摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof: wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, a ethenylene group, a ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally; or a methylene group optionally substituted; R1 represents a pyrimidine group optionally substituted; R2 may represent a C 1-6 alkyl group optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group ; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, an indanyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents each independently a hydrogen atom, C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, an ethenylene group, an ethynylene group or a methylene group optionally substituted by one or two groups chosen from a C 1-6 alkyl group, a hydroxy group or a C 1-4 alkoxy group; R1 represents a 2, 4 or 5-pyrimidine ring optionally; R2 represents a heterocyclic bicyclic rings, having 1-4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and having 5-9 carbon atoms, of formula
R3 represents a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R4 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-4 alkoxy group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
摘要翻译:本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示任选被一个或两个选自C 1-6烷基,羟基或C 1-4烷氧基的基团取代的键,亚乙烯基,亚乙炔基或亚甲基; R1代表任选的2,4或5-嘧啶环; R 2表示具有1-4个选自氧原子,硫原子和氮原子并且具有5-9个碳原子的杂原子的杂环二环,式 R 3表示氢原子,C 1-6烷基 ,羟基,C 1-4烷氧基或卤素原子; R4表示氢原子,C1-6烷基,C1-4烷氧基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。
摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, an ethenylene group, an ethynylene group or a methylene group optionally substituted; R1 represents a 2, 3 or 4-pyridine ring optionally substituted; R2 represents a heterocyclic bicyclic rings, having 1-4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and having 5-9 carbon atoms, of formula
R3 represents a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R4 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-4 alkoxy group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
摘要翻译:本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基或任选取代的亚甲基; R1表示任选取代的2,3或4-吡啶环; R 2表示具有1-4个选自氧原子,硫原子和氮原子并且具有5-9个碳原子的杂原子的杂环二环,式 R 3表示氢原子,C 1-6烷基 ,羟基,C 1-4烷氧基或卤素原子; R 4表示氢原子,C 1-6烷基,C 1-4烷氧基或卤素原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。
摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, an ethenylene group, an ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a hydroxyiminomethylene group, a dioxolan group, a nitrogen atom being optionally substituted; or a methylene group optionally substituted; R1 represents a 2, 3 or 4-pyridine ring optionally substituted; R2 may represent a C 1-6 alkyl group optionally; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents, each independently, a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; with the proviso that when R3 and R4 represent each a hydrogen atom then R5 is not a hydrogen atom. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSk3β and cdk5/p25, such as Alzheimer disease.
摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof: wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, a ethenylene group, a ethynylene group, a an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally substituted by a C 1-6 alkyl group, a phenyl or a benzyl group; or a methylene group optionally substituted; R1 represents a pyrimidine group; when Y represents a bond, a methylene group optionally substituted or a carbonyl group then R2 represents a C 1-6 alkyl group optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group ; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; when Y represents a double bond, a triple bond, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted then R2 represents a C 1-6 alkyl group (optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group), a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents each independently a hydrogen atom, C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
摘要:
The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein:
X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; Y represents a bond, an ethenylene group, an ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a hydroxyiminomethylene group, a dioxolan group, a nitrogen atom being optionally substituted; or a methylene group optionally substituted; R1 represents a 2, 3 or 4-pyridyl group optionally substituted by a C 3-6 cycloalkyl group, a C 1-4 alkyl group, a C 1-4 alkoxy group, a benzyl group or a halogen atom; when Y represents a bond, a methylene group optionally substituted , a hydroxyiminomethylene group, a dioxolan group or a carbonyl group then R2 represents a C 1-6 alkyl group optionally; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; when Y represents a ethenylene group, a ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted then R2 represents a C 1-6 alkyl group optionally substituted by a hydroxy group, a C 6,10 aryloxy or a C 6,10 arylamino group; a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a C 6,10 arylamino, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents, each independently, a hydrogen atom, a C 1-6 alkyl group, a hydroxy group, a C 1-4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom; with the proviso that when R3 and R4 represent each a hydrogen atom then R5 is not a hydrogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
摘要翻译:本发明涉及由式(I)表示的嘧啶酮衍生物或其盐,其中:X表示两个氢原子,硫原子,氧原子或C 1-2烷基和氢原子; Y表示键,亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基,羰基,羟基亚氨基亚甲基,二氧戊环,任选取代的氮原子; 或任选取代的亚甲基; R 1表示任选被C 3-6环烷基,C 1-4烷基,C 1-4烷氧基,苄基或卤素原子取代的2,3或4-吡啶基; 当Y表示键时,可以被取代的亚甲基,羟基亚氨基亚甲基,二氧戊环或羰基,则R2表示C1-6烷基; C 3-6环烷基,C 1-4烷硫基,C 1-4烷氧基,C1-2全卤代烷基,C 1-3卤代烷基,苯硫基,苄基,苯环, 5,6,7,8-四氢萘基环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; 当Y表示任选被取代的亚乙烯基,亚乙炔基,氧原子,硫原子,磺酰基,亚砜基或氮原子时,R 2表示任选被羟基取代的C 1-6烷基, C6,10芳氧基或C6,10芳基氨基; C 3-6环烷基,C1-2全卤代烷基,C1-3卤代烷基,苄基,苯环,5,6,7,8-四氢萘基环,萘环,C6, 10芳基氨基,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环; R 3和R 4各自独立地表示氢原子,C 1-6烷基,羟基,C 1-4烷氧基或卤素原子; R5表示氢原子,C1-6烷基或卤素原子; 条件是当R 3和R 4各自表示氢原子时,R 5不是氢原子; 本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β或GSK3β和cdk5 / p25的异常活性引起的神经退行性疾病,例如 阿尔茨海默病。
摘要:
The invention relates to a dihydroimidazo[1,2- a ]pyrimidone derivative represented by formula (I) or a salt thereof: wherein :
X represents hydrogen atoms, a sulphur atom or an oxygen atom; Y represents a bond, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group, a carbonyl group, a nitrogen atom being optionally substituted or a methylene group optionally substituted; R1 represents a 2, 3 or 4-pyridyl group optionally substituted;
when Y represents a bond, a methylene group optionally substituted or a carbonyl group, then R2 represents a C 1-6 alkyl group, a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a naphthyl group, a phenylthio group, a benzyl group, a phenyl ring, a pyridyl ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; the benzyl group, the phenyls, the naphthyl or the rings being optionally substituted by 1 to 3 substituents; when Y represents an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted, then R2 represents a C 1-6 alkyl group, a C 3-6 cycloalkyl group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a naphthyl group, a benzyl group, a phenyl ring, a pyridyl ring, an indole ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring; the benzyl group, the phenyls, the naphthyl or the rings being optionally substituted by 1 to 3 substituents;
and n represents 0 to 3.
The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β.
摘要翻译:本发明涉及由式(I)表示的二氢咪唑并[1,2-a]嘧啶酮衍生物或其盐:其中:X表示氢原子,硫原子或氧原子; Y表示键,氧原子,硫原子,磺酰基,亚砜基,羰基,任选取代的氮原子或任选取代的亚甲基; R1表示任选取代的2,3或4-吡啶基; 当Y表示键,亚甲基任意取代或羰基时,则R2表示C1-6烷基,C3-6环烷基,C1-2全卤代烷基,C1-3卤代烷基, C 1-4烷硫基,C 1-4烷氧基,萘基,苯硫基,苄基,苯环,吡啶环,吲哚环,吡咯环,噻吩环,呋喃环或 咪唑环; 苄基,苯基,萘基或环任选被1至3个取代基取代; 当Y表示氧原子,硫原子,磺酰基,亚砜基或任选被取代的氮原子时,则R2表示C1-6烷基,C3-6环烷基,C1-2全卤代烷基 C 1-3卤代烷基,萘基,苄基,苯环,吡啶环,吲哚环,吡咯环,噻吩环,呋喃环或咪唑环; 苄基,苯基,萘基或环任选被1至3个取代基取代; 并且n表示0至3.本发明还涉及包含所述衍生物或其盐作为活性成分的药物,其用于预防和/或治疗由GSK3β的异常活性引起的神经变性疾病。
摘要:
The invention relates to 3-ketoester of formula (IV)
wherein R1 represents a 2, 3 or 4-pyridine ring optionally substituted by a C 3-6 cycloalkyl group, a C 1-4 alkyl group, a C 1-4 alkoxy group, a benzyl group or a halogen atom, R5 is an halogen atom and R is an alkyl.
摘要翻译:本发明涉及式(IV)的3-酮酯,其中R 1表示任选被C 3-6环烷基取代的2,3或4-吡啶环,C 1-4烷基, C 1-4烷氧基,苄基或卤素原子,R 5为卤素原子,R为烷基。
摘要:
The invention relates to 3-ketoester of formula (IV)
wherein R1 represents a 2, 3 or 4-pyridine ring optionally substituted by a C 3-6 cycloalkyl group, a C 1-4 alkyl group, a C 1-4 alkoxy group, a benzyl group or a halogen atom, R5 is an halogen atom and R is an alkyl.
摘要翻译:本发明涉及式(IV)的3-酮酯,其中R 1表示任选被C 3-6环烷基取代的2,3或4-吡啶环,C 1-4烷基, C 1-4烷氧基,苄基或卤素原子,R 5为卤素原子,R为烷基。