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Indole Derivatives as CCK Receptor Antagonists as CCK Receptor Antagonists

机译:吲哚衍生物作为CCK受体拮抗剂

摘要

The present invention describes novel cholestyocyte antagonists of formula (I) which are useful as obesity agents, gastric hyperplasia in gastrointestinal tracts, therapeutic agents for gastrin-dependent tumors or therapeutic agents for psychosis and having excellent bioavailability. In addition, the compound is an anxiolytic and an anti-ulcer agent. Nicotine, diazepam, alcohol, cocaine, coffee or an opioid (opioid). The compounds of the present invention are also useful for treating and / or preventing panic attacks. Pharmaceutical compositions and methods of making the same are also described. An important characteristic of the present invention is the absolute oral bioavailability of the compound.
机译:本发明描述了式(I)的新型胆囊细胞拮抗剂,其可用作肥胖剂,胃肠道中的胃增生,用于胃泌素依赖性肿瘤的治疗剂或用于精神病的治疗剂并且具有优异的生物利用度。另外,该化合物是抗焦虑药和抗溃疡药。尼古丁,地西epa,酒精,可卡因,咖啡或阿片类药物(阿片类药物)。本发明的化合物也可用于治疗和/或预防惊恐发作。还描述了药物组合物及其制备方法。本发明的重要特征是该化合物的绝对口服生物利用度。

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