PHENANTHRYL PIPERAZINYL DICARBOXYLIC ACIDS AS SELECTIVE NMDA RECEPTOR MODULATING AGENTS
    4.
    发明申请
    PHENANTHRYL PIPERAZINYL DICARBOXYLIC ACIDS AS SELECTIVE NMDA RECEPTOR MODULATING AGENTS 审中-公开
    作为选择性NMDA受体调节剂的苯丙氨酸二苯甲酸

    公开(公告)号:WO0144205A3

    公开(公告)日:2002-02-21

    申请号:PCT/US0034137

    申请日:2000-12-18

    CPC classification number: G01N33/9466 A61K51/0459 C07D241/04

    Abstract: Disclosed are compounds of formula (I) wherein : L is (a) optionally substituted by replacement of one or more of the hydrogen atoms on the phenanthrene ring system by one or more groups other than hydrogen; A is CH2, SO2 or C=O; X is CO2H, PO3H2, PO2H2, PO2HR , PO2HOR , SO3H, SO2H, or tetrazole; and R , R , R , R and R are independently selected from H, alkyl, alkenyl, alkynyl, aryl and aralkyl; or a pharmaceutically acceptable acid salt or base addition salt or an in vivo hydrolysable ester or amide thereof. Compounds of formula (I) are selective NMDA receptor modulating agents and, therefore, may be used to advantage in vitro in neuroassays and in vivo in the treatment of disorders of the CNS.

    Abstract translation: 公开了式(I)的化合物,其中:L是(a)任选地被一个或多个除氢之外的基团取代菲环体系中的一个或多个氢原子; A是CH 2,SO 2或C = O; X是CO2H,PO3H2,PO2H2,PO2HR5,PO2HOR5,SO3H,SO2H或四唑; R 1,R 2,R 3,R 4和R 5独立地选自H,烷基,烯基,炔基,芳基和芳烷基; 或其药学上可接受的酸盐或碱加成盐或其体内可水解的酯或酰胺。 式(I)的化合物是选择性NMDA受体调节剂,因此可以在神经分析和体内用于CNS的疾病的治疗中有利地用于体外 。

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