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
-
- 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
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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
- A61P25/24—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)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (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) |
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| JP2014510055A (ja) | 2011-02-18 | 2014-04-24 | アラーガン インコーポレイテッド | ホスホジエステラーゼ１０（ｐｄｅ１０ａ）阻害剤としての置換６，７−ジアルコキシ−３−イソキノリノール誘導体 |
| BR112014009348A2 (pt) * | 2011-10-20 | 2017-04-18 | Glaxosmithkline Llc | aza-heterociclos substituídos bicíclicos e análogos como moduladores de sirtuina |
| WO2013059589A1 (en) * | 2011-10-20 | 2013-04-25 | Sirtris Pharmaceuticals, Inc. | Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators |
| KR20140077963A (ko) | 2011-10-20 | 2014-06-24 | 글락소스미스클라인 엘엘씨 | 시르투인 조절제로서의 치환된 비시클릭 아자-헤테로사이클 및 유사체 |
| RU2638112C2 (ru) * | 2012-08-17 | 2017-12-15 | Ф. Хоффманн-Ля Рош Аг | Способ получения производных пиразолкарбоновой кислоты |
| WO2014071044A1 (en) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
| WO2014072261A1 (en) * | 2012-11-07 | 2014-05-15 | F. Hoffmann-La Roche Ag | Triazolo compounds |
| 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 |
| AU2014221799B2 (en) | 2013-02-27 | 2017-09-28 | Mochida Pharmaceutical Co., Ltd. | Novel pyrazole derivative |
| BR112015025140A2 (pt) * | 2013-05-23 | 2017-07-18 | Hoffmann La Roche | 2-fenilimidazo[1,2-a]pirimidinas como agentes de imagem |
| WO2015006689A1 (en) | 2013-07-12 | 2015-01-15 | University Of South Alabama | Treatment and diagnosis of cancer and precancerous conditions using pde10a inhibitors and methods to measure pde10a expression |
| CA2920068A1 (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 |
| DK3355699T3 (da) * | 2015-09-29 | 2021-06-07 | Onco Therapy Science Inc | Bicyklisk forbindelse og anvendelse deraf til inhibering af suv39h2 |
| ES2928164T3 (es) | 2015-10-19 | 2022-11-15 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| ES2928856T3 (es) | 2015-11-19 | 2022-11-23 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| TW201726623A (zh) | 2015-12-17 | 2017-08-01 | 英塞特公司 | 作為免疫調節劑之雜環化合物 |
| EP3394033B1 (en) | 2015-12-22 | 2020-11-25 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| ES2906460T3 (es) | 2016-05-06 | 2022-04-18 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
| EP3464279B1 (en) | 2016-05-26 | 2021-11-24 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| CA3028685A1 (en) | 2016-06-20 | 2017-12-28 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2018013789A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2018044783A1 (en) | 2016-08-29 | 2018-03-08 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| ES2874756T3 (es) | 2016-12-22 | 2021-11-05 | Incyte Corp | Derivados de triazolo[1,5-A]piridina como inmunomoduladores |
| MX391980B (es) | 2016-12-22 | 2025-03-21 | Incyte Corp | Derivados de tetrahidro imidazo [4,5-c] piridina como inductores de internalización de ligando 1 de muerte programada (pd-l1). |
| TW201835049A (zh) | 2016-12-22 | 2018-10-01 | 美商英塞特公司 | 作為免疫調節劑之雜環化合物 |
| EP3558973B1 (en) | 2016-12-22 | 2021-09-15 | Incyte Corporation | Pyridine derivatives as immunomodulators |
| PE20191532A1 (es) | 2016-12-22 | 2019-10-23 | Incyte Corp | Compuestos heterociclicos como inmunomoduladores |
| 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 |
| 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 |
| IL313101A (en) | 2018-03-30 | 2024-07-01 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| MD3790877T2 (ro) | 2018-05-11 | 2023-08-31 | Incyte Corp | Derivați de tetrahidro-imidazo[4,5-c]piridină în calitate de imunomodulatori PD-L1 |
| BR112020013697A2 (pt) | 2018-11-06 | 2020-12-01 | H. Lundbeck A/S | compostos para tratamento de sintomas negativos e comprometimentos cognitivos |
| 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 |
| TW202115059A (zh) | 2019-08-09 | 2021-04-16 | 美商英塞特公司 | Ｐｄ—１／ｐｄ—ｌ１抑制劑之鹽 |
| JP7559059B2 (ja) | 2019-09-30 | 2024-10-01 | インサイト・コーポレイション | 免疫調節剤としてのピリド［３，２－ｄ］ピリミジン化合物 |
| EP4049662A4 (en) * | 2019-10-21 | 2023-11-01 | SK Biopharmaceuticals Co., Ltd. | USE OF IMIDAZOPYRIMIDINE OR IMIDAZOTRIAZINE COMPOUNDS TO PREVENT, RELIEF OR TREAT COGNITIVE DISORDERS OR TO IMPROVE COGNITIVE FUNCTION |
| WO2021096849A1 (en) | 2019-11-11 | 2021-05-20 | Incyte Corporation | Salts and crystalline forms of a pd-1/pd-l1 inhibitor |
| EP4100023A4 (en) * | 2020-02-07 | 2024-03-13 | University of South Florida | Inhibition of beta-arrestin oligomerization in tauopathy |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| TW202233615A (zh) | 2020-11-06 | 2022-09-01 | 美商英塞特公司 | Ｐｄ—１／ｐｄ—ｌ１抑制劑之結晶形式 |
| JP2023548859A (ja) | 2020-11-06 | 2023-11-21 | インサイト・コーポレイション | Ｐｄ－１／ｐｄ－ｌ１阻害剤ならびにその塩及び結晶形態を作製するためのプロセス |
| 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 |
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| 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 |
| ATE288915T1 (de) * | 1999-11-10 | 2005-02-15 | Ortho Mcneil Pharm Inc | Substituierte 2-aryl-3-(heteroaryl)-imidazo(1,2- alpha)pyrimidine und ihren verwandten arzneimittel und verfahren |
| CA2410037C (en) | 2000-05-24 | 2009-11-03 | Merck Sharp & Dohme Limited | 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 |
| EP1660500B1 (en) * | 2003-07-30 | 2007-12-12 | Laboratorios S.A.L.V.A.T., S.A. | Substituted imidazopyrimidines for the prevention and treatment of cancer |
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| WO2007034282A2 (en) * | 2005-09-19 | 2007-03-29 | Pfizer Products Inc. | Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists |
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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 PH PH1/2012/501772A patent/PH12012501772A1/en unknown
- 2011-03-23 CN CN201180013745.6A patent/CN102791714B/zh not_active Expired - Fee Related
- 2011-03-23 NZ NZ600927A patent/NZ600927A/xx not_active IP Right Cessation
- 2011-03-23 AU AU2011231668A patent/AU2011231668A1/en not_active Abandoned
- 2011-03-23 ES ES11711068.4T patent/ES2478448T3/es active Active
- 2011-03-23 BR BR112012024199A patent/BR112012024199A2/pt active Search and Examination
- 2011-03-23 MA MA35218A patent/MA34069B1/fr unknown
- 2011-03-23 WO PCT/EP2011/054385 patent/WO2011117264A1/en not_active Ceased
- 2011-03-23 AR ARP110100945A patent/AR080785A1/es unknown
- 2011-03-23 JP JP2013501753A patent/JP5764196B2/ja not_active Expired - Fee Related
- 2011-03-23 CA CA2786213A patent/CA2786213A1/en not_active Abandoned
- 2011-03-23 KR KR1020127027825A patent/KR20130073876A/ko not_active Ceased
- 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 SG SG2012064044A patent/SG183824A1/en 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 PE PE2012001636A patent/PE20130382A1/es not_active Application Discontinuation
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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 |
|---|---|
| JP2013523673A (ja) | 2013-06-17 |
| US8410117B2 (en) | 2013-04-02 |
| ES2478448T3 (es) | 2014-07-22 |
| TWI478924B (zh) | 2015-04-01 |
| EP2552918A1 (en) | 2013-02-06 |
| CR20120443A (es) | 2012-10-11 |
| AU2011231668A1 (en) | 2012-07-19 |
| SG183824A1 (en) | 2012-10-30 |
| BR112012024199A2 (pt) | 2016-07-05 |
| ECSP12012174A (es) | 2012-10-30 |
| MA34069B1 (fr) | 2013-03-05 |
| CN102791714B (zh) | 2015-03-25 |
| CA2786213A1 (en) | 2011-09-29 |
| CL2012002497A1 (es) | 2013-03-22 |
| US20110237564A1 (en) | 2011-09-29 |
| RU2562066C2 (ru) | 2015-09-10 |
| UA108640C2 (uk) | 2015-05-25 |
| PH12012501772A1 (en) | 2017-07-26 |
| HK1173440A1 (en) | 2013-05-16 |
| NZ600927A (en) | 2013-08-30 |
| EP2552918B1 (en) | 2014-06-11 |
| JP5764196B2 (ja) | 2015-08-12 |
| MX2012010880A (es) | 2012-10-15 |
| TW201136937A (en) | 2011-11-01 |
| WO2011117264A1 (en) | 2011-09-29 |
| RU2012143794A (ru) | 2014-05-10 |
| ZA201206257B (en) | 2013-05-29 |
| KR20130073876A (ko) | 2013-07-03 |
| CN102791714A (zh) | 2012-11-21 |
| IL220932A0 (en) | 2012-09-24 |
| PE20130382A1 (es) | 2013-03-30 |
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