid secretion in rats. Many compounds tested were potent inhibitors of (H+ + K+)ATPase. Most compounds showed antisecretory activity. The antiulcer activity against water-immersion stress-induced gastric ulcer, aspirin-induced gastric ulcer and gastric necrosis induced by hydrochloric acid also were tested in the rat. Some of these compounds, in particular, 4-(N-allyl-N-methylamino)-1-ethyl-8-[(5-fluoro-6-methoxy-2-benzimidazoly l) sulfinylmethyl]-1-ethyl-1,2,3,4-tetrahydroquinoline (XVIIx) were found to have potent activity. The structure-activity relationships are discussed.
合成了一系列4-取代的8-[(2-苯并咪唑基)亚磺酰甲基]-1,2,3,4-四氢喹啉,并检测了它们对大鼠组胺诱导胃酸分泌的(H⁺ + K⁺)腺苷三磷酸酶(ATP酶)抑制活性和抗分泌活性。许多受试化合物是(H⁺ + K⁺)ATP酶的强效抑制剂。大多数化合物表现出抗分泌活性。还在大鼠中测试了这些化合物对水浸应激诱导的胃溃疡、阿司匹林诱导的胃溃疡和盐酸诱导的胃坏死的抗溃疡活性。发现其中一些化合物,特别是4-(N-烯丙基-N-甲氨基)-1-乙基-8-[(5-氟-6-甲氧基-2-苯并咪唑基)亚磺酰甲基]-1-乙基-1,2,3,4-四氢喹啉(XVIIx)具有强效活性。讨论了构效关系。