MA32656B1 - Nouveaux composes chimiques - Google Patents
Nouveaux composes chimiquesInfo
- Publication number
- MA32656B1 MA32656B1 MA33729A MA33729A MA32656B1 MA 32656 B1 MA32656 B1 MA 32656B1 MA 33729 A MA33729 A MA 33729A MA 33729 A MA33729 A MA 33729A MA 32656 B1 MA32656 B1 MA 32656B1
- Authority
- MA
- Morocco
- Prior art keywords
- chemical compounds
- new chemical
- novel compounds
- compounds
- excessive
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 230000004663 cell proliferation Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
L'invention concerne de nouveaux composés représentés par la formule (i) dans laquelle les groupes r1 à r3, x1, x2, x3 et l1 ont la signification donnée dans la revendication 1, ces nouveaux composés étant appropriés pour traiter des maladies caractérisées par une prolifération cellulaire excessive ou anormale; et l'utilisation de tels composés dans un tel traitement.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08165437 | 2008-09-29 | ||
| PCT/EP2009/062551 WO2010034838A2 (fr) | 2008-09-29 | 2009-09-28 | Nouveaux composés chimiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32656B1 true MA32656B1 (fr) | 2011-09-01 |
Family
ID=40019293
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33729A MA32656B1 (fr) | 2008-09-29 | 2011-03-28 | Nouveaux composes chimiques |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8778929B2 (fr) |
| EP (1) | EP2350052B1 (fr) |
| JP (1) | JP5603869B2 (fr) |
| KR (1) | KR20110063574A (fr) |
| CN (1) | CN102227421A (fr) |
| AR (1) | AR073700A1 (fr) |
| AU (1) | AU2009295855A1 (fr) |
| BR (1) | BRPI0920608A2 (fr) |
| CA (1) | CA2738448A1 (fr) |
| CL (1) | CL2011000691A1 (fr) |
| CO (1) | CO6351739A2 (fr) |
| EA (1) | EA201100564A1 (fr) |
| EC (1) | ECSP11010930A (fr) |
| IL (1) | IL211744A0 (fr) |
| MA (1) | MA32656B1 (fr) |
| MX (1) | MX2011003292A (fr) |
| PE (1) | PE20110294A1 (fr) |
| TW (1) | TW201018670A (fr) |
| UY (1) | UY32146A (fr) |
| WO (1) | WO2010034838A2 (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20090837A1 (es) * | 2007-07-02 | 2009-07-24 | Boehringer Ingelheim Int | Nuevos compuestos quimicos |
| TW201014860A (en) | 2008-09-08 | 2010-04-16 | Boehringer Ingelheim Int | New chemical compounds |
| MX2011003292A (es) | 2008-09-29 | 2011-04-21 | Boehringer Ingelheim Int | Compuestos antiproliferativos. |
| CA2752265A1 (fr) | 2009-02-17 | 2010-08-26 | Boehringer Ingelheim International Gmbh | Derives pyrimido-[5,4-d]-pyrimidine pour l'inhibition des tyrosine-kinases |
| JP2011057661A (ja) | 2009-08-14 | 2011-03-24 | Bayer Cropscience Ag | 殺虫性カルボキサミド類 |
| AR077975A1 (es) | 2009-08-28 | 2011-10-05 | Irm Llc | Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina |
| EP2552905B1 (fr) | 2010-03-26 | 2016-10-05 | Boehringer Ingelheim International GmbH | Inhibiteurs de la kinase B-Raf |
| WO2011117382A1 (fr) * | 2010-03-26 | 2011-09-29 | Boehringer Ingelheim International Gmbh | Pyridyltriazoles |
| US8710055B2 (en) | 2010-12-21 | 2014-04-29 | Boehringer Ingelheim International Gmbh | Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| US8889684B2 (en) | 2011-02-02 | 2014-11-18 | Boehringer Ingelheim International Gmbh | Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| ES2882807T3 (es) | 2011-09-16 | 2021-12-02 | Novartis Ag | Heterociclil carboxamidas N-sustituidas |
| AU2012335663B2 (en) | 2011-11-11 | 2015-12-24 | Array Biopharma Inc. | Method of treating a proliferative disease |
| AR088936A1 (es) | 2011-11-23 | 2014-07-16 | Novartis Ag | Formulaciones farmaceuticas |
| CA2769821C (fr) | 2012-02-28 | 2020-08-11 | Michael Hatzinikolas | Ensemble structurel a liberation automatique |
| SG11201407152XA (en) | 2012-05-15 | 2014-11-27 | Novartis Ag | Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1 |
| CN104379574B (zh) | 2012-05-15 | 2017-03-01 | 诺华股份有限公司 | 用于抑制abl1、abl2和bcr‑abl1的活性的苯甲酰胺衍生物 |
| BR112014027584B1 (pt) | 2012-05-15 | 2023-01-24 | Novartis Ag | Uso de inibidores da atividade de abl1, abl2 e bcr-abl1, e composição farmacêutica |
| EA201492007A1 (ru) | 2012-05-15 | 2015-03-31 | Новартис Аг | Производные бензамида для ингибирования активности abl1, abl2 и bcr-abl1 |
| US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
| US20180194769A1 (en) | 2015-07-06 | 2018-07-12 | Rodin Therapeutics, Inc. | Hetero-halo inhibitors of histone deacetylase |
| WO2017069226A1 (fr) * | 2015-10-23 | 2017-04-27 | 田辺三菱製薬株式会社 | Nouveau composé hétérocyclique aromatique contenant de l'azote |
| CN106316864A (zh) * | 2016-08-22 | 2017-01-11 | 苏州天马精细化学品股份有限公司 | 4‑甲基‑3‑三氟甲基苯胺的制备方法 |
| DK3570834T3 (en) | 2017-01-11 | 2022-02-28 | Alkermes Inc | Bicyclic inhibitors of histone deacetylase |
| AU2018313094A1 (en) | 2017-08-07 | 2020-02-20 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
| CN108707147A (zh) * | 2018-06-20 | 2018-10-26 | 桑文军 | 一种新型微管蛋白抑制剂及其在抗肿瘤药物中的应用 |
| MA53225A (fr) * | 2018-08-14 | 2021-06-23 | Biogen Ma Inc | Agents inhibiteurs d'ask1 |
| CA3121202A1 (fr) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Composes pyrrole et pyrazole et leurs procedes d'utilisation |
| WO2022188792A1 (fr) * | 2021-03-12 | 2022-09-15 | 四川科伦博泰生物医药股份有限公司 | Composé hétérocyclique ayant une activité inhibitrice de protéine kinase, composition pharmaceutique le comprenant, son procédé de préparation et son utilisation |
| CN115772121A (zh) * | 2021-09-06 | 2023-03-10 | 南通诺泰生物医药技术有限公司 | 2-甲胺基-3-羟甲基吡啶的制备方法 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU507066B1 (en) | 1977-09-06 | 1980-01-31 | Sumitomo Chemical Company, Limited | 2-Substituted-5-Hydroxy-1h-Imidazole 4-Carbozamide Derivatives |
| JPH03174153A (ja) | 1989-09-20 | 1991-07-29 | Fuji Photo Film Co Ltd | カラー画像形成方法 |
| PL184490B1 (pl) | 1995-02-02 | 2002-11-29 | Smithkline Beecham Plc | Nowe pochodne indolu jako antagonista receptora T |
| WO1997003967A1 (fr) | 1995-07-22 | 1997-02-06 | Rhone-Poulenc Rorer Limited | Composes aromatiques substitues et leur utilisation pharmaceutique |
| WO2000047194A2 (fr) | 1999-02-09 | 2000-08-17 | 3-Dimensional Pharmaceuticals, Inc. | METHODES DE TRAITEMENT DE MALADIES ET PATHOLOGIES INDUITES PAR C1s, COMPOSES ET COMPOSITIONS PREPARES A CET EFFET |
| UA71971C2 (en) | 1999-06-04 | 2005-01-17 | Agoron Pharmaceuticals Inc | Diaminothiazoles, composition based thereon, a method for modulation of protein kinases activity, a method for the treatment of diseases mediated by protein kinases |
| US6531478B2 (en) | 2000-02-24 | 2003-03-11 | Cheryl P. Kordik | Amino pyrazole derivatives useful for the treatment of obesity and other disorders |
| CA2437248A1 (fr) * | 2001-02-02 | 2002-08-15 | Takeda Chemical Industries, Ltd. | Inhibiteur de jnk |
| ES2338539T3 (es) | 2001-11-01 | 2010-05-10 | Icagen, Inc. | Pirazolamidas para uso en el tratamiento del dolor. |
| US20040010027A1 (en) | 2001-12-17 | 2004-01-15 | Pharmacia & Upjohn Spa | Hydroxphenyl-pyrazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical comositions comprising them |
| JP2005162612A (ja) | 2002-01-09 | 2005-06-23 | Ajinomoto Co Inc | アシルスルホンアミド誘導体 |
| EP1567507B1 (fr) | 2002-11-27 | 2006-06-14 | Boehringer Ingelheim Pharmaceuticals Inc. | Inhibiteurs de cytokines a base de derives de 1, 2, 3- triazole-amides |
| BRPI0414313A (pt) | 2003-09-11 | 2006-11-07 | Kemia Inc | inibidores de citocinas |
| WO2005030705A1 (fr) | 2003-09-24 | 2005-04-07 | Methylgene, Inc. | Inhibiteurs d'histone deacetylase |
| WO2005040152A1 (fr) | 2003-10-20 | 2005-05-06 | E.I. Dupont De Nemours And Company | Azolecarboxamides substitues par heterocyclylphenyle et heterocyclylpyridile |
| ES2360292T3 (es) | 2003-12-03 | 2011-06-02 | Boehringer Ingelheim Pharmaceuticals Inc. | Derivados de 1,2,3-triazol amida como inhibidores de la producción de citoquinas. |
| ATE432273T1 (de) | 2004-03-09 | 2009-06-15 | Boehringer Ingelheim Pharma | 3-ä4-heterocyclyl-1,2,3-triazol-1-ylü-n- arylbenzamide als inhibitoren der cytokinenproduktion für die behandlung von chronischen entzündlichen erkrankungen |
| US7485657B2 (en) | 2004-05-12 | 2009-02-03 | Boehringer Ingelheim Pharmaceuticals, Inc. | Anti-cytokine heterocyclic compounds |
| US7531560B2 (en) | 2004-11-10 | 2009-05-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Anti-cytokine heterocyclic compounds |
| TW200628159A (en) | 2004-11-10 | 2006-08-16 | Synta Pharmaceuticals Corp | IL-12 modulatory compounds |
| JP2007076376A (ja) | 2005-09-09 | 2007-03-29 | Yanmar Co Ltd | トラクタ |
| WO2007056016A2 (fr) | 2005-11-02 | 2007-05-18 | Kemia, Inc. | Inhibiteurs de cytokine bisamide |
| WO2007075896A2 (fr) | 2005-12-22 | 2007-07-05 | Kemia, Inc. | Inhibiteurs de cytokine heterocycliques |
| US20070155746A1 (en) * | 2005-12-23 | 2007-07-05 | Kalypsys, Inc. | Novel substituted pyridinyloxy and pyrimidinyloxy amides useful as inhibitors of protein kinases |
| CA2647266A1 (fr) | 2006-04-18 | 2007-10-25 | Boehringer Ingelheim International Gmbh | Procede de preparation de composes inhibiteurs des cytokines contenant des cycles 4- et 5-imidazolyle et leurs intermediaires |
| PE20080068A1 (es) | 2006-05-15 | 2008-03-17 | Boehringer Ingelheim Int | Compuestos derivados de pirimidina como inhibidores de la quinasa aurora |
| EP2041138B1 (fr) | 2006-07-07 | 2014-06-25 | Bristol-Myers Squibb Company | Inhibiteurs de pyrrolotriazine kinase |
| PE20080553A1 (es) | 2006-07-07 | 2008-05-16 | Schering Corp | Ciclobuten-1,2-dionas 3,4-di-sustituidas como ligandos de receptores de quimiocinas cxc |
| NZ574621A (en) | 2006-07-07 | 2012-03-30 | Boehringer Ingelheim Int | Phenyl substituted heteroaryl-derivatives and use thereof as anti-tumour agents |
| US8030487B2 (en) | 2006-07-07 | 2011-10-04 | Targegen, Inc. | 2-amino—5-substituted pyrimidine inhibitors |
| PE20080906A1 (es) * | 2006-08-17 | 2008-07-05 | Kemia Inc | Derivados heteroarilo como inhibidores de citocina |
| WO2008079909A1 (fr) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Composés et méthodes de modulation des kinases, et indications connexes |
| WO2008089034A2 (fr) | 2007-01-11 | 2008-07-24 | Kemia, Inc. | Inhibiteurs de cytokine |
| AU2008221263B2 (en) * | 2007-03-01 | 2012-02-23 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| JP2010531850A (ja) | 2007-07-02 | 2010-09-30 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規化合物 |
| PE20090837A1 (es) | 2007-07-02 | 2009-07-24 | Boehringer Ingelheim Int | Nuevos compuestos quimicos |
| AU2008276063B2 (en) | 2007-07-17 | 2013-11-28 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| BRPI0916356B1 (pt) | 2008-07-24 | 2022-08-23 | Nerviano Medical Sciences S.R.L | 3,4-diaril pirazois como inibidores da proteína quinase |
| TW201014860A (en) | 2008-09-08 | 2010-04-16 | Boehringer Ingelheim Int | New chemical compounds |
| MX2011003292A (es) | 2008-09-29 | 2011-04-21 | Boehringer Ingelheim Int | Compuestos antiproliferativos. |
| CA2752265A1 (fr) | 2009-02-17 | 2010-08-26 | Boehringer Ingelheim International Gmbh | Derives pyrimido-[5,4-d]-pyrimidine pour l'inhibition des tyrosine-kinases |
| WO2011117382A1 (fr) | 2010-03-26 | 2011-09-29 | Boehringer Ingelheim International Gmbh | Pyridyltriazoles |
| EP2552905B1 (fr) | 2010-03-26 | 2016-10-05 | Boehringer Ingelheim International GmbH | Inhibiteurs de la kinase B-Raf |
| US8710055B2 (en) | 2010-12-21 | 2014-04-29 | Boehringer Ingelheim International Gmbh | Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| US20130023531A1 (en) | 2011-01-27 | 2013-01-24 | Boehringer Ingelheim International Gmbh | Pyrimido[5,4-d]pyrimidylamino phenyl sulfonamides as serine/threonine kinase inhibitors |
| US8889684B2 (en) | 2011-02-02 | 2014-11-18 | Boehringer Ingelheim International Gmbh | Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors |
-
2009
- 2009-09-28 MX MX2011003292A patent/MX2011003292A/es not_active Application Discontinuation
- 2009-09-28 AU AU2009295855A patent/AU2009295855A1/en not_active Abandoned
- 2009-09-28 US US13/121,241 patent/US8778929B2/en active Active
- 2009-09-28 TW TW098132738A patent/TW201018670A/zh unknown
- 2009-09-28 KR KR1020117009679A patent/KR20110063574A/ko not_active Withdrawn
- 2009-09-28 EP EP09783505.2A patent/EP2350052B1/fr active Active
- 2009-09-28 PE PE2011000796A patent/PE20110294A1/es not_active Application Discontinuation
- 2009-09-28 BR BRPI0920608A patent/BRPI0920608A2/pt not_active IP Right Cessation
- 2009-09-28 JP JP2011528358A patent/JP5603869B2/ja active Active
- 2009-09-28 UY UY0001032146A patent/UY32146A/es not_active Application Discontinuation
- 2009-09-28 AR ARP090103730A patent/AR073700A1/es unknown
- 2009-09-28 CA CA2738448A patent/CA2738448A1/fr not_active Abandoned
- 2009-09-28 CN CN2009801476559A patent/CN102227421A/zh active Pending
- 2009-09-28 WO PCT/EP2009/062551 patent/WO2010034838A2/fr not_active Ceased
- 2009-09-28 EA EA201100564A patent/EA201100564A1/ru unknown
-
2011
- 2011-03-15 IL IL211744A patent/IL211744A0/en unknown
- 2011-03-25 CO CO11036947A patent/CO6351739A2/es not_active Application Discontinuation
- 2011-03-28 MA MA33729A patent/MA32656B1/fr unknown
- 2011-03-29 CL CL2011000691A patent/CL2011000691A1/es unknown
- 2011-03-29 EC EC2011010930A patent/ECSP11010930A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2009295855A1 (en) | 2010-04-01 |
| MX2011003292A (es) | 2011-04-21 |
| AR073700A1 (es) | 2010-11-24 |
| EP2350052A2 (fr) | 2011-08-03 |
| CA2738448A1 (fr) | 2010-04-01 |
| EP2350052B1 (fr) | 2014-08-13 |
| UY32146A (es) | 2010-04-30 |
| CN102227421A (zh) | 2011-10-26 |
| JP5603869B2 (ja) | 2014-10-08 |
| US8778929B2 (en) | 2014-07-15 |
| PE20110294A1 (es) | 2011-05-26 |
| US20110312939A1 (en) | 2011-12-22 |
| TW201018670A (en) | 2010-05-16 |
| WO2010034838A3 (fr) | 2010-11-18 |
| WO2010034838A2 (fr) | 2010-04-01 |
| KR20110063574A (ko) | 2011-06-10 |
| CO6351739A2 (es) | 2011-12-20 |
| EA201100564A1 (ru) | 2011-12-30 |
| CL2011000691A1 (es) | 2011-07-29 |
| JP2012504114A (ja) | 2012-02-16 |
| ECSP11010930A (es) | 2011-04-29 |
| IL211744A0 (en) | 2011-06-30 |
| BRPI0920608A2 (pt) | 2019-09-24 |
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| EP2571876A4 (fr) | Composés hétérocycliques substitués à sept chaînons en tant qu'inhibiteurs de la dipeptidyl-peptidase iv pour le traitement du diabète | |
| MA30402B1 (fr) | Acides carboxyliques substitues par des phenylamino-benzoxazoles, leur procede de production et leur utilisation comme medicaments | |
| MA26697A1 (fr) | Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenant | |
| MA27946A1 (fr) | Omega-carboxyaryldiphenyluree fluoro-substituee pour le traitement et la prevention de maladies et d'etats pathologiques. | |
| EP1305024A4 (fr) | Procede de traitement des maladies fibreuses ou autres indications | |
| MA31076B1 (fr) | Dérivés de l'isoquinoléine et de l'isoquinoléinone substitués par une cycloalkylamine. | |
| MA31024B1 (fr) | Nouveaux derives de l'isoquinoleine et de l'isoquinoleinone substituees | |
| MA31075B1 (fr) | Dérivés d'isoquinolone substitués par une cycloalkylamine. | |
| MA27734A1 (fr) | DERIVES HEXAHYDROPYRAZINO [1,2-a]PYRIMIDINE-4,7-DIONE SUBSTITUES SUR L'AZOTE, METHODE POUR LEUR PRODUCTION ET LEUR UTILISATION EN TANT QUE MEDICAMENTS | |
| MA30609B1 (fr) | Imidazolidine-2,4-diones arylaminoaryl-alkyl-substituees, leur procede de synthese, les medicaments comprenant ces composes, et leurs applications. | |
| TN2015000547A1 (fr) | Composes heteroaromatiques et leur utilisation comme ligands de dopamine d1 | |
| MA26723A1 (fr) | Acides oxamiques nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant | |
| MA31834B1 (fr) | 5-[(3,3,3-trifluoro-2-hydroxy-1-arylpropyl)amino]-1h-quinolin-2-ones, leur procédé de production et leur utilisation comme anti-inflammatoires | |
| MA31570B1 (fr) | Oxazolidinones substitués et leur utilisation | |
| TN2009000138A1 (fr) | Biaryl-ether-urees | |
| EP2190428A4 (fr) | Composés hétérocycliques en tant qu'inhibiteurs de dipeptidylpeptidase-iv pour le traitement ou la prévention des diabètes | |
| TNSN05073A1 (fr) | Quinazolinones spirocondensees nouvelles et leur utilisation comme inhibiteurs de phosphodiesterase |