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Substituted tricyclic 1,4-benzodiazepinone derivatives as allosteric modulators of the Group II metabotropic glutamate receptors

机译:取代的三环1,4-苯并二氮杂酮衍生物作为II组代谢型谷氨酸受体的变构调节剂

摘要

The present invention provides novel tricyclic 1,4-benzodiazepinone derivatives of formula I and pharmaceutical compositions containing them. Moreover, the compounds of formula I and pharmaceutical compositions containing them can be used for the treatment of conditions which may be influenced by altered glutamate activity signaling and / or function-related conditions and / or glutamate concentrations or signaling in the mammal, and / It is provided for use in prevention. The tricyclic 1,4-benzodiazepinone derivatives of formula (I) above may act as modulators of glutamate-sensitive nervous system receptors, particularly as modulators of metabotropic glutamate receptors (mGluRs), which cause acute and chronic neurological And / or for the treatment and / or prevention of psychiatric disorders. The present invention further provides a tricyclic 1,4-benzodiazepinone derivative of formula I, which is a modulator of metabotropic glutamate receptor (mGluR), particularly a positive allosteric modulator of mGluR, more particularly a positive allosteric modulator of mGluR3 do.Formula I ;
机译:本发明提供了式I的新型三环1,4-苯并二氮杂醌衍生物和包含它们的药物组合物。此外,式I化合物和包含它们的药物组合物可用于治疗可能受到改变的谷氨酸活性信号和/或功能相关条件和/或谷氨酸浓度或信号在哺乳动物中影响的疾病,和/提供用于预防。上式(I)的三环的1,4-苯并二氮杂酮衍生物可以用作谷氨酸敏感性神经系统受体的调节剂,尤其是代谢型谷氨酸受体(mGluRs)的调节剂,其引起急性和慢性神经系统疾病和/或用于治疗和/或预防精神疾病。本发明进一步提供式I的三环1,4-苯并二氮杂pin酮衍生物,其为代谢型谷氨酸受体(mGluR)的调节剂,特别是mGluR的正变构调节剂,更特别是mGluR3 do的正变构调节剂。

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