Phenyl-alkyl-imidazoles
    1.
    发明授权
    Phenyl-alkyl-imidazoles 失效
    苯基 - 烷基 - 咪唑

    公开(公告)号:US06034251A

    公开(公告)日:2000-03-07

    申请号:US185972

    申请日:1998-11-05

    CPC分类号: C07D233/64

    摘要: Disclosed are novel phenyl-alkyl-imidazoles of the formula ##STR1## wherein R.sup.1, R.sup.7, m, n, p, q, X, Y, Z, R and R.sup.15 are as defined in the specification.Also disclosed are pharmaceutical compositions comprising the compounds of formula I.Further disclosed are methods of treating allergy, inflammation, hypotension, glaucoma, sleeping disorders, states of hyper and hypo motility of the gastrointestinal tract, hypo and hyperactivity of the central nervous system, Alzheimer's, schizophrenia, obesity and migraines by administering compounds of formula I.Also disclosed are methods for treatment of upper airway allergic responses comprising administering a compound, or salt or solvate thereof, of formula I in combination or admixture with a histamine H.sub.1 receptor antagonist.

    摘要翻译: 公开了下式的新型苯基 ​​- 烷基 - 咪唑:其中R1,R7,m,n,p,q,X,Y,Z,R和R15如说明书中所定义。 还公开了包含式I化合物的药物组合物。进一步公开的是治疗过敏,炎症,低血压,青光眼,睡眠障碍,胃肠道超低运动状态,中枢神经系统低血压和多动症,阿尔茨海默病 ,精神分裂症,肥胖症和偏头痛。还公开了治疗上呼吸道过敏反应的方法,包括与组胺H1受体拮抗剂组合或混合施用式I化合物或其盐或溶剂合物。

    Substituted aniline derivatives useful as histamine H3 antagonists
    9.
    发明授权
    Substituted aniline derivatives useful as histamine H3 antagonists 失效
    用作组胺H3拮抗剂的取代苯胺衍生物

    公开(公告)号:US07879880B2

    公开(公告)日:2011-02-01

    申请号:US11641153

    申请日:2006-12-19

    摘要: Disclosed are compounds of the formula or a pharmaceutically acceptable salt thereof, wherein M1 is M2 is N; X is a bond, optionally substituted alkylene, alkenylene, —O—, —CH2N(R12)—, —N(R12)CH2—, —N(R12)—, —NHC(O)—, —OCH2—, —CH2O—, or —S(O)0-2—; and Y is —(CH2)1-2—, —C(═O)—, —C(═NOR13)— or —SO0-2—; or M1 is N; M2 is N or CH; X is a bond, alkylene, alkenylene, —C(O)—, —NHC(O)—, —OC(O)— or —S(O)1-2—; Y is —(CH2)1-2—, —C(═O)— or —SO0-2—; and when M2 is CH, Y is also Y is —O— or —C(═NOR13)—; Z is a bond or optionally substituted alkylene or alkenylene; U and W are CH, or one is CH and one is N; R1 is optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl, heterocycloalkyl; R2 is optionally substituted alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or heterocycloalkyl; and the remaining variables are as defined in the specification; and compositions and methods of treating obesity, metabolic syndrome and a cognition deficit disorder, alone or in combination with other agents.

    摘要翻译: 公开了下式的化合物或其药学上可接受的盐,其中M 1为M 2为N; X是一个键,任选取代的亚烷基,亚烯基,-O - , - CH2-(R12) - , - N(R12)CH2-,-N(R12) - , - NHC(O) - , - OCH2 - - 或-S(O)0-2-; 并且Y是 - (CH 2)1-2 - , - C(= O) - , - C(= NOR 13) - 或-SOO 2 - ; 或M1为N; M2为N或CH; X是键,亚烷基,亚烯基,-C(O) - , - NHC(O) - , - OC(O) - 或-S(O)1-2 - Y是 - (CH 2)1-2 - , - C(= O) - 或-SOO 2 - ; 当M2是CH时,Y也是Y是-O-或-C(= NROR13) - ; Z是键或任选取代的亚烷基或亚烯基; U和W是CH,或一个是CH,一个是N; R 1是任选取代的烷基,环烷基,芳基,芳基烷基,杂芳基,杂环烷基; R 2是任选取代的烷基,烯基,芳基,芳基烷基,杂芳基,杂芳基烷基,环烷基或杂环烷基; 剩余的变量如规范中所定义; 以及单独或与其他药物组合治疗肥胖症,代谢综合征和认知缺陷障碍的组合物和方法。