1-aza-2-alky-6-aryl-cycloalkanes
    1.
    发明授权
    1-aza-2-alky-6-aryl-cycloalkanes 失效
    1-氮杂-2-烷基-6-芳基 - 环烷烃

    公开(公告)号:US06451789B1

    公开(公告)日:2002-09-17

    申请号:US09964085

    申请日:2001-09-26

    IPC分类号: A61K3155

    摘要: Compound of formula (I): wherein: n represents 0 or 1, R1 represents hydrogen, arylalkyl, alkyl, acyl, alkoxycarbonyl, arylalkoxycarbonyl or trifluoroacetyl, R2 represents alkyl, X represents oxygen, chlorine, OR3, SR4 or NOR5, R3 represents hydrogen , alkyl, acyl, alkoxycarbonyl or arylalkoxycarbonyl, R4 represents hydrogen, alkyl or aryl, R5 represents hydrogen or optionally substituted alkyl, represents a single or double bond, Ar represents aryl or heteroaryl, its isomers and addition salts thereof with a pharmaceutically acceptable acid, and medicinal products containing the same which are useful as facilitators of memory and cognition and antalgic agents.

    摘要翻译: 式(I)化合物:其中:n表示0或1,R1表示氢,芳基烷基,烷基,酰基,烷氧基羰基,芳基烷氧基羰基或三氟乙酰基,R2表示烷基,X表示氧,氯,OR3,SR4或NOR5,R3表示氢 烷基,酰基,烷氧基羰基或芳基烷氧基羰基,R4代表氢,烷基或芳基,R5代表氢或任选取代的烷基,CUSTOM-CHARACTER FILE =“US06451789-20020917-P00900.TIF”ALT =“custom character”HE =“20 “WI =”20“ID =”CUSTOM-CHARACTER-00001“/>表示单键或双键,Ar表示芳基或杂芳基,其异构体和其药学上可接受的酸的加成盐,以及含有它们的药物 有用作记忆和认知和安踏药剂的促进者。

    2,3-dihydro-4(1H)-pyridone derivatives , method for production thereof and pharmaceutical composition comprising the same
    3.
    发明申请
    2,3-dihydro-4(1H)-pyridone derivatives , method for production thereof and pharmaceutical composition comprising the same 审中-公开
    2,3-二氢-4(1H) - 吡啶酮衍生物,其制备方法和包含其的药物组合物

    公开(公告)号:US20060019995A1

    公开(公告)日:2006-01-26

    申请号:US10533784

    申请日:2003-11-04

    摘要: A compound selected from those of formula (I): wherein: R1 represents hydrogen, aryl(C1-C6)alkyl, linear or branched (C1-C6)alkyl, linear or branched (C1-C6)acyl, linear or branched (C1-C6)alkoxycarbonyl, aryl(C1-C6)alkoxycarbonyl, or trifluoroacetyl, R2 represents hydrogen, linear or branched (C1-C6)alkyl, X represents oxygen or NOR3, R3 represents hydrogen, linear or branched (C1-C6)alkyl optionally substituted by one or more identical or different groups selected from hydroxy, amino and linear or branched (C1-C6)alkoxy, Ar represents aryl or heteroaryl, its isomers, and addition salts thereof with a pharmaceutically acceptable acid or base, and medicinal products containing the same which are useful in the treatment of cognitive disorders and which possess antalgic properties.

    摘要翻译: 选自式(I)的化合物的化合物:其中:R 1表示氢,芳基(C 1 -C 6 -C 6)烷基,直链 或支链(C 1 -C 6 -C 6)烷基,直链或支链(C 1 -C 6 -C 6)酰基(C 1 -C 6 -C 6) ,直链或支链(C 1 -C 6)烷氧基羰基,芳基(C 1 -C 6 -C 6)烷氧基羰基 ,或三氟乙酰基,R 2表示氢,直链或支链(C 1 -C 6 -C 6)烷基,X表示氧或NOR 3,R 3表示氢,任选被一个或多个相同的(C 1 -C 6)烷基取代的直链或支链(C 1 -C 6 -C 6)烷基, 或选自羟基,氨基和直链或支链(C 1 -C 6 -C 6)烷氧基的不同基团,Ar表示芳基或杂芳基,其异构体及其加成盐与 药学上可接受的酸或碱,以及含有该化合物的医药产品,其可用于治疗认知障碍并且具有止痛药 红酒

    Thiadiazine derivatives and use thereof as positive ampa receptor modulators
    8.
    发明申请
    Thiadiazine derivatives and use thereof as positive ampa receptor modulators 失效
    噻二嗪衍生物及其作为正安培受体调节剂的用途

    公开(公告)号:US20070004709A1

    公开(公告)日:2007-01-04

    申请号:US10555743

    申请日:2004-05-04

    IPC分类号: A61K31/549 C07D498/02

    CPC分类号: C07D513/04

    摘要: Compounds of formula (I): wherein: A represents thienyl, furyl, pyrrolyl, oxathiol, thiazole, isothiazole, oxazole or imidazole, represents a single bond or a double bond, R1 represents hydrogen, linear or branched (C1-C6)alkyl optionally substituted by one or more groups selected from halogen or (C1-C6)alkoxy-(C1-C6)alkyl, R2 represents hydrogen or linear or branched (C1-C6)alkyl group optionally substituted by one or more halogen, R3 represents hydrogen or a group selected from linear or branched (C1-C6)alkyl, CONHR′ and SO2NHR′ wherein R′ represents linear or branched (C1-C6)alkyl, its enantiomers and diastereoisomers, and addition salts thereof with a pharmaceutically acceptable acid or base. Medicinal products containing the same, which are useful as AMPA inhibitors.

    摘要翻译: 式(I)化合物:其中:A表示噻吩基,呋喃基,吡咯基,氧硫杂环戊烷,噻唑,异噻唑,恶唑或咪唑,表示单键或双键,R <1 表示任选被一个或多个选自卤素或(C 1 -C 6)烷基的基团取代的直链或支链(C 1 -C 6 -C 6)烷基, -C 6 -C 6烷氧基 - (C 1 -C 6 -C 6)烷基,R 2表示氢或直链或 任选被一个或多个卤素取代的支链(C 1 -C 6 -C 6)烷基,R 3 3表示氢或选自直链或 支链(C 1 -C 6 -C 6)烷基,CONHR'和SO 2 NHR',其中R'表示直链或支链(C 1 -C 6) 1 -C 6烷基,其对映体和非对映异构体及其加成盐w 具有药学上可接受的酸或碱。 含有该药物的药物,可用作AMPA抑制剂。