HK1032050A1 - Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas. - Google Patents
Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas.Info
- Publication number
- HK1032050A1 HK1032050A1 HK01102468A HK01102468A HK1032050A1 HK 1032050 A1 HK1032050 A1 HK 1032050A1 HK 01102468 A HK01102468 A HK 01102468A HK 01102468 A HK01102468 A HK 01102468A HK 1032050 A1 HK1032050 A1 HK 1032050A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- kinase
- inhibition
- symmetrical
- diphenyl ureas
- unsymmetrical diphenyl
- 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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- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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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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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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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 |
Publications (1)
Publication Number | Publication Date |
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HK1032050A1 true HK1032050A1 (en) | 2001-07-06 |
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Family Applications (1)
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HK01102468A HK1032050A1 (en) | 1997-12-22 | 2001-04-07 | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas. |
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EP (2) | EP1616865A1 (es) |
JP (1) | JP3887769B2 (es) |
AT (1) | ATE297383T1 (es) |
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CA (1) | CA2315715C (es) |
DE (2) | DE1042305T1 (es) |
DK (1) | DK1042305T3 (es) |
ES (1) | ES2154252T3 (es) |
HK (1) | HK1032050A1 (es) |
IL (3) | IL136737A0 (es) |
PT (1) | PT1042305E (es) |
WO (1) | WO1999032463A1 (es) |
Families Citing this family (153)
Publication number | Priority date | Publication date | Assignee | Title |
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US6696475B2 (en) | 1997-04-22 | 2004-02-24 | Neurosearch A/S | Substituted phenyl derivatives, their preparation and use |
DE69829412T2 (de) * | 1997-12-22 | 2005-07-28 | Bayer Pharmaceuticals Corp., West Haven | Hemmung der raf-kinase unter verwendung von symmetrisch und unsymmetrisch substituierten harnstoffen |
NZ510098A (en) * | 1998-10-22 | 2003-09-26 | Neurosearch As | Substituted phenyl derivatives, pharmaceuticals thereof and their use as blockers of the chloride channel |
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
EP1158985B1 (en) * | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS 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 |
CA2549558C (en) * | 1999-01-13 | 2010-08-31 | Bayer Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
US20020065296A1 (en) * | 1999-01-13 | 2002-05-30 | Bayer Corporation | Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors |
AU2004200566B2 (en) * | 1999-01-13 | 2006-08-17 | Bayer Pharmaceuticals Corporation | Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
EP1157026A1 (en) | 1999-02-22 | 2001-11-28 | Boehringer Ingelheim Pharmaceuticals Inc. | Polycyclo heterocyclic derivatives as antiinflammatory agents |
WO2000055152A1 (en) * | 1999-03-12 | 2000-09-21 | Boehringer Ingelheim Pharmaceuticals, Inc. | Aromatic heterocyclic compounds as anti-inflammatory agents |
RU2242474C2 (ru) | 1999-03-12 | 2004-12-20 | Бёрингер Ингельхайм Фармасьютиклз, Инк. | Соединения, пригодные в качестве противовоспалительных агентов |
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 |
MXPA02000314A (es) | 1999-07-09 | 2004-06-22 | Boehringer Ingelheim Pharma | Proceso novedoso para la sintesis de compuestos de urea substituidos con heteroarilo. |
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 |
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 |
US6492393B1 (en) | 1999-11-16 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as anti-inflammatory agents |
JP2003513995A (ja) * | 1999-11-19 | 2003-04-15 | アクスクシーマ ファルマシューティカルス アクチェンゲゼルシャフト | ヘリコバクターピロリにより誘発される胃腸疾患の阻害剤 |
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 |
US6645990B2 (en) | 2000-08-15 | 2003-11-11 | Amgen Inc. | Thiazolyl urea compounds and methods of uses |
PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
US6849409B2 (en) | 2000-10-16 | 2005-02-01 | Axxima Pharmaceuticals Ag | Cellular kinases involved in Cytomegalovirus infection and their inhibition |
US7238813B2 (en) | 2000-11-29 | 2007-07-03 | Smithkline Beecham Corporation | Chemical compounds |
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ES2154252T1 (es) | 2001-04-01 |
DK1042305T3 (da) | 2005-09-19 |
EP1616865A1 (en) | 2006-01-18 |
EP1042305A4 (en) | 2003-05-14 |
IL136737A (en) | 2006-12-10 |
AU1939999A (en) | 1999-07-12 |
JP2001526276A (ja) | 2001-12-18 |
ES2154252T3 (es) | 2005-12-01 |
DE69830513T2 (de) | 2006-03-16 |
JP3887769B2 (ja) | 2007-02-28 |
CA2315715A1 (en) | 1999-07-01 |
ATE297383T1 (de) | 2005-06-15 |
IL170235A (en) | 2010-04-15 |
CA2315715C (en) | 2010-06-22 |
PT1042305E (pt) | 2005-10-31 |
EP1042305A1 (en) | 2000-10-11 |
DE1042305T1 (de) | 2001-04-19 |
DE69830513D1 (de) | 2005-07-14 |
IL136737A0 (en) | 2001-06-14 |
WO1999032463A1 (en) | 1999-07-01 |
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