MA35893B1 - Dérivés d'amide hétérocyclique comme antagonistes du récepteur p2x7 - Google Patents
Dérivés d'amide hétérocyclique comme antagonistes du récepteur p2x7Info
- Publication number
- MA35893B1 MA35893B1 MA37252A MA37252A MA35893B1 MA 35893 B1 MA35893 B1 MA 35893B1 MA 37252 A MA37252 A MA 37252A MA 37252 A MA37252 A MA 37252A MA 35893 B1 MA35893 B1 MA 35893B1
- Authority
- MA
- Morocco
- Prior art keywords
- amide derivatives
- receptor antagonists
- heterocyclic amide
- heterocyclic
- derivatives
- Prior art date
Links
- -1 Heterocyclic amide Chemical class 0.000 title abstract 2
- 102100037602 P2X purinoceptor 7 Human genes 0.000 title 1
- 101710189965 P2X purinoceptor 7 Proteins 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne des dérivés d'amide hétérocyclique de formule (i), dans laquelle r1, r2, r3, x et n sont tels que définis dans la description, leur préparation et leur utilisation comme composés pharmaceutiquement actifs.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2012050282 | 2012-01-20 | ||
| PCT/IB2013/050479 WO2013108227A1 (fr) | 2012-01-20 | 2013-01-18 | Dérivés d'amide hétérocyclique comme antagonistes du récepteur p2x7 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35893B1 true MA35893B1 (fr) | 2014-12-01 |
Family
ID=47757670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA37252A MA35893B1 (fr) | 2012-01-20 | 2014-07-31 | Dérivés d'amide hétérocyclique comme antagonistes du récepteur p2x7 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US9409917B2 (fr) |
| EP (1) | EP2804865B1 (fr) |
| JP (1) | JP6111268B2 (fr) |
| KR (1) | KR102033190B1 (fr) |
| CN (1) | CN104066737B (fr) |
| AR (1) | AR089753A1 (fr) |
| AU (1) | AU2013210682B2 (fr) |
| BR (1) | BR112014017735B1 (fr) |
| CA (1) | CA2863228C (fr) |
| CL (1) | CL2014001772A1 (fr) |
| EA (1) | EA024204B1 (fr) |
| ES (1) | ES2563189T3 (fr) |
| HK (1) | HK1203932A1 (fr) |
| IL (1) | IL233662A0 (fr) |
| MA (1) | MA35893B1 (fr) |
| MX (1) | MX336247B (fr) |
| NZ (1) | NZ628910A (fr) |
| PH (1) | PH12014501415A1 (fr) |
| PL (1) | PL2804865T3 (fr) |
| SG (1) | SG11201403933UA (fr) |
| TW (1) | TWI576347B (fr) |
| WO (1) | WO2013108227A1 (fr) |
| ZA (1) | ZA201406085B (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101995088B1 (ko) | 2011-07-22 | 2019-07-02 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 헤테로시클릭 아미드 유도체 |
| US9718774B2 (en) | 2012-12-12 | 2017-08-01 | Idorsia Pharmaceuticals Ltd | Indole carboxamide derivatives as P2X7 receptor antagonist |
| AR094053A1 (es) | 2012-12-18 | 2015-07-08 | Actelion Pharmaceuticals Ltd | Derivados de indol carboxamida como antagonistas del receptor p2x₇ |
| EP2956135B1 (fr) | 2013-01-22 | 2016-11-16 | Actelion Pharmaceuticals Ltd. | Dérivés d'amides hétérocycliques utilisés comme antagonistes du récepteur p2x7 |
| KR102220847B1 (ko) | 2013-01-22 | 2021-02-26 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 헤테로시클릭 아미드 유도체 |
| EP3122347B1 (fr) * | 2014-03-26 | 2020-06-03 | The Children's Medical Center Corporation | Celastrol derivées destinées au traitement de l'obésité |
| PT3609868T (pt) | 2017-03-13 | 2023-12-18 | Raqualia Pharma Inc | Derivados de tetra-hidroquinolina como antagonistas do recetor p2x7 |
| MD3740481T3 (ro) | 2018-01-19 | 2025-06-30 | Cytokinetics Inc | Analogi de dihidrobenzofuran și inden în calitate de inhibitori ai sarcomerului cardiac |
| JP7610985B2 (ja) | 2018-06-26 | 2025-01-09 | サイトキネティックス, インコーポレイテッド | 心臓サルコメア阻害剤 |
| JP7438148B2 (ja) | 2018-06-26 | 2024-02-26 | サイトキネティックス, インコーポレイテッド | 心臓サルコメア阻害剤 |
| JP2024508526A (ja) | 2021-03-04 | 2024-02-27 | サイトキネティックス, インコーポレイテッド | 心筋サルコメア阻害剤 |
Family Cites Families (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ20013608A3 (cs) | 1999-04-09 | 2002-05-15 | Astrazeneca Ab | Adamantanové deriváty |
| SE9904505D0 (sv) | 1999-12-09 | 1999-12-09 | Astra Pharma Prod | Novel compounds |
| TWI258462B (en) | 1999-12-17 | 2006-07-21 | Astrazeneca Ab | Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same |
| GB0013737D0 (en) | 2000-06-07 | 2000-07-26 | Astrazeneca Ab | Novel compounds |
| PA8557501A1 (es) | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | Benzamida, heteroarilamida y amidas inversas |
| WO2003042190A1 (fr) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | Derives de n-adamantylalkyle benzamide en tant qu'antagonistes du recepteur p2x7 |
| SE0103836D0 (sv) | 2001-11-16 | 2001-11-16 | Astrazeneca Ab | Novel compounds |
| SE0200920D0 (sv) | 2002-03-25 | 2002-03-25 | Astrazeneca Ab | Novel compounds |
| BR0317844A (pt) | 2002-12-31 | 2005-12-06 | Pfizer Prod Inc | Inibidores de benzamida do receptor p2x7 |
| PA8591801A1 (es) | 2002-12-31 | 2004-07-26 | Pfizer Prod Inc | Inhibidores benzamidicos del receptor p2x7. |
| SE0300480D0 (sv) | 2003-02-21 | 2003-02-21 | Astrazeneca Ab | Novel compounds |
| MXPA05012086A (es) | 2003-05-12 | 2006-02-22 | Pfizer Prod Inc | Inhibidores de benzamida del receptor p2x7. |
| GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
| SE0302139D0 (sv) | 2003-07-28 | 2003-07-28 | Astrazeneca Ab | Novel compounds |
| KR20060120053A (ko) * | 2003-10-30 | 2006-11-24 | 코닌클리케 필립스 일렉트로닉스 엔.브이. | 입력 예측 방법 |
| JP2007535553A (ja) * | 2004-04-29 | 2007-12-06 | アボット・ラボラトリーズ | アミノ−テトラゾール類縁体および使用方法 |
| SA05260265A (ar) | 2004-08-30 | 2005-12-03 | استرازينيكا ايه بي | مركبات جديدة |
| SE0402925D0 (sv) | 2004-11-30 | 2004-11-30 | Astrazeneca Ab | Novel Compounds |
| EP1844003A4 (fr) | 2005-01-27 | 2010-09-22 | Astrazeneca Ab | Nouveaux composes biaromatiques, inhibiteurs du recepteur p2x7 |
| WO2006086464A2 (fr) | 2005-02-10 | 2006-08-17 | Bristol-Myers Squibb Company | Dihydroquinazolinones utilisees comme modulateurs de la 5ht |
| US7402596B2 (en) | 2005-03-24 | 2008-07-22 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| WO2007055374A1 (fr) * | 2005-11-14 | 2007-05-18 | Mitsubishi Tanabe Pharma Corporation | Agent therapeutique pour l'osteoporose |
| WO2007109154A2 (fr) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Composés de bicyclohétéroaryle en tant que modulateurs de p2x7 modulators et leurs utilisations |
| US20100184802A1 (en) | 2006-03-16 | 2010-07-22 | Kelly Michael G | Bicycloheteroaryl Compounds as P2X7 Modulators and Uses Thereof |
| WO2007109182A2 (fr) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Composés de bicyclohétéroaryle en tant que modulateurs de p2x7 et leurs utilisations |
| WO2007109160A2 (fr) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Composés de bicyclohétéroaryle en tant que modulateurs de p2x7 et leurs utilisations |
| TWI464148B (zh) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為p2x7調節劑之雙環雜芳基化合物與其用途 |
| US8546579B2 (en) | 2006-03-16 | 2013-10-01 | Evotec (Us) Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| GB0611154D0 (en) | 2006-06-06 | 2006-07-19 | Glaxo Group Ltd | Novel receptor antagonists and their methods of use |
| JP2009539795A (ja) | 2006-06-06 | 2009-11-19 | グラクソ グループ リミテッド | 疼痛、炎症および神経変性の治療のためのp2x7アンタゴニストとしてのn−(フェニルメチル)−2−(1h−ピラゾール−4−イル)アセトアミド誘導体 |
| US7718693B2 (en) | 2006-07-06 | 2010-05-18 | Glaxo Group Limited | Receptor antagonists and their methods of use |
| EP2096923B1 (fr) | 2006-11-27 | 2014-01-22 | H. Lundbeck A/S | Dérivés d'hétéroaryl-amides |
| TW200838516A (en) | 2007-01-31 | 2008-10-01 | Merck & Co Inc | Substituted pyrano[2,3-B]pyridine derivatives as cannabinoid-1 receptor modulators |
| CA2680275C (fr) | 2007-03-09 | 2016-08-23 | Renovis, Inc. | Composes de bicycloheteroaryle utilises comme modulateurs de p2x7 et leurs utilisations |
| PE20091225A1 (es) | 2007-03-22 | 2009-09-16 | Astrazeneca Ab | Derivados de quinolina como antagonistas del receptor p2x7 |
| GB0705882D0 (en) | 2007-03-27 | 2007-05-02 | Glaxo Group Ltd | Novel compounds |
| US20100168171A1 (en) | 2007-03-28 | 2010-07-01 | Paul John Beswick | Piperidinone Carboxamide Derivatives as P2X7 Modulators |
| JP2010522710A (ja) | 2007-03-29 | 2010-07-08 | グラクソ グループ リミテッド | P2x7調節因子としてのオキサゾリジンおよびモルホリンカルボキサミド誘導体 |
| CN101679291A (zh) | 2007-04-03 | 2010-03-24 | 葛兰素集团有限公司 | 作为p2x7调节剂的咪唑烷甲酰胺衍生物 |
| CN101772498A (zh) | 2007-04-10 | 2010-07-07 | H.隆德贝克有限公司 | 作为p2x7拮抗剂的杂芳基酰胺类似物 |
| WO2008125600A2 (fr) | 2007-04-11 | 2008-10-23 | Glaxo Group Limited | Dérivés de pyrazole utilisés comme modulateurs de p2x7 |
| US20110046137A1 (en) | 2007-05-10 | 2011-02-24 | Glaxo Group Limited | Pyrazole Derivatives as P2X7 Modulators |
| SG187396A1 (en) | 2007-07-19 | 2013-02-28 | Lundbeck & Co As H | 5-membered heterocyclic amides and related compounds |
| BRPI0812594A2 (pt) * | 2007-08-10 | 2015-06-23 | Lundbeck & Co As H | Composto ou sal ou hidrato do mesmo, composição farmacêutica, métodos para modulação da atividade de um receptor p2x7, para tratamento de uma condição responsiva á modulação do receptor p2x7 em um paciente, para inibição de morte de células gangliônicas retinais em um paciente, para determinação da presença ou ausência de receptor p2x7 em uma amostra, preparação farmacêutica acondicionada, e, uso de um composto ou sal ou hidrato do mesmo. |
| PE20091036A1 (es) | 2007-11-30 | 2009-08-15 | Astrazeneca Ab | Derivado de quinolina como antagonista del receptor p2x7 |
| GB0724258D0 (en) | 2007-12-12 | 2008-01-30 | Glaxo Group Ltd | Novel combinations |
| WO2009074518A1 (fr) | 2007-12-12 | 2009-06-18 | Glaxo Group Limited | Combinaisons formées de modulateurs au prolinamide du récepteur p2x7 et d'autres agents thérapeutiques |
| GB0724625D0 (en) | 2007-12-18 | 2008-01-30 | Glaxo Group Ltd | Novel compounds |
| KR20100099178A (ko) | 2007-12-18 | 2010-09-10 | 글락소 그룹 리미티드 | P2x7 조절제로서의 5-옥소-3-피롤리딘카르복스아미드 유도체 |
| WO2009108551A2 (fr) | 2008-02-25 | 2009-09-03 | H. Lundbeck A/S | Analogues d’hétéroarylamide |
| US8232290B2 (en) | 2008-03-25 | 2012-07-31 | Affectis Pharmaceuticals Ag | P2X7R antagonists and their use |
| CA2722035C (fr) | 2008-04-22 | 2016-10-11 | Janssen Pharmaceutica Nv | Antagonistes de p2x7 substitues par une quinoline ou isoquinoline |
| EP2243772B1 (fr) | 2009-04-14 | 2012-01-18 | Affectis Pharmaceuticals AG | Nouveaux antagonistes P2X7R et leur utilisation |
| GB0919594D0 (en) | 2009-11-09 | 2009-12-23 | Glaxo Group Ltd | Compounds |
| US20120157494A1 (en) | 2010-12-16 | 2012-06-21 | Harris Iii Ralph New | Isoindolyl compounds |
| JP2014513671A (ja) | 2011-02-22 | 2014-06-05 | アクテリオン ファーマシューティカルズ リミテッド | P2x7受容体アンタゴニストとしてのベンズアミド誘導体 |
| WO2012163792A1 (fr) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Nouveaux antagonistes de p2x7r et leur utilisation |
| KR101995088B1 (ko) * | 2011-07-22 | 2019-07-02 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 헤테로시클릭 아미드 유도체 |
| US9718774B2 (en) | 2012-12-12 | 2017-08-01 | Idorsia Pharmaceuticals Ltd | Indole carboxamide derivatives as P2X7 receptor antagonist |
| AR094053A1 (es) | 2012-12-18 | 2015-07-08 | Actelion Pharmaceuticals Ltd | Derivados de indol carboxamida como antagonistas del receptor p2x₇ |
| KR102220847B1 (ko) | 2013-01-22 | 2021-02-26 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 헤테로시클릭 아미드 유도체 |
| EP2956135B1 (fr) | 2013-01-22 | 2016-11-16 | Actelion Pharmaceuticals Ltd. | Dérivés d'amides hétérocycliques utilisés comme antagonistes du récepteur p2x7 |
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2013
- 2013-01-18 MX MX2014008736A patent/MX336247B/es unknown
- 2013-01-18 EP EP13707053.8A patent/EP2804865B1/fr active Active
- 2013-01-18 CN CN201380005966.8A patent/CN104066737B/zh not_active Expired - Fee Related
- 2013-01-18 WO PCT/IB2013/050479 patent/WO2013108227A1/fr not_active Ceased
- 2013-01-18 KR KR1020147022934A patent/KR102033190B1/ko not_active Expired - Fee Related
- 2013-01-18 JP JP2014552736A patent/JP6111268B2/ja not_active Expired - Fee Related
- 2013-01-18 AU AU2013210682A patent/AU2013210682B2/en not_active Ceased
- 2013-01-18 AR ARP130100155A patent/AR089753A1/es unknown
- 2013-01-18 NZ NZ628910A patent/NZ628910A/en not_active IP Right Cessation
- 2013-01-18 TW TW102102130A patent/TWI576347B/zh not_active IP Right Cessation
- 2013-01-18 US US14/373,338 patent/US9409917B2/en not_active Expired - Fee Related
- 2013-01-18 BR BR112014017735-0A patent/BR112014017735B1/pt not_active IP Right Cessation
- 2013-01-18 ES ES13707053.8T patent/ES2563189T3/es active Active
- 2013-01-18 CA CA2863228A patent/CA2863228C/fr active Active
- 2013-01-18 SG SG11201403933UA patent/SG11201403933UA/en unknown
- 2013-01-18 HK HK15104330.4A patent/HK1203932A1/xx unknown
- 2013-01-18 EA EA201400822A patent/EA024204B1/ru not_active IP Right Cessation
- 2013-01-18 PL PL13707053T patent/PL2804865T3/pl unknown
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2014
- 2014-06-20 PH PH12014501415A patent/PH12014501415A1/en unknown
- 2014-07-01 CL CL2014001772A patent/CL2014001772A1/es unknown
- 2014-07-16 IL IL233662A patent/IL233662A0/en unknown
- 2014-07-31 MA MA37252A patent/MA35893B1/fr unknown
- 2014-08-19 ZA ZA2014/06085A patent/ZA201406085B/en unknown
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