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)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (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 (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2014000894A (es) | 2011-07-22 | 2014-02-27 | Actelion Pharmaceuticals Ltd | Derivados de amidas heterociclicas como antagonistas de receptores p2x7. |
| KR102232742B1 (ko) | 2012-12-12 | 2021-03-26 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 인돌 카르복사미드 유도체 |
| WO2014097140A1 (fr) | 2012-12-18 | 2014-06-26 | Actelion Pharmaceuticals Ltd | Dérivés d'indole carboxamide utilisés en tant qu'antagonistes du récepteur p2x7 |
| JP6282016B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしての複素環アミド誘導体 |
| JP6282017B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしての複素環アミド誘導体 |
| BR112016021985B1 (pt) * | 2014-03-26 | 2022-08-30 | The General Hospital Corporation | Formulação farmacêutica |
| AU2018235561B2 (en) | 2017-03-13 | 2020-06-18 | Asahi Kasei Pharma Corporation | Tetrahydroquinoline derivatives as P2X7 receptor antagonists |
| SG11202006296YA (en) | 2018-01-19 | 2020-08-28 | Cytokinetics Inc | Dihydrobenzofuran and inden analogs as cardiac sarcomere inhibitors |
| 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 |
| EP3814343B1 (fr) | 2018-06-26 | 2023-01-11 | Cytokinetics, Inc. | Inhibiteurs de sarcomères cardiaques |
| KR20240015622A (ko) | 2021-03-04 | 2024-02-05 | 싸이토키네틱스, 인코포레이티드 | 심장 근절 억제제 |
| CN122301820A (zh) * | 2026-06-02 | 2026-06-30 | 辽宁龙田化工科技有限公司 | 一种高收率苯并呋喃-2,3-二酮3-(o-甲基肟)2-肟的合成方法 |
Family Cites Families (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TR200102911T2 (tr) | 1999-04-09 | 2002-01-21 | Astrazeneca Ab | Adamantan türevleri. |
| 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 |
| WO2003042190A1 (fr) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | Derives de n-adamantylalkyle benzamide en tant qu'antagonistes du recepteur p2x7 |
| PA8557501A1 (es) | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | Benzamida, heteroarilamida y amidas inversas |
| SE0103836D0 (sv) | 2001-11-16 | 2001-11-16 | Astrazeneca Ab | Novel compounds |
| SE0200920D0 (sv) | 2002-03-25 | 2002-03-25 | Astrazeneca Ab | Novel compounds |
| AU2003288640A1 (en) | 2002-12-31 | 2004-07-22 | Pfizer Products Inc. | Benzamide inhibitors of the p2x7 receptor |
| 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 |
| EP1626962B1 (fr) | 2003-05-12 | 2007-02-28 | Pfizer Products Inc. | Inhibiteurs benzamidiques du recepteur 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 |
| EP1683043A1 (fr) * | 2003-10-30 | 2006-07-26 | Koninklijke Philips Electronics N.V. | Methode de prediction de saisie |
| WO2005111003A1 (fr) * | 2004-04-29 | 2005-11-24 | Abbott Laboratories | Analogues d’amino-tétrazoles et méthodes d’utilisation |
| 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 |
| US20100298285A1 (en) | 2006-03-16 | 2010-11-25 | Kelly Michael G | Biclycloheteroaryl Compounds as P2x7 Modulators and Uses Thereof |
| 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 |
| CA2645556C (fr) | 2006-03-16 | 2016-05-24 | Renovis, Inc. | Composes de bicycloheteroaryle en tant que modulateurs de p2x7 et leurs utilisations |
| CA2645652A1 (fr) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Composes de bicycloheteroaryle 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 |
| ES2596532T3 (es) | 2006-03-16 | 2017-01-10 | Second Genome, Inc. | Compuestos de bicicloheteroarilo como moduladores de P2X7 y usos de los mismos |
| GB0611154D0 (en) | 2006-06-06 | 2006-07-19 | Glaxo Group Ltd | Novel receptor antagonists and their methods of use |
| EP2040700B1 (fr) | 2006-06-06 | 2010-11-24 | Glaxo Group Limited | Dérivés de n- (phénylméthyl) -2- (1h-pyraz0l-4-yl) acétamide utilisés comme antagonistes fp2x7 pour le traitement de la douleur, de l'inflammation et de la neurodégénérescence |
| AU2007271182B2 (en) | 2006-07-06 | 2012-03-15 | Glaxo Group Limited | Substituted N-phenylmethyl -5-oxo-proline-2-amides as P2X7-receptor antagonists and their methods of use |
| CA2670636A1 (fr) | 2006-11-27 | 2008-06-05 | H. Lundbeck A/S | Derives d'heteroaryl-amides |
| TW200838516A (en) | 2007-01-31 | 2008-10-01 | Merck & Co Inc | Substituted pyrano[2,3-B]pyridine derivatives as cannabinoid-1 receptor modulators |
| US8093265B2 (en) | 2007-03-09 | 2012-01-10 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| RU2460727C2 (ru) | 2007-03-22 | 2012-09-10 | Астразенека Аб | Хинолиновые производные для лечения воспалительных заболеваний |
| GB0705882D0 (en) | 2007-03-27 | 2007-05-02 | Glaxo Group Ltd | Novel compounds |
| EP2139858A1 (fr) | 2007-03-28 | 2010-01-06 | Glaxo Group Limited | Dérivés pipéridone carboxamide comme modulateurs du p2x7 |
| EP2139875A2 (fr) | 2007-03-29 | 2010-01-06 | Glaxo Group Limited | Dérivés d'oxazolidine et de morpholine carboxamide comme modulateurs de p2x7 |
| EA200970912A1 (ru) | 2007-04-03 | 2010-02-26 | Глэксо Груп Лимитед | Карбоксамидные производные имидазолидина в качестве модуляторов p2x7 |
| CN103204852A (zh) | 2007-04-10 | 2013-07-17 | H.隆德贝克有限公司 | 作为p2x7拮抗剂的杂芳基酰胺类似物 |
| JP2010523623A (ja) | 2007-04-11 | 2010-07-15 | グラクソ グループ リミテッド | P2x7調節因子としてのピラゾール誘導体 |
| WO2008138876A1 (fr) | 2007-05-10 | 2008-11-20 | Glaxo Group Limited | Dérivés du pyrazole utilisés comme modulateurs de p2x7 |
| CN101711245B (zh) | 2007-07-19 | 2015-03-25 | H.隆德贝克有限公司 | 5元杂环酰胺及相关的化合物 |
| EP2185560A4 (fr) * | 2007-08-10 | 2011-10-05 | Lundbeck & Co As H | Analogues d'hétéroarylamides |
| 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 |
| US20100292295A1 (en) | 2007-12-18 | 2010-11-18 | Glaxo Group Limited | 5-oxo-3-pyrrolidinecarboxamide derivatives as p2x7 modulators |
| WO2009108551A2 (fr) | 2008-02-25 | 2009-09-03 | H. Lundbeck A/S | Analogues d’hétéroarylamide |
| AU2009228649B2 (en) * | 2008-03-25 | 2014-05-22 | Affectis Pharmaceuticals Ag | Novel P2X7R antagonists and their use |
| JP5369173B2 (ja) | 2008-04-22 | 2013-12-18 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | キノリン若しくはイソキノリン置換p2x7アンタゴニスト |
| DK2243772T3 (da) | 2009-04-14 | 2012-02-13 | Affectis Pharmaceuticals Ag | Hidtil ukendte P2X7R-antagonister og deres anvendelse |
| 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 |
| US20140073651A1 (en) | 2011-02-22 | 2014-03-13 | Actelion Pharmaceuticals Ltd. | Benzamide derivatives as p2x7 receptor antagonists |
| WO2012163792A1 (fr) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Nouveaux antagonistes de p2x7r et leur utilisation |
| MX2014000894A (es) * | 2011-07-22 | 2014-02-27 | Actelion Pharmaceuticals Ltd | Derivados de amidas heterociclicas como antagonistas de receptores p2x7. |
| KR102232742B1 (ko) | 2012-12-12 | 2021-03-26 | 이도르시아 파마슈티컬스 리미티드 | P2x7 수용체 길항제로서의 인돌 카르복사미드 유도체 |
| WO2014097140A1 (fr) | 2012-12-18 | 2014-06-26 | Actelion Pharmaceuticals Ltd | Dérivés d'indole carboxamide utilisés en tant qu'antagonistes du récepteur p2x7 |
| JP6282017B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしての複素環アミド誘導体 |
| JP6282016B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしての複素環アミド誘導体 |
-
2013
- 2013-01-18 TW TW102102130A patent/TWI576347B/zh not_active IP Right Cessation
- 2013-01-18 AU AU2013210682A patent/AU2013210682B2/en not_active Ceased
- 2013-01-18 NZ NZ628910A patent/NZ628910A/en not_active IP Right Cessation
- 2013-01-18 BR BR112014017735-0A patent/BR112014017735B1/pt not_active IP Right Cessation
- 2013-01-18 MX MX2014008736A patent/MX336247B/es unknown
- 2013-01-18 JP JP2014552736A patent/JP6111268B2/ja not_active Expired - Fee Related
- 2013-01-18 CN CN201380005966.8A patent/CN104066737B/zh not_active Expired - Fee Related
- 2013-01-18 US US14/373,338 patent/US9409917B2/en not_active Expired - Fee Related
- 2013-01-18 SG SG11201403933UA patent/SG11201403933UA/en unknown
- 2013-01-18 EA EA201400822A patent/EA024204B1/ru not_active IP Right Cessation
- 2013-01-18 PL PL13707053T patent/PL2804865T3/pl unknown
- 2013-01-18 HK HK15104330.4A patent/HK1203932A1/xx unknown
- 2013-01-18 CA CA2863228A patent/CA2863228C/fr active Active
- 2013-01-18 AR ARP130100155A patent/AR089753A1/es unknown
- 2013-01-18 WO PCT/IB2013/050479 patent/WO2013108227A1/fr not_active Ceased
- 2013-01-18 ES ES13707053.8T patent/ES2563189T3/es active Active
- 2013-01-18 EP EP13707053.8A patent/EP2804865B1/fr not_active Not-in-force
- 2013-01-18 KR KR1020147022934A patent/KR102033190B1/ko not_active Expired - Fee Related
-
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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| MA37519B1 (fr) | Composés et compositions pour inhiber l'activité d'abl1, abl2 et bcr-abl1 | |
| MA37891B1 (fr) | Alcoxypyrazoles comme activateurs de guanylate cyclase soluble | |
| MA31953B1 (fr) | Nouveaux derives du thiophene. | |
| EA201490912A1 (ru) | Производные [1,2,3]триазоло[4,5-d]пиримидина в качестве агонистов каннабиноидного рецептора 2 | |
| MA34069B1 (fr) | Dérivés de n-(imidazopyrimidin-7-yl)hétéroarylamide et leur utilisation comme inhibiteurs de pde10a) | |
| MA37142A3 (fr) | Dérivés de dihydro-benzo-oxazine et de dihydro-pyrido-oxazine | |
| MA38540A1 (fr) | Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6 | |
| MA34819B1 (fr) | Dérivés bicyclo[3.2.1]octylamide et leurs utilisations | |
| MA37405A1 (fr) | Composés hétérocyclyle | |
| MA33528B1 (fr) | Derives pyridin-4-yliques | |
| EA201690019A1 (ru) | Производное аминотриазина и содержащая его фармацевтическая композиция | |
| EA201591008A1 (ru) | Пиридин-2-амиды, пригодные в качестве агонистов каннабиноидного рецептора 2 | |
| MA33420B1 (fr) | Dérivés fluorés de l'aminotriazole | |
| MA35816B1 (fr) | Dérivés d'aniline, leur préparation et leur application thérapeutique | |
| PH12014501415A1 (en) | Heterocyclic amide derivatives as p2x7 receptor antagonists | |
| MA38192A1 (fr) | Dérivés d'indole carboxamide utilisés en tant qu'antagonistes du récepteur p2x7 | |
| MA35663B1 (fr) | Dérivés de [1, 2, 3]triazolo [4, 5 -d] pyrimidine comme agonistes des récepteurs aux cannabinoïdes 2 | |
| MX2013006418A (es) | Derivados de oxazolil-metileter como agonistas del receptor de alx. | |
| EA201401259A1 (ru) | Фторированные мостиковые производные спиро[2,4]гептана в качестве агонистов рецептора alx | |
| MX2013006420A (es) | Derivados de aminotriazol hidrolixado como agonistas del receptor de alx. | |
| MA38679B1 (fr) | Modulateurs du récepteur de cxcr7 | |
| MA20150280A2 (fr) | Dérivés d'aryléthynyle | |
| EA201001842A1 (ru) | Новые соединения, обладающие активностью антагонистов мускариновых рецепторов | |
| ATE546448T1 (de) | Urotensin-ii-rezeptorantagonisten | |
| MA38010B1 (fr) | Dérivés d'éthynyl utilisés en tant que modulateurs de l'activité des récepteurs mglur5 |