EA201170829A1 - Замещенные бициклические производные имидазола в качестве модуляторов гамма-секретазы - Google Patents
Замещенные бициклические производные имидазола в качестве модуляторов гамма-секретазыInfo
- Publication number
- EA201170829A1 EA201170829A1 EA201170829A EA201170829A EA201170829A1 EA 201170829 A1 EA201170829 A1 EA 201170829A1 EA 201170829 A EA201170829 A EA 201170829A EA 201170829 A EA201170829 A EA 201170829A EA 201170829 A1 EA201170829 A1 EA 201170829A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- gamma secretase
- substituted bicyclic
- imidazol
- bicyclic derivatives
- secretase modulator
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- C07D403/02—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
- C07D455/02—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing not further condensed quinolizine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Настоящее изобретение относится к новым замещенным бициклическим производным имидазола формулы (I), где R, R, R, R, X, A, A, A, A, Y, Yи Yимеют значения, определенные в формуле изобретения. Соединения согласно настоящему изобретению применимы в качестве модуляторов гамма секретазы. Кроме того, изобретение относится к получению подобных новых соединений, фармацевтических композиций, содержащих указанное новое соединение в качестве активного ингредиента, а также к использованию указанных соединений в качестве лекарственного средства.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08172202 | 2008-12-18 | ||
PCT/EP2009/067321 WO2010070008A1 (en) | 2008-12-18 | 2009-12-16 | Substituted bicyclic imidazole derivatives as gamma secretase modulators |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201170829A1 true EA201170829A1 (ru) | 2011-12-30 |
EA018625B1 EA018625B1 (ru) | 2013-09-30 |
Family
ID=40451180
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201170829A EA018625B1 (ru) | 2008-12-18 | 2009-12-16 | Замещенные бициклические производные имидазола в качестве модуляторов гамма-секретазы |
Country Status (21)
Country | Link |
---|---|
US (1) | US8546440B2 (ru) |
EP (1) | EP2379552B1 (ru) |
JP (2) | JP2012512831A (ru) |
KR (1) | KR20110102455A (ru) |
CN (1) | CN102256974B (ru) |
AP (1) | AP2011005692A0 (ru) |
AR (1) | AR074771A1 (ru) |
AU (1) | AU2009327103B2 (ru) |
BR (1) | BRPI0922664A2 (ru) |
CA (1) | CA2742914A1 (ru) |
EA (1) | EA018625B1 (ru) |
ES (1) | ES2460642T3 (ru) |
IL (1) | IL213563A (ru) |
MX (1) | MX2011006543A (ru) |
NZ (1) | NZ594036A (ru) |
PA (1) | PA8854101A1 (ru) |
SG (1) | SG172213A1 (ru) |
TW (1) | TWI438203B (ru) |
UA (1) | UA104151C2 (ru) |
WO (1) | WO2010070008A1 (ru) |
ZA (1) | ZA201104504B (ru) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7868001B2 (en) * | 2007-11-02 | 2011-01-11 | Hutchison Medipharma Enterprises Limited | Cytokine inhibitors |
KR20110082189A (ko) | 2008-11-06 | 2011-07-18 | 아스트라제네카 아베 | 아밀로이드 베타의 조절제 |
PA8854101A1 (es) | 2008-12-18 | 2010-07-27 | Ortho Mcneil Janssen Pharm | Derivados de imidazol bicíclicos sustituidos como moduladores de gamma secretasa |
NZ593951A (en) | 2009-02-06 | 2013-01-25 | Ortho Mcneil Janssen Pharm | Novel substituted bicyclic heterocyclic compounds as 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 |
US8835482B2 (en) | 2009-05-07 | 2014-09-16 | Janssen Pharmaceuticals, Inc. | Substituted indazole and aza-indazole derivatives as gamma secretase modulators |
TWI625121B (zh) | 2009-07-13 | 2018-06-01 | 基利科學股份有限公司 | 調節細胞凋亡信號之激酶的抑制劑 |
CA2778517A1 (en) | 2009-07-15 | 2011-01-20 | Janssen Pharmaceuticals, Inc. | Substituted triazole and imidazole derivatives as gamma secretase modulators |
ES2512840T3 (es) | 2010-01-15 | 2014-10-24 | Janssen Pharmaceuticals, Inc. | Derivados de triazol bicíclicos sustituidos novedosos como moduladores de gamma-secretasa |
CN103384670B (zh) | 2010-07-28 | 2016-05-25 | 拜耳知识产权有限责任公司 | 取代的咪唑并[1,2-b]哒嗪 |
MX2013010970A (es) | 2011-03-24 | 2013-10-17 | Cellzome Ltd | Novedosos derivados de triazolil piperazina y triazolil piperidina sustituidos como moduladores de gamma-secretasa. |
WO2012131539A1 (en) | 2011-03-31 | 2012-10-04 | Pfizer Inc. | Novel bicyclic pyridinones |
EP2694500B1 (en) | 2011-04-06 | 2015-05-27 | Bayer Pharma Aktiengesellschaft | Substituted imidazopyridines and intermediates thereof |
JO3068B1 (ar) | 2011-04-07 | 2017-03-15 | Bayer Ip Gmbh | إيميدازوبيريميدينات كمثبطات كيناز akt |
CA2841102C (en) | 2011-07-15 | 2019-08-13 | Janssen Pharmaceuticals, Inc. | Novel substituted indole derivatives as gamma secretase modulators |
CA2852939A1 (en) * | 2011-10-20 | 2013-04-25 | Glaxosmithkline Llc | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
US9957271B2 (en) | 2011-10-20 | 2018-05-01 | Glaxosmithkline Llc | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
JP6173327B2 (ja) * | 2011-11-01 | 2017-08-02 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | イミダゾピリダジン化合物 |
KR20140108594A (ko) | 2012-01-10 | 2014-09-11 | 에프. 호프만-라 로슈 아게 | 피리다진 아미드 화합물 및 syk 저해제로서의 이의 용도 |
AU2013261023B2 (en) * | 2012-05-16 | 2016-11-24 | Cellzome Limited | Substituted 3, 4 - dihydro - 2H - pyrido [1, 2 -a] pyrazine - 1, 6 - dione derivatives useful for the treatment of (inter alia) Alzheimer's disease |
FR2993564B1 (fr) | 2012-07-20 | 2014-08-22 | Metabrain Res | Derives d'imidazopyridine utiles dans le traitement du diabete |
UA110688C2 (uk) | 2012-09-21 | 2016-01-25 | Пфайзер Інк. | Біциклічні піридинони |
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 |
EP2945944B1 (en) | 2013-01-17 | 2016-11-09 | Janssen Pharmaceutica, N.V. | Novel substituted pyrido-piperazinone derivatives as gamma secretase modulators |
CN105452251B (zh) * | 2013-06-12 | 2017-12-26 | 詹森药业有限公司 | 作为β‑分泌酶(BACE)抑制剂的4‑氨基‑6‑苯基‑5,6‑二氢咪唑并[1,5‑A]吡嗪‑3(2H)‑酮衍生物 |
WO2014198853A1 (en) * | 2013-06-12 | 2014-12-18 | Janssen Pharmaceutica Nv | 4-amino-6-phenyl-5,6-dihydroimidazo[1,5-a]pyrazine derivatives as inhibitors of beta-secretase (bace) |
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 |
WO2015166370A1 (en) | 2014-04-28 | 2015-11-05 | Pfizer Inc. | Heteroaromatic compounds and their use as dopamine d1 ligands |
KR20170095881A (ko) | 2014-12-18 | 2017-08-23 | 얀센 파마슈티카 엔.브이. | 베타―세크레타제의 2,3,4,5―테트라히드로피리딘―6―아민 및 3,4―디히드로―2h―피롤―5―아민 화합물 억제제 |
MA41252A (fr) | 2014-12-23 | 2017-10-31 | Gilead Sciences Inc | Formes solides d'un inhibiteur d'ask 1 |
PL3237404T3 (pl) * | 2014-12-23 | 2021-05-04 | Gilead Sciences, Inc. | Procesy wytwarzania inhibitorów ask1 |
PE20171318A1 (es) | 2015-02-03 | 2017-09-07 | Pfizer | Ciclopropabenzofuranil-piridopirazindionas novedosas |
JP6740239B2 (ja) * | 2015-03-12 | 2020-08-12 | エフ エム シー コーポレーションFmc Corporation | 複素環置換二環式アゾール殺有害生物剤 |
BR112021006329B1 (pt) * | 2018-10-05 | 2023-04-18 | E. I. Du Pont De Nemours And Company | Método de preparação de certas sulfonamidas nematicidas |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2406383A1 (en) * | 2000-04-13 | 2001-10-25 | Mayo Foundation For Medical Education And Research | A.beta.42 lowering agents |
DE10238002A1 (de) | 2002-08-20 | 2004-03-04 | Merck Patent Gmbh | Benzimidazolderivate |
US7244739B2 (en) | 2003-05-14 | 2007-07-17 | Torreypines Therapeutics, Inc. | Compounds and uses thereof in modulating amyloid beta |
US7884112B2 (en) | 2004-03-08 | 2011-02-08 | Stuart Edward Bradley | Pyrrolopyridine-2-carboxylic acid hydrazides |
EP2261218B1 (en) | 2004-05-26 | 2013-04-03 | Eisai R&D Management Co., Ltd. | Imidazole compound for use as an intermediate in the production of cinnamide compounds |
ES2338904T3 (es) * | 2004-10-26 | 2010-05-13 | EISAI R&D MANAGEMENT CO., LTD. | Forma amorfa de compuestos de cinamida. |
US7572807B2 (en) | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
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 |
JP4987873B2 (ja) | 2005-10-11 | 2012-07-25 | ケムチュア コーポレイション | 二芳香族アミン |
US20090163482A1 (en) | 2006-03-13 | 2009-06-25 | Mchardy Stanton Furst | 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 |
WO2008065199A1 (en) * | 2006-12-01 | 2008-06-05 | Galapagos N.V. | Imidazolopyridine compounds useful for the treatment of degenerative and inflammatory diseases |
US20100298314A1 (en) * | 2006-12-20 | 2010-11-25 | Schering Corporation | Novel jnk inhibitors |
JP2010518080A (ja) | 2007-02-08 | 2010-05-27 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療薬 |
RU2009144998A (ru) | 2007-05-07 | 2011-06-20 | Шеринг Корпорейшн (US) | Модуляторы гамма-секретазы |
RU2009140182A (ru) * | 2007-05-11 | 2011-06-20 | Ф. Хоффманн-Ля Рош Аг (Ch) | Гетариланилины в качестве модуляторов для бета-амилоида |
WO2008156580A1 (en) | 2007-06-13 | 2008-12-24 | Merck & Co., Inc. | Triazole derivatives for treating alzheimer's disease and related conditions |
US20110053918A1 (en) | 2007-06-29 | 2011-03-03 | Zhaoning Zhu | Gamma secretase modulators |
US7935815B2 (en) * | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
WO2009032277A1 (en) | 2007-09-06 | 2009-03-12 | Schering Corporation | Gamma secretase modulators |
RU2010119950A (ru) | 2007-10-19 | 2011-11-27 | Эрак Ас (No) | Комплексы s100a12 c устойчивостью к эдта (erac) |
JP2011506335A (ja) | 2007-12-06 | 2011-03-03 | シェーリング コーポレイション | γ−セクレターゼ調節剤 |
EP2227471A1 (en) | 2007-12-11 | 2010-09-15 | Schering Corporation | Gamma secretase modulators |
JP5328816B2 (ja) | 2008-02-22 | 2013-10-30 | エフ.ホフマン−ラ ロシュ アーゲー | アミロイドβの調節薬 |
WO2010010188A1 (en) | 2008-07-25 | 2010-01-28 | Galapagos Nv | Novel compounds useful for the treatment of degenerative and inflammatory diseases. |
US20120129846A1 (en) * | 2008-11-06 | 2012-05-24 | Zhaoning Zhu | Gamma secretase modulators |
CN102239165A (zh) | 2008-12-03 | 2011-11-09 | 维尔制药公司 | 二酰甘油酰基转移酶抑制剂 |
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 |
NZ593951A (en) | 2009-02-06 | 2013-01-25 | Ortho Mcneil Janssen Pharm | Novel substituted bicyclic heterocyclic compounds as 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 |
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 |
AU2010241929A1 (en) | 2009-04-27 | 2011-10-06 | High Point Pharmaceuticals, Llc | Substituted imidazo[1,2-a]pyridine derivatives, pharmaceutical compositions, and methods of use as beta-secretase inhibitors |
US8835482B2 (en) | 2009-05-07 | 2014-09-16 | 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 |
CA2778517A1 (en) | 2009-07-15 | 2011-01-20 | Janssen Pharmaceuticals, Inc. | Substituted triazole and imidazole derivatives as gamma secretase modulators |
-
2009
- 2009-12-15 PA PA20098854101A patent/PA8854101A1/es unknown
- 2009-12-16 EP EP09797025.5A patent/EP2379552B1/en active Active
- 2009-12-16 UA UAA201105485A patent/UA104151C2/ru unknown
- 2009-12-16 NZ NZ594036A patent/NZ594036A/xx not_active IP Right Cessation
- 2009-12-16 KR KR1020117016065A patent/KR20110102455A/ko not_active Application Discontinuation
- 2009-12-16 EA EA201170829A patent/EA018625B1/ru not_active IP Right Cessation
- 2009-12-16 WO PCT/EP2009/067321 patent/WO2010070008A1/en active Application Filing
- 2009-12-16 JP JP2011541412A patent/JP2012512831A/ja active Pending
- 2009-12-16 AU AU2009327103A patent/AU2009327103B2/en not_active Ceased
- 2009-12-16 ES ES09797025.5T patent/ES2460642T3/es active Active
- 2009-12-16 CN CN200980151827.XA patent/CN102256974B/zh active Active
- 2009-12-16 SG SG2011044310A patent/SG172213A1/en unknown
- 2009-12-16 BR BRPI0922664A patent/BRPI0922664A2/pt not_active IP Right Cessation
- 2009-12-16 MX MX2011006543A patent/MX2011006543A/es active IP Right Grant
- 2009-12-16 CA CA2742914A patent/CA2742914A1/en not_active Abandoned
- 2009-12-16 US US13/133,027 patent/US8546440B2/en active Active
- 2009-12-16 AP AP2011005692A patent/AP2011005692A0/xx unknown
- 2009-12-17 TW TW098143263A patent/TWI438203B/zh not_active IP Right Cessation
- 2009-12-17 AR ARP090104939A patent/AR074771A1/es not_active Application Discontinuation
-
2011
- 2011-06-15 IL IL213563A patent/IL213563A/en not_active IP Right Cessation
- 2011-06-17 ZA ZA2011/04504A patent/ZA201104504B/en unknown
-
2015
- 2015-06-25 JP JP2015127609A patent/JP2015164969A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
BRPI0922664A2 (pt) | 2016-01-05 |
SG172213A1 (en) | 2011-07-28 |
CN102256974B (zh) | 2014-07-30 |
UA104151C2 (ru) | 2014-01-10 |
US8546440B2 (en) | 2013-10-01 |
KR20110102455A (ko) | 2011-09-16 |
PA8854101A1 (es) | 2010-07-27 |
ES2460642T3 (es) | 2014-05-14 |
CN102256974A (zh) | 2011-11-23 |
US20110237580A1 (en) | 2011-09-29 |
IL213563A0 (en) | 2011-07-31 |
IL213563A (en) | 2015-06-30 |
AP2011005692A0 (en) | 2011-06-30 |
AU2009327103B2 (en) | 2014-12-04 |
WO2010070008A1 (en) | 2010-06-24 |
AU2009327103A1 (en) | 2011-07-21 |
ZA201104504B (en) | 2014-01-29 |
CA2742914A1 (en) | 2010-06-24 |
MX2011006543A (es) | 2011-07-20 |
EP2379552A1 (en) | 2011-10-26 |
JP2012512831A (ja) | 2012-06-07 |
EA018625B1 (ru) | 2013-09-30 |
EP2379552B1 (en) | 2014-02-26 |
AR074771A1 (es) | 2011-02-09 |
JP2015164969A (ja) | 2015-09-17 |
TW201035093A (en) | 2010-10-01 |
TWI438203B (zh) | 2014-05-21 |
NZ594036A (en) | 2012-10-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA201170829A1 (ru) | Замещенные бициклические производные имидазола в качестве модуляторов гамма-секретазы | |
EA201270166A1 (ru) | Замещенные производные триазола и имидазола в качестве модуляторов гамма-секретазы | |
EA201290654A1 (ru) | Новые замещенные триазольные производные как модуляторы гамма-секретазы | |
EA201171008A1 (ru) | Новые замещенные бициклические гетероциклические соединения в качестве модуляторов гамма-секретазы | |
EA201171363A1 (ru) | Новые замещенные производные индазола и азаиндазола в качестве модуляторов гамма-секретазы | |
EA201490287A1 (ru) | Новые замещенные производные индола в качестве модуляторов гамма-секретазы | |
EA201171066A1 (ru) | Новые замещенные производные бензоксазола, бензимидазола, оксазолопиридина и имидазопиридина в качестве модуляторов гамма-секретазы | |
EA201492112A1 (ru) | ЗАМЕЩЕННЫЕ 3,4-ДИГИДРО-2H-ПИРИДО[1,2-a]ПИРАЗИН-1,6-ДИОНОВЫЕ ПРОИЗВОДНЫЕ, ПРИМЕНИМЫЕ ДЛЯ ЛЕЧЕНИЯ (В ТОМ ЧИСЛЕ) БОЛЕЗНИ АЛЬЦГЕЙМЕРА | |
EA201590118A1 (ru) | Производные пирролидина и их применение в качестве модуляторов пути активации комплемента | |
MA32508B1 (fr) | Composes organiques | |
EA201891179A1 (ru) | N-замещенные индольные производные в качестве модуляторов pge2 рецепторов | |
EA200970156A1 (ru) | Пиридизиноновые производные | |
GEP20146146B (en) | Pyrrolopyrimidine compounds as inhibitors of cdk4/6 | |
BRPI1009333B8 (pt) | compostos inibidores de beta-secretase, seus usos, bem como composição farmacêutica | |
UY32156A (es) | Derivados sustituidos de la n2 - [1-(5 - fluoropirimidin -2-il) etil] - n4 - (1-metil - 1h-imidazol - 4 - il)) - pirimidina - 2,4 - diaminas y sus sales farmacéuticamente aceptables, proceso de preparación, composiciones conteniéndolos y aplicaciones. | |
EA201201050A1 (ru) | Пиразолы в качестве антагонистов crth2 | |
UY30316A1 (es) | Derivados sustituidos de benzamidas, nicotinamidas, propanamidas, acetamidas y carboxamidas n-(2-(piperidin-1-ilmetil)ciclohexil)sustituidas, procesos de preparacion, composiciones conteniéndolos y aplicaciones | |
CA2891755C (en) | Substituted pyrido-piperazinone derivatives as gamma secretase modulators | |
EA201070588A1 (ru) | Производные 1,2,3-триазола для применения в качестве ингибиторов стеароил-соа десатуразы | |
EA201992679A1 (ru) | N-замещенные индольные производные | |
EA201071224A1 (ru) | Ингибиторы limk2, композиции, содержащие их, и способы их применения | |
BR112012009310B8 (pt) | composto derivados de 2-oxo-1-pirrolidinil imidazotiadiazol, uso dos mesmos e composição farmacêutica compreendendo os mesmos | |
EA201001859A1 (ru) | Гетероциклические производные мочевины и способы их применеия | |
UA107455C2 (ru) | Производные индола как противораковые агенты | |
EA201000703A1 (ru) | Производные пиразола в качестве ингибиторов 5-lo |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
HC1A | Change in name of an applicant in a eurasian application | ||
PC1A | Registration of transfer to a eurasian application by force of assignment | ||
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |
|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): RU |