AR080785A1 - 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. - Google Patents
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.Info
- Publication number
- AR080785A1 AR080785A1 ARP110100945A ARP110100945A AR080785A1 AR 080785 A1 AR080785 A1 AR 080785A1 AR P110100945 A ARP110100945 A AR P110100945A AR P110100945 A ARP110100945 A AR P110100945A AR 080785 A1 AR080785 A1 AR 080785A1
- Authority
- AR
- Argentina
- Prior art keywords
- lower alkyl
- heteroaryl
- optionally substituted
- alkoxy
- heterocyclyl
- Prior art date
Links
Classifications
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- 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
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- 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
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- 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
-
- 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
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- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Anesthesiology (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (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)
Abstract
Reivindicacion 1: Un compuesto de la formula (1) en la que R1 es fenilo o tienilo, dichos fenilo y tienilo están opcionalmente sustituidos de 1 a 3 veces por sustituyentes elegidos con independencia entre el grupo formado por hidroxilo, halogeno, alquilo inferior, alcoxi inferior, haloalquilo inferior, haloalcoxi inferior, (alcoxi inferior)-alquilo inferior, -OC(O)-alquilo inferior, -OCH2C(O)-alcoxi inferior y fenilo; R2 es un heteroarilo monocíclico de 5 o 6 eslabones que tiene de 1 a 3 heteroátomos elegidos con independencia entre N y O, dicho heteroarilo está opcionalmente sustituido de 1 a 3 veces por sustituyentes elegidos con independencia entre el grupo formado el resto de formula (2), halogeno, hidroxilo, nitro, alquilo inferior, alquenilo inferior, alcoxi inferior, alcoxi inferior-C(O)-, hidroxialquilo inferior, haloalquilo inferior, (alcoxi inferior)-alquilo inferior, (alquilo inferior)-C(O)-, cicloalquilo, heterociclilo, arilo, heteroarilo y amino opcionalmente sustituido por heteroarilo, en el que dos sustituyentes de R2, junto con dicho heteroarilo al que están unidos, pueden formar un anillo bicíclico de 9 o 10 eslabones; R3 y R3' son con independencia hidrogeno, alquilo inferior, hidroxialquilo inferior, cianoalquilo inferior, haloalquilo inferior, (alcoxi inferior)-alquilo inferior, cicloalquilo, cianocicloalquilo, heterociclilo o arilo, dicho alquilo inferior está opcionalmente sustituido por haloalcoxi inferior, cicloalquilo, arilo o heteroarilo, dicho heteroarilo está opcionalmente sustituido de 1 a 3 veces por sustituyentes elegidos con independencia entre el grupo formado por halogeno, nitro, ciano, alquilo inferior, haloalquilo inferior, alcoxi inferior y cicloalquilo y dicho heterociclilo está opcionalmente sustituido por alquilo inferior, o R3 y R3', junto con el átomo de nitrogeno al que están unidos, forman un heterociclilo, 2,5-dihidro-1H-pirrol, 2-metil-2,4,5,6-tetrahidropirrolo[3,4-c]pirazol o 2-oxa-6-aza-espiro[3.3]heptano, dicho heterociclilo está opcionalmente sustituido de 1 a 3 veces por halogeno, hidroxilo, oxo, alquilo inferior o heteroarilo; R8 es hidrogeno, alquilo inferior, alcoxi inferior o (alcoxi inferior)-alquilo inferior; o sus sales farmacéuticamente aceptables.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10158011 | 2010-03-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR080785A1 true AR080785A1 (es) | 2012-05-09 |
Family
ID=43989818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP110100945A AR080785A1 (es) | 2010-03-26 | 2011-03-23 | 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. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8410117B2 (es) |
| EP (1) | EP2552918B1 (es) |
| JP (1) | JP5764196B2 (es) |
| KR (1) | KR20130073876A (es) |
| CN (1) | CN102791714B (es) |
| AR (1) | AR080785A1 (es) |
| AU (1) | AU2011231668A1 (es) |
| BR (1) | BR112012024199A2 (es) |
| CA (1) | CA2786213A1 (es) |
| CL (1) | CL2012002497A1 (es) |
| CR (1) | CR20120443A (es) |
| EC (1) | ECSP12012174A (es) |
| ES (1) | ES2478448T3 (es) |
| IL (1) | IL220932A0 (es) |
| MA (1) | MA34069B1 (es) |
| MX (1) | MX2012010880A (es) |
| NZ (1) | NZ600927A (es) |
| PE (1) | PE20130382A1 (es) |
| PH (1) | PH12012501772A1 (es) |
| RU (1) | RU2562066C2 (es) |
| SG (1) | SG183824A1 (es) |
| TW (1) | TWI478924B (es) |
| UA (1) | UA108640C2 (es) |
| WO (1) | WO2011117264A1 (es) |
| ZA (1) | ZA201206257B (es) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2013009575A (es) | 2011-02-18 | 2014-10-14 | Exonhit Therapeutics Sa | Derivados de 6, 7-dialcoxi-3-isoquinolinol sustituidos como inhibidores de fosfodiesterasa 10 (pdei0a). |
| EP2768834B1 (en) * | 2011-10-20 | 2016-04-27 | Glaxosmithkline LLC | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
| JP2014530872A (ja) * | 2011-10-20 | 2014-11-20 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC | サーチュイン調節因子としての置換された二環式アザ複素環およびアナログ |
| RU2014120166A (ru) | 2011-10-20 | 2015-11-27 | ГЛЭКСОСМИТКЛАЙН ЭлЭлСи | Замещенные бициклические аза-гетероциклы и их аналоги в качестве модуляторов сиртуина |
| JP6122118B2 (ja) * | 2012-08-17 | 2017-04-26 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ピラゾールカルボン酸誘導体を調製するための方法 |
| WO2014071044A1 (en) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
| MX2015005375A (es) * | 2012-11-07 | 2015-07-21 | Hoffmann La Roche | Compuestos de triazolo. |
| CN102964308B (zh) * | 2012-11-30 | 2015-03-18 | 中国药科大学 | 新型嘧啶类化合物、其制备方法、包含此类化合物的药物组合物及其用途 |
| HUE043059T2 (hu) | 2013-02-27 | 2019-07-29 | Mochida Pharm Co Ltd | Új pirazolszármazék |
| SG11201509503QA (en) | 2013-05-23 | 2015-12-30 | Hoffmann La Roche | 2-phenylimidazo[1,2-a]pyrimidines as imaging agents |
| US10039764B2 (en) | 2013-07-12 | 2018-08-07 | University Of South Alabama | Treatment and diagnosis of cancer and precancerous conditions using PDE10A inhibitors and methods to measure PDE10A expression |
| WO2015044095A1 (en) * | 2013-09-26 | 2015-04-02 | F. Hoffmann-La Roche Ag | Imidazo[1,2-a]pyridin-7-amines as imaging tools |
| US9200016B2 (en) | 2013-12-05 | 2015-12-01 | Allergan, Inc. | Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A) |
| PL408251A1 (pl) | 2014-05-19 | 2015-11-23 | Celon Pharma Spółka Z Ograniczoną Odpowiedzialnością | Skondensowane pochodne triazolu jako inhibitory fosfodiesterazy 10A |
| WO2016017711A1 (ja) * | 2014-07-30 | 2016-02-04 | 持田製薬株式会社 | ピラゾール誘導体の製造方法 |
| BR112018006005A2 (pt) * | 2015-09-29 | 2018-10-30 | Oncotherapy Science Inc | composto bicíclico e uso do mesmo para inibição de suv39h2 |
| ES2928164T3 (es) | 2015-10-19 | 2022-11-15 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| MD3377488T2 (ro) | 2015-11-19 | 2023-02-28 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
| MA44075A (fr) | 2015-12-17 | 2021-05-19 | Incyte Corp | Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation en tant que modulateurs des interactions protéine/protéine pd-1/pd-l1 |
| MY199705A (en) | 2015-12-22 | 2023-11-20 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| WO2017192961A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| KR102685249B1 (ko) | 2016-06-20 | 2024-07-17 | 인사이트 코포레이션 | 면역조절제로서의 복소환식 화합물 |
| MA45669A (fr) | 2016-07-14 | 2019-05-22 | Incyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
| WO2018044783A1 (en) | 2016-08-29 | 2018-03-08 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| EP3558973B1 (en) | 2016-12-22 | 2021-09-15 | Incyte Corporation | Pyridine derivatives as immunomodulators |
| WO2018119224A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Tetrahydro imidazo[4,5-c]pyridine derivatives as pd-l1 internalization inducers |
| CA3047991A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Bicyclic heteroaromatic compounds as immunomodulators |
| PE20191532A1 (es) | 2016-12-22 | 2019-10-23 | Incyte Corp | Compuestos heterociclicos como inmunomoduladores |
| EP3558989B1 (en) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
| TWI752155B (zh) * | 2017-02-01 | 2022-01-11 | 德商菲尼克斯製藥股份有限公司 | 芳香烴受體(AhR)調節劑化合物 |
| TWI674260B (zh) | 2017-02-01 | 2019-10-11 | 德商菲尼克斯製藥股份有限公司 | 芳基烴受體(AhR)調節劑化合物 |
| RS64055B1 (sr) | 2018-03-30 | 2023-04-28 | Incyte Corp | Heterociklična jedinjenja kao imunomodulatori |
| MD3790877T2 (ro) | 2018-05-11 | 2023-08-31 | Incyte Corp | Derivați de tetrahidro-imidazo[4,5-c]piridină în calitate de imunomodulatori PD-L1 |
| TW202031250A (zh) | 2018-11-06 | 2020-09-01 | 丹麥商H 朗德貝克公司 | 用於治療負性症狀和認知損傷之pde10a抑制劑 |
| WO2020094592A1 (en) | 2018-11-06 | 2020-05-14 | H. Lundbeck A/S | Compounds for treating negative symptoms and cognitive impairments |
| JP7665593B2 (ja) | 2019-08-09 | 2025-04-21 | インサイト・コーポレイション | Pd-1/pd-l1阻害剤の塩 |
| AR120109A1 (es) | 2019-09-30 | 2022-02-02 | Incyte Corp | Compuestos de pirido[3,2-d]pirimidina como inmunomoduladores |
| WO2021080312A1 (ko) * | 2019-10-21 | 2021-04-29 | 에스케이바이오팜 주식회사 | 인지 장애의 예방, 경감 또는 치료, 또는 인지 기능 향상을 위한 이미다조피리미딘 또는 이미다조트리아진 화합물의 용도 |
| PE20230407A1 (es) | 2019-11-11 | 2023-03-07 | Incyte Corp | Sales y formas cristalinas de un inhibidor de pd-1/pd-l1 |
| CN115427050B (zh) * | 2020-02-07 | 2025-02-14 | 南佛罗里达大学 | 对tau蛋白病中的β-抑制蛋白寡聚化的抑制 |
| WO2022099018A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process of preparing a pd-1/pd-l1 inhibitor |
| TW202233616A (zh) | 2020-11-06 | 2022-09-01 | 美商英塞特公司 | 用於製備pd-1/pd-l1抑制劑以及其鹽及結晶形式之方法 |
| WO2022099075A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Crystalline form of a pd-1/pd-l1 inhibitor |
| CN115572282B (zh) * | 2021-07-05 | 2024-07-09 | 华东理工大学 | 含芳杂环结构的吡唑酰胺类化合物及其制备方法和应用 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES493459A0 (es) | 1980-07-17 | 1981-07-01 | Consejo Superior Investigacion | Procedimiento para la preparacion de 3(6 5)-formilpira- zol-4-carboxilatos de alquilo |
| RU2264403C2 (ru) * | 1999-11-10 | 2005-11-20 | Орто-Макнейл Фармасьютикал, Инк. | Замещенные 2-арил-3-(гетероарил) имидазо [1,2-а] пиримидины, содержащие их фармацевтические композиции и связанные с ними способы |
| EP1294723A1 (en) | 2000-05-24 | 2003-03-26 | MERCK SHARP & DOHME LTD. | 3-phenyl-imidazo-pyrimidine derivatives as ligands for gaba receptors |
| US6596731B2 (en) | 2001-03-27 | 2003-07-22 | Hoffmann-La Roche Inc. | Substituted imidazo[1,2-A] pyridine derivatives |
| FR2825705B1 (fr) | 2001-06-08 | 2005-05-20 | Aventis Pharma Sa | Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens |
| WO2005014598A1 (en) * | 2003-07-30 | 2005-02-17 | Laboratorios S.A.L.V.A.T., S.A. | Substituted imidazopyrimidines for the prevention and treatment of cancer |
| WO2005012485A2 (en) | 2003-07-31 | 2005-02-10 | Bayer Pharmaceuticals Corporation | Methods for treating diabetes and related disorders using pde10a inhibitors |
| WO2007034282A2 (en) * | 2005-09-19 | 2007-03-29 | Pfizer Products Inc. | Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists |
| AU2007207053B2 (en) * | 2006-01-17 | 2012-05-24 | F. Hoffmann-La Roche Ag | Aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine useful for the treatment of Alzheimer's disease via GABA receptors |
| US7951824B2 (en) | 2006-02-17 | 2011-05-31 | Hoffman-La Roche Inc. | 4-aryl-pyridine-2-carboxyamide derivatives |
| ES2560435T3 (es) * | 2006-11-22 | 2016-02-19 | Incyte Holdings Corporation | Imidazotriazinas e imidazopirimidinas como inhibidores de la quinasa |
| EP1964841A1 (en) * | 2007-02-28 | 2008-09-03 | sanofi-aventis | Imidazo[1,2-a]azine and their use as pharmaceuticals |
| DE102007048716A1 (de) * | 2007-10-11 | 2009-04-23 | Merck Patent Gmbh | Imidazo[1,2-a]pyrimidinderivate |
| FR2926556B1 (fr) * | 2008-01-22 | 2010-02-19 | Sanofi Aventis | Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique |
| TWI501965B (zh) * | 2008-06-20 | 2015-10-01 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之新穎苯基咪唑衍生物 |
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2011
- 2011-03-17 US US13/049,941 patent/US8410117B2/en not_active Expired - Fee Related
- 2011-03-22 TW TW100109761A patent/TWI478924B/zh active
- 2011-03-23 AU AU2011231668A patent/AU2011231668A1/en not_active Abandoned
- 2011-03-23 CN CN201180013745.6A patent/CN102791714B/zh not_active Expired - Fee Related
- 2011-03-23 JP JP2013501753A patent/JP5764196B2/ja not_active Expired - Fee Related
- 2011-03-23 PH PH1/2012/501772A patent/PH12012501772A1/en unknown
- 2011-03-23 MX MX2012010880A patent/MX2012010880A/es active IP Right Grant
- 2011-03-23 EP EP11711068.4A patent/EP2552918B1/en not_active Not-in-force
- 2011-03-23 ES ES11711068.4T patent/ES2478448T3/es active Active
- 2011-03-23 KR KR1020127027825A patent/KR20130073876A/ko not_active Ceased
- 2011-03-23 PE PE2012001636A patent/PE20130382A1/es not_active Application Discontinuation
- 2011-03-23 CA CA2786213A patent/CA2786213A1/en not_active Abandoned
- 2011-03-23 AR ARP110100945A patent/AR080785A1/es unknown
- 2011-03-23 RU RU2012143794/04A patent/RU2562066C2/ru not_active IP Right Cessation
- 2011-03-23 UA UAA201211970A patent/UA108640C2/uk unknown
- 2011-03-23 MA MA35218A patent/MA34069B1/fr unknown
- 2011-03-23 BR BR112012024199A patent/BR112012024199A2/pt active Search and Examination
- 2011-03-23 NZ NZ600927A patent/NZ600927A/xx not_active IP Right Cessation
- 2011-03-23 WO PCT/EP2011/054385 patent/WO2011117264A1/en not_active Ceased
- 2011-03-23 SG SG2012064044A patent/SG183824A1/en unknown
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2012
- 2012-07-12 IL IL220932A patent/IL220932A0/en unknown
- 2012-08-20 ZA ZA2012/06257A patent/ZA201206257B/en unknown
- 2012-08-24 CR CR20120443A patent/CR20120443A/es unknown
- 2012-09-10 CL CL2012002497A patent/CL2012002497A1/es unknown
- 2012-09-24 EC ECSP12012174 patent/ECSP12012174A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2478448T3 (es) | 2014-07-22 |
| WO2011117264A1 (en) | 2011-09-29 |
| TWI478924B (zh) | 2015-04-01 |
| HK1173440A1 (en) | 2013-05-16 |
| UA108640C2 (uk) | 2015-05-25 |
| JP5764196B2 (ja) | 2015-08-12 |
| ECSP12012174A (es) | 2012-10-30 |
| CR20120443A (es) | 2012-10-11 |
| RU2562066C2 (ru) | 2015-09-10 |
| JP2013523673A (ja) | 2013-06-17 |
| TW201136937A (en) | 2011-11-01 |
| PH12012501772A1 (en) | 2017-07-26 |
| MA34069B1 (fr) | 2013-03-05 |
| US8410117B2 (en) | 2013-04-02 |
| CA2786213A1 (en) | 2011-09-29 |
| CN102791714A (zh) | 2012-11-21 |
| AU2011231668A1 (en) | 2012-07-19 |
| BR112012024199A2 (pt) | 2016-07-05 |
| EP2552918A1 (en) | 2013-02-06 |
| CL2012002497A1 (es) | 2013-03-22 |
| KR20130073876A (ko) | 2013-07-03 |
| NZ600927A (en) | 2013-08-30 |
| PE20130382A1 (es) | 2013-03-30 |
| US20110237564A1 (en) | 2011-09-29 |
| ZA201206257B (en) | 2013-05-29 |
| CN102791714B (zh) | 2015-03-25 |
| IL220932A0 (en) | 2012-09-24 |
| EP2552918B1 (en) | 2014-06-11 |
| RU2012143794A (ru) | 2014-05-10 |
| SG183824A1 (en) | 2012-10-30 |
| MX2012010880A (es) | 2012-10-15 |
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