首页> 外国专利> SUBSTITUTED TRICYCLIC 1,4-BENZODIAZEPINONE DERIVATIVES AS ALLOSTERIC MODULATORS OF GROUP II METABOTROPIC GLUTAMATE RECEPTORS

SUBSTITUTED TRICYCLIC 1,4-BENZODIAZEPINONE DERIVATIVES AS ALLOSTERIC MODULATORS OF GROUP II METABOTROPIC GLUTAMATE RECEPTORS

机译:取代的三环1,4-二氮杂二酮衍生物作为II类代谢型谷氨酸受体的变位调节剂

摘要

The present invention provides novel tricyclic 1,4-benzodiazepinone derivatives of the general formula (I) and pharmaceutical compositions containing them. Moreover, the compounds of formula (I) and the pharmaceutical compositions containing them are provided for use in the treatment and/or prophylaxis of conditions associated with altered glutamatergic signalling and/or functions, and/or conditions which can be affected by alteration of glutamate level or signalling in mammals. The tricyclic 1,4-benzodiazepinone derivatives of formula (I) can act as modulators of nervous system receptors sensitive to glutamate, in particular as modulators of metabotropic glutamate receptors (mGluRs), which makes them particularly suitable for the treatment and/or prophylaxis of acute and chronic neurological and/or psychiatric disorders. The present invention further provides tricyclic 1,4-benzodiazepinone derivatives of formula (I) that are modulators of metabotropic glutamate receptors (mGluRs), particularly positive allosteric modulators of mGluRs, and more specifically positive allosteric modulators of mGluR3. (I)
机译:本发明提供了通式(I)的新型三环1,4-苯并二氮杂醌衍生物和含有它们的药物组合物。此外,提供了式(I)的化合物和包含它们的药物组合物,用于治疗和/或预防与改变的谷氨酸能信号传导和/或功能有关的病症,和/或可能受谷氨酸改变影响的病症。哺乳动物体内的水平或信号。式(I)的三环1,4-苯并二氮杂酮衍生物可以用作对谷氨酸敏感的神经系统受体的调节剂,特别是作为代谢型谷氨酸受体(mGluRs)的调节剂,这使得它们特别适合于治疗和/或预防糖尿病。急性和慢性神经和/或精神疾病。本发明进一步提供式(I)的三环的1,4-苯并二氮杂pin酮衍生物,其为亲代谢型谷氨酸受体(mGluRs)的调节剂,特别是mGluRs的正变构调节剂,更具体地是mGluR3的正变构调节剂。 (一世)

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