发明申请
US20070167435A1 Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists
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苯氧基哌啶及其类似物可用作组胺H3拮抗剂
- 专利标题: Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists
- 专利标题(中): 苯氧基哌啶及其类似物可用作组胺H3拮抗剂
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申请号: US11641175申请日: 2006-12-19
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公开(公告)号: US20070167435A1公开(公告)日: 2007-07-19
- 发明人: Mwangi Mutahi , Robert Aslanian , Michael Berlin , Christopher Boyce , Manuel de Lera Ruiz , Kevin McCormick , Daniel Solomon , Henry Vaccaro , Junying Zheng , Purakkattle Biju , Younong Yu , Wei Zhou , Xiaohong Zhu
- 申请人: Mwangi Mutahi , Robert Aslanian , Michael Berlin , Christopher Boyce , Manuel de Lera Ruiz , Kevin McCormick , Daniel Solomon , Henry Vaccaro , Junying Zheng , Purakkattle Biju , Younong Yu , Wei Zhou , Xiaohong Zhu
- 专利权人: Schering Corporation
- 当前专利权人: Schering Corporation
- 主分类号: A61K31/551
- IPC分类号: A61K31/551 ; A61K31/501 ; A61K31/506 ; A61K31/4745 ; C07D471/02
摘要:
Disclosed are compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: M is CH or N; U and W are each CH, or one of U and W is CH and the other is N; X is a bond, alkylene, —C(O)—, —C(N—OR5)—, —C(N—OR5)—CH(R6)—, —CH(R6)—C(N—OR5)—, —O—, —OCH2—, —CH2O— or —S(O)0-2—; Y is —O—, —(CH2)2—, —C(═O)—, —C(═NOR7)— or —SO0-2—; Z is a bond, optionally substituted alkylene or alkylene interrupted by a heteroatom or heterocyclic group; R1 is optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl, heterocycloalkyl, or benzimidazolyl or a derivative thereof; R2 is optionally substituted alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or heterocycloalkyl; and the remaining variables are as defined in the specification; compositions and methods for treating an allergy-induced airway response, congestion, diabetes, obesity, an obesity-related disorder, metabolic syndrome and a cognition deficit disorder using said compounds, alone or in combination with other agents.
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