PE20120172A1 - Compuestos heterociclicos fusionados que contiene nitrogeno como inhibidores de la produccion de beta-amiloide - Google Patents
Compuestos heterociclicos fusionados que contiene nitrogeno como inhibidores de la produccion de beta-amiloideInfo
- Publication number
- PE20120172A1 PE20120172A1 PE2011001502A PE2011001502A PE20120172A1 PE 20120172 A1 PE20120172 A1 PE 20120172A1 PE 2011001502 A PE2011001502 A PE 2011001502A PE 2011001502 A PE2011001502 A PE 2011001502A PE 20120172 A1 PE20120172 A1 PE 20120172A1
- Authority
- PE
- Peru
- Prior art keywords
- pyridine
- beta
- methylimidazol
- triazolo
- pyridin
- Prior art date
Links
- 150000002391 heterocyclic compounds Chemical class 0.000 title abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title 2
- 102000013455 Amyloid beta-Peptides Human genes 0.000 title 1
- 108010090849 Amyloid beta-Peptides Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 229910052757 nitrogen Inorganic materials 0.000 title 1
- -1 PHENYL GROUP Chemical group 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 206010012289 Dementia Diseases 0.000 abstract 1
- 201000010374 Down Syndrome Diseases 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical group C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- 206010044688 Trisomy 21 Diseases 0.000 abstract 1
- 206010002022 amyloidosis Diseases 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical group COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07D417/14—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 three or more hetero rings
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61P25/28—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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/18—Bridged systems
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
REFERIDA A UN COMPUESTO HETEROCICLICO DE FORMULA (I), DONDE R1 Y R2 SON ALQUILO C1-C6, CICLOALQUILO C3-C8, ALQUENILO C2-C6, ALCOXI C1-C6, ENTRE OTROS; EL ANILLO A ES UN GRUPO HETEROCICLICLO AROMATICO DE 5 MIEMBROS FUSIONADO CON UN ANILLO NO AROMATICO DE 5 A 14 MIEMBROS, OPCIONALMENTE SUSTITUIDO ALQUILO C1-C6, ALQUENILO C2-C6, ENTRE OTROS; X1 ES UN ENLACE INDIVIDUAL, UN GRUPO ALQUILENO C1-C6, UN GRUPO VINILENO, ENTRE OTROS; EL ANILLO B ES UN GRUPO FENILO, PIRIDINA, OXAZOL, FURANO, ENTRE OTROS; m ES UN ENTERO DE 0 A 3; n ES UN ENTERO DE 0 A 2; W ES N O C. SON COMPUESTOS PREFERIDOS: (+)-8-(5-ISOPROPIL-4-METOXI-2-METILFENIL)-2-[6-METOXI-5-(4-METILIMIDAZOL-1-IL)PIRIDIN-2-IL-5,6,7,8-TETRAHIDRO[1,2,4]TRIAZOLO[1,5-a]PIRIDINA, (-)-2-[5-METOXI-6-(4-METILIMIDAZOL-1-IL)PIRIDIN-3-IL]-8-(2-TRIFLUOROMETILFENIL)-5,6,7,8-TETRAHIDRO[1,2,4]TRIAZOLO[1,5-a]PIRIDINA, (-)-8-(4-BROMO-2-TRIFLUOROMETILFENIL)-2-[6-METOXI-5-(4-METILIMIDAZOL-1-IL)PIRIDIN-2-IL]-5,6,7,8-TETRAHIDRO[1,2,4]TRIAZOLO[1,5-a]PIRIDINA, ENTRE OTROS. DICHOS COMPUESTOS INHIBEN LA PRODUCCION DE BETA-AMILOIDES Y SON UTILES EN EL TRATAMIENTO DE LA ENFERMEDAD DE ALZHEIMER, SINDROME DE DOWN, DEMENCIA Y AMILOIDOSIS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15569709P | 2009-02-26 | 2009-02-26 | |
| JP2009043337 | 2009-02-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20120172A1 true PE20120172A1 (es) | 2012-03-08 |
Family
ID=42331601
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2011001502A PE20120172A1 (es) | 2009-02-26 | 2010-02-24 | Compuestos heterociclicos fusionados que contiene nitrogeno como inhibidores de la produccion de beta-amiloide |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8754100B2 (es) |
| EP (2) | EP2615090A1 (es) |
| JP (1) | JP2012519152A (es) |
| KR (1) | KR20110122746A (es) |
| CN (1) | CN102333777B (es) |
| AR (1) | AR075606A1 (es) |
| AU (1) | AU2010218714A1 (es) |
| CA (1) | CA2753696A1 (es) |
| IL (1) | IL214780A (es) |
| MX (1) | MX2011008501A (es) |
| NZ (1) | NZ594776A (es) |
| PE (1) | PE20120172A1 (es) |
| RU (1) | RU2515976C2 (es) |
| SG (1) | SG173710A1 (es) |
| TW (1) | TW201035101A (es) |
| WO (1) | WO2010098487A1 (es) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10164139A1 (de) | 2001-12-27 | 2003-07-10 | Bayer Ag | 2-Heteroarylcarbonsäureamide |
| CN101952275B (zh) | 2008-02-22 | 2014-06-18 | 弗·哈夫曼-拉罗切有限公司 | β-淀粉样蛋白的调节剂 |
| MX2011003246A (es) | 2008-10-09 | 2011-04-21 | Hoffmann La Roche | Moduladores de beta amiloide. |
| BRPI0921348A2 (pt) | 2008-11-10 | 2019-09-24 | Hoffmann La Roche | moduladores heterocíclicos da gama secretase |
| PL2540297T3 (pl) | 2008-11-19 | 2015-12-31 | Forum Pharmaceuticals Inc | Leczenie zaburzeń funkcji poznawczych(R)-7-chloro-N-(chinuklidyn-3-ylo)benzo[b]tiofeno-2-karboksyamidem i jego farmaceutyczne dopuszczalnymi solami |
| KR20110113197A (ko) | 2009-02-06 | 2011-10-14 | 오르토-맥닐-얀센 파마슈티칼스 인코포레이티드 | 감마 세크레타제 조절제로서의 신규 치환된 비사이클릭 헤테로사이클릭 화합물 |
| EP2427453B1 (en) | 2009-05-07 | 2013-07-17 | Janssen Pharmaceuticals, Inc. | Substituted indazole and aza-indazole derivatives as gamma secretase modulators |
| CN102802620A (zh) * | 2009-05-11 | 2012-11-28 | 英维沃医药有限公司 | 使用某种α-7烟酸受体与乙酰胆碱酯酶抑制剂结合治疗认知障碍 |
| US20120142672A1 (en) * | 2009-07-13 | 2012-06-07 | Tatsuki Koike | Heterocyclic compound and use thereof |
| CN102482227A (zh) * | 2009-07-15 | 2012-05-30 | 杨森制药公司 | 作为γ分泌酶调节剂的取代的三唑和咪唑衍生物 |
| EP2523949B1 (en) | 2010-01-15 | 2014-08-20 | Janssen Pharmaceuticals Inc. | Novel substituted triazole derivatives as gamma secretase modulators |
| US20110190269A1 (en) | 2010-02-01 | 2011-08-04 | Karlheinz Baumann | Gamma secretase modulators |
| US8486967B2 (en) | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
| KR101698250B1 (ko) | 2010-05-17 | 2017-01-19 | 포럼 파마슈티칼즈 인크. | (R)-7-클로로-N-(퀴누클리딘-3-일)벤조[b]티오펜-2-카르복사미드 히드로클로리드 모노히드레이트의 결정질 형태 |
| JP6069661B2 (ja) | 2010-06-24 | 2017-02-01 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | 種々のアミロイドβペプチドアロフォームレベルの調節における組成物及びその使用 |
| EP2611805A1 (en) * | 2010-09-02 | 2013-07-10 | Takeda Pharmaceutical Company Limited | Fused triazoles for the treatment or prophylaxis of mild cognitive impairment |
| ES2536442T3 (es) | 2011-03-24 | 2015-05-25 | Janssen Pharmaceuticals, Inc. | Derivados novedosos de triazolil piperazina y triazolil piperidina como moduladores de la gamma secretasa |
| WO2013005354A1 (ja) * | 2011-07-01 | 2013-01-10 | 武田薬品工業株式会社 | 複素環化合物 |
| JP6068464B2 (ja) * | 2011-07-15 | 2017-01-25 | ヤンセン ファーマシューティカルズ,インコーポレーテッド | γ−セクレターゼ調節剤としての新規な置換インドール誘導体 |
| WO2013106328A1 (en) * | 2012-01-09 | 2013-07-18 | Envivo Pharmaceuticals, Inc. | Tetrasubstituted benzenes for treatment of early onset alzheimer's disease |
| RU2635522C2 (ru) | 2012-05-08 | 2017-11-13 | Форум Фармасьютикалз, Инк. | Способы поддержания, лечения или улучшения когнитивной функции |
| MX355164B (es) | 2012-05-16 | 2018-04-06 | Janssen Pharmaceuticals Inc | Derivados de 3,4-dihidro-2h-pirido[1,2-a]pirazin-1,6-diona sustituidos utiles para el tratamiento de la enfermedad de alzheimer (inter alia). |
| EP2687528A1 (en) * | 2012-07-17 | 2014-01-22 | Ares Trading S.A. | Fused triazole derivatives as gamma secretase modulators |
| KR102209418B1 (ko) | 2012-12-20 | 2021-01-29 | 얀센 파마슈티카 엔.브이. | 감마 세크레타제 조절 인자로서의 신규 삼환 3,4-디하이드로-2H-피리도[1,2-α]피라진-1,6-디온 유도체 |
| CN104936958B (zh) | 2013-01-17 | 2019-07-26 | 詹森药业有限公司 | 作为γ分泌酶调节剂的新颖的经取代的吡啶并-哌嗪酮衍生物 |
| US9938263B2 (en) | 2013-03-12 | 2018-04-10 | The General Hospital Corporation | Gamma-secretase modulators |
| 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 |
| CN103910781B (zh) * | 2014-03-18 | 2016-02-17 | 重庆大学 | 一种Aβ聚集抑制剂 |
| JP6672296B2 (ja) | 2014-10-31 | 2020-03-25 | ザ ジェネラル ホスピタル コーポレイション | 強力なγ−セクレターゼモジュレータ |
| EP3031458A1 (en) | 2014-12-09 | 2016-06-15 | Iproteos S.L. | Use of 1-[(2-phenylcycloprop-1-yl)carbonyl]-2-[(1,3-thiazolidin-3-yl)carbonyl]perhydroindole in the treatment of schizophrenia-associated cognitive deficits |
| TWI696617B (zh) * | 2015-04-28 | 2020-06-21 | 大陸商上海復尚慧創醫藥研究有限公司 | 特定蛋白質激酶抑制劑 |
| CR20210104A (es) | 2018-09-03 | 2021-04-19 | Hoffmann La Roche | Derivados de heteroarilo bicíclicos |
| PT3894411T (pt) | 2018-12-13 | 2024-08-08 | Hoffmann La Roche | Derivados da 7-fenoxi-n-(3-azabiciclo[3.2.1]octan-8-il)-6,7-dihidro-5h-pirrolo[1,2-b][1,2,4]triazol-2-amina e compostos relacionados enquanto moduladores da gama-secretase para o tratamento da doença de alzheimer |
| CN110642689B (zh) * | 2019-09-05 | 2022-06-24 | 南通大学 | 一种3,6-二溴-2-甲基苯甲醛及其化学合成方法 |
| CN112661639A (zh) * | 2020-12-07 | 2021-04-16 | 浙江工业大学 | 一种4-乙酰丁酸酯类化合物合成方法 |
| WO2022207123A1 (de) * | 2021-04-03 | 2022-10-06 | Symrise Ag | Herstellungsverfahren für polycyclische riechstoffe |
| CN116621846B (zh) * | 2023-07-24 | 2023-10-17 | 华润医药研究院(深圳)有限公司 | 双环杂环及三环杂环类化合物及其制备方法和医药用途 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE210132T1 (de) * | 1995-04-21 | 2001-12-15 | Neurosearch As | Benzmidazolverbindungen und ihre verwendung als modulatoren des gabaa-rezeptor-komplexes |
| HUP0001434A3 (en) * | 1997-04-16 | 2001-01-29 | Abbott Lab | 5,7-disubstituted 4-aminopyrido[2,3-d]pyrimidine compounds, pharmaceutical compouads thereof and process for their preparation |
| CA2525547C (en) * | 2003-05-14 | 2012-07-03 | Torreypines Therapeutics, Inc. | Compounds and uses thereof in modulating amyloid beta |
| MY149038A (en) | 2004-05-26 | 2013-07-15 | Eisai R&D Man Co Ltd | Cinnamide compound |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
| JP5221144B2 (ja) | 2005-11-24 | 2013-06-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | モルホリンタイプ・シンナミド化合物 |
| EP1992618B1 (en) | 2006-03-09 | 2012-01-18 | Eisai R&D Management Co., Ltd. | Polycyclic cinnamide derivative |
| TWI378091B (en) | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
| JP2009184924A (ja) | 2006-05-31 | 2009-08-20 | Eisai R & D Management Co Ltd | 生物学的試薬用化合物 |
| PE20081791A1 (es) | 2007-02-28 | 2009-02-07 | Eisai Randd Man Co Ltd | Dos derivados ciclicos de oxomorfolina |
| AR068121A1 (es) | 2007-08-31 | 2009-11-04 | Eisai R&D Man Co Ltd | Compuestos multiciclicos para tratar enfermedades neurodegenerativas |
| US7935815B2 (en) | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
| CN101939315A (zh) | 2007-12-06 | 2011-01-05 | 先灵公司 | γ分泌酶调节剂 |
| RU2011111534A (ru) | 2008-08-27 | 2012-10-10 | ЭЙСАЙ Ар энд Ди МЕНЕДЖМЕНТ КО., ЛТД. (JP) | Способ получения определенных цинниамидных соединений |
| 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 |
| 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 |
| JP5629274B2 (ja) | 2009-02-26 | 2014-11-19 | 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 | ブラジキニンb1アンタゴニストとしての化合物 |
| CN102388039B (zh) | 2009-02-26 | 2015-07-15 | 葛兰素集团有限公司 | 用作ccr4受体拮抗剂的吡唑衍生物 |
| JP5580816B2 (ja) | 2009-02-26 | 2014-08-27 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | テトラヒドロトリアゾロピリジン誘導体の塩およびその結晶 |
| CN102482227A (zh) | 2009-07-15 | 2012-05-30 | 杨森制药公司 | 作为γ分泌酶调节剂的取代的三唑和咪唑衍生物 |
| WO2011031984A2 (en) | 2009-09-11 | 2011-03-17 | Simplisse, Inc. | Nipple shield |
-
2010
- 2010-02-24 CN CN201080009288.9A patent/CN102333777B/zh not_active Expired - Fee Related
- 2010-02-24 SG SG2011058864A patent/SG173710A1/en unknown
- 2010-02-24 US US13/138,504 patent/US8754100B2/en not_active Expired - Fee Related
- 2010-02-24 MX MX2011008501A patent/MX2011008501A/es active IP Right Grant
- 2010-02-24 TW TW099105284A patent/TW201035101A/zh unknown
- 2010-02-24 NZ NZ594776A patent/NZ594776A/xx not_active IP Right Cessation
- 2010-02-24 EP EP13162886.9A patent/EP2615090A1/en not_active Withdrawn
- 2010-02-24 KR KR1020117022134A patent/KR20110122746A/ko not_active Withdrawn
- 2010-02-24 PE PE2011001502A patent/PE20120172A1/es not_active Application Discontinuation
- 2010-02-24 RU RU2011139132/04A patent/RU2515976C2/ru not_active IP Right Cessation
- 2010-02-24 JP JP2011536639A patent/JP2012519152A/ja not_active Ceased
- 2010-02-24 WO PCT/JP2010/053368 patent/WO2010098487A1/en not_active Ceased
- 2010-02-24 CA CA2753696A patent/CA2753696A1/en not_active Abandoned
- 2010-02-24 EP EP10708824.7A patent/EP2401276B1/en active Active
- 2010-02-24 AU AU2010218714A patent/AU2010218714A1/en not_active Abandoned
- 2010-02-25 AR ARP100100548A patent/AR075606A1/es not_active Application Discontinuation
-
2011
- 2011-08-22 IL IL214780A patent/IL214780A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| HK1165954A1 (en) | 2012-10-12 |
| CN102333777A (zh) | 2012-01-25 |
| TW201035101A (en) | 2010-10-01 |
| IL214780A0 (en) | 2011-11-30 |
| AU2010218714A1 (en) | 2011-09-08 |
| CA2753696A1 (en) | 2010-09-02 |
| RU2515976C2 (ru) | 2014-05-20 |
| EP2615090A1 (en) | 2013-07-17 |
| JP2012519152A (ja) | 2012-08-23 |
| MX2011008501A (es) | 2011-09-01 |
| RU2011139132A (ru) | 2013-04-20 |
| EP2401276A1 (en) | 2012-01-04 |
| IL214780A (en) | 2014-06-30 |
| US8754100B2 (en) | 2014-06-17 |
| US20120053171A1 (en) | 2012-03-01 |
| CN102333777B (zh) | 2014-06-25 |
| AR075606A1 (es) | 2011-04-20 |
| WO2010098487A1 (en) | 2010-09-02 |
| EP2401276B1 (en) | 2013-06-05 |
| KR20110122746A (ko) | 2011-11-10 |
| NZ594776A (en) | 2013-05-31 |
| SG173710A1 (en) | 2011-09-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20120172A1 (es) | Compuestos heterociclicos fusionados que contiene nitrogeno como inhibidores de la produccion de beta-amiloide | |
| PE20091833A1 (es) | Derivados heterociclicos espiro biciclicos o heterociclicos biciclicos, puenteados, de pirazolo [1,5-a]pirimidinas como inhibidores de quinasas raf y metodos para su preparacion | |
| PE20061424A1 (es) | Compuestos triciclicos de base 1,6-dihidro-1-3,5,6-tetraaza-as-indaceno y composiciones farmaceuticas que comprenden los mismos | |
| AR080785A1 (es) | Derivados de imidazo[1,2-a]pirimidina ,proceso para prepararlos e intermediarios de dicha sintesis, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de patologias del sistema nervioso central,tales como esquizofrenia y parkinson, entre otros. | |
| PE20130012A1 (es) | Derivados de pirazol como inhibidores de jak | |
| PE20180500A1 (es) | Derivados de 2,3-dihidro-4h-1,3-benzoxazin-4-ona como moduladores del receptor muscarinico colinergico m1 | |
| PE20130651A1 (es) | Derivados de imidazopiridina y su procedimiento de preparacion | |
| PE20081612A1 (es) | Analogos de las pterinas | |
| PE20130234A1 (es) | Derivados de heteroaril imidazolona como inhibidores de jak | |
| PE20121815A1 (es) | Compuestos de pirrolo-pirimidina como inhibidores de cdk4/6 | |
| PE20030010A1 (es) | Triazolopiridinas como inhibidores de quinasas | |
| AR085960A1 (es) | 1,3-oxazinas como inhibidores de la bace1 y/o de la bace2 | |
| AR082154A1 (es) | DERIVADOS DE PIRAZOLO[1,5-a]PIRIMIDINA COMO MODULADORES DE IRAK4 | |
| AR063081A1 (es) | Derivados de 3- aza- biciclo [3.1.0] hexano y su uso para la preparacion de medicamentos | |
| AR054560A1 (es) | Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer | |
| PE20091349A1 (es) | Compuestos derivados de espiro 1,3,4-tiadiazol como inhibidores de la actividad quinesina ksp | |
| ES2600636T3 (es) | Spiro-[1,3]-oxazinas y spiro-[1,4]-oxazepinas como inhibidores de BACE1 y/o BACE2 | |
| AR049331A1 (es) | Derivados de imidazopiridinas, imidazoquinolinas e iimidazonaftiridinas sustituidas con amidas como moduladores de biosintesis de citoquinas. composiciones farmaceuticas. | |
| PE20120534A1 (es) | PIRIMIDINAS FUSIONADAS COMO INHIBIDORES DE Akt | |
| MA32249B1 (fr) | Dérivés polysubstitues de 2-heteroaryl-6-phenyl-imidazo[1,2- a]pyridines, leur préparation et leur application en thérapeutique | |
| PE20130401A1 (es) | Heteroaril-ciclohexil-tetraazabenzo[e]azulenos | |
| ES2530884T3 (es) | Derivados de imidazopiridina o imidazopirimidina como inhibidores de fosfodiesterasa 10A | |
| ECSP11011257A (es) | Derivados de triazolo [4,3-b] piridazina y sus usos para el cáncer de próstata | |
| CO6640266A2 (es) | Proceso para preparar derivados de dihidropirrol | |
| CO6230982A2 (es) | Compuestos triciclicos que contienen actividad antagonista de factor de liberacion de corticotropina y composiciones farmaceuticas que los contienen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD | Application declared void or lapsed |