DE60309344D1 - Derivate von ä6, 7-dihydro -5h-imidazoä1,2 - aüimidazol -3 -sulfonylaminoü-propionamid und deren verwendung als inhibitoren der interaktion von cams und leukointreginen - Google Patents
Derivate von ä6, 7-dihydro -5h-imidazoä1,2 - aüimidazol -3 -sulfonylaminoü-propionamid und deren verwendung als inhibitoren der interaktion von cams und leukointreginenInfo
- Publication number
- DE60309344D1 DE60309344D1 DE60309344T DE60309344T DE60309344D1 DE 60309344 D1 DE60309344 D1 DE 60309344D1 DE 60309344 T DE60309344 T DE 60309344T DE 60309344 T DE60309344 T DE 60309344T DE 60309344 D1 DE60309344 D1 DE 60309344D1
- Authority
- DE
- Germany
- Prior art keywords
- sulfonylaminoü
- leukoin
- imidazoä1
- aimidazole
- propionamide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 208000013641 Cerebrofacial arteriovenous metameric syndrome Diseases 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 230000003993 interaction Effects 0.000 title 1
- 229940080818 propionamide Drugs 0.000 title 1
Classifications
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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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
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- 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
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-
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- A61P11/16—Central respiratory analeptics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- 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
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- 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
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42244602P | 2002-10-30 | 2002-10-30 | |
| US422446P | 2002-10-30 | ||
| PCT/US2003/033865 WO2004041827A2 (en) | 2002-10-30 | 2003-10-27 | DERIVATIVES OF [6,7-DIHYDRO-5H-IMIDAZO[1,2-α] IMIDAZOLE-3-SULFONYLAMINO]-PROPIONAMIDE AND THEIR USE AS INHIBITORS UPON THE INTERACTION OF CAMS AND LEUKO INTEGRINS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60309344D1 true DE60309344D1 (de) | 2006-12-07 |
| DE60309344T2 DE60309344T2 (de) | 2007-02-08 |
Family
ID=32312506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60309344T Expired - Fee Related DE60309344T2 (de) | 2002-10-30 | 2003-10-27 | Derivate von ä6, 7-dihydro -5h-imidazoä1,2 - aüimidazol -3 -sulfonylaminoü-propionamid und deren verwendung als inhibitoren der interaktion von cams und leukointreginen |
Country Status (32)
| Country | Link |
|---|---|
| US (4) | US6844360B2 (de) |
| EP (1) | EP1560830B1 (de) |
| JP (1) | JP4366477B2 (de) |
| KR (1) | KR20050067426A (de) |
| CN (1) | CN1708500A (de) |
| AR (1) | AR041854A1 (de) |
| AT (1) | ATE343582T1 (de) |
| AU (1) | AU2003284938A1 (de) |
| BR (1) | BR0315836A (de) |
| CA (1) | CA2504219A1 (de) |
| CO (1) | CO5690604A2 (de) |
| CY (1) | CY1106258T1 (de) |
| DE (1) | DE60309344T2 (de) |
| DK (1) | DK1560830T3 (de) |
| EA (1) | EA008443B1 (de) |
| EC (1) | ECSP055823A (de) |
| ES (1) | ES2276134T3 (de) |
| HR (1) | HRP20050387A2 (de) |
| MX (1) | MXPA05004480A (de) |
| MY (1) | MY136822A (de) |
| NO (1) | NO20052579L (de) |
| NZ (1) | NZ540269A (de) |
| PE (1) | PE20040782A1 (de) |
| PL (1) | PL375709A1 (de) |
| PT (1) | PT1560830E (de) |
| RS (1) | RS20050327A (de) |
| SI (1) | SI1560830T1 (de) |
| TW (1) | TW200424204A (de) |
| UA (1) | UA80160C2 (de) |
| UY (1) | UY28049A1 (de) |
| WO (1) | WO2004041827A2 (de) |
| ZA (1) | ZA200502701B (de) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6492408B1 (en) * | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| 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 |
| 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 |
| EP1712553A3 (de) * | 2002-10-30 | 2006-11-02 | Boehringer Ingelheim Pharmaceuticals, Inc. | Derivate von [6,7-dihydro-5h-imidazo[1,2-alpha]imidazol-3-sulfonylamino]-Propionamid und deren Verwendung als Inhibitoren der Interaktion von CAMS und Leukointegrinen |
| US8699508B2 (en) * | 2003-12-18 | 2014-04-15 | Intel Corporation | Response scheduling for multiple receivers |
| KR20070047798A (ko) * | 2004-07-27 | 2007-05-07 | 베링거 인겔하임 인터내셔날 게엠베하 | 6,7-디하이드로-5H-이미다조[1,2-a]이미다졸-3-설폰산아미드의 합성 |
| WO2006107941A1 (en) * | 2005-04-06 | 2006-10-12 | Boehringer Ingelheim International Gmbh | DERIVATIVES OF [6,7-DIHYDRO-5HIMIDAZO [l,2-ALPHA] IMIDAZOLE-3-SULFONYL]-AZETEDINE-CARBOXYLIC ACIDS, ESTERS AND AMIDES AND USE THEREOF AS ANTI-INFLAMMATORY AGENTS |
| CN101166743A (zh) * | 2005-05-19 | 2008-04-23 | 贝林格尔·英格海姆国际有限公司 | 6,7-二氢-5H-咪唑并[1,2-α]咪唑-3-磺酸的衍生物 |
| WO2007084882A2 (en) * | 2006-01-20 | 2007-07-26 | Boehringer Ingelheim International Gmbh | Process for the preparation of 6,7-dihydro-5h-imidazo[1,2-a]imidazole-3-sulfonic acid amides and intermediates used therein |
| RS53602B1 (sr) * | 2007-11-29 | 2015-02-27 | Boehringer Ingelheim International Gmbh | DERIVATI AMIDA 6,7-DIHIDRO-5H-IMIDAZO[1,2-α]IMIDAZOL-3-KARBOKSILNE KISELINE |
| JP5384732B2 (ja) * | 2009-06-02 | 2014-01-08 | 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 | 6,7−ジヒドロ−5H−イミダゾ[1,2−a]イミダゾール−3−カルボン酸アミドの誘導体 |
| WO2010141330A1 (en) | 2009-06-02 | 2010-12-09 | Boehringer Ingelheim International Gmbh | DERIVATIVES OF 6,7-DIHYDRO-5H-IMIDAZO[1,2-a]IMIDAZOLE-3-CARBOXYLIC ACID AMIDES |
| WO2021217040A1 (en) * | 2020-04-24 | 2021-10-28 | Immvention Therapeutix | Carbamate and urea derivatives |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EE9900481A (et) | 1997-03-03 | 2000-06-15 | Boehringer Ingelheim Pharmaceuticals, Inc. | Väikesed molekulid, mida kasutatakse põletikuliste haiguste raviks |
| 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 |
| US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| US6414161B1 (en) * | 2000-08-09 | 2002-07-02 | Boehringer Ingelheim Pharmaceuticals, Inc. | Synthesis of (R)-3-(4-Bromobenzyl)-1-(3,5-dichlorophenyl)-5-iodo-3-methyl-1-H-imidazo[1,2-a]imidazol-2-one |
| 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 |
-
2003
- 2003-10-15 US US10/686,073 patent/US6844360B2/en not_active Expired - Lifetime
- 2003-10-27 RS YUP-2005/0327A patent/RS20050327A/sr unknown
- 2003-10-27 ES ES03779257T patent/ES2276134T3/es not_active Expired - Lifetime
- 2003-10-27 NZ NZ540269A patent/NZ540269A/en unknown
- 2003-10-27 MX MXPA05004480A patent/MXPA05004480A/es active IP Right Grant
- 2003-10-27 DK DK03779257T patent/DK1560830T3/da active
- 2003-10-27 BR BR0315836-5A patent/BR0315836A/pt not_active IP Right Cessation
- 2003-10-27 HR HR20050387A patent/HRP20050387A2/xx not_active Application Discontinuation
- 2003-10-27 DE DE60309344T patent/DE60309344T2/de not_active Expired - Fee Related
- 2003-10-27 PL PL03375709A patent/PL375709A1/xx not_active Application Discontinuation
- 2003-10-27 EA EA200500603A patent/EA008443B1/ru not_active IP Right Cessation
- 2003-10-27 JP JP2004550109A patent/JP4366477B2/ja not_active Expired - Fee Related
- 2003-10-27 WO PCT/US2003/033865 patent/WO2004041827A2/en not_active Ceased
- 2003-10-27 CA CA002504219A patent/CA2504219A1/en not_active Abandoned
- 2003-10-27 SI SI200330574T patent/SI1560830T1/sl unknown
- 2003-10-27 CN CNA2003801024910A patent/CN1708500A/zh active Pending
- 2003-10-27 AT AT03779257T patent/ATE343582T1/de not_active IP Right Cessation
- 2003-10-27 PT PT03779257T patent/PT1560830E/pt unknown
- 2003-10-27 KR KR1020057007452A patent/KR20050067426A/ko not_active Withdrawn
- 2003-10-27 AU AU2003284938A patent/AU2003284938A1/en not_active Abandoned
- 2003-10-27 UA UAA200505014A patent/UA80160C2/uk unknown
- 2003-10-27 EP EP03779257A patent/EP1560830B1/de not_active Expired - Lifetime
- 2003-10-28 TW TW092129932A patent/TW200424204A/zh unknown
- 2003-10-28 MY MYPI20034095A patent/MY136822A/en unknown
- 2003-10-28 PE PE2003001088A patent/PE20040782A1/es not_active Application Discontinuation
- 2003-10-28 UY UY28049A patent/UY28049A1/es not_active Application Discontinuation
- 2003-10-29 AR ARP030103945A patent/AR041854A1/es unknown
-
2004
- 2004-10-20 US US10/969,105 patent/US7345074B2/en not_active Expired - Lifetime
-
2005
- 2005-01-13 US US11/034,701 patent/US7304067B2/en not_active Expired - Lifetime
- 2005-04-04 ZA ZA200502701A patent/ZA200502701B/en unknown
- 2005-05-26 CO CO05051551A patent/CO5690604A2/es not_active Application Discontinuation
- 2005-05-27 NO NO20052579A patent/NO20052579L/no not_active Application Discontinuation
- 2005-05-30 EC EC2005005823A patent/ECSP055823A/es unknown
-
2006
- 2006-11-09 CY CY20061101615T patent/CY1106258T1/el unknown
-
2007
- 2007-10-15 US US11/872,276 patent/US7589115B2/en not_active Expired - Lifetime
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