-
1.Heteroaryl substituted spirocyclic sulfamides for inhibition of gamma secretase 审中-公开
标题翻译: 用于抑制γ分泌酶的杂芳基取代的螺环磺酰胺公开(公告)号:US20080070895A1
公开(公告)日:2008-03-20
申请号:US11899844
申请日:2007-09-07
申请人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
发明人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
IPC分类号: C07D285/14 , A61K31/397 , A61K31/433 , A61K31/4439 , C07D417/00 , C07D401/00 , A61K31/5377 , A61P25/28
CPC分类号: C07D285/14 , C07D417/04 , C07D417/06 , C07D417/12 , C07D417/14 , C07D491/04
摘要: Compounds of formula I are disclosed: in which X is a 5-membered heteroaryl ring and R is as defined herein. The compounds are inhibitors of the processing of APP by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.
摘要翻译: 公开了式I化合物:其中X是5元杂芳基环,R如本文所定义。 这些化合物是通过γ-分泌酶处理APP的抑制剂,因此可用于治疗或预防阿尔茨海默氏病。
-
2.Heteroaryl substituted spirocyclic sulfamides for inhibition of gamma secretase 有权
标题翻译: 用于抑制γ分泌酶的杂芳基取代的螺环磺酰胺公开(公告)号:US20060173054A1
公开(公告)日:2006-08-03
申请号:US11366866
申请日:2006-03-02
申请人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
发明人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
IPC分类号: A61K31/433 , C07D417/02
CPC分类号: C07D285/14 , C07D417/04 , C07D417/06 , C07D417/12 , C07D417/14 , C07D491/04
摘要: Compounds of formula I are disclosed: in which X is a 5-membered heteroaryl ring and R is as defined herein. The compounds are inhibitors of the processing of APP by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.
摘要翻译: 公开了式I化合物:其中X是5元杂芳基环,R如本文所定义。 这些化合物是通过γ-分泌酶处理APP的抑制剂,因此可用于治疗或预防阿尔茨海默氏病。
-
3.Heteroaryl substituted spriocyclic sulfamides for inhibition of gamma secretase 有权
标题翻译: 用于抑制γ分泌酶的杂芳基取代的三环磺酰胺公开(公告)号:US20050182109A1
公开(公告)日:2005-08-18
申请号:US10512810
申请日:2003-04-24
申请人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
发明人: Ian Collins , Laura Cooper , Timothy Harrison , Linda Keown , Andrew Madin , Mark Ridgill
IPC分类号: A61K31/433 , A61P25/28 , C07D285/14 , C07D417/02 , C07D417/04 , C07D417/14 , C07D491/04
CPC分类号: C07D285/14 , C07D417/04 , C07D417/06 , C07D417/12 , C07D417/14 , C07D491/04
摘要: Compounds of formula I are disclosed: in which X is a 5-membered heteroaryl ring and R is as defined herein. The compounds are inhibitors of the processing of APP by gamma-secretase, and hence are useful in the treatment or prevention of Alzheimer's disease.
摘要翻译: 公开了式I化合物:其中X是5元杂芳基环,R如本文所定义。 这些化合物是通过γ-分泌酶处理APP的抑制剂,因此可用于治疗或预防阿尔茨海默氏病。
-
公开(公告)号:US20060135570A1
公开(公告)日:2006-06-22
申请号:US10533272
申请日:2003-10-31
申请人: Ian Collins , Joanne Hannam , Timothy Harrison , Andrew Madin , Mark Ridgill
发明人: Ian Collins , Joanne Hannam , Timothy Harrison , Andrew Madin , Mark Ridgill
IPC分类号: A61K31/433 , C07D271/12
CPC分类号: C07D417/10
摘要: Compounds of formula I: inhibit the processing of AP by gamma-secretase, and hence are useful for treatment or prevention of Alzheimer's disease.
摘要翻译: 式I化合物:通过γ-分泌酶抑制AP的加工,因此可用于治疗或预防阿尔茨海默氏病。
-
公开(公告)号:US20060293373A1
公开(公告)日:2006-12-28
申请号:US10571717
申请日:2004-09-16
申请人: Ian Collins , Joanne Hannam , Andrew Madin , Mark Ridgill
发明人: Ian Collins , Joanne Hannam , Andrew Madin , Mark Ridgill
IPC分类号: A01N43/80
CPC分类号: C07D233/64 , C07D249/08 , C07D409/12 , C07D417/04 , C07D417/12
摘要: Compounds of formula I: are potent inhibitors of gamma-secretase and hence find use in treatment or prevention of diseases associated with deposition of β-amyloid.
-
6.Alkenyl-substituted spirocyclic sulfamides as inhibitors of gamma-secretase 失效
标题翻译: 烯基取代的螺环磺酰胺作为γ-分泌酶的抑制剂公开(公告)号:US20050182111A1
公开(公告)日:2005-08-18
申请号:US10511507
申请日:2003-04-24
申请人: Jose Pineiro , Joanne Hannam , Timothy Harrison , Andrew Madin , Mark Ridgill
发明人: Jose Pineiro , Joanne Hannam , Timothy Harrison , Andrew Madin , Mark Ridgill
IPC分类号: A61P25/28 , C07D285/14 , C07D417/06 , A61K31/433 , C07D498/10
CPC分类号: C07D285/14 , C07D417/06
摘要: Compounds of formula (I) are disclosed: wherein R4 is an alkenyl group of defined structure. The compounds inhibit gamma-secretase, and hence are useful for treatment of Alzheimer's disease.
摘要翻译: 公开了式(I)的化合物:其中R 4是定义结构的烯基。 该化合物抑制γ-分泌酶,因此可用于治疗阿尔茨海默氏病。
-
7.
公开(公告)号:US20080021043A1
公开(公告)日:2008-01-24
申请号:US11664678
申请日:2005-10-20
申请人: Joanne Hannam , Janusz Kulagowski , Andrew Madin , Mark Ridgill , Eileen Seward
发明人: Joanne Hannam , Janusz Kulagowski , Andrew Madin , Mark Ridgill , Eileen Seward
IPC分类号: A61K31/451 , A61K31/439 , A61K31/454 , A61K31/496 , A61P25/28 , C07D211/34 , C07D211/60 , C07D241/04 , C07D401/06 , C07D451/02
CPC分类号: C07D471/08 , C07D207/08 , C07D211/34 , C07D211/60 , C07D211/62 , C07D241/04 , C07D401/06
摘要: Compounds of formula I: selectively inhibit production of Aβ(1-42) and hence are useful in treatment or prevention of disease associated with deposition of β-amyloid in the brain.
摘要翻译: 式I化合物:选择性抑制Aβ(1-42)的产生,因此可用于治疗或预防与脑中沉淀β-淀粉样蛋白相关的疾病。
-
公开(公告)号:US07365196B2
公开(公告)日:2008-04-29
申请号:US10239233
申请日:2001-03-15
申请人: Patrice Charles Belanger , Ian James Collins , Joanne Claire Hannam , Timothy Harrison , Stephen John Lewis , Andrew Madin , Edward Giles McIver , Alan John Nadin , Joseph George Neduvelil , Mark Steven Shearman , Adrian Leonard Smith , Timothy Jason Sparey , Graeme Irvine Stevenson , Martin Richard Teall
发明人: Patrice Charles Belanger , Ian James Collins , Joanne Claire Hannam , Timothy Harrison , Stephen John Lewis , Andrew Madin , Edward Giles McIver , Alan John Nadin , Joseph George Neduvelil , Mark Steven Shearman , Adrian Leonard Smith , Timothy Jason Sparey , Graeme Irvine Stevenson , Martin Richard Teall
IPC分类号: C07D413/14 , C07D413/12 , C07D213/71 , C07D213/52 , C07D333/34 , C07D409/14 , C07D409/12 , C07D249/12 , C07D233/84 , C07D207/48 , C07D277/16 , C07D307/64 , A61P25/28
CPC分类号: C07D213/30 , A61K31/18 , A61K31/40 , C07C311/07 , C07C311/09 , C07C311/11 , C07C311/14 , C07C311/20 , C07C311/24 , C07C323/67 , C07C2601/08 , C07C2601/14 , C07C2602/44 , C07C2602/46 , C07C2603/72 , C07C2603/78 , C07D207/36 , C07D211/14 , C07D211/18 , C07D213/71 , C07D213/81 , C07D215/12 , C07D223/32 , C07D231/12 , C07D233/56 , C07D249/08 , C07D271/107 , C07D277/36 , C07D285/14 , C07D285/16 , C07D295/088 , C07D295/135 , C07D295/26 , C07D307/64 , C07D307/81 , C07D319/18 , C07D333/34 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/06 , C07D417/12 , C07D417/14 , C07D487/04 , C07D487/08 , C07D491/08 , C07D491/10 , C07D513/10
摘要: A class of compounds is disclosed, comprising sulphonamido-substituted bridged bicycloalkyl structures. The compounds are inhibitors of gamma-secretase, and hence are useful in the treatment of and/or prevention of Alzheimer's disease.
摘要翻译: 公开了一类化合物,其包含磺酰氨基取代的桥连双环烷基结构。 这些化合物是γ-分泌酶的抑制剂,因此可用于治疗和/或预防阿尔茨海默氏病。
-
公开(公告)号:US07205434B2
公开(公告)日:2007-04-17
申请号:US10484290
申请日:2002-07-31
IPC分类号: C07C303/00 , A61K31/18
CPC分类号: C07D333/34
摘要: There is disclosed a novel class of sulphonamido-substituted bridged bicycloalkyl derivatives comprising a substitute on the bridgehead position. The compounds modulate the production of the β-amyloid precursor protein, and hence are useful in the treatment of Alzheimer's Disease.
摘要翻译: 公开了一种新型磺酰胺取代的桥连双环烷基衍生物,其包含在桥头头位置上的替代物。 该化合物调节β-淀粉样蛋白前体蛋白的产生,因此可用于治疗阿尔茨海默病。
-
公开(公告)号:US07105509B2
公开(公告)日:2006-09-12
申请号:US10296428
申请日:2001-05-21
申请人: Jose Luis Castro Pineiro , Ian Churcher , Alexander Richard Guiblin , Timothy Harrison , Sonia Kerrard , Andrew Madin , Alan John Nadin , Andrew Pate Owens , Timothy Jason Sparey , Martin Richard Teall , Susannah Williams
发明人: Jose Luis Castro Pineiro , Ian Churcher , Alexander Richard Guiblin , Timothy Harrison , Sonia Kerrard , Andrew Madin , Alan John Nadin , Andrew Pate Owens , Timothy Jason Sparey , Martin Richard Teall , Susannah Williams
IPC分类号: C07D243/24 , C07D243/12 , C07D417/04 , A61K31/55 , A61P25/28
CPC分类号: C07D401/04 , A61K31/55 , C07D243/14 , C07D243/24 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/12 , C07D417/06 , C07D417/12 , C07D487/04 , C07D491/10
摘要: A novel class of 1,4- and 1,5-benzodiazepines of formula (I) is disclosed. The compounds modulate the processing of amyloid precursor protein by γ-secretase, and hence find use in the treatment or prevention of conditions associated with the deposition of β-amyloid, such as Alzheimer's disease
摘要翻译: 公开了一类新颖的式(I)的1,4-和1,5-苯并二氮杂。 该化合物通过γ-分泌酶调节淀粉样前体蛋白的加工,因此可用于治疗或预防与β-淀粉样蛋白沉积相关的病症,例如阿尔茨海默病
-
-
-
-
-
-
-
-
-