BRPI1011190A8 - Derivados de indazol e aza-indazol substituídos como moduladores de gama secretase - Google Patents
Derivados de indazol e aza-indazol substituídos como moduladores de gama secretaseInfo
- Publication number
- BRPI1011190A8 BRPI1011190A8 BRPI1011190A BRPI1011190A BRPI1011190A8 BR PI1011190 A8 BRPI1011190 A8 BR PI1011190A8 BR PI1011190 A BRPI1011190 A BR PI1011190A BR PI1011190 A BRPI1011190 A BR PI1011190A BR PI1011190 A8 BRPI1011190 A8 BR PI1011190A8
- Authority
- BR
- Brazil
- Prior art keywords
- indazole
- aza
- gamma secretase
- secretase modulators
- substituted
- Prior art date
Links
- VHNYOQKVZQVBLC-RTCGXNAVSA-N (4r,7e,9as)-7-[[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]methylidene]-4-(3,4,5-trifluorophenyl)-1,3,4,8,9,9a-hexahydropyrido[2,1-c][1,4]oxazin-6-one Chemical compound C1([C@@H]2COC[C@@H]3CC\C(C(N32)=O)=C/C=2C=C(C(=CC=2)N2C=C(C)N=C2)OC)=CC(F)=C(F)C(F)=C1 VHNYOQKVZQVBLC-RTCGXNAVSA-N 0.000 title abstract 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 title abstract 3
- 229940124648 γ-Secretase Modulator Drugs 0.000 title abstract 3
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical class C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000002473 indoazoles Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
DERIVADOS DE INDAZOL E AZA-INDAZOL SUBSTITUÍDOS COMO MODULADORES DE GAMA SECRETASE A presente invenção refere-se aos novos derivados de indazol e aza-indazol substituídos da Fórmula (I), em que R1, R2 , R3 , R4, Y, A1, A2 , A3 , A4, x1, X2 , X3 e Het1 têm o significado definido nas reivindicações. Os compostos de acordo com a presente invenção são úteis como moduladores de gama secretase. A invenção ainda diz respeito aos processos para preparar tais novos compostos, composições farmacêuticas compreendendo os ditos compostos como um ingrediente ativo como também o uso dos ditos compostos como um medicamento.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09159615 | 2009-05-07 | ||
| PCT/EP2010/056074 WO2010145883A1 (en) | 2009-05-07 | 2010-05-05 | Novel substituted indazole and aza-indazole derivatives as gamma secretase modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BRPI1011190A2 BRPI1011190A2 (pt) | 2016-03-15 |
| BRPI1011190A8 true BRPI1011190A8 (pt) | 2016-11-16 |
Family
ID=40786448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI1011190A BRPI1011190A8 (pt) | 2009-05-07 | 2010-05-05 | Derivados de indazol e aza-indazol substituídos como moduladores de gama secretase |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8835482B2 (pt) |
| EP (1) | EP2427453B1 (pt) |
| JP (1) | JP5559309B2 (pt) |
| KR (1) | KR20120024555A (pt) |
| CN (1) | CN102439005B (pt) |
| AR (1) | AR076850A1 (pt) |
| AU (1) | AU2010262036B2 (pt) |
| BR (1) | BRPI1011190A8 (pt) |
| CA (1) | CA2755467A1 (pt) |
| EA (1) | EA019702B1 (pt) |
| ES (1) | ES2431619T3 (pt) |
| IL (1) | IL216113A (pt) |
| MX (1) | MX2011011753A (pt) |
| MY (1) | MY152998A (pt) |
| NZ (1) | NZ596843A (pt) |
| SG (1) | SG175317A1 (pt) |
| TW (1) | TWI461419B (pt) |
| UA (1) | UA105377C2 (pt) |
| WO (1) | WO2010145883A1 (pt) |
| ZA (1) | ZA201108117B (pt) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PA8854101A1 (es) | 2008-12-18 | 2010-07-27 | Ortho Mcneil Janssen Pharm | Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa |
| AP2011005779A0 (en) | 2009-02-06 | 2011-08-31 | Ortho Mcneil Janssen Pharm | Novel susbstituted bicyclic heterocyclic compoundsas gamma secretase modulators. |
| TWI461425B (zh) | 2009-02-19 | 2014-11-21 | Janssen Pharmaceuticals Inc | 作為伽瑪分泌酶調節劑之新穎經取代的苯并唑、苯并咪唑、唑并吡啶及咪唑并吡啶衍生物類 |
| EP2427453B1 (en) | 2009-05-07 | 2013-07-17 | Janssen Pharmaceuticals, Inc. | Substituted indazole and aza-indazole derivatives as gamma secretase modulators |
| BR112012000915A2 (pt) | 2009-07-15 | 2019-09-24 | Janssen Pharmaceuticals Inc | derivados de triazol e imidazol substituídos como moduladores de gama secretase. |
| EP2523955B1 (en) | 2010-01-15 | 2014-07-16 | Janssen Pharmaceuticals, Inc. | Novel substituted bicyclic triazole derivatives as gamma secretase modulators |
| JP2014508794A (ja) | 2011-03-24 | 2014-04-10 | ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド | γ−セクレターゼ調節剤としての新規な置換トリアゾリルピペラジンおよびトリアゾリルピペラジン誘導体 |
| AU2012285931B2 (en) | 2011-07-15 | 2017-01-12 | Cellzome Limited | Novel substituted indole derivatives as gamma secretase modulators |
| CN104583208B (zh) | 2012-05-16 | 2016-09-28 | 杨森制药公司 | 可用于治疗(尤其是)阿尔茨海默病的取代的3,4-二氢-2H-吡啶并[1,2-a]吡嗪-1,6-二酮衍生物 |
| WO2014096212A1 (en) | 2012-12-20 | 2014-06-26 | Janssen Pharmaceutica Nv | NOVEL TRICYCLIC 3,4-DIHYDRO-2H-PYRIDO[1,2-α]PYRAZINE-1,6-DIONE DERIVATIVES AS GAMMA SECRETASE MODULATORS |
| KR102171710B1 (ko) | 2013-01-17 | 2020-10-30 | 얀센 파마슈티카 엔.브이. | 감마 세크레타제 조절 인자로서의 신규 치환 피리도-피페라지논 유도체 |
| JP6072308B2 (ja) * | 2013-02-21 | 2017-02-01 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ジヒドロプテリジノンii |
| US10562897B2 (en) | 2014-01-16 | 2020-02-18 | Janssen Pharmaceutica Nv | Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators |
| CN103880683B (zh) * | 2014-02-26 | 2018-06-22 | 南通大学 | 一种3-溴-2-硝基苯甲醛的化学合成方法 |
| EP3347363B1 (en) * | 2015-09-09 | 2020-01-01 | H. Hoffnabb-La Roche Ag | N-(3-azabicyclo[3.2.1]octan-8-yl)-8-(4-phenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[l,5-a]pyridin-2-amine derivatives as gamma-secretase modulators for treating alzheimer's disease |
| CN105585547A (zh) * | 2016-03-09 | 2016-05-18 | 中国科学院广州生物医药与健康研究院 | 一种4-五氟化硫苯酚类化合物及制备方法以及五氟化硫取代苯并吡喃类化合物的制备方法 |
| CN114195702A (zh) * | 2020-09-18 | 2022-03-18 | 瑞博(杭州)医药科技有限公司 | 一种用于合成抗肿瘤药物尼拉帕利的中间体及其制备方法 |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5767144A (en) | 1994-08-19 | 1998-06-16 | Abbott Laboratories | Endothelin antagonists |
| EA004405B1 (ru) | 1999-06-10 | 2004-04-29 | Уорнер-Ламберт Компани | Способ ингибирования агрегации амилоидных белков и визуализации амилоидных отложений с использованием производных изоиндолина |
| AU5702201A (en) | 2000-04-13 | 2001-10-30 | Mayo Foundation | Abeta<sub>42</sub> lowering agents |
| US20030176454A1 (en) | 2000-05-15 | 2003-09-18 | Akira Yamada | N-coating heterocyclic compounds |
| DE10238002A1 (de) | 2002-08-20 | 2004-03-04 | Merck Patent Gmbh | Benzimidazolderivate |
| RU2005129550A (ru) | 2003-02-27 | 2006-07-27 | Ф.Хоффманн-Ля Рош Аг (Ch) | Антагонисты рецептора ccr-3 |
| MXPA05012281A (es) * | 2003-05-14 | 2006-05-19 | Torreypines Therapeutics Inc | Compuestos y uso de los mismos en la modulacion beta amiloide. |
| JP2007502257A (ja) | 2003-08-14 | 2007-02-08 | エフ.ホフマン−ラ ロシュ アーゲー | γアミノ酪酸作動性モジュレーター |
| ATE483708T1 (de) | 2004-03-08 | 2010-10-15 | Prosidion Ltd | Pyrrolopyridin-2-carbonsäurehydrazide als inhibitoren von glykogenphosphorylase |
| EP1757591A4 (en) | 2004-05-26 | 2010-05-05 | Eisai R&D Man Co Ltd | ZIMTSÄUREAMIDVERBINDUNG |
| CN100577657C (zh) | 2004-10-26 | 2010-01-06 | 卫材R&D管理有限公司 | 肉桂酰胺化合物的无定形物 |
| US7572807B2 (en) | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
| BRPI0616150A2 (pt) | 2005-09-22 | 2011-06-07 | Sanofi Aventis | derivados de amino-alquil-amida como lìquidos receptores de ccr3 |
| US20070078136A1 (en) | 2005-09-22 | 2007-04-05 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
| WO2007043786A1 (en) | 2005-10-10 | 2007-04-19 | Seiyang Yang | Dynamic-based verification apparatus for verification from electronic system level to gate level, and verification method using the same |
| CN101283031B (zh) | 2005-10-11 | 2012-10-10 | 科聚亚公司 | 二芳基胺 |
| EP2007749A2 (en) | 2006-03-13 | 2008-12-31 | Pfizer Products Inc. | Tetralines antagonists of the h-3 receptor |
| GB0606774D0 (en) | 2006-04-03 | 2006-05-10 | Novartis Ag | Organic compounds |
| US7893058B2 (en) | 2006-05-15 | 2011-02-22 | Janssen Pharmaceutica Nv | Imidazolopyrazine compounds useful for the treatment of degenerative and inflammatory diseases |
| EP2099798A1 (en) | 2006-12-01 | 2009-09-16 | Galapagos N.V. | Imidazolopyridine compounds useful for the treatment of degenerative and inflammatory diseases |
| MX2009006863A (es) | 2006-12-20 | 2009-08-28 | Schering Corp | Inhibidores novedosos de c-jun-n-terminal cinasas. |
| WO2008097538A1 (en) | 2007-02-08 | 2008-08-14 | Merck & Co., Inc. | Therapeutic agents |
| WO2008100412A1 (en) | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Piperidine derivatives |
| CA2676715A1 (en) * | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Piperazine derivatives for treatment of ad and related conditions |
| MX2009012177A (es) | 2007-05-07 | 2009-11-23 | Schering Corp | Moduladores de gamma-secretasa. |
| CA2686754C (en) * | 2007-05-11 | 2014-10-28 | F. Hoffmann-La Roche Ag | Hetarylanilines as modulators for amyloid beta |
| WO2008156580A1 (en) | 2007-06-13 | 2008-12-24 | Merck & Co., Inc. | Triazole derivatives for treating alzheimer's disease and related conditions |
| EP2178857A1 (en) | 2007-06-29 | 2010-04-28 | Schering Corporation | Gamma secretase modulators |
| US7935815B2 (en) | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
| US8518975B2 (en) | 2007-09-06 | 2013-08-27 | Merck Sharp + Dohme Corp. | Gamma secretase modulators |
| RU2010119950A (ru) | 2007-10-19 | 2011-11-27 | Эрак Ас (No) | Комплексы s100a12 c устойчивостью к эдта (erac) |
| WO2009073777A1 (en) | 2007-12-06 | 2009-06-11 | Schering Corporation | Gamma secretase modulators |
| MX2010006378A (es) | 2007-12-11 | 2010-09-07 | Schering Corp | Moduladores de gamma secretasa. |
| MX2010008700A (es) | 2008-02-22 | 2010-08-30 | Hoffmann La Roche | Moduladores de beta-amiloide. |
| US20100137320A1 (en) | 2008-02-29 | 2010-06-03 | Schering Corporation | Gamma secretase modulators |
| WO2010010188A1 (en) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Novel compounds useful for the treatment of degenerative and inflammatory diseases. |
| AU2009313527A1 (en) | 2008-11-06 | 2010-05-14 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
| CN102209537A (zh) | 2008-11-10 | 2011-10-05 | 弗·哈夫曼-拉罗切有限公司 | 杂环γ分泌酶调节剂 |
| AU2009322774A1 (en) | 2008-12-03 | 2011-06-30 | Via Pharmaceuticals, Inc | Inhibitors of diacylglycerol acyltransferase |
| PA8854101A1 (es) | 2008-12-18 | 2010-07-27 | Ortho Mcneil Janssen Pharm | Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa |
| TW201030002A (en) | 2009-01-16 | 2010-08-16 | Bristol Myers Squibb Co | Bicyclic compounds for the reduction of beta-amyloid production |
| AP2011005779A0 (en) | 2009-02-06 | 2011-08-31 | Ortho Mcneil Janssen Pharm | Novel susbstituted bicyclic heterocyclic compoundsas gamma secretase modulators. |
| TWI461425B (zh) | 2009-02-19 | 2014-11-21 | Janssen Pharmaceuticals Inc | 作為伽瑪分泌酶調節劑之新穎經取代的苯并唑、苯并咪唑、唑并吡啶及咪唑并吡啶衍生物類 |
| JP2012051807A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | アリールイミダゾール化合物 |
| US8754100B2 (en) | 2009-02-26 | 2014-06-17 | Eisai R&D Management Co., Ltd. | Nitrogen-containing fused heterocyclic compounds and their use as beta amyloid production inhibitors |
| JP2012051806A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | イミダゾリルピラジン誘導体 |
| WO2010100606A1 (en) | 2009-03-03 | 2010-09-10 | Pfizer Inc. | Novel phenyl imidazoles and phenyl triazoles as gamma-secretase modulators |
| JPWO2010106745A1 (ja) | 2009-03-16 | 2012-09-20 | パナソニック株式会社 | アプリケーション実行装置 |
| EA201171306A1 (ru) | 2009-04-27 | 2012-05-30 | ХАЙ ПОЙНТ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи | ЗАМЕЩЕННЫЕ ПРОИЗВОДНЫЕ ИМИДАЗО[1,2-α]ПИРИДИНА, ФАРМАЦЕВТИЧЕСКИЕ КОМПОЗИЦИИ И СПОСОБЫ ПРИМЕНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ β-СЕКРЕТАЗЫ |
| EP2427453B1 (en) | 2009-05-07 | 2013-07-17 | Janssen Pharmaceuticals, Inc. | Substituted indazole and aza-indazole derivatives as gamma secretase modulators |
| JP2010274429A (ja) | 2009-05-26 | 2010-12-09 | Ihi Corp | アライメントステージ |
| BR112012000915A2 (pt) | 2009-07-15 | 2019-09-24 | Janssen Pharmaceuticals Inc | derivados de triazol e imidazol substituídos como moduladores de gama secretase. |
| EP2523955B1 (en) | 2010-01-15 | 2014-07-16 | Janssen Pharmaceuticals, Inc. | Novel substituted bicyclic triazole derivatives as gamma secretase modulators |
| JP2014508794A (ja) | 2011-03-24 | 2014-04-10 | ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド | γ−セクレターゼ調節剤としての新規な置換トリアゾリルピペラジンおよびトリアゾリルピペラジン誘導体 |
| ES2602794T3 (es) | 2011-03-31 | 2017-02-22 | Pfizer Inc | Piridinonas bicíclicas novedosas |
| AU2012285931B2 (en) | 2011-07-15 | 2017-01-12 | Cellzome Limited | Novel substituted indole derivatives as gamma secretase modulators |
-
2010
- 2010-05-05 EP EP10719325.2A patent/EP2427453B1/en active Active
- 2010-05-05 ES ES10719325T patent/ES2431619T3/es active Active
- 2010-05-05 CN CN201080020131.6A patent/CN102439005B/zh not_active Expired - Fee Related
- 2010-05-05 JP JP2012509024A patent/JP5559309B2/ja not_active Expired - Fee Related
- 2010-05-05 EA EA201171363A patent/EA019702B1/ru not_active IP Right Cessation
- 2010-05-05 CA CA2755467A patent/CA2755467A1/en not_active Abandoned
- 2010-05-05 US US13/263,860 patent/US8835482B2/en active Active
- 2010-05-05 BR BRPI1011190A patent/BRPI1011190A8/pt not_active IP Right Cessation
- 2010-05-05 WO PCT/EP2010/056074 patent/WO2010145883A1/en not_active Ceased
- 2010-05-05 MX MX2011011753A patent/MX2011011753A/es active IP Right Grant
- 2010-05-05 UA UAA201110540A patent/UA105377C2/uk unknown
- 2010-05-05 NZ NZ596843A patent/NZ596843A/xx not_active IP Right Cessation
- 2010-05-05 KR KR1020117024948A patent/KR20120024555A/ko not_active Ceased
- 2010-05-05 SG SG2011077518A patent/SG175317A1/en unknown
- 2010-05-05 MY MYPI2011005324 patent/MY152998A/en unknown
- 2010-05-05 AU AU2010262036A patent/AU2010262036B2/en not_active Ceased
- 2010-05-06 TW TW099114456A patent/TWI461419B/zh not_active IP Right Cessation
- 2010-05-06 AR ARP100101549A patent/AR076850A1/es not_active Application Discontinuation
-
2011
- 2011-11-03 IL IL216113A patent/IL216113A/en not_active IP Right Cessation
- 2011-11-04 ZA ZA2011/08117A patent/ZA201108117B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TWI461419B (zh) | 2014-11-21 |
| US8835482B2 (en) | 2014-09-16 |
| CA2755467A1 (en) | 2010-12-23 |
| ES2431619T3 (es) | 2013-11-27 |
| KR20120024555A (ko) | 2012-03-14 |
| AU2010262036B2 (en) | 2014-10-30 |
| BRPI1011190A2 (pt) | 2016-03-15 |
| AU2010262036A1 (en) | 2011-09-22 |
| SG175317A1 (en) | 2011-11-28 |
| IL216113A0 (en) | 2012-01-31 |
| EP2427453B1 (en) | 2013-07-17 |
| IL216113A (en) | 2015-02-26 |
| TW201105658A (en) | 2011-02-16 |
| MY152998A (en) | 2014-12-31 |
| EA201171363A1 (ru) | 2012-04-30 |
| EA019702B1 (ru) | 2014-05-30 |
| CN102439005B (zh) | 2015-07-22 |
| EP2427453A1 (en) | 2012-03-14 |
| MX2011011753A (es) | 2011-11-29 |
| US20120095036A1 (en) | 2012-04-19 |
| JP2012526078A (ja) | 2012-10-25 |
| JP5559309B2 (ja) | 2014-07-23 |
| ZA201108117B (en) | 2015-06-24 |
| WO2010145883A1 (en) | 2010-12-23 |
| UA105377C2 (uk) | 2014-05-12 |
| CN102439005A (zh) | 2012-05-02 |
| NZ596843A (en) | 2012-12-21 |
| AR076850A1 (es) | 2011-07-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BRPI1011190A8 (pt) | Derivados de indazol e aza-indazol substituídos como moduladores de gama secretase | |
| BRPI1008473A2 (pt) | compostos heterocíclicos bicíclicos substituídos como moduladores de gama secretase | |
| BR112014000713A2 (pt) | derivados de indol substituído como moduladores de gama secretase | |
| PH12012501382A1 (en) | Novel substituted triazole derivatives as gamma secretase modulators | |
| BR112013023984A2 (pt) | derivados triazolil piperazina e triazolil piperidina substituidos como moduladores de gama secretase | |
| PA8854101A1 (es) | Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa | |
| EA201270166A1 (ru) | Замещенные производные триазола и имидазола в качестве модуляторов гамма-секретазы | |
| UY33201A (es) | Compuestos de pirazol como antagonistas de crth2. | |
| BR112018076169A2 (pt) | derivados azabenzimidazol como inibidores de pi3k beta | |
| UY31069A1 (es) | Nuevos derivados de imidazoquinola, composiciones conteniendolos, proceso de preparacion y aplicaciones | |
| ECSP10010419A (es) | Derivados heterocíclicos de urea y métodos de uso de los mismos-211 | |
| CR11802A (es) | Derivados de indazoles sustituidos con fenilo o piridinilo | |
| BR112012009310B8 (pt) | composto derivados de 2-oxo-1-pirrolidinil imidazotiadiazol, uso dos mesmos e composição farmacêutica compreendendo os mesmos | |
| UY31905A (es) | Derivados de benzoxazinona, procesos de preparación, composiciones farmacéuticas conteniéndolos y aplicaciones. | |
| BRPI1008855B8 (pt) | derivados de indol, seu uso como agentes anticâncer, seu processo para preparação e composição farmacêutica que os compreende | |
| BR112012009670A2 (pt) | compostos de cumarina como moduladores de receptor com utilidade terapêutica | |
| ECSP10010664A (es) | Derivados de urea heterocíclicos para el tratamiento de infecciones bacterianas | |
| BR112015012716A2 (pt) | derivados de feniletilpiridina como inibidores de pde4 | |
| BR112018007068A2 (pt) | derivados de quinoxalina e piridopirazina como inibidores de pi3kbeta | |
| BR112015024971A2 (pt) | derivados de n-(2,3-di-hidro-1h-pirrolo[2,3-b]piridin-5-il)-4-quinazolinamina e n-(2,3-di-hidro-1h-indol-5-il)-4-quinazolinamina como inibidores de perk | |
| UY32856A (es) | Derivados heterocíclicos de urea y métodos de uso de los mismos | |
| UA118562C2 (uk) | Модулятори рецептора cxcr7 | |
| UY32694A (es) | Derivados heterocíclicos de urea y métodos de uso de los mismos | |
| BR112017012930A2 (pt) | derivados de imidazopiridazina como inibidores de pi3kbeta. | |
| CL2010001432A1 (es) | Compuestos derivados de 2-oxo-alquil-1-piperazin-2-ona, afines por los receptores p75ntr; procedimiento para preparar los compuestos; compuesto intermediario; medicamento y composicion farmaceutica que comprende a uno de los compuestos; y su uso en la preparacion de medicamentos utiles para tratar enfermedades neurodegenerativas. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B25A | Requested transfer of rights approved |
Owner name: JANSSEN PHARMACEUTICALS, INC (US) , CELLZOME LIMIT |
|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 7A ANUIDADE. |
|
| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |