JP2010504301A - Ikk2阻害物質としてのピロロ[2,3−b]ピリジン−4−イル−ベンゼンスルホンアミド化合物 - Google Patents
Ikk2阻害物質としてのピロロ[2,3−b]ピリジン−4−イル−ベンゼンスルホンアミド化合物 Download PDFInfo
- Publication number
- JP2010504301A JP2010504301A JP2009528719A JP2009528719A JP2010504301A JP 2010504301 A JP2010504301 A JP 2010504301A JP 2009528719 A JP2009528719 A JP 2009528719A JP 2009528719 A JP2009528719 A JP 2009528719A JP 2010504301 A JP2010504301 A JP 2010504301A
- Authority
- JP
- Japan
- Prior art keywords
- pyrrolo
- pyridin
- compound
- alkyl
- methyl
- 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.)
- Pending
Links
- 0 *c([n]1)cc2c1nccc2-c1ccc(*)cc1 Chemical compound *c([n]1)cc2c1nccc2-c1ccc(*)cc1 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N OC(C(F)(F)F)=O Chemical compound OC(C(F)(F)F)=O DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- RIUXWEGBWYUUEF-UHFFFAOYSA-N Brc1ccnc2c1cc(C1CC1)[nH]2 Chemical compound Brc1ccnc2c1cc(C1CC1)[nH]2 RIUXWEGBWYUUEF-UHFFFAOYSA-N 0.000 description 1
- ZYIUZWKLXOVOQL-UHFFFAOYSA-N C(C1)CC1c([nH]1)cc2c1nccc2 Chemical compound C(C1)CC1c([nH]1)cc2c1nccc2 ZYIUZWKLXOVOQL-UHFFFAOYSA-N 0.000 description 1
- PXZQMSHGNGQPID-UHFFFAOYSA-N C(CN1CCCC1)c(cc1)ccc1-c1ccnc2c1cc(C[n]1nccn1)[nH]2 Chemical compound C(CN1CCCC1)c(cc1)ccc1-c1ccnc2c1cc(C[n]1nccn1)[nH]2 PXZQMSHGNGQPID-UHFFFAOYSA-N 0.000 description 1
- XKAPOJQKLRKFFV-UHFFFAOYSA-N CC(C)(C)OC(NC(CC1)CCS1(=O)=O)=O Chemical compound CC(C)(C)OC(NC(CC1)CCS1(=O)=O)=O XKAPOJQKLRKFFV-UHFFFAOYSA-N 0.000 description 1
- QVOUECHCQNPJAY-UHFFFAOYSA-N CC(C)NC(Cc([nH]c1ncc2)cc1c2-c(cc1)ccc1NS(C)(=O)=O)=O Chemical compound CC(C)NC(Cc([nH]c1ncc2)cc1c2-c(cc1)ccc1NS(C)(=O)=O)=O QVOUECHCQNPJAY-UHFFFAOYSA-N 0.000 description 1
- AOKRXIIIYJGNNU-UHFFFAOYSA-O CC(CC1)CC1=[OH+] Chemical compound CC(CC1)CC1=[OH+] AOKRXIIIYJGNNU-UHFFFAOYSA-O 0.000 description 1
- VFNAXOCHFCRPOU-UHFFFAOYSA-N CC(CNS(c(cc1)ccc1-c1c(cc(C)[nH]2)c2ncc1)(=O)=O)O Chemical compound CC(CNS(c(cc1)ccc1-c1c(cc(C)[nH]2)c2ncc1)(=O)=O)O VFNAXOCHFCRPOU-UHFFFAOYSA-N 0.000 description 1
- NZANNALXDKRTAW-UHFFFAOYSA-N CC(CO)NS(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(=O)=O Chemical compound CC(CO)NS(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(=O)=O NZANNALXDKRTAW-UHFFFAOYSA-N 0.000 description 1
- FCWAYRSKYGFAFN-UHFFFAOYSA-O CC1(C)OB(c(cc2)ccc2S(NC2C[SH+]CC2)(=O)=O)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2S(NC2C[SH+]CC2)(=O)=O)OC1(C)C FCWAYRSKYGFAFN-UHFFFAOYSA-O 0.000 description 1
- NPEZYINXFHTEIV-UHFFFAOYSA-N CC1(CC1)c1cc2ccc[n+]([O-])c2[nH]1 Chemical compound CC1(CC1)c1cc2ccc[n+]([O-])c2[nH]1 NPEZYINXFHTEIV-UHFFFAOYSA-N 0.000 description 1
- PYGDYDRATIAEEN-UHFFFAOYSA-N CCC(CO)NS(c(cc1)ccc1-c1c(cc(C2CC2)[nH]2)c2ncc1)(=O)=O Chemical compound CCC(CO)NS(c(cc1)ccc1-c1c(cc(C2CC2)[nH]2)c2ncc1)(=O)=O PYGDYDRATIAEEN-UHFFFAOYSA-N 0.000 description 1
- UCLDSUYQTQAEBR-UHFFFAOYSA-N CCC(N(C)COC)=O Chemical compound CCC(N(C)COC)=O UCLDSUYQTQAEBR-UHFFFAOYSA-N 0.000 description 1
- NZANNALXDKRTAW-JTQLQIEISA-N C[C@@H](CO)NS(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(=O)=O Chemical compound C[C@@H](CO)NS(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(=O)=O NZANNALXDKRTAW-JTQLQIEISA-N 0.000 description 1
- JJENTBUOWPUYHO-UHFFFAOYSA-N NCCNS(c(cc1)ccc1-c1ccnc2c1cc(C#CCO)[nH]2)(=O)=O Chemical compound NCCNS(c(cc1)ccc1-c1ccnc2c1cc(C#CCO)[nH]2)(=O)=O JJENTBUOWPUYHO-UHFFFAOYSA-N 0.000 description 1
- OZEAONXTWCNARP-UHFFFAOYSA-N NCCNS(c(cc1)ccc1-c1ccnc2c1cc(C(F)(F)F)[nH]2)(=O)=O Chemical compound NCCNS(c(cc1)ccc1-c1ccnc2c1cc(C(F)(F)F)[nH]2)(=O)=O OZEAONXTWCNARP-UHFFFAOYSA-N 0.000 description 1
- UXMRTJBZVCBOFF-UHFFFAOYSA-N O=S(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(NC1CCNCC1)=O Chemical compound O=S(c(cc1)ccc1-c1c(cc(C(F)(F)F)[nH]2)c2ncc1)(NC1CCNCC1)=O UXMRTJBZVCBOFF-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- 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
- A61P19/00—Drugs for skeletal disorders
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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]
-
- 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
-
- 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
-
- 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
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Virology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Dermatology (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0618776A GB0618776D0 (en) | 2006-09-22 | 2006-09-22 | Novel compounds |
| GB0704012A GB0704012D0 (en) | 2007-03-01 | 2007-03-01 | Novel compounds |
| GB0717170A GB0717170D0 (en) | 2007-09-04 | 2007-09-04 | Novelcompounds |
| PCT/EP2007/059933 WO2008034860A1 (en) | 2006-09-22 | 2007-09-20 | Pyrrolo[2, 3-b]pyridin-4-yl-benzenesulfonamide compounds as ikk2 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010504301A true JP2010504301A (ja) | 2010-02-12 |
| JP2010504301A5 JP2010504301A5 (enExample) | 2010-11-18 |
Family
ID=39092148
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009528719A Pending JP2010504301A (ja) | 2006-09-22 | 2007-09-20 | Ikk2阻害物質としてのピロロ[2,3−b]ピリジン−4−イル−ベンゼンスルホンアミド化合物 |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US20080176891A1 (enExample) |
| EP (1) | EP2069341B1 (enExample) |
| JP (1) | JP2010504301A (enExample) |
| AR (1) | AR062928A1 (enExample) |
| AT (1) | ATE493411T1 (enExample) |
| CL (1) | CL2007002708A1 (enExample) |
| DE (1) | DE602007011645D1 (enExample) |
| PE (1) | PE20080925A1 (enExample) |
| TW (1) | TW200836724A (enExample) |
| UY (1) | UY30600A1 (enExample) |
| WO (1) | WO2008034860A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016514113A (ja) * | 2013-03-14 | 2016-05-19 | アッヴィ・インコーポレイテッド | ピロロ[2,3−b]ピリジンcdk9キナーゼ阻害剤 |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0400895D0 (en) * | 2004-01-15 | 2004-02-18 | Smithkline Beecham Corp | Chemical compounds |
| AR050253A1 (es) * | 2004-06-24 | 2006-10-11 | Smithkline Beecham Corp | Compuesto derivado de indazol carboxamida, composicion que lo comprende y su uso para la preparacion de un medicamento |
| US8063071B2 (en) * | 2007-10-31 | 2011-11-22 | GlaxoSmithKline, LLC | Chemical compounds |
| PE20081889A1 (es) | 2007-03-23 | 2009-03-05 | Smithkline Beecham Corp | Indol carboxamidas como inhibidores de ikk2 |
| GB0804591D0 (en) * | 2008-03-12 | 2008-04-16 | Glaxo Group Ltd | Novel compounds |
| GB0804592D0 (en) * | 2008-03-12 | 2008-04-16 | Glaxo Group Ltd | Novel compounds |
| WO2010025236A1 (en) * | 2008-08-27 | 2010-03-04 | Alexander Goldin | Composition and method for treating colds |
| WO2010102968A1 (en) | 2009-03-10 | 2010-09-16 | Glaxo Group Limited | Indole derivatives as ikk2 inhibitors |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| JP2014516084A (ja) * | 2011-06-10 | 2014-07-07 | グラクソスミスクライン、インテレクチュアル、プロパティー、リミテッド | 新規化合物 |
| SMT201700146T1 (it) | 2012-06-13 | 2017-05-08 | Incyte Holdings Corp | Composti triciclici sostituiti come inibitori di fgfr |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014139328A1 (en) * | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Pyrrolo[2,3-b]pyridine cdk9 kinase inhibitors |
| CA2909207C (en) | 2013-04-19 | 2021-11-02 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| UA121669C2 (uk) | 2015-02-20 | 2020-07-10 | Інсайт Корпорейшн | Біциклічні гетероцикли як інгібітори fgfr |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| SG11202010882XA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Salts of an fgfr inhibitor |
| SMT202400507T1 (it) | 2018-05-04 | 2025-01-14 | Incyte Corp | Forme solide di un inibitore di fgfr e procedimenti per preparare le stesse |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CA3157361A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| WO2021113462A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| EP4352060A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CN114210133B (zh) * | 2021-12-13 | 2023-01-24 | 广德辉龙环保科技有限公司 | 一种抗紫外线过滤袋及其制备方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2460680A1 (en) * | 2001-09-19 | 2003-05-01 | Pharmacia Corporation | Substituted indazole compounds for the treatment of inflammation |
| GB0308466D0 (en) * | 2003-04-11 | 2003-05-21 | Novartis Ag | Organic compounds |
-
2007
- 2007-09-20 WO PCT/EP2007/059933 patent/WO2008034860A1/en not_active Ceased
- 2007-09-20 CL CL200702708A patent/CL2007002708A1/es unknown
- 2007-09-20 AT AT07820377T patent/ATE493411T1/de not_active IP Right Cessation
- 2007-09-20 US US11/858,144 patent/US20080176891A1/en not_active Abandoned
- 2007-09-20 DE DE602007011645T patent/DE602007011645D1/de active Active
- 2007-09-20 US US12/442,012 patent/US20100035917A1/en not_active Abandoned
- 2007-09-20 TW TW096135178A patent/TW200836724A/zh unknown
- 2007-09-20 PE PE2007001270A patent/PE20080925A1/es not_active Application Discontinuation
- 2007-09-20 EP EP07820377A patent/EP2069341B1/en active Active
- 2007-09-20 JP JP2009528719A patent/JP2010504301A/ja active Pending
- 2007-09-20 AR ARP070104169A patent/AR062928A1/es not_active Application Discontinuation
- 2007-09-20 US US11/858,143 patent/US20080146606A1/en not_active Abandoned
- 2007-09-20 UY UY30600A patent/UY30600A1/es unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016514113A (ja) * | 2013-03-14 | 2016-05-19 | アッヴィ・インコーポレイテッド | ピロロ[2,3−b]ピリジンcdk9キナーゼ阻害剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW200836724A (en) | 2008-09-16 |
| EP2069341B1 (en) | 2010-12-29 |
| US20080146606A1 (en) | 2008-06-19 |
| US20100035917A1 (en) | 2010-02-11 |
| PE20080925A1 (es) | 2008-09-04 |
| ATE493411T1 (de) | 2011-01-15 |
| AR062928A1 (es) | 2008-12-17 |
| EP2069341A1 (en) | 2009-06-17 |
| WO2008034860A1 (en) | 2008-03-27 |
| UY30600A1 (es) | 2008-05-02 |
| US20080176891A1 (en) | 2008-07-24 |
| DE602007011645D1 (de) | 2011-02-10 |
| CL2007002708A1 (es) | 2008-04-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010504301A (ja) | Ikk2阻害物質としてのピロロ[2,3−b]ピリジン−4−イル−ベンゼンスルホンアミド化合物 | |
| JP2010529002A (ja) | ピロロピリジン化合物、その調製方法、および医薬としてのその使用 | |
| JP5502076B2 (ja) | 新規化合物 | |
| TWI466884B (zh) | 6-(1h-吲哚-4-基)-4-(5-{[4-(1-甲基乙基)-1-哌嗪基]甲基}-1,3-噁唑-2-基)-1h-吲唑、其醫藥組合物及作為激酶活性抑制劑之用途 | |
| JP5965402B2 (ja) | N−[5−[4−(5−{[(2r,6s)−2,6−ジメチル−4−モルホリニル]メチル}−1,3−オキサゾール−2−イル)−1h−インダゾール−6−イル]−2−(メチルオキシ)−3−ピリジニル]メタンスルホンアミドの多形体および塩 | |
| JP5502858B2 (ja) | Pi3キナーゼの阻害剤として有用な4−カルボキサミドインダゾール誘導体 | |
| US20120245171A1 (en) | Benzpyrazole derivatives as inhibitors of pi3 kinases | |
| JP2013512880A (ja) | Pi3−キナーゼ阻害剤としてのインダゾール誘導体 | |
| TW200811111A (en) | Novel compounds | |
| TW200811116A (en) | Compounds | |
| WO2011110575A1 (en) | Derivatives of 2-[2-(benzo- or pyrido-) thiazolylamino]-6-aminopyridine, useful in the treatment of respiratoric, allergic or inflammatory diseases | |
| JP2019524792A (ja) | 化合物 | |
| JP6916195B2 (ja) | キナーゼ活性の阻害剤としての化合物 | |
| WO2009112473A1 (en) | Novel compounds | |
| US8354539B2 (en) | Indole derivatives as IKK2 inhibitors | |
| JP7080900B2 (ja) | Pi3-キナーゼ活性の阻害剤としてのオキセピノピラゾール誘導体 | |
| ES2358299T3 (es) | Compuestos pirrolo[2,3-b]piridin-4-il-bencenosulfonamida como inhibidores de ikk2. | |
| WO2009112475A1 (en) | Pyrrolo [2, 3-b] pyridin derivatives as ikk2 inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100917 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100917 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20121211 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130305 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130312 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20131029 |