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INHIBITORS OF CATECHOL-O-METHYLTRANSFERASE AND THEREOF APPLICATION IN TREATMENT OF PSYCHIC DISORDERS

机译:儿茶酚-O-甲基转移酶抑制剂及其在精神分裂症治疗中的应用

摘要

FIELD: medicine, pharmaceutics.SUBSTANCE: claimed invention relates to novel compounds of 4-pyrimidinone of structural formula I and II, which possess properties of catechol-O-methyltransferase (COMT) inhibitor. Compounds can be applied in treatment and prevention of neurological, psychic disorders and diseases, which COMT fragment is involved in, such as negative and positive symptoms of schizophrenia, depression, depressive phase of bipolar disorder, diseases, associated with DA deficiency, such as ADD/ADHD, and addiction, such as opiate, drug and tobacco-addiction, as well as against growth of weight/sense of hunger, associated with cessation of smoking of use of antipsychotics. In formulaandcompounds A represents hydrogen or Calkyl; X represents hydrogen or halogen; Rrepresents phenyl or heterocyclyl, selected from 6-membered unsaturated heterocyclyl with one nitrogen atom in cycle, where said phenyl and heterocyclyl is substituted with 1-3 groups R; Rrepresents Calkyl, N(CH), (CH)Cheterocyclyl, (CH)Caryl, where said aryl and heterocyclyl is optionally substituted with 1-2 groups R; Rrepresents halogen, C-alkinyl, (CH)CF, CN, NHSOR, OR, (CH)C-heterocyclyl, containing 1-2 nitrogen atoms and possibly additionally oxygen or sulphur atom in ring, (CH)Caryl, O(CH)Caryl, where said aryl represents phenyl, where said alkinyl, heterocyclyl and aryl is optionally substituted with 1-3 groups R; Rrepresents Calkyl, OCalkyl, halogen, CHF, OCHF, -O-, (CH)Caryl, (CH)Cheterocyclyl, containing 3 heteroatoms in cycle, selected from nitrogen and oxygen, OR, (CH)CF, where said heterocycle is optionally substituted with 1 or several Calkyls; and n equals 0-1.EFFECT: invention relates to pharmaceutical composition, containing claimed invention compounds and possibly additionally containing monoamine oxidase inhibitor (MAOI), selected from moclobemide.16 cl, 1 tbl, 8 ex
机译:具有儿茶酚-O-甲基转移酶(COMT)抑制剂性质的新颖的结构式I和II的4-嘧啶酮化合物。化合物可用于治疗和预防与COMT片段有关的神经,精神疾病和疾病,例如精神分裂症的阴性和阳性症状,抑郁症,躁郁症的抑郁期,与DA缺乏症相关的疾病,例如ADD / ADHD和成瘾,例如鸦片,毒品和烟草成瘾,以及防止体重增加/饥饿感,与停止使用抗精神病药有关。式中化合物A代表氢或C 1-6烷基; X代表氢或卤素; R表示苯基或杂环基,其选自在一个环中具有一个氮原子的6-元不饱和杂环基,其中所述苯基和杂环基被1-3个R基团取代; R代表C 1-6烷基,N(CH),(CH)杂环基,(CH)C芳基,其中所述芳基和杂环基任选地被1-2个R基团取代; R代表卤素,C-炔基,(CH)CF,CN,NHSOR或OR,(CH)C杂环基,在环中含有1-2个氮原子并且可能还包含氧或硫原子,(CH)Caryl,O(CH)芳基,其中所述芳基代表苯基,其中所述炔基,杂环基和芳基任选地被1-3个基团R取代; R代表C烷基,OC烷基,卤素,CHF,OCHF,-O-,(CH)芳基,(CH)杂环基,循环中包含3个杂原子,选自氮和氧,OR,(CH)CF,其中所述杂环被任选取代具有1个或多个C 1-6烷基;并且n等于0-1。功效:本发明涉及药物组合物,其包含要求保护的发明化合物并且可能还包含选自莫氯贝胺的单胺氧化酶抑制剂(MAOI)。16cl,1 tbl,8 ex

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