BR0013551A - Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnas - Google Patents
Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnasInfo
- Publication number
- BR0013551A BR0013551A BR0013551-8A BR0013551A BR0013551A BR 0013551 A BR0013551 A BR 0013551A BR 0013551 A BR0013551 A BR 0013551A BR 0013551 A BR0013551 A BR 0013551A
- Authority
- BR
- Brazil
- Prior art keywords
- inhibitors
- jnk
- kinases
- cjun
- terminal
- Prior art date
Links
- 102000001253 Protein Kinase Human genes 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 108060006633 protein kinase Proteins 0.000 title abstract 3
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000012825 JNK inhibitor Substances 0.000 abstract 1
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 abstract 1
- 230000030833 cell death Effects 0.000 abstract 1
- 230000004663 cell proliferation Effects 0.000 abstract 1
- 230000036755 cellular response Effects 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 239000003909 protein kinase inhibitor Substances 0.000 abstract 1
Classifications
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- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A—HUMAN NECESSITIES
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- 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
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- 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
- A61K31/4192—1,2,3-Triazoles
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- A—HUMAN NECESSITIES
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- 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
- A61K31/42—Oxazoles
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- A—HUMAN NECESSITIES
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Psychology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
Abstract
"INIBIDORES DE CINASES DE N-TERMINAL c-JUN (JNK) E OUTRAS CINASES DE PROTEìNA". A presente invenção refere-se aos compostos da fórmula (I) onde R^ 1^ é H CONH~ 2~, T~ (n)~-R ou T~ (n)~-Ar^ 2^, n pode ser zero ou um, e G, XYZ, e Q são como descritos abaixo. Estes compostos são inibidores da cinase de proteína, particularmente inibidores de JNK, uma cinase de proteína de mamífero envolveu proliferação de célula, morte de célula e resposta aos estímulos extracelulares. A invenção da mesma forma relata aos métodos para produção destes inibidores. A invenção da mesma forma fornece composições farmacêuticas compreendendo os inibidores da invenção e métodos de utilização daquelas composições no tratamento e prevenção de vários distúrbios.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14879599P | 1999-08-13 | 1999-08-13 | |
| US16692299P | 1999-11-22 | 1999-11-22 | |
| US21151700P | 2000-06-14 | 2000-06-14 | |
| PCT/US2000/022445 WO2001012621A1 (en) | 1999-08-13 | 2000-08-11 | INHIBITORS OF c-JUN N-TERMINAL KINASES (JNK) AND OTHER PROTEIN KINASES |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR0013551A true BR0013551A (pt) | 2003-06-17 |
Family
ID=27386739
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR0013551-8A BR0013551A (pt) | 1999-08-13 | 2000-08-11 | Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnas |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US6693108B2 (pt) |
| EP (1) | EP1218369B1 (pt) |
| JP (1) | JP2003531103A (pt) |
| KR (1) | KR20020030791A (pt) |
| CN (1) | CN1222520C (pt) |
| AR (1) | AR032130A1 (pt) |
| AT (1) | ATE402163T1 (pt) |
| AU (1) | AU6909600A (pt) |
| BR (1) | BR0013551A (pt) |
| CA (1) | CA2381882C (pt) |
| CO (1) | CO5200770A1 (pt) |
| CZ (1) | CZ2002534A3 (pt) |
| DE (1) | DE60039616D1 (pt) |
| HK (1) | HK1045507A1 (pt) |
| HU (1) | HUP0300340A3 (pt) |
| MX (1) | MXPA02001565A (pt) |
| MY (1) | MY133159A (pt) |
| NO (1) | NO20020713L (pt) |
| NZ (1) | NZ517694A (pt) |
| PL (1) | PL366110A1 (pt) |
| SK (1) | SK3572002A3 (pt) |
| WO (1) | WO2001012621A1 (pt) |
Families Citing this family (103)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1169038B9 (en) | 1999-04-15 | 2013-07-10 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
| US7125875B2 (en) | 1999-04-15 | 2006-10-24 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
| US7119114B1 (en) | 1999-08-19 | 2006-10-10 | Signal Pharmaceuticals, Llc | Pyrazoloanthrone and derivatives thereof as JNK inhibitors and compositions and methods related thereto |
| US20040072888A1 (en) | 1999-08-19 | 2004-04-15 | Bennett Brydon L. | Methods for treating inflammatory conditions or inhibiting JNK |
| US7211594B2 (en) | 2000-07-31 | 2007-05-01 | Signal Pharmaceuticals, Llc | Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith |
| US6897231B2 (en) | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
| WO2002022605A1 (en) | 2000-09-15 | 2002-03-21 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US7473691B2 (en) | 2000-09-15 | 2009-01-06 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US6660731B2 (en) | 2000-09-15 | 2003-12-09 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US7122544B2 (en) * | 2000-12-06 | 2006-10-17 | Signal Pharmaceuticals, Llc | Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto |
| US7129242B2 (en) | 2000-12-06 | 2006-10-31 | Signal Pharmaceuticals, Llc | Anilinopyrimidine derivatives as JNK pathway inhibitors and compositions and methods related thereto |
| US7429599B2 (en) | 2000-12-06 | 2008-09-30 | Signal Pharmaceuticals, Llc | Methods for treating or preventing an inflammatory or metabolic condition or inhibiting JNK |
| US6989385B2 (en) | 2000-12-21 | 2006-01-24 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US7199124B2 (en) | 2001-02-02 | 2007-04-03 | Takeda Pharmaceutical Company Limited | JNK inhibitor |
| US6987184B2 (en) | 2001-02-15 | 2006-01-17 | Signal Pharmaceuticals, Llc | Isothiazoloanthrones, isoxazoloanthrones, isoindolanthrones and derivatives thereof as JNK inhibitors and compositions and methods related |
| WO2002083668A1 (en) * | 2001-04-10 | 2002-10-24 | Vertex Pharmaceuticals Incorporated | Isoxaxole derivatives as inhibitors of src and other protein kinases |
| AU2002338642A1 (en) * | 2001-04-13 | 2002-10-28 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
| CN1300116C (zh) | 2001-04-16 | 2007-02-14 | 卫材株式会社 | 1h-吲唑化合物 |
| US6727364B2 (en) * | 2001-04-30 | 2004-04-27 | The Procter & Gamble Company | Triazole compounds useful in treating diseases associated with unwanted cytokine activity |
| US6787555B2 (en) | 2001-04-30 | 2004-09-07 | The Procter & Gamble Company | Triazole compounds useful in treating diseases associated with unwanted cytokine activity |
| US7018999B2 (en) | 2001-05-16 | 2006-03-28 | Cephalon, Inc. | Methods for the treatment and prevention of pain |
| US6790846B2 (en) * | 2001-05-24 | 2004-09-14 | The Procter & Gamble Company | Isoxazolone compounds useful in treating diseases associated with unwanted cytokine activity |
| CA2450769A1 (en) * | 2001-06-15 | 2002-12-27 | Vertex Pharmaceuticals Incorporated | 5-(2-aminopyrimidin-4-yl) benzisoxazoles as protein kinase inhibitors |
| US6589997B2 (en) * | 2001-06-29 | 2003-07-08 | North Shore-Long Island Jewish Health System | Small-molecule modulators of hepatocyte growth factor/scatter factor activities |
| ATE337312T1 (de) * | 2001-07-03 | 2006-09-15 | Vertex Pharma | Isoxazolyl-pyrimidines als inhibitoren von src- und lck-protein-kinasen |
| JP4414219B2 (ja) | 2001-07-23 | 2010-02-10 | メルク セローノ ソシエテ アノニム | C−jun−n−末端キナーゼ(jnk)インヒビターとしてのアリールスルホンアミド誘導体 |
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2000
- 2000-08-11 BR BR0013551-8A patent/BR0013551A/pt not_active IP Right Cessation
- 2000-08-11 SK SK357-2002A patent/SK3572002A3/sk unknown
- 2000-08-11 CN CNB008141789A patent/CN1222520C/zh not_active Expired - Fee Related
- 2000-08-11 AR ARP000104188A patent/AR032130A1/es not_active Application Discontinuation
- 2000-08-11 JP JP2001517519A patent/JP2003531103A/ja active Pending
- 2000-08-11 AT AT00957485T patent/ATE402163T1/de not_active IP Right Cessation
- 2000-08-11 NZ NZ517694A patent/NZ517694A/en unknown
- 2000-08-11 KR KR1020027001947A patent/KR20020030791A/ko not_active Withdrawn
- 2000-08-11 HK HK02106918.4A patent/HK1045507A1/zh unknown
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- 2000-08-11 AU AU69096/00A patent/AU6909600A/en not_active Abandoned
- 2000-08-11 HU HU0300340A patent/HUP0300340A3/hu unknown
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| CN1222520C (zh) | 2005-10-12 |
| NZ517694A (en) | 2005-03-24 |
| CA2381882A1 (en) | 2001-02-22 |
| MY133159A (en) | 2007-10-31 |
| JP2003531103A (ja) | 2003-10-21 |
| US20030149051A1 (en) | 2003-08-07 |
| US6693108B2 (en) | 2004-02-17 |
| US20050026967A1 (en) | 2005-02-03 |
| HK1045507A1 (zh) | 2002-11-29 |
| AR032130A1 (es) | 2003-10-29 |
| ATE402163T1 (de) | 2008-08-15 |
| CA2381882C (en) | 2011-01-25 |
| EP1218369A4 (en) | 2005-06-22 |
| EP1218369A1 (en) | 2002-07-03 |
| PL366110A1 (en) | 2005-01-24 |
| CZ2002534A3 (cs) | 2002-07-17 |
| AU6909600A (en) | 2001-03-13 |
| SK3572002A3 (en) | 2002-07-02 |
| CN1378541A (zh) | 2002-11-06 |
| EP1218369B1 (en) | 2008-07-23 |
| HUP0300340A2 (hu) | 2003-06-28 |
| MXPA02001565A (es) | 2005-07-14 |
| HUP0300340A3 (en) | 2005-04-28 |
| WO2001012621A1 (en) | 2001-02-22 |
| KR20020030791A (ko) | 2002-04-25 |
| NO20020713L (no) | 2002-04-12 |
| NO20020713D0 (no) | 2002-02-12 |
| DE60039616D1 (de) | 2008-09-04 |
| US7169798B2 (en) | 2007-01-30 |
| CO5200770A1 (es) | 2002-09-27 |
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