SG162790A1 - Aspartyl protease inhibitors - Google Patents
Aspartyl protease inhibitorsInfo
- Publication number
- SG162790A1 SG162790A1 SG201004170-5A SG2010041705A SG162790A1 SG 162790 A1 SG162790 A1 SG 162790A1 SG 2010041705 A SG2010041705 A SG 2010041705A SG 162790 A1 SG162790 A1 SG 162790A1
- Authority
- SG
- Singapore
- Prior art keywords
- aspartyl protease
- disclosed
- protease inhibitors
- compounds
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- AIDS & HIV (AREA)
- Oncology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69053705P | 2005-06-14 | 2005-06-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG162790A1 true SG162790A1 (en) | 2010-07-29 |
Family
ID=37114557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG201004170-5A SG162790A1 (en) | 2005-06-14 | 2006-06-12 | Aspartyl protease inhibitors |
Country Status (18)
Country | Link |
---|---|
US (1) | US7868000B2 (fr) |
EP (1) | EP1896478B1 (fr) |
JP (2) | JP2008543849A (fr) |
KR (1) | KR20080029965A (fr) |
CN (1) | CN101228163A (fr) |
AR (1) | AR054617A1 (fr) |
AU (1) | AU2006259572A1 (fr) |
BR (1) | BRPI0612072A2 (fr) |
CA (1) | CA2609582A1 (fr) |
EC (1) | ECSP078003A (fr) |
IL (1) | IL187814A0 (fr) |
MX (1) | MX2007016180A (fr) |
NO (1) | NO20080187L (fr) |
PE (1) | PE20070135A1 (fr) |
RU (1) | RU2008100165A (fr) |
SG (1) | SG162790A1 (fr) |
TW (2) | TW201004961A (fr) |
WO (1) | WO2006138264A2 (fr) |
Families Citing this family (70)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0220581D0 (en) * | 2002-09-04 | 2002-10-09 | Novartis Ag | Organic Compound |
US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
PE20060437A1 (es) * | 2004-06-18 | 2006-06-08 | Novartis Ag | COMPUESTOS AZA-BICICLONONANOS COMO LIGANDOS COLINERGICOS DE nAChR |
GB0415746D0 (en) | 2004-07-14 | 2004-08-18 | Novartis Ag | Organic compounds |
AR056865A1 (es) | 2005-06-14 | 2007-10-31 | Schering Corp | Heterociclos nitrogenados y su uso como inhibidores de proteasas, composiciones farmaceuticas |
CA2610812A1 (fr) * | 2005-06-14 | 2006-12-28 | Schering Corporation | Inhibiteurs de l'aspartyl protease |
WO2006138264A2 (fr) | 2005-06-14 | 2006-12-28 | Schering Corporation | Inhibiteurs d'aspartyl protease |
GB0521508D0 (en) * | 2005-10-21 | 2005-11-30 | Novartis Ag | Organic compounds |
WO2007050721A2 (fr) | 2005-10-27 | 2007-05-03 | Schering Corporation | Inhibiteurs heterocycliques d'aspartyle protease |
GB0525672D0 (en) | 2005-12-16 | 2006-01-25 | Novartis Ag | Organic compounds |
GB0525673D0 (en) * | 2005-12-16 | 2006-01-25 | Novartis Ag | Organic compounds |
EP2032542A2 (fr) | 2006-06-12 | 2009-03-11 | Schering Corporation | Inhibiteurs d'aspartyl protéase hétérocycliques |
TW200815349A (en) | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
CN101631779A (zh) * | 2006-12-12 | 2010-01-20 | 先灵公司 | 含有三环系统的天冬氨酰蛋白酶抑制剂 |
AU2007332754A1 (en) * | 2006-12-12 | 2008-06-19 | Schering Corporation | Aspartyl protease inhibitors |
TW200902499A (en) | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
CA2698341A1 (fr) | 2007-09-06 | 2009-03-12 | Schering Corporation | Modulateurs de la gamma secretase |
US8487099B2 (en) | 2007-11-05 | 2013-07-16 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
CA2708300A1 (fr) | 2007-12-11 | 2009-06-18 | Schering Corporation | Modulateurs de gamma secretase |
AR071385A1 (es) * | 2008-04-22 | 2010-06-16 | Schering Corp | Compuestos de 2-imino-3-metil pirrolopirimidinona sustituida con tiofenilo,composiciones farmaceuticas que los contienen,y uso de los mismos para el tratamiento de patologias asociadas con la proteina beta amiloide,tales como alzheimer y otros formas de demencia. |
MX2011005046A (es) | 2008-11-13 | 2011-06-01 | Schering Corp | Moduladores de gamma secretasa. |
TW201020244A (en) | 2008-11-14 | 2010-06-01 | Astrazeneca Ab | New compounds |
AR074702A1 (es) | 2008-12-22 | 2011-02-02 | Schering Corp | Moduladores de gamma secretasa y composiciones farmaceuticas que los contienen |
CA2747744A1 (fr) | 2008-12-22 | 2010-07-01 | Theodros Asberom | Modulateurs de gamma secretase |
FR2944011B1 (fr) | 2009-04-03 | 2011-05-20 | Pf Medicament | Derives d'aminocyclobutane ou d'aminocyclobutene, leur procede de preparation et leur utilisation a titre de medicaments. |
US20120238546A1 (en) | 2009-06-16 | 2012-09-20 | Zhaoning Zhu | Gamma secretase modulators |
WO2010147975A1 (fr) | 2009-06-16 | 2010-12-23 | Schering Corporation | Modulateurs de gamma sécrétase |
WO2010147973A1 (fr) | 2009-06-16 | 2010-12-23 | Schering Corporation | Modulateurs de gamma sécrétase |
GB0912777D0 (en) * | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydropyrimidone derivatives |
GB0912778D0 (en) | 2009-07-22 | 2009-08-26 | Eisai London Res Lab Ltd | Fused aminodihydro-oxazine derivatives |
EP2281824A1 (fr) | 2009-08-07 | 2011-02-09 | Noscira, S.A. | Dérivés de furan-imidazolone pour le traitement de maladies ou de troubles cognitifs, neurodégénératifs ou neuronaux |
EP2485590B1 (fr) | 2009-10-08 | 2015-01-07 | Merck Sharp & Dohme Corp. | Composés hétérocycliques de type imino-pentafluorosulfure utilisés en tant qu'inhibiteurs de bace1, compositions en contenant et leur utilisation |
US8569310B2 (en) | 2009-10-08 | 2013-10-29 | Merck Sharp & Dohme Corp. | Pentafluorosulfur imino heterocyclic compounds as BACE-1 inhibitors, compositions and their use |
UA108363C2 (uk) | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
EP2485591B1 (fr) | 2009-10-08 | 2016-03-23 | Merck Sharp & Dohme Corp. | Composés de type dioxyde d'imino-thiadiazine utilisés en tant qu'inhibiteurs de bace, compositions en contenant et leur utilisation |
EP2511269A4 (fr) * | 2009-12-11 | 2013-04-24 | Shionogi & Co | Composé hétérocyclique fusionné comportant un groupement amino |
EP2643299B1 (fr) | 2010-11-22 | 2016-06-22 | Noscira, S.A. | Dérivés de bipyridine-sulfonamide pour le traitement de maladies et d'affections neurodégénératives |
US8415483B2 (en) | 2010-12-22 | 2013-04-09 | Astrazeneca Ab | Compounds and their use as BACE inhibitors |
GB201100181D0 (en) | 2011-01-06 | 2011-02-23 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
GB201101139D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
GB201101140D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
ES2624288T3 (es) | 2011-01-21 | 2017-07-13 | Eisai R&D Management Co., Ltd. | Métodos y compuestos útiles en la síntesis de derivados de aminodihidrotiazina condensados |
WO2012138734A1 (fr) | 2011-04-07 | 2012-10-11 | Merck Sharp & Dohme Corp. | Composés de dioxyde de thiadiazine condensés avec des dérivés oxacycliques en c5-c6 comme inhibiteurs de bace, compositions, et utilisation use |
US9145426B2 (en) | 2011-04-07 | 2015-09-29 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use |
US9181236B2 (en) | 2011-08-22 | 2015-11-10 | Merck Sharp & Dohme Corp. | 2-spiro-substituted iminothiazines and their mono-and dioxides as bace inhibitors, compositions and their use |
WO2013054108A1 (fr) | 2011-10-10 | 2013-04-18 | Astrazeneca Ab | Inhibiteurs de mono fluoro-bêta-secretase |
KR102160388B1 (ko) | 2012-03-19 | 2020-09-28 | 버크 인스티튜트 포 리서치 온 에이징 | App 특이적 bace 억제제(asbi) 및 이의 용도 |
JO3143B1 (ar) | 2012-04-03 | 2017-09-20 | Lilly Co Eli | مركبات تتراهيدرو بيرولو ثيازين |
WO2013180265A1 (fr) | 2012-06-01 | 2013-12-05 | 武田薬品工業株式会社 | Composé hétérocyclique |
US9000183B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cyclohexane-1,2′-indene-1′,2″-imidazol compounds and their use as BACE inhibitors |
US9000184B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cyclohexane-1,2′-naphthalene-1′,2″-imidazol compounds and their use as BACE inhibitors |
US9000182B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | 2H-imidazol-4-amine compounds and their use as BACE inhibitors |
US9000185B2 (en) | 2012-06-20 | 2015-04-07 | Astrazeneca Ab | Cycloalkyl ether compounds and their use as BACE inhibitors |
US10548882B2 (en) | 2012-06-21 | 2020-02-04 | Astrazeneca Ab | Camsylate salt |
EP2908824B1 (fr) | 2012-10-17 | 2018-05-02 | Merck Sharp & Dohme Corp. | Composés de dioxyde de thiadiazine substituée tricyclique utilisés en tant qu'inhibiteurs de bace, compositions et leur utilisation |
US9422277B2 (en) | 2012-10-17 | 2016-08-23 | Merck Sharp & Dohme Corp. | Tricyclic substituted thiadiazine dioxide compounds as BACE inhibitors, compositions and their use |
PT2912041T (pt) | 2012-10-26 | 2017-02-13 | Lilly Co Eli | Inibidores de bace |
WO2014099788A1 (fr) | 2012-12-21 | 2014-06-26 | Merck Sharp & Dohme Corp. | Dioxydes d'iminothiadiazine spiro c5 utilisés en tant qu'inhibiteurs de bace |
KR102220259B1 (ko) | 2013-02-12 | 2021-02-25 | 버크 인스티튜트 포 리서치 온 에이징 | Bace 매개 app 처리과정을 조절하는 히단토인 |
TWI593692B (zh) * | 2013-03-12 | 2017-08-01 | 美國禮來大藥廠 | 四氫吡咯并噻嗪化合物 |
JO3318B1 (ar) | 2013-06-18 | 2019-03-13 | Lilly Co Eli | مثبطات bace |
EP3082823B1 (fr) | 2013-12-18 | 2020-04-22 | Merck Sharp & Dohme Corp. | Composés de dioxyde d'iminothiadiazépane utilisés en tant qu'inhibiteurs de bace, compositions et leur utilisation |
AR103680A1 (es) | 2015-02-23 | 2017-05-24 | Lilly Co Eli | Inhibidores selectivos de bace1 |
CN104761557B (zh) * | 2015-04-08 | 2017-02-22 | 河南师范大学 | 六氢‑1H‑吡咯并[3,4‑d]嘧啶类化合物及其制备方法 |
AR104241A1 (es) | 2015-04-29 | 2017-07-05 | Lilly Co Eli | Derivados de tetrahidrofuro tiazina como inhibidores de bace1 selectivos |
EP3414253B1 (fr) | 2016-02-11 | 2021-07-21 | Merck Sharp & Dohme Corp. | Composés de dioxyde d'iminothiazine condensé oxacylique en c5 a c6 portant un lieur éther en tant qu'inhibiteurs de bace, compositions et leur utilisation |
CN107892697B (zh) | 2016-12-26 | 2020-11-03 | 郑州泰基鸿诺医药股份有限公司 | 一种[1,3]噻嗪-2-胺类化合物及应用,药物组合物 |
CN111741948B (zh) | 2018-02-28 | 2023-11-10 | 日本烟草产业株式会社 | 饱和环稠合的二氢嘧啶酮或二氢三嗪酮化合物及其药物用途 |
Family Cites Families (100)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL92011A0 (en) | 1988-10-19 | 1990-07-12 | Abbott Lab | Heterocyclic peptide renin inhibitors |
AU2436792A (en) | 1991-08-16 | 1993-03-16 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
US5610294A (en) * | 1991-10-11 | 1997-03-11 | The Du Pont Merck Pharmaceutical Company | Substituted cyclic carbonyls and derivatives thereof useful as retroviral protease inhibitors |
IT1270008B (it) | 1994-09-23 | 1997-04-16 | Ist Superiore Sanita | Derivati purinici ed 8-azapurinici atti al trattamento terapeutico dell'aids |
IL117149A0 (en) | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
US5889006A (en) | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
US5935958A (en) | 1996-07-01 | 1999-08-10 | Schering Corporation | Muscarinic antagonists |
US5952349A (en) | 1996-07-10 | 1999-09-14 | Schering Corporation | Muscarinic antagonists for treating memory loss |
US5977138A (en) | 1996-08-15 | 1999-11-02 | Schering Corporation | Ether muscarinic antagonists |
WO1999065870A2 (fr) * | 1998-06-19 | 1999-12-23 | Vertex Pharmaceuticals Incorporated | Inhibiteurs sulfonamides d'aspartyle protease |
US6066636A (en) | 1998-06-30 | 2000-05-23 | Schering Corporation | Muscarinic antagonists |
US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
US6294554B1 (en) | 1999-09-22 | 2001-09-25 | Schering Corporation | Muscarinic antagonists |
JP2004505978A (ja) | 2000-08-09 | 2004-02-26 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | (R)−3−(4−ブロモベンジル)−1−(3,5−ジクロロフェニル)−5−ヨード−3−メチル−1−H−イミダゾ[1,2−a]イミダゾール−2−オンの合成 |
CN1481360A (zh) | 2000-12-22 | 2004-03-10 | ���鹫˾ | 蕈毒碱拮抗剂 |
US7560482B2 (en) | 2001-03-15 | 2009-07-14 | The Johns Hopkins University | Inhibitors of plasmepsins |
US6831089B2 (en) | 2001-10-10 | 2004-12-14 | Schering Corporation | Muscarinic antagonists |
EP1660443B1 (fr) | 2003-08-08 | 2009-03-04 | Schering Corporation | Inhibiteurs bace-1 amines cycliques a substituant benzamide |
TW200524910A (en) | 2003-08-08 | 2005-08-01 | Schering Corp | Cyclic amine BACE-1 inhibitors having a heterocyclic substituent |
US20050171112A1 (en) | 2003-11-03 | 2005-08-04 | Probiodrug Ag | Combinations useful for the treatment of neuronal disorders |
US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
CN102627609B (zh) | 2003-12-15 | 2016-05-04 | 默沙东公司 | 杂环天冬氨酰蛋白酶抑制剂 |
US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
EP1740575A2 (fr) | 2004-04-22 | 2007-01-10 | Eli Lilly And Company | Inhibiteurs de la bace |
AU2005264917A1 (en) | 2004-06-16 | 2006-01-26 | Wyeth | Diphenylimidazopyrimidine and -imidazole amines as inhibitors of B-secretase |
CN1968945A (zh) | 2004-06-16 | 2007-05-23 | 惠氏公司 | 用于抑制β分泌酶的氨基-5,5-二苯基咪唑酮衍生物 |
MX2007000760A (es) | 2004-07-22 | 2007-04-09 | Schering Corp | Amida sustituida inhibidora de b secretasa. |
ES2306200T3 (es) | 2004-07-28 | 2008-11-01 | Schering Corporation | Inhibidores macrociclicos de beta-secretasa. |
CN101035770B (zh) | 2004-08-06 | 2011-02-23 | 詹森药业有限公司 | 可用作β-分泌酶(BACE)抑制剂的2-氨基-喹唑啉衍生物 |
JP4898677B2 (ja) | 2004-08-06 | 2012-03-21 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | β−セクレターゼ(BACE)のインヒビターとして有用な2−アミノ−キナゾリン誘導体 |
US8436006B2 (en) | 2004-08-06 | 2013-05-07 | Jansssen Pharmaceutica N.V. | 2-amino-quinazoline derivatives useful as inhibitors of β-secretase (BACE) |
WO2006044492A2 (fr) | 2004-10-14 | 2006-04-27 | Ingenious Targeting Laboratory, Inc. | Methodes de generation de lignees cellulaires derivees d'embryons de rats et de modification genetique de genome de rats |
JP2008516946A (ja) | 2004-10-15 | 2008-05-22 | アストラゼネカ・アクチエボラーグ | 置換されたアミノ−ピリミドンおよびそれらの使用 |
WO2006041404A1 (fr) | 2004-10-15 | 2006-04-20 | Astrazeneca Ab | Composes amino substitues et utilisation de ces compose |
BRPI0606690A2 (pt) | 2005-01-14 | 2009-07-14 | Wyeth Corp | composto; uso do composto para o tratamento de uma doença ou distúrbio associado com uma atividade excessiva de bace; e composição farmacêutica |
CA2610812A1 (fr) | 2005-06-14 | 2006-12-28 | Schering Corporation | Inhibiteurs de l'aspartyl protease |
AR056865A1 (es) | 2005-06-14 | 2007-10-31 | Schering Corp | Heterociclos nitrogenados y su uso como inhibidores de proteasas, composiciones farmaceuticas |
WO2006138264A2 (fr) | 2005-06-14 | 2006-12-28 | Schering Corporation | Inhibiteurs d'aspartyl protease |
ATE489370T1 (de) | 2005-06-14 | 2010-12-15 | Schering Corp | Herstellung und verwendung von verbindungen als aspartylproteasehemmer |
JP2008543846A (ja) | 2005-06-14 | 2008-12-04 | シェーリング コーポレイション | プロテアーゼ阻害剤として化合物の調製およびその使用 |
AU2006259609A1 (en) | 2005-06-14 | 2006-12-28 | Pharmacopeia, Inc. | Aspartyl protease inhibitors |
CN101193892A (zh) | 2005-06-14 | 2008-06-04 | 先灵公司 | 大环杂环天冬氨酰基蛋白酶抑制剂 |
AU2006266167A1 (en) | 2005-06-30 | 2007-01-11 | Wyeth | Amino-5-(6-membered)heteroarylimidazolone compounds and the use thereof for beta-secretase modulation |
TW200738683A (en) | 2005-06-30 | 2007-10-16 | Wyeth Corp | Amino-5-(5-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation |
TW200730523A (en) | 2005-07-29 | 2007-08-16 | Wyeth Corp | Cycloalkyl amino-hydantoin compounds and use thereof for β-secretase modulation |
CA2623245A1 (fr) | 2005-09-26 | 2007-04-05 | Wyeth | Composes d'amino-5-[4-(difluoromethoxy) phenyl]-5-phenylimidazolone utilises comme inhibiteurs de la beta-secretase (bace) |
CN103936690B (zh) | 2005-10-25 | 2016-06-08 | 盐野义制药株式会社 | 氨基二氢噻嗪衍生物 |
ATE502036T1 (de) | 2005-10-25 | 2011-04-15 | Janssen Pharmaceutica Nv | Als inhibitoren von beta-sekretase (bace) geeignete 2-amino-3,4-dihydropyridoä3,4- düpyrimidinderivate |
WO2007050721A2 (fr) | 2005-10-27 | 2007-05-03 | Schering Corporation | Inhibiteurs heterocycliques d'aspartyle protease |
EP1943246A1 (fr) | 2005-10-31 | 2008-07-16 | Schering Corporation | Inhibiteurs de l aspartyle protease |
EP1951680A4 (fr) | 2005-11-15 | 2011-08-10 | Astrazeneca Ab | Nouveaux derives de 2-aminopyrimidinone et leur utilisation |
CN101360721A (zh) | 2005-11-15 | 2009-02-04 | 阿斯利康(瑞典)有限公司 | 新颖的2-氨基嘧啶酮衍生物或2-氨基吡啶酮衍生物及其用途 |
TW200804290A (en) | 2005-11-15 | 2008-01-16 | Astrazeneca Ab | Compounds and uses thereof |
TW200734311A (en) | 2005-11-21 | 2007-09-16 | Astrazeneca Ab | New compounds |
EP1954682A4 (fr) | 2005-11-21 | 2011-11-09 | Astrazeneca Ab | Nouveaux composes 2-amino-imidazole-4-one et leur utilisation dans la fabrication d'un medicament destine a etre utilise dans le traitement d'une deficience cognitive, la maladie d'alzheimer, le neurodegenerescence et la demence |
AR058381A1 (es) | 2005-12-19 | 2008-01-30 | Astrazeneca Ab | Compuestos derivados de 2-aminopiridin-4-onas y una composicion farmaceutica |
EP1966185A2 (fr) | 2005-12-19 | 2008-09-10 | Wyeth a Corporation of the State of Delaware | DÉRIVÉS DE 2-AMINO-5-PIPÉRIDINYLIMIDAZOLONE ET APPLICATIONS À LA MODULATION DE LA ß-SECRÉTASE |
WO2007092839A2 (fr) | 2006-02-06 | 2007-08-16 | Janssen Pharmaceutica N.V. | DÉRIVÉS MACROCYCLIQUES UTILES COMME INHIBITEURS DE LA β-SÉCRÉTASE (BACE) |
WO2007092846A2 (fr) | 2006-02-06 | 2007-08-16 | Janssen Pharmaceutica N.V. | DÉRIVÉS DE 2-AMINO-3,4-DIHYDRO-QUINOLÉINE UTILES COMME INHIBITEURS DE LA β-SÉCRÉTASE (BACE) |
US7868022B2 (en) | 2006-02-06 | 2011-01-11 | Janssen Pharmaceutica Nv | 2-amino-quinoline derivatives useful as inhibitors of β-secretase (BACE) |
WO2007100536A1 (fr) | 2006-02-24 | 2007-09-07 | Wyeth | COMPOSES DE DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] POUR L'INHIBITION DE LA β-SECRETASE |
EP2004630A4 (fr) | 2006-04-05 | 2010-05-19 | Astrazeneca Ab | 2-aminopyrimidin-4-ones et leur utilisation pour le traitement ou la prevention de pathologies liees a la proteine a |
EP2032542A2 (fr) | 2006-06-12 | 2009-03-11 | Schering Corporation | Inhibiteurs d'aspartyl protéase hétérocycliques |
TW200808796A (en) | 2006-06-14 | 2008-02-16 | Astrazeneca Ab | New compounds III |
TW200815447A (en) | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds IV |
TW200815449A (en) | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds II |
US20080051420A1 (en) | 2006-06-14 | 2008-02-28 | Astrazeneca Ab | New Compounds 317 |
TW200815443A (en) | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds I |
TW200815349A (en) | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
TW200817406A (en) | 2006-08-17 | 2008-04-16 | Wyeth Corp | Imidazole amines as inhibitors of β-secretase |
WO2008063114A1 (fr) | 2006-11-20 | 2008-05-29 | Astrazeneca Ab | Amino-imidazolones et utilisation thérapeutique de ces composés pour traiter les troubles cognitifs, la maladie d'alzheimer, la neurodégénérescence et la démence |
AU2007332754A1 (en) * | 2006-12-12 | 2008-06-19 | Schering Corporation | Aspartyl protease inhibitors |
CN101631779A (zh) * | 2006-12-12 | 2010-01-20 | 先灵公司 | 含有三环系统的天冬氨酰蛋白酶抑制剂 |
WO2008076044A1 (fr) | 2006-12-20 | 2008-06-26 | Astrazeneca Ab | Nouveaux 2-amino-5, 5-diaryl-imidazol-4-ones |
TW200831091A (en) | 2006-12-20 | 2008-08-01 | Astrazeneca Ab | New compounds |
TW200831484A (en) | 2006-12-20 | 2008-08-01 | Astrazeneca Ab | New compounds |
PE20090160A1 (es) | 2007-03-20 | 2009-02-11 | Wyeth Corp | COMPUESTOS AMINO-5-[4-(DIFLUOROMETOXI)FENIL SUSTITUIDO]-5-FENILIMIDAZOLONA COMO INHIBIDORES DE ß-SECRETASA |
AR065814A1 (es) | 2007-03-23 | 2009-07-01 | Wyeth Corp | Derivados de 5-fenilimidazolona,inhibidores de beta-secretasa,composiciones farmaceuticas que los contienen y usos para prevenir y/o tratar trastornos asociados a niveles beta-amiloides elevados. |
JP5383483B2 (ja) | 2007-04-24 | 2014-01-08 | 塩野義製薬株式会社 | アルツハイマー症治療用医薬組成物 |
EP2147914B1 (fr) | 2007-04-24 | 2014-06-04 | Shionogi&Co., Ltd. | Dérivés d'aminodihydrothiazine substitués par des groupes cycliques |
UY31083A1 (es) | 2007-05-15 | 2009-01-05 | Astrazeneca Ab | Derivados de sulfoximinas para la inhibicion de b-secretasa |
TW200902499A (en) | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
WO2009005471A1 (fr) | 2007-07-05 | 2009-01-08 | Astrazeneca Ab | Dérivés d'isoindole substitués aryle et hétéroaryle en tant qu'inhibiteurs de la bace |
WO2009005470A1 (fr) | 2007-07-05 | 2009-01-08 | Astrazeneca Ab | Dérivés d'isoindole substitués aryle et hétéroaryle en tant qu'inhibiteurs de la bace |
US8222264B2 (en) | 2007-07-06 | 2012-07-17 | Boehringer Ingelheim International Gmbh | Substituted amino-quinazolinones, medicaments comprising said compound, their use and their method of manufacture |
RU2476431C2 (ru) | 2008-01-18 | 2013-02-27 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Конденсированное производное аминодигидротиазина |
TW200932218A (en) | 2008-01-22 | 2009-08-01 | Boehringer Ingelheim Int | Substituted amino-benzimidazoles, medicaments comprising said compound, their use and their method of manufacture |
MX2010008202A (es) | 2008-01-28 | 2010-12-06 | Janssen Pharmaceutica Nv | Derivados de tio-2-aminoquinolina 6-sustituida utiles como inhibidores de beta-secretasa (bace). |
CN101970429B (zh) | 2008-01-29 | 2013-05-29 | 詹森药业有限公司 | 可用作β-分泌酶(BACE)抑制剂的2-氨基喹啉衍生物 |
MX2010008347A (es) | 2008-02-18 | 2010-11-12 | Hoffmann La Roche | Derivados de 4,5-dihidro-oxazol-2-ilamina. |
AR071385A1 (es) | 2008-04-22 | 2010-06-16 | Schering Corp | Compuestos de 2-imino-3-metil pirrolopirimidinona sustituida con tiofenilo,composiciones farmaceuticas que los contienen,y uso de los mismos para el tratamiento de patologias asociadas con la proteina beta amiloide,tales como alzheimer y otros formas de demencia. |
TWI431004B (zh) | 2008-05-02 | 2014-03-21 | Lilly Co Eli | Bace抑制劑 |
ES2738123T3 (es) | 2008-06-13 | 2020-01-20 | Shionogi & Co | Derivado heterocíclico que contiene azufre que tiene actividad inhibitoria de ß-secretasa |
WO2010013794A1 (fr) | 2008-07-28 | 2010-02-04 | Eisai R&D Management Co., Ltd. | Dérivés de spiroaminodihydrothiazine |
WO2010013302A1 (fr) | 2008-07-28 | 2010-02-04 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Dérivé de spiroaminodihydrothiazine |
AR073406A1 (es) | 2008-09-30 | 2010-11-03 | Eisai R&D Man Co Ltd | Aminodihidrotiazinas fusionadas con tetrahidropiranos,inhibidoras de bace1 y de la produccion de abeta amiloide, composiciones farmaceuticas que las contienen y usos de las mismas para el tratamiento de enfermedades neurodegenerativas,tales como alzheimer. |
JPWO2010047372A1 (ja) | 2008-10-22 | 2012-03-22 | 塩野義製薬株式会社 | Bace1阻害活性を有する2−アミノピリミジン−4−オンおよび2−アミノピリジン誘導体 |
US20100125081A1 (en) | 2008-11-14 | 2010-05-20 | Astrazeneca Ab | New compounds 574 |
EP2376083A4 (fr) | 2008-11-20 | 2012-06-20 | Purdue Research Foundation | Inhibiteurs de bace 1 à base de quinazoline et procédés d'utilisation |
-
2006
- 2006-06-12 WO PCT/US2006/022918 patent/WO2006138264A2/fr active Application Filing
- 2006-06-12 PE PE2006000655A patent/PE20070135A1/es not_active Application Discontinuation
- 2006-06-12 TW TW098137006A patent/TW201004961A/zh unknown
- 2006-06-12 EP EP06784807.7A patent/EP1896478B1/fr active Active
- 2006-06-12 MX MX2007016180A patent/MX2007016180A/es active IP Right Grant
- 2006-06-12 TW TW095120854A patent/TWI332005B/zh active
- 2006-06-12 AR ARP060102461A patent/AR054617A1/es not_active Application Discontinuation
- 2006-06-12 AU AU2006259572A patent/AU2006259572A1/en not_active Abandoned
- 2006-06-12 CA CA002609582A patent/CA2609582A1/fr not_active Abandoned
- 2006-06-12 JP JP2008516997A patent/JP2008543849A/ja active Pending
- 2006-06-12 RU RU2008100165/04A patent/RU2008100165A/ru not_active Application Discontinuation
- 2006-06-12 KR KR1020077029300A patent/KR20080029965A/ko not_active Application Discontinuation
- 2006-06-12 BR BRPI0612072-5A patent/BRPI0612072A2/pt not_active IP Right Cessation
- 2006-06-12 CN CNA2006800215030A patent/CN101228163A/zh active Pending
- 2006-06-12 US US11/451,541 patent/US7868000B2/en active Active
- 2006-06-12 SG SG201004170-5A patent/SG162790A1/en unknown
-
2007
- 2007-12-02 IL IL187814A patent/IL187814A0/en unknown
- 2007-12-12 EC EC2007008003A patent/ECSP078003A/es unknown
-
2008
- 2008-01-11 NO NO20080187A patent/NO20080187L/no not_active Application Discontinuation
- 2008-03-05 JP JP2008055596A patent/JP2008201784A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
NO20080187L (no) | 2008-03-14 |
AR054617A1 (es) | 2007-07-04 |
MX2007016180A (es) | 2008-03-07 |
WO2006138264A3 (fr) | 2007-03-01 |
TWI332005B (en) | 2010-10-21 |
AU2006259572A1 (en) | 2006-12-28 |
WO2006138264A2 (fr) | 2006-12-28 |
TW201004961A (en) | 2010-02-01 |
JP2008201784A (ja) | 2008-09-04 |
EP1896478B1 (fr) | 2014-05-21 |
US20070060575A1 (en) | 2007-03-15 |
CN101228163A (zh) | 2008-07-23 |
EP1896478A2 (fr) | 2008-03-12 |
KR20080029965A (ko) | 2008-04-03 |
CA2609582A1 (fr) | 2006-12-28 |
RU2008100165A (ru) | 2009-07-20 |
ECSP078003A (es) | 2008-01-23 |
TW200716642A (en) | 2007-05-01 |
BRPI0612072A2 (pt) | 2010-10-19 |
IL187814A0 (en) | 2008-08-07 |
PE20070135A1 (es) | 2007-03-09 |
JP2008543849A (ja) | 2008-12-04 |
US7868000B2 (en) | 2011-01-11 |
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