摘要:
Disclosed are compounds of the formula: where variables Q, Z, X, R 15 , R 2 , R 3 , and R c are defined herein. Compounds disclosed herein are inhibitors of the beta-secretase enzyme and are therefore useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal.
摘要:
The invention relates to novel compounds and methods of treating diseases, disorders, and conditions associated with amyloidosis. Amyloidosis refers to a colletion of diseases, disorders, and conditions associated with abnormal deposition of A-beta protein.
摘要:
Novel cinnamic acid-related compounds and salts thereof which are useful as drugs, specifically, compounds represented by the general formula [1] and salts thereof: [1] wherein A is a six-membered hydrocarbon ring or a six-membered heterocycle; R
摘要:
The invention relates to novel compounds and also to methods of treating at least one disease, disorder, or condition associated with amyloidosis using such compounds. Amyloidosis refers to a collection of diseases, disorders, and conditions associated with abnormal deposition of A-beta protein.
摘要:
The invention relates to compounds of formula (I). Useful in treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal. The compounds of the invention are useful in pharmaceutical compositions and methods of treatment to reduce A beta peptide formation.
摘要:
Disclosed are compounds of the formula: (I) where variables Z, X, R15, R2, R3, and Rc are defined herein. Compounds disclosed herein are inhibitors of the beta-secretase enzyme and are therefore useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal.
摘要:
The N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein n represents an integer being 1 or 2; R and R each independently represents hydrogen C1-4alkyl, NR R , C1-4alkyloxy; or R and R taken together with the carbon atom with which they are attached form a C3-6cycloalkyl; and where n is 2, either R or R may be absent to form an unsaturated bond; R represents a C6-12cycloalkyl, preferably selected from cylo-octanyl and cyclohexyl or R represents a monovalent radical having one of the following formulae, wherein said C6-12cycloalkyl or monovalent radical may optionally be substituted with one, or where possible two, three or more substituents selected from the group consisting of C1-4alkyl, C1-4alkyloxy, halo or hydroxy; Q represents Het or Ar wherein said C3-8cycloalkyl, Het or Ar are optionally substituted with one or where possible two or more substituents selected from halo, C1-4alkyl, C1-4alkyloxy, hydroxy, nitro, NR R , C1-4alkyloxy substituted with one or where possible two, three or more substituents each independently selected from hydroxycarbonyl, Het and NR R , and C1-4alkyl substituted with one or where possible two or three halo substituents, preferably trifluoromethyl; R and R each independently represent hydrogen, C1-4alkyl, or C1-4alkyl substituted with phenyl; R and R each independently represent hydrogen or C1-4alkyl; R9 and R10 each independently represent hydrogen, C1-4alkyl or Cl-4alkyloxycarbonyl; L represents C1-4alkyl; Het represents a heterocycle selected from pyridinyl, thiophenyl, or 1,3-benzodioxolyl; Het represents piperidinyl, pyrrolidinyl or morpholinyl; Ar represents phenyl, naphtyl or indenyl.
摘要翻译:N-氧化物形式,其药学上可接受的加成盐和立体化学异构形式,其中n代表1或2的整数; R 1和R 2各自独立地表示氢C 1-4烷基,NR 9 R 10,C 1-4烷氧基; 或者R 1和R 2与它们所连接的碳原子一起形成C 3-6环烷基; 并且其中n是2时,可以不存在R 1或R 2以形成不饱和键; R 3代表C 6-12环烷基,优选选自环辛基和环己基,或者R 3代表具有下式之一的一价基团,其中所述C 6-12环烷基或一价基团可以任选被一个,或者 在可能的情况下两个,三个或更多个选自C 1-4烷基,C 1-4烷氧基,卤素或羟基的取代基; Q代表Het 1或Ar 2,其中所述C 3-8环烷基,Het 1或Ar 2任选被一个或在可能的情况下被两个或更多个选自卤素,C 1-4烷基,C 1-4烷氧基, 羟基,硝基,NR 5 R 6,被一个或在可能的情况下被两个,三个或更多个取代基取代的C 1-4烷氧基,所述取代基各自独立地选自羟基羰基,Het 2和NR 7 R 8,以及C1 被一个或在可能的情况下被两个或三个卤素取代基取代的芳基, R 5和R 6各自独立地表示氢,C 1-4烷基或被苯基取代的C 1-4烷基; R 1和R 8各自独立地表示氢或C 1-4烷基; R9和R10各自独立地表示氢,C1-4烷基或C1-4烷氧基羰基; L代表C 1-4烷基; Het 1表示选自吡啶基,噻吩基或1,3-苯并二氧杂环戊烯基的杂环; Het 2代表哌啶基,吡咯烷基或吗啉基; Ar 2代表苯基,萘基或茚基。
摘要:
The invention relates to compounds of formula (I). Useful in treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disease and other diseases characterized by deposition of A beta peptide in a mammal. The compounds of the invention are useful in pharmaceutical compositions and methods of treatment to reduce A beta peptide formation.
摘要:
Compounds, compositions and methods useful for treating cellular proliferative diseases and disorders, for example, by modulating the activity of KSP, are disclosed.
摘要:
The current invention relates to methods for treating hyperlipidemia in mammals, including humans. More specifically, the current invention relates to the use of retinoid or retinoid derivative that is able to act as an antagonist or inverse agonist of a retinoid receptor to treat hyperlipidemia.