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PIPERIDINE DERIVATIVES USEFUL AS HISTAMINE H3 ANTAGONISTS.

机译:哌啶衍生物可作为组胺H3拮抗剂使用。

摘要

Disclosed are novel compounds of the formula (I) or a pharmaceutically acceptable salt thereof, wherein: Msup1/sup and Msup3/sup are CH or N; Msup2/sup is CH, CF or N; Y is -C(=O)-, -C(=S)-, -(CHsub2/sub)subq/sub-, -C(=NORsup7/sup)- or -SOsub1-2/sub-; Z is a bond or optionally substituted alkylene or alkenylene; Rsup1/sup is H, or alkyl, cycloalkyl, aryl, heteroaryl, heterocycloalkyl, all optionally substituted, or a group of the formula (II) where ring A is a heteroaryl ring; Rsup2/sup is optionally substituted alkyl, alkenyl, aryl, heteroaryl, cycloalkyl or heterocycloalkyl; Rsup3/sup is H, -C(O)NHsub2/sub, or alkyl, aryl, cycloalkyl, heterocycloalkyl or heteroaryl, all optionally substituted; and the remaining variables are as defined in the specification; compositions and methods of treating allergy-induced airway responses, congestion, obesity, metabolic syndrome, alcoholic fatty liver disease, hepatic steatosis, nonalcoholic steatohepatitis, cirrhosis, hepatacellular carcinoma and cognition deficit disorders using said compounds, alone or in combination with other agents.
机译:公开了式(I)的新型化合物或其药学上可接受的盐,其中:M 1 和M 3 是CH或N; M 2 是CH,CF或N; Y是-C(= O)-,-C(= S)-,-(CH 2 q -,-C(= NOR 7 < / sup>)-或-SO 1-2 -; Z为键或任选取代的亚烷基或亚烯基; R 1 s为H,或为烷基,环烷基,芳基,杂芳基,杂环烷基,所有任选取代的基团或式(II)的基团,其中环A为杂芳基环; R 2 是任选取代的烷基,烯基,芳基,杂芳基,环烷基或杂环烷基; R 3 是H,-C(O)NH 2 或烷基,芳基,环烷基,杂环烷基或杂芳基,它们全部是任选取代的;其余变量如规范中所定义;单独或与其他药物组合使用的化合物治疗过敏性气道反应,充血,肥胖,代谢综合症,酒精性脂肪肝病,肝脂肪变性,非酒精性脂肪性肝炎,肝硬化,肝细胞癌和认知缺陷疾病的组合物和方法。

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