KR20120100913A - 아세틸콜린 수용체에 관련된 질환의 치료를 위한 축합 아진 - 유도체 - Google Patents
아세틸콜린 수용체에 관련된 질환의 치료를 위한 축합 아진 - 유도체 Download PDFInfo
- Publication number
- KR20120100913A KR20120100913A KR1020127009340A KR20127009340A KR20120100913A KR 20120100913 A KR20120100913 A KR 20120100913A KR 1020127009340 A KR1020127009340 A KR 1020127009340A KR 20127009340 A KR20127009340 A KR 20127009340A KR 20120100913 A KR20120100913 A KR 20120100913A
- Authority
- KR
- South Korea
- Prior art keywords
- diazabicyclo
- methyl
- nonan
- alkyl
- mmol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 0 CC(C)NC(C*C(c1c(*)ccc(F)c1)=O)=O Chemical compound CC(C)NC(C*C(c1c(*)ccc(F)c1)=O)=O 0.000 description 4
- GUPLUDGNBXNASI-UHFFFAOYSA-N CC(C)(CN(C(c1cc(Cl)ccc1F)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)CO Chemical compound CC(C)(CN(C(c1cc(Cl)ccc1F)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)CO GUPLUDGNBXNASI-UHFFFAOYSA-N 0.000 description 1
- CITUJCDCMDHNEP-UHFFFAOYSA-N CC(C)NC(CN(C(C1CCCCC1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O Chemical compound CC(C)NC(CN(C(C1CCCCC1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O CITUJCDCMDHNEP-UHFFFAOYSA-N 0.000 description 1
- QUBKQLVWKZSYOC-UHFFFAOYSA-N CC(C)NC(CN(C(c1cc(F)cc(F)c1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O Chemical compound CC(C)NC(CN(C(c1cc(F)cc(F)c1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O QUBKQLVWKZSYOC-UHFFFAOYSA-N 0.000 description 1
- KSLDDCLRYOABGF-UHFFFAOYSA-N CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O Chemical compound CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O KSLDDCLRYOABGF-UHFFFAOYSA-N 0.000 description 1
- GDYFMOROHDHJMV-UHFFFAOYSA-N CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1CC(CN(C3)C(OC(C)(C)C)=O)C3C1)C2=O)=O Chemical compound CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1CC(CN(C3)C(OC(C)(C)C)=O)C3C1)C2=O)=O GDYFMOROHDHJMV-UHFFFAOYSA-N 0.000 description 1
- CIUSAKIVYAVQKY-UHFFFAOYSA-N CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1CC(CNC3)C3C1)C2=O)=O Chemical compound CC(C)NC(CN(C(c1ccccc1)=Nc(cc1)c2cc1N1CC(CNC3)C3C1)C2=O)=O CIUSAKIVYAVQKY-UHFFFAOYSA-N 0.000 description 1
- RKDDUWNJMDSYLK-UHFFFAOYSA-N CC(C)NC(CN(C(c1ccccc1F)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O Chemical compound CC(C)NC(CN(C(c1ccccc1F)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O)=O RKDDUWNJMDSYLK-UHFFFAOYSA-N 0.000 description 1
- LMHHIAMMWMTQKO-UHFFFAOYSA-N CC(C)NC(CN(C=Nc(cc1)c2cc1N1CC(CN(C3)C(OC(C)(C)C)=O)C3C1)C2=O)=O Chemical compound CC(C)NC(CN(C=Nc(cc1)c2cc1N1CC(CN(C3)C(OC(C)(C)C)=O)C3C1)C2=O)=O LMHHIAMMWMTQKO-UHFFFAOYSA-N 0.000 description 1
- VGAMLXPQIKJIRV-UHFFFAOYSA-N CCC(N1C2CCC2)=Nc(ccc(N2C(CC3)CCN3CC2)c2)c2C1=O Chemical compound CCC(N1C2CCC2)=Nc(ccc(N2C(CC3)CCN3CC2)c2)c2C1=O VGAMLXPQIKJIRV-UHFFFAOYSA-N 0.000 description 1
- SOEPRDVVUFTACN-UHFFFAOYSA-N CCC(N1CC(N(C)C)=O)=Nc(ccc(N2C(CC3)CCN3CC2)c2)c2C1=O Chemical compound CCC(N1CC(N(C)C)=O)=Nc(ccc(N2C(CC3)CCN3CC2)c2)c2C1=O SOEPRDVVUFTACN-UHFFFAOYSA-N 0.000 description 1
- NKXSDZNKLCXPFA-UHFFFAOYSA-N CN(C(c1cc(C#N)ccc1)=Nc1c2ccc(N3C(CC4)CCN4CC3)c1)C2=O Chemical compound CN(C(c1cc(C#N)ccc1)=Nc1c2ccc(N3C(CC4)CCN4CC3)c1)C2=O NKXSDZNKLCXPFA-UHFFFAOYSA-N 0.000 description 1
- PPHIAYQNEAQCMX-UHFFFAOYSA-N CN(C(c1cc(Cl)ccc1)=Nc1c2cc(N3C(CC4)CCN4CC3)nc1)C2=O Chemical compound CN(C(c1cc(Cl)ccc1)=Nc1c2cc(N3C(CC4)CCN4CC3)nc1)C2=O PPHIAYQNEAQCMX-UHFFFAOYSA-N 0.000 description 1
- YFMQERMVMZKDCJ-UHFFFAOYSA-N CN(C(c1ccncc1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O Chemical compound CN(C(c1ccncc1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O YFMQERMVMZKDCJ-UHFFFAOYSA-N 0.000 description 1
- DNFFAFCULSITDH-UHFFFAOYSA-N CN(C(c1cnc[s]1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O Chemical compound CN(C(c1cnc[s]1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O DNFFAFCULSITDH-UHFFFAOYSA-N 0.000 description 1
- TZEGGLAQRXWSCY-UHFFFAOYSA-N CN(C1)CC2C1CN(C)C2 Chemical compound CN(C1)CC2C1CN(C)C2 TZEGGLAQRXWSCY-UHFFFAOYSA-N 0.000 description 1
- WSGVYRVTJRTQIQ-GJZGRUSLSA-N CN(C[C@@H]1C2)[C@@H]2CN1c(cc1)cc2c1N=C(c1cc(F)ccc1F)N(C)C2=O Chemical compound CN(C[C@@H]1C2)[C@@H]2CN1c(cc1)cc2c1N=C(c1cc(F)ccc1F)N(C)C2=O WSGVYRVTJRTQIQ-GJZGRUSLSA-N 0.000 description 1
- NRGUSJXTCUQTBB-RYUDHWBXSA-N CN(C[C@@H]1C2)[C@@H]2CN1c(cc1)cc2c1N=CN(C)C2=O Chemical compound CN(C[C@@H]1C2)[C@@H]2CN1c(cc1)cc2c1N=CN(C)C2=O NRGUSJXTCUQTBB-RYUDHWBXSA-N 0.000 description 1
- CMGDFEIKBFFGLS-BQBZGAKWSA-N CN1[C@@H](C2)CN(C)[C@@H]2C1 Chemical compound CN1[C@@H](C2)CN(C)[C@@H]2C1 CMGDFEIKBFFGLS-BQBZGAKWSA-N 0.000 description 1
- SRWDHJYCKZRAJU-UHFFFAOYSA-N COC1C(CC2)CCN2C1 Chemical compound COC1C(CC2)CCN2C1 SRWDHJYCKZRAJU-UHFFFAOYSA-N 0.000 description 1
- LOQXPUJLHUJHPJ-UHFFFAOYSA-N COCCN(C(C1CC1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O Chemical compound COCCN(C(C1CC1)=Nc(cc1)c2cc1N1C(CC3)CCN3CC1)C2=O LOQXPUJLHUJHPJ-UHFFFAOYSA-N 0.000 description 1
- RIJGJDHIZJRUAZ-UHFFFAOYSA-N Cc1cc(C(N2CC3(CO)CCC3)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)ccc1 Chemical compound Cc1cc(C(N2CC3(CO)CCC3)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)ccc1 RIJGJDHIZJRUAZ-UHFFFAOYSA-N 0.000 description 1
- LSAYLIOEQNLKRY-UHFFFAOYSA-N Cc1cncc(C(N2C)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)c1 Chemical compound Cc1cncc(C(N2C)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)c1 LSAYLIOEQNLKRY-UHFFFAOYSA-N 0.000 description 1
- KBUWZOJACCKYCI-UHFFFAOYSA-N Cc1nc(C(N2CC3(CO)CCC3)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)ccc1 Chemical compound Cc1nc(C(N2CC3(CO)CCC3)=Nc(ccc(N3C(CC4)CCN4CC3)c3)c3C2=O)ccc1 KBUWZOJACCKYCI-UHFFFAOYSA-N 0.000 description 1
- CVFYVFHDOVOTOM-UHFFFAOYSA-N OCC1(CN(C(C2CC2)=Nc(cc2)c3cc2N2C(CC4)CCN4CC2)C3=O)CCC1 Chemical compound OCC1(CN(C(C2CC2)=Nc(cc2)c3cc2N2C(CC4)CCN4CC2)C3=O)CCC1 CVFYVFHDOVOTOM-UHFFFAOYSA-N 0.000 description 1
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
- C07D471/08—Bridged 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25110109P | 2009-10-13 | 2009-10-13 | |
| US61/251,101 | 2009-10-13 | ||
| EP09172872.5 | 2009-10-13 | ||
| EP09172872 | 2009-10-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20120100913A true KR20120100913A (ko) | 2012-09-12 |
Family
ID=42040651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127009340A Withdrawn KR20120100913A (ko) | 2009-10-13 | 2010-10-11 | 아세틸콜린 수용체에 관련된 질환의 치료를 위한 축합 아진 - 유도체 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8841289B2 (enExample) |
| EP (1) | EP2488520B1 (enExample) |
| JP (1) | JP2013507417A (enExample) |
| KR (1) | KR20120100913A (enExample) |
| CN (1) | CN102666540A (enExample) |
| AU (1) | AU2010305825A1 (enExample) |
| BR (1) | BR112012008518A2 (enExample) |
| CA (1) | CA2776835A1 (enExample) |
| IN (1) | IN2012DN02968A (enExample) |
| MX (1) | MX2012004289A (enExample) |
| RU (1) | RU2012119488A (enExample) |
| WO (1) | WO2011045258A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2012291133A1 (en) | 2011-07-29 | 2014-02-20 | Taisho Pharmaceutical Co., Ltd. | Amidine compound or salt thereof |
| WO2013132253A1 (en) | 2012-03-07 | 2013-09-12 | Institute Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| AU2013264943B2 (en) * | 2012-05-22 | 2018-02-01 | King Abdullah University Of Science And Technology | Combination comprising parthenolide for use in the treatment of Alzheimer's Disease and other neurodegenerative disorders |
| EP3044221B1 (en) | 2013-09-11 | 2018-02-21 | Institute of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| WO2016034703A1 (en) | 2014-09-05 | 2016-03-10 | AbbVie Deutschland GmbH & Co. KG | Fused heterocyclic or carbocyclic compounds carrying a substituted cycloaliphatic radical and use thereof for treating vasopressin-related diseases |
| ES2764660T3 (es) | 2014-12-16 | 2020-06-04 | Axovant Sciences Gmbh | Compuestos de amida de quinuclidina sustituida geminal como agonistas de receptores alfa-7 nicotínicos de acetilcolina |
| AR103297A1 (es) | 2014-12-30 | 2017-05-03 | Forma Therapeutics Inc | Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina |
| MA41291A (fr) | 2014-12-30 | 2017-11-07 | Forma Therapeutics Inc | Dérivés de la pyrrolotriazinone et de l'imidazotriazinone en tant qu'inhibiteurs de la protéase spécifique de l'ubiquitine n° 7 (usp7) pour le traitement d'un cancer |
| JP2018504430A (ja) | 2015-02-05 | 2018-02-15 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的プロテアーゼ7阻害物質としてのキナゾリノン及びアザキナゾリノン |
| WO2016126929A1 (en) | 2015-02-05 | 2016-08-11 | Forma Therapeutics, Inc. | Thienopyrimidinones as ubiquitin-specific protease 7 inhibitors |
| US9938300B2 (en) | 2015-02-05 | 2018-04-10 | Forma Therapeutics, Inc. | Isothiazolopyrimidinones, pyrazolopyrimidinones, and pyrrolopyrimidinones as ubiquitin-specific protease 7 inhibitors |
| CN106146410B (zh) * | 2015-04-03 | 2018-10-12 | 中南大学 | 6-氨基-4(3h)-喹唑啉酮衍生物及其合成方法和用途 |
| CN106279211B (zh) | 2015-06-03 | 2020-09-15 | 北京大学 | 一种噻唑并嘧啶酮化合物及其制备方法和应用 |
| WO2016201096A1 (en) | 2015-06-10 | 2016-12-15 | Forum Pharmaceuticals, Inc. | Aminobenzisoxazole compounds as agonists of a7-nicotinic acetylcholine receptors |
| HK1253295A1 (zh) | 2015-08-12 | 2019-06-14 | Axovant Sciences Gmbh | 作为7-烟碱乙酰胆碱受体的激动剂的偕取代的氨基苯并异恶唑化合物 |
| JP7071917B2 (ja) | 2015-12-09 | 2022-05-19 | カデント セラピューティクス,インコーポレーテッド | ヘテロ芳香族nmda受容体モジュレーターおよびその使用 |
| EP3386990B1 (en) | 2015-12-09 | 2023-04-19 | Novartis AG | Thienopyrimidinone nmda receptor modulators and uses thereof |
| EP3558318B1 (en) | 2016-12-22 | 2023-12-20 | Novartis AG | Nmda receptor modulators and uses thereof |
| BR112020026637A2 (pt) * | 2018-06-27 | 2021-03-30 | Reborna Biosciences, Inc. | Agente profilático ou terapêutico para atrofia muscular espinhal |
| HU231414B1 (hu) | 2018-07-13 | 2023-08-28 | Richter Gedeon Nyrt. | Tiadiazin származékok |
| AU2019309448B2 (en) | 2018-07-26 | 2024-08-29 | Domain Therapeutics | Substituted quinazolinone derivatives and their use as positive allosteric modulators of mGluR4 |
| JOP20210020A1 (ar) | 2018-08-03 | 2021-01-25 | Cadent Therapeutics Inc | معدلات عطرية غير متجانسة لمستقبل nmda واستخداماتها |
| WO2021198191A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| WO2021198188A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| WO2022047145A1 (en) | 2020-08-28 | 2022-03-03 | Arvinas Operations, Inc. | Rapidly accelerating fibrosarcoma protein degrading compounds and associated methods of use |
| CN112898290B (zh) * | 2021-01-29 | 2022-08-05 | 中南大学 | 异噁唑甲酰胺基-4(3h)-喹唑啉酮衍生物及其合成方法和用途 |
| EP4584258A1 (en) | 2022-09-07 | 2025-07-16 | Arvinas Operations, Inc. | Rapidly accelerated fibrosarcoma (raf) degrading compounds and associated methods of use |
| TW202539670A (zh) * | 2024-02-23 | 2025-10-16 | 大陸商海思科醫藥集團股份有限公司 | Braf抑制劑的製備方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0000540D0 (sv) | 2000-02-18 | 2000-02-18 | Astrazeneca Ab | New compounds |
| JP2005504730A (ja) * | 2001-04-20 | 2005-02-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | Gsk−3インヒビターとして有用な組成物 |
| US7148236B2 (en) * | 2002-01-17 | 2006-12-12 | Merck & Co., Inc. | Modulators of acetylcholine receptors |
| GB0220581D0 (en) | 2002-09-04 | 2002-10-09 | Novartis Ag | Organic Compound |
| TW200536830A (en) * | 2004-02-06 | 2005-11-16 | Chugai Pharmaceutical Co Ltd | 1-(2H)-isoquinolone derivative |
| ES2423006T3 (es) * | 2005-07-26 | 2013-09-17 | Sanofi | Derivados de isoquinolona sustituidos con piperidinilo como inhibidores de la cinasa Rho |
| JP5256202B2 (ja) * | 2006-09-11 | 2013-08-07 | エム・エス・ディー・オス・ベー・フェー | キナゾリノンおよびイソキノリノンアセトアミド誘導体 |
| ATE502027T1 (de) * | 2006-12-27 | 2011-04-15 | Sanofi Aventis | Substituierte isochinoline und ihre verwendung als rho-kinase-inhibitoren |
| JP2010229035A (ja) * | 2007-08-01 | 2010-10-14 | Taisho Pharmaceutical Co Ltd | ピリドピリミジン−4−オン誘導体 |
| US8343960B2 (en) * | 2007-11-14 | 2013-01-01 | Neurosearch A/S | 1,4-diaza-bicyclo[3.2.2]nonyl pyrimidine derivatives and their medical use |
| CN101960691B (zh) | 2008-02-29 | 2013-04-24 | 核心技术国际有限公司 | 电池组的充电装置和电池组的品质判断装置 |
-
2010
- 2010-10-11 IN IN2968DEN2012 patent/IN2012DN02968A/en unknown
- 2010-10-11 BR BR112012008518A patent/BR112012008518A2/pt not_active Application Discontinuation
- 2010-10-11 CA CA2776835A patent/CA2776835A1/en not_active Abandoned
- 2010-10-11 US US13/501,587 patent/US8841289B2/en active Active
- 2010-10-11 AU AU2010305825A patent/AU2010305825A1/en not_active Abandoned
- 2010-10-11 MX MX2012004289A patent/MX2012004289A/es not_active Application Discontinuation
- 2010-10-11 CN CN2010800465507A patent/CN102666540A/zh active Pending
- 2010-10-11 EP EP10771062.6A patent/EP2488520B1/en active Active
- 2010-10-11 WO PCT/EP2010/065160 patent/WO2011045258A1/en not_active Ceased
- 2010-10-11 KR KR1020127009340A patent/KR20120100913A/ko not_active Withdrawn
- 2010-10-11 RU RU2012119488/04A patent/RU2012119488A/ru unknown
- 2010-10-11 JP JP2012533593A patent/JP2013507417A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013507417A (ja) | 2013-03-04 |
| WO2011045258A1 (en) | 2011-04-21 |
| US20120208796A1 (en) | 2012-08-16 |
| EP2488520A1 (en) | 2012-08-22 |
| RU2012119488A (ru) | 2013-11-20 |
| US8841289B2 (en) | 2014-09-23 |
| IN2012DN02968A (enExample) | 2015-07-31 |
| MX2012004289A (es) | 2012-06-12 |
| BR112012008518A2 (pt) | 2016-04-05 |
| CA2776835A1 (en) | 2011-04-21 |
| CN102666540A (zh) | 2012-09-12 |
| AU2010305825A1 (en) | 2012-04-19 |
| EP2488520B1 (en) | 2015-09-02 |
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