DK1042305T3 - Inhibering af p38-kinase ved anvendelse af symmetriske og asymmetriske diphenylurinstoffer - Google Patents
Inhibering af p38-kinase ved anvendelse af symmetriske og asymmetriske diphenylurinstofferInfo
- Publication number
- DK1042305T3 DK1042305T3 DK98964221T DK98964221T DK1042305T3 DK 1042305 T3 DK1042305 T3 DK 1042305T3 DK 98964221 T DK98964221 T DK 98964221T DK 98964221 T DK98964221 T DK 98964221T DK 1042305 T3 DK1042305 T3 DK 1042305T3
- Authority
- DK
- Denmark
- Prior art keywords
- diphenylureas
- kinase
- asymmetric
- symmetric
- inhibition
- Prior art date
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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| US99574997A | 1997-12-22 | 1997-12-22 | |
| PCT/US1998/027265 WO1999032463A1 (en) | 1997-12-22 | 1998-12-22 | INHIBITION OF p38 KINASE USING SYMMETRICAL AND UNSYMMETRICAL DIPHENYL UREAS |
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| DK1042305T3 true DK1042305T3 (da) | 2005-09-19 |
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| DK98964221T DK1042305T3 (da) | 1997-12-22 | 1998-12-22 | Inhibering af p38-kinase ved anvendelse af symmetriske og asymmetriske diphenylurinstoffer |
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| CA2315646C (en) * | 1997-12-22 | 2010-02-09 | Bayer Corporation | Inhibition of raf kinase using symmetrical and unsymmetrical substituted diphenyl ureas |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| US7329670B1 (en) | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
| EP1123274B1 (en) * | 1998-10-22 | 2004-12-29 | Neurosearch A/S | Substituted phenyl derivatives, their preparation and use |
| US7351834B1 (en) | 1999-01-13 | 2008-04-01 | Bayer Pharmaceuticals Corporation | ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| SI1690853T1 (sl) * | 1999-01-13 | 2010-07-30 | Bayer Healthcare Llc | Uporaba omega-karboksiarilno substituiranih difenilsečnin kot inhibitorjev raf-kinaze |
| ATE556713T1 (de) * | 1999-01-13 | 2012-05-15 | Bayer Healthcare Llc | Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| AU2004200566B2 (en) * | 1999-01-13 | 2006-08-17 | Bayer Pharmaceuticals Corporation | Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
| US20020065296A1 (en) * | 1999-01-13 | 2002-05-30 | Bayer Corporation | Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors |
| EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
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| CA2360934A1 (en) | 1999-02-22 | 2000-08-31 | Lin-Hua Zhang | Polycyclo heterocyclic derivatives as antiinflammatory agents |
| EE04799B1 (et) | 1999-03-12 | 2007-04-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Ühendid, mis on kasulikud põletikuvastaste vahenditena, nende ühendite valmistamise meetodid ja neid sisaldavad farmatseutilised kompositsioonid |
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| US6337418B1 (en) * | 1999-04-09 | 2002-01-08 | Eastman Chemical Co. | Preparation of C1-C5 alkyl esters of nitro or thioether substituted aromatic carboxylic acids |
| DE60024830T2 (de) | 1999-07-09 | 2006-06-14 | Boehringer Ingelheim Pharma | Verfahren zur herstellung heteroarylsubstituierter ureaverbindungen |
| US7030109B2 (en) | 1999-07-19 | 2006-04-18 | Pharmacia & Upjohn Company | 1,2,3,4,5,6-Hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position |
| MY122278A (en) | 1999-07-19 | 2006-04-29 | Upjohn Co | 1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position |
| EP1232150B1 (en) | 1999-11-16 | 2007-10-10 | Boehringer Ingelheim Pharmaceuticals Inc. | Urea derivatives as anti-inflammatory agents |
| EP1229925A2 (en) * | 1999-11-19 | 2002-08-14 | Axxima Pharmaceuticals Aktiengesellschaft | Inhibitors of helicobacter pylori induced gastrointestinal diseases |
| US6525046B1 (en) | 2000-01-18 | 2003-02-25 | Boehringer Ingelheim Pharmaceuticals, Inc. | Aromatic heterocyclic compounds as antiinflammatory agents |
| US6608052B2 (en) | 2000-02-16 | 2003-08-19 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as anti-inflammatory agents |
| GB0010757D0 (en) | 2000-05-05 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
| US20040077605A1 (en) | 2001-06-20 | 2004-04-22 | Salvati Mark E. | Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
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- 1998-12-22 JP JP2000525400A patent/JP3887769B2/ja not_active Expired - Fee Related
- 1998-12-22 DK DK98964221T patent/DK1042305T3/da active
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- 2005-08-11 IL IL170235A patent/IL170235A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL136737A0 (en) | 2001-06-14 |
| DE1042305T1 (de) | 2001-04-19 |
| DE69830513T2 (de) | 2006-03-16 |
| EP1042305B1 (en) | 2005-06-08 |
| DE69830513D1 (de) | 2005-07-14 |
| EP1042305A1 (en) | 2000-10-11 |
| WO1999032463A1 (en) | 1999-07-01 |
| EP1616865A1 (en) | 2006-01-18 |
| EP1042305A4 (en) | 2003-05-14 |
| CA2315715C (en) | 2010-06-22 |
| CA2315715A1 (en) | 1999-07-01 |
| HK1032050A1 (en) | 2001-07-06 |
| ATE297383T1 (de) | 2005-06-15 |
| ES2154252T3 (es) | 2005-12-01 |
| IL136737A (en) | 2006-12-10 |
| IL170235A (en) | 2010-04-15 |
| JP3887769B2 (ja) | 2007-02-28 |
| PT1042305E (pt) | 2005-10-31 |
| ES2154252T1 (es) | 2001-04-01 |
| AU1939999A (en) | 1999-07-12 |
| JP2001526276A (ja) | 2001-12-18 |
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