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    • 7. 发明申请
    • NOVEL 1,3-DIHYDRO-BENZOIMIDAZOL-2-ONES AS M1 AGONISTS
    • 新的1,3-二氢苯并咪唑-2-酮作为M1激发剂
    • WO2009124883A1
    • 2009-10-15
    • PCT/EP2009/054000
    • 2009-04-03
    • H. LUNDBECK A/SBANG-ANDERSEN, BennyMIKKELSEN, Gitte, Kobberøe
    • BANG-ANDERSEN, BennyMIKKELSEN, Gitte, Kobberøe
    • C07D401/04A61K31/454
    • C07D401/04
    • The present invention relates to novel MI agonistic compounds of the present invention. wherein R1 and R3 are idenpendently selected from H, cyano, halogen, such as F or C1, C 1-6 alkoxy, such as methoxy, or C 1-6 alkyI, such as methyl R2 is selected from H and halogen, such as F or C1; Y and Y' are individually selected from C 1-3 alkyl, or Y and Y' together with the carbon atom to which they are attached, form a C 3-7 cyctoalkyl group; and wherein each C 1-3 alkyl and C 3-7 cycloalkyl group may be optionally substituted with one or two substituents Z; Z is selected from hydrogen, C 1-3 alkyl and halogen, such as F or C1; and their use in the treatment of cognitive impairment associated 1 a. w ith schizophrenia and in the treatment of other diseases mediated b> the muscarinic MI receptor
    • 本发明涉及本发明的新型MI激动剂化合物。 其中R 1和R 3独立地选自H,氰基,卤素如F或C 1,C 1-6烷氧基如甲氧基或C 1-6烷基,例如甲基R 2选自H和卤素,例如F或 C1; Y和Y'分别选自C 1-3烷基或Y和Y'与它们所连接的碳原子一起形成C 3-7环烷基; 并且其中每个C 1-3烷基和C 3-7环烷基可以任选被一个或两个取代基Z取代; Z选自氢,C 1-3烷基和卤素,例如F或C 1; 及其在治疗认知功能障碍中的应用1 a。 与精神分裂症和治疗其他疾病介导b>毒蕈碱性MI受体