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    • 2. 发明授权
    • Pyrrolopyridazine compounds
    • 吡咯并哒嗪化合物
    • US06734181B2
    • 2004-05-11
    • US10215246
    • 2002-08-08
    • Haruo IwabuchiMasahiko HagiharaNobuhiko ShibakawaKeiji MatsunobuHiroshi Fujiwara
    • Haruo IwabuchiMasahiko HagiharaNobuhiko ShibakawaKeiji MatsunobuHiroshi Fujiwara
    • A61K315025
    • C07D487/04A61K31/5025
    • A pyrrolopyridazine compound having the formula (I) or a pharmaceutically acceptable salt thereof: wherein, R1 is a C2-C6 alkenyl group, a halogeno C2-C6 alkenyl group, a C3-C7 cycloalkyl group which may be optionally substituted or a C3-C7 cycloalkyl- C1-C6 alkyl group which may be optionally substituted. R2 is a C1-C6 alkyl group. R3 is a hydroxymethyl group, a C2-C6 aliphatic acyloxymethyl group, a C6-C10 arylcarbonyloxymethyl group which may be optionally substituted, a C1-C6 alkoxycarbonyloxymethyl group, a formyl group, a carboxyl group, a C1-C6 alkoxycarbonyl group or a C6-C10 aryloxycarbonyl group which may be optionally substituted. R4 is a C6-C10 aryl group which may be optionally substituted. A is an imino group, an oxygen atom or a sulfur atom. These compounds exhibit excellent gastric acid secretory inhibition activity and gastric mucous membrane protection activity etc. They are useful for prevention or treatment of ulcerative diseases and for Helicobacter pylori infections.
    • 具有式(I)的吡咯并哒嗪化合物或其药学上可接受的盐:其中R 1为C 2 -C 6烯基,卤代C 2 -C 6烯基,可任意取代的C 3 -C 7环烷基或 可以任意取代的C 3 -C 7环烷基-C 1 -C 6烷基。 R 2是C 1 -C 6烷基。 R 3是羟甲基,C 2 -C 6脂族酰氧基甲基,可以任意取代的C 6 -C 10芳基羰基氧基甲基,C 1 -C 6烷氧基羰基氧基甲基,甲酰基,羧基,C 1 -C 6烷氧基羰基 或可任意取代的C 6 -C 10芳氧基羰基。 R 4是可以任选取代的C 6 -C 10芳基。 A是亚氨基,氧原子或硫原子。 这些化合物表现出优异的胃酸分泌抑制活性和胃粘膜保护活性等,它们可用于预防或治疗溃疡性疾病和幽门螺杆菌感染。