MA31905B1 - DERIVES D'AMIDES DE L'ACIDE 6,7-DIHYDRO-5H-IMIDAZO[1,2-alpha] IMIDAZOLE-3-CARBOXYLIQUE - Google Patents
DERIVES D'AMIDES DE L'ACIDE 6,7-DIHYDRO-5H-IMIDAZO[1,2-alpha] IMIDAZOLE-3-CARBOXYLIQUEInfo
- Publication number
- MA31905B1 MA31905B1 MA32900A MA32900A MA31905B1 MA 31905 B1 MA31905 B1 MA 31905B1 MA 32900 A MA32900 A MA 32900A MA 32900 A MA32900 A MA 32900A MA 31905 B1 MA31905 B1 MA 31905B1
- Authority
- MA
- Morocco
- Prior art keywords
- imidazo
- dihydro
- imidazole
- carboxylic acid
- amide derivatives
- Prior art date
Links
- OKRROXQXGNEUSS-UHFFFAOYSA-N 1h-imidazol-1-ium-1-carboxylate Chemical compound OC(=O)N1C=CN=C1 OKRROXQXGNEUSS-UHFFFAOYSA-N 0.000 title 1
- 150000001408 amides Chemical class 0.000 title 1
- -1 amide derivatives of 6,7-dihydro-5h-imidazo [1,2-a] imidazole-3-carboxylic acid Chemical class 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 102000006495 integrins Human genes 0.000 abstract 1
- 108010044426 integrins Proteins 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 210000000265 leukocyte Anatomy 0.000 abstract 1
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
-
- 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
- A61P11/06—Antiasthmatics
-
- 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
- A61P11/16—Central respiratory analeptics
-
- 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
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- 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
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- 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
-
- 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
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
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- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Toxicology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne des dérivés d'amide de l'acide 6,7-dihydro-5h-imidazo[1,2-a]imidazole-3-carboxylique qui présentent un bon effet d'inhibition sur l'interaction des cam (molécules d'adhésion cellulaire) et des intégrines leucocytaires et sont donc utiles dans le traitement d'une maladie inflammatoire.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99096007P | 2007-11-29 | 2007-11-29 | |
| US4795708P | 2008-04-25 | 2008-04-25 | |
| PCT/US2008/084149 WO2009070485A1 (fr) | 2007-11-29 | 2008-11-20 | Dérivés d'amides de l'acide 6,7-dihydro-5h-imidazo[1,2-α]imidazole-3-carboxylique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31905B1 true MA31905B1 (fr) | 2010-12-01 |
Family
ID=40193954
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32900A MA31905B1 (fr) | 2007-11-29 | 2010-06-09 | DERIVES D'AMIDES DE L'ACIDE 6,7-DIHYDRO-5H-IMIDAZO[1,2-alpha] IMIDAZOLE-3-CARBOXYLIQUE |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US8552205B2 (fr) |
| EP (1) | EP2225238B1 (fr) |
| JP (1) | JP5485164B2 (fr) |
| KR (1) | KR20100101095A (fr) |
| CN (1) | CN101889011B (fr) |
| AR (1) | AR069513A1 (fr) |
| AU (1) | AU2008329909B2 (fr) |
| BR (1) | BRPI0819831A2 (fr) |
| CA (1) | CA2705583A1 (fr) |
| CL (1) | CL2008003576A1 (fr) |
| CO (1) | CO6210701A2 (fr) |
| CY (1) | CY1115857T1 (fr) |
| DK (1) | DK2225238T3 (fr) |
| EA (1) | EA017688B1 (fr) |
| EC (1) | ECSP10010196A (fr) |
| ES (1) | ES2525237T3 (fr) |
| HR (1) | HRP20141171T1 (fr) |
| IL (1) | IL205189A (fr) |
| MA (1) | MA31905B1 (fr) |
| MX (1) | MX2010004995A (fr) |
| MY (1) | MY151004A (fr) |
| NZ (1) | NZ585640A (fr) |
| PE (1) | PE20091427A1 (fr) |
| PL (1) | PL2225238T3 (fr) |
| PT (1) | PT2225238E (fr) |
| RS (1) | RS53602B1 (fr) |
| SI (1) | SI2225238T1 (fr) |
| TN (1) | TN2010000240A1 (fr) |
| TW (2) | TWI475991B (fr) |
| UY (1) | UY31493A1 (fr) |
| WO (1) | WO2009070485A1 (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010141330A1 (fr) * | 2009-06-02 | 2010-12-09 | Boehringer Ingelheim International Gmbh | Dérivés d'amides d'acide 6,7-dihydro-5h-imidazo [1,2-a] imidazole-3-carboxylique |
| BRPI1012581A2 (pt) | 2009-06-02 | 2016-03-29 | Boehringer Ingelheim Int | derivados de amidas de ácido 6, 7-di-hidro-5h-imidazol[1,2-a]imidazol-3-carboxílico |
| PH12012500775A1 (en) | 2009-10-21 | 2012-11-26 | Boehringer Ingelheim Int | Indazole and pyrazolopyridine compounds as ccr1 receptor antagonists |
| US8912221B2 (en) * | 2010-12-27 | 2014-12-16 | Hoffmann-La Roche Inc. | Biaryl amide derivatives |
| US8916594B2 (en) * | 2011-04-27 | 2014-12-23 | Shionogi & Co., Ltd. | 5-membered ring heteroaromatic derivatives having NPY Y5 receptor antagonistic activity |
| CN103874697A (zh) | 2011-08-03 | 2014-06-18 | 协和发酵麒麟株式会社 | 二苯并氧杂*衍生物 |
| DK2763992T3 (en) | 2011-10-03 | 2016-04-25 | Euroscreen Sa | NOVEL CHIRAL N-acyl-5,6,7, (8-substituted) -tetrahydro [1,2,4] triazolo [4,3-a] pyrazines as selective NK-3 receptor antagonists, PHARMACEUTICAL COMPOSITION AND METHODS FOR THE use in the NK-3 receptor mediated diseases |
| EP3207018B1 (fr) | 2014-10-14 | 2018-07-25 | Syngenta Participations AG | Procédé de préparation de 1- (3,5-dichloro-4-fluorophényl) -2,2,2-trifluoro-éthanone |
| JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
| CN106631827B (zh) * | 2016-12-30 | 2018-10-23 | 上海毕得医药科技有限公司 | 一种(1-环丙基-1-甲基)乙基胺及其盐酸盐的合成方法 |
| CN109369432B (zh) * | 2018-11-02 | 2021-06-25 | 永农生物科学有限公司 | (s)-4-氯-2-氨基丁酸酯的制备方法 |
| CN118496197A (zh) | 2019-12-20 | 2024-08-16 | 拜耳公司 | 取代的噻吩甲酰胺、噻吩甲酸及其衍生物 |
| CN111848521A (zh) * | 2020-08-26 | 2020-10-30 | 韶远科技(上海)有限公司 | 一种2-取代-4-烷氧基咪唑化合物的制备方法 |
| EP4554931A1 (fr) * | 2022-07-12 | 2025-05-21 | Adama Makhteshim Ltd. | Procédé de préparation de benzamides substitués |
| WO2025021943A1 (fr) | 2023-07-26 | 2025-01-30 | Neuralis | Quinazolinone, benzoxazinone et dérivés de benzoxazépinone utilisés en tant qu'inhibiteurs de protéine kinase |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2015493A1 (fr) | 1968-08-12 | 1970-04-30 | Sumitomo Chemical Co | |
| DK123717B (da) | 1968-11-25 | 1972-07-24 | Sumitomo Chemical Co | 3-(3',5'-Dihalogenphenyl)-imidazolidin-2,4-dionderivater med mirobicid virkning. |
| JPS5136332B1 (fr) | 1970-12-09 | 1976-10-07 | ||
| EP0091596B1 (fr) | 1982-04-08 | 1991-09-11 | Shell Internationale Researchmaatschappij B.V. | Hydantoins, préparation et application |
| JPS63270665A (ja) | 1987-04-30 | 1988-11-08 | Wakamoto Pharmaceut Co Ltd | イミダゾ−ル誘導体 |
| JPS63270667A (ja) | 1987-04-30 | 1988-11-08 | Wakamoto Pharmaceut Co Ltd | 1−ベンジルイミダゾ−ル誘導体 |
| IE62214B1 (en) | 1988-05-25 | 1995-01-11 | Warner Lambert Co | Arylmethylenyl derivatives of thiazolidinones, imidazolidinones and oxazolidinones useful as antiallergy agents and antiinflammatory agents |
| US5306822A (en) | 1988-05-25 | 1994-04-26 | Warner-Lambert Company | Arylmethylenyl derivatives of oxazolidinone |
| US5208250A (en) | 1988-05-25 | 1993-05-04 | Warner-Lambert Company | Known and selected novel arylmethylenyl derivatives of thiazolidinones, imidazolidinones and oxazolidinones useful as antiallergy agents and anti-inflammatory agents |
| US4977270A (en) | 1988-12-01 | 1990-12-11 | Ici Americas Inc. | Substituted 2,4-dioxodiazolidines and -thiadiazolidines and their use as herbicides |
| US4911748A (en) | 1988-12-22 | 1990-03-27 | Ici Americas Inc. | Herbicidal 5-substituted-3-phenyl-imidazolidine-2,4-diones |
| JPH04273877A (ja) | 1991-02-28 | 1992-09-30 | Sumitomo Pharmaceut Co Ltd | 新規なイミダゾール誘導体 |
| CA2083891A1 (fr) | 1991-12-03 | 1993-06-04 | Angus Murray Macleod | Composes heterocycliques, compositions et utilisation therapeutique |
| JPH05188631A (ja) | 1992-01-10 | 1993-07-30 | Mita Ind Co Ltd | 電子写真感光体 |
| TW521073B (en) | 1994-01-05 | 2003-02-21 | Hoechst Marion Roussel Inc | New optionally substituted phenylimidazolidines, their preparation process, their use as anti-androgenic agent and the pharmaceutical compositions containing them |
| US20040006011A1 (en) | 1996-07-12 | 2004-01-08 | Gour Barbara J. | Peptidomimetic modulators of cell adhesion |
| NZ507848A (en) | 1996-10-28 | 2005-01-28 | Univ Washington | Method of increasing the mutation rate of a virus in a non-human by administering an RNA nucleoside analogue to a virally infected cell |
| ES2191286T3 (es) | 1997-03-03 | 2003-09-01 | Boehringer Ingelheim Pharma | Moleculas pequeñas, utiles en el tratamiento de enfermedades inflamatorias. |
| US6355664B1 (en) | 1997-03-03 | 2002-03-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Phenylpyrrolidines, phenylimidazolidines, 3-phenyl-1,3-oxizolidines and 3-phenyl-1,3-thiazolidines and their use in the treatment of inflammatory disease |
| NZ502872A (en) | 1997-08-28 | 2002-10-25 | Novartis Ag | Mevinolin and compaction as LFA-1 antagonists for treating autoimmune diseases |
| JP2002509881A (ja) | 1998-03-27 | 2002-04-02 | ジェネンテク・インコーポレイテッド | Cd11/cd18接着レセプター媒介疾患の治療用アンタゴニスト |
| WO2001007044A1 (fr) | 1999-07-21 | 2001-02-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Petites molecules utiles pour le traitement de maladies inflammatoires |
| JP3833532B2 (ja) | 1999-07-21 | 2006-10-11 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | 炎症性疾患の治療において有用な小分子 |
| WO2001007048A1 (fr) | 1999-07-21 | 2001-02-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Petites molecules utiles pour le traitement de troubles inflammatoires |
| WO2001007052A1 (fr) | 1999-07-21 | 2001-02-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Petites molecules des plus utiles dans le traitement de maladies inflammatoires |
| US6492408B1 (en) * | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| ES2240201T3 (es) | 1999-10-20 | 2005-10-16 | Tanabe Seiyaku Co., Ltd. | Inhibidores de la adhesion molecular mediada por la alfa-l beta-2. |
| WO2002050080A1 (fr) | 2000-12-19 | 2002-06-27 | Boehringer Ingelheim Pharmaceuticals, Inc. | Petites molecules utiles dans le traitement de maladies inflammatoires |
| KR20040034594A (ko) * | 2001-01-26 | 2004-04-28 | 브리스톨-마이어스스퀴브컴파니 | 코르티코트로핀 방출 인자 억제제로서의 이미다졸릴 유도체 |
| US20030232817A1 (en) | 2002-05-29 | 2003-12-18 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful for the treatment of inflammatory disease |
| US6844360B2 (en) * | 2002-10-30 | 2005-01-18 | Boehringer Ingelheim Pharmaceuticals, Inc. | Derivatives of [6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonylamino]-propionamide |
| US6852748B1 (en) | 2002-10-30 | 2005-02-08 | Boehringer Ingelheim Pharmaceuticals, Inc. | Derivatives of [6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonyl]-pyrrolidine-2-carboxylic acid amide |
| RU2007106927A (ru) | 2004-07-27 | 2008-09-10 | БЕРИНГЕР ИНГЕЛЬХАЙМ ИНТЕРНАЦИОНАЛЬ ГмбХ (DE) | Синтез амидов 6,7,-дигидро-5н-имидазо [1.2-а] имидазол-3-сульфоновой кислоты |
| EP1869012A1 (fr) | 2005-04-05 | 2007-12-26 | Boehringer Ingelheim International Gmbh | Benzylimidazoles substituees utilisees dans le traitement de maladies inflammatoires |
| WO2006107941A1 (fr) | 2005-04-06 | 2006-10-12 | Boehringer Ingelheim International Gmbh | Derives d'amides, esters et acides [6,7-dihydro-5h-imidazo [1,2-alpha]imidazole-3-sulfonyl]-azetedino-carboxyliques et leur utilisation comme anti-inflammatoires |
| WO2007027233A2 (fr) | 2005-05-19 | 2007-03-08 | Boehringer Ingelheim International, Gmbh | Derives d'acide 6,7-dihydro-5h-imidazo[1,2-a]imidazole-3-sulfonique |
| TW200831488A (en) | 2006-11-29 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
| JP2009149609A (ja) | 2007-11-29 | 2009-07-09 | Sumitomo Chemical Co Ltd | アミド化合物及びその用途 |
| EP2225253B1 (fr) | 2007-11-29 | 2012-06-27 | Actelion Pharmaceuticals Ltd. | Dérivés d'acide phosphonique et leur utilisation en tant qu'antagonistes du récepteur p2y12 |
| EP2080758A3 (fr) | 2007-11-29 | 2009-08-26 | Bayer CropScience AG | Delta-1-pyrrolines substituées par halogène |
| AR069740A1 (es) | 2007-11-29 | 2010-02-17 | Metabasis Therapeutics Inc | Compuestos nucleosidos antivirales |
| BRPI1012581A2 (pt) | 2009-06-02 | 2016-03-29 | Boehringer Ingelheim Int | derivados de amidas de ácido 6, 7-di-hidro-5h-imidazol[1,2-a]imidazol-3-carboxílico |
| WO2010141330A1 (fr) | 2009-06-02 | 2010-12-09 | Boehringer Ingelheim International Gmbh | Dérivés d'amides d'acide 6,7-dihydro-5h-imidazo [1,2-a] imidazole-3-carboxylique |
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2008
- 2008-11-20 MX MX2010004995A patent/MX2010004995A/es active IP Right Grant
- 2008-11-20 CA CA2705583A patent/CA2705583A1/fr not_active Abandoned
- 2008-11-20 NZ NZ585640A patent/NZ585640A/en not_active IP Right Cessation
- 2008-11-20 BR BRPI0819831A patent/BRPI0819831A2/pt not_active IP Right Cessation
- 2008-11-20 PL PL08853791T patent/PL2225238T3/pl unknown
- 2008-11-20 RS RSP20140622 patent/RS53602B1/sr unknown
- 2008-11-20 AU AU2008329909A patent/AU2008329909B2/en not_active Ceased
- 2008-11-20 PT PT88537915T patent/PT2225238E/pt unknown
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