JP5047164B2 - IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物 - Google Patents
IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物 Download PDFInfo
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- JP5047164B2 JP5047164B2 JP2008511281A JP2008511281A JP5047164B2 JP 5047164 B2 JP5047164 B2 JP 5047164B2 JP 2008511281 A JP2008511281 A JP 2008511281A JP 2008511281 A JP2008511281 A JP 2008511281A JP 5047164 B2 JP5047164 B2 JP 5047164B2
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- Prior art keywords
- alkyl
- heteroaryl
- aryl
- cycloalkyl
- heterocyclo
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- 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.)
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- 0 Cc([n]1*)c(*)c2c1nc(*)c1c2[n](*)c(*)n1 Chemical compound Cc([n]1*)c(*)c2c1nc(*)c1c2[n](*)c(*)n1 0.000 description 4
- DSIMMIXWWRTDLE-UHFFFAOYSA-N Bc1nc(C(C)NC(C)=O)ccc1 Chemical compound Bc1nc(C(C)NC(C)=O)ccc1 DSIMMIXWWRTDLE-UHFFFAOYSA-N 0.000 description 1
- VSWICNJIUPRZIK-UHFFFAOYSA-N C1CNC=CC1 Chemical compound C1CNC=CC1 VSWICNJIUPRZIK-UHFFFAOYSA-N 0.000 description 1
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- YDGFHFMRNSUOFT-UHFFFAOYSA-N CC(NCc1cccc(-c2cc3c4[n](C)cnc4c(NC)nc3[nH]2)c1)=O Chemical compound CC(NCc1cccc(-c2cc3c4[n](C)cnc4c(NC)nc3[nH]2)c1)=O YDGFHFMRNSUOFT-UHFFFAOYSA-N 0.000 description 1
- DBRGPHMGORJZPO-UHFFFAOYSA-O CC(c1cccc(-c2cc3c4[n](C)cnc4c([NH3+])nc3[nH]2)n1)N Chemical compound CC(c1cccc(-c2cc3c4[n](C)cnc4c([NH3+])nc3[nH]2)n1)N DBRGPHMGORJZPO-UHFFFAOYSA-O 0.000 description 1
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- YIGYLEOPRNZMCB-UHFFFAOYSA-N CCC(c1nc(Br)ccc1)N Chemical compound CCC(c1nc(Br)ccc1)N YIGYLEOPRNZMCB-UHFFFAOYSA-N 0.000 description 1
- WLWNLADYKGZCEZ-UHFFFAOYSA-N CCCC(c1cc(C#C)ccc1)NC(C)=O Chemical compound CCCC(c1cc(C#C)ccc1)NC(C)=O WLWNLADYKGZCEZ-UHFFFAOYSA-N 0.000 description 1
- DLMDCWZFVXTHET-UHFFFAOYSA-N CNCCNC(OCc1cccc(-c2cc3c4[n](C)cnc4c(NC)nc3[nH]2)n1)=O Chemical compound CNCCNC(OCc1cccc(-c2cc3c4[n](C)cnc4c(NC)nc3[nH]2)n1)=O DLMDCWZFVXTHET-UHFFFAOYSA-N 0.000 description 1
- XXAVVAWFKBYMEW-UHFFFAOYSA-N CNc1c2nc[n](C)c2c(cc(-c2cc(F)cc(C#N)c2)[n]2CCNCCOCCO)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2cc(F)cc(C#N)c2)[n]2CCNCCOCCO)c2n1 XXAVVAWFKBYMEW-UHFFFAOYSA-N 0.000 description 1
- LRIPMYFBYHQQSY-UHFFFAOYSA-N CNc1c2nc[n](C)c2c(cc(-c2cc(F)cc(CNC(N3CCOCC3)=O)c2)[nH]2)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2cc(F)cc(CNC(N3CCOCC3)=O)c2)[nH]2)c2n1 LRIPMYFBYHQQSY-UHFFFAOYSA-N 0.000 description 1
- YLBRZLSBMYSGRX-INIZCTEOSA-N CNc1c2nc[n](C)c2c(cc(-c2cccc([C@H](CO)NC(COC)=O)c2)[nH]2)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2cccc([C@H](CO)NC(COC)=O)c2)[nH]2)c2n1 YLBRZLSBMYSGRX-INIZCTEOSA-N 0.000 description 1
- QOHYPCMJIOABQV-UHFFFAOYSA-N CNc1c2nc[n](C)c2c(cc(-c2ccccc2)[n]2C)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2ccccc2)[n]2C)c2n1 QOHYPCMJIOABQV-UHFFFAOYSA-N 0.000 description 1
- VPMDFGAXSDHVNQ-UHFFFAOYSA-N CNc1c2nc[n](C)c2c(cc(-c2ccccc2)[n]2CC(CO)O)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2ccccc2)[n]2CC(CO)O)c2n1 VPMDFGAXSDHVNQ-UHFFFAOYSA-N 0.000 description 1
- YGUWEBIKTIAOFQ-UHFFFAOYSA-N CNc1c2nc[n](C)c2c(cc(-c2nc(COC(COC)=O)ccc2)[nH]2)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(-c2nc(COC(COC)=O)ccc2)[nH]2)c2n1 YGUWEBIKTIAOFQ-UHFFFAOYSA-N 0.000 description 1
- QCAUUKHBNBWGIP-ZDUSSCGKSA-N CNc1c2nc[n](C)c2c(cc(C2CCCCC2)[n]2C[C@@H](CO)O)c2n1 Chemical compound CNc1c2nc[n](C)c2c(cc(C2CCCCC2)[n]2C[C@@H](CO)O)c2n1 QCAUUKHBNBWGIP-ZDUSSCGKSA-N 0.000 description 1
- WLLSVGJANXTBHH-CWQZNGJJSA-N C[C@@H](CO)NC(C[n]1c2nc(NC)c3nc[n](C)c3c2cc1-c1cc(F)cc(C#N)c1)C#N Chemical compound C[C@@H](CO)NC(C[n]1c2nc(NC)c3nc[n](C)c3c2cc1-c1cc(F)cc(C#N)c1)C#N WLLSVGJANXTBHH-CWQZNGJJSA-N 0.000 description 1
- VAMVNSMGEFGYRJ-ZDUSSCGKSA-N C[C@@H](CO)NCC[n]1c2nc(NC)c3nc[n](C)c3c2cc1-c1cc(F)cc(C#N)c1 Chemical compound C[C@@H](CO)NCC[n]1c2nc(NC)c3nc[n](C)c3c2cc1-c1cc(F)cc(C#N)c1 VAMVNSMGEFGYRJ-ZDUSSCGKSA-N 0.000 description 1
- DNCPRRALJDKXID-UHFFFAOYSA-N C[Si](C)(C)C#Cc1cc(C#N)cc(F)c1 Chemical compound C[Si](C)(C)C#Cc1cc(C#N)cc(F)c1 DNCPRRALJDKXID-UHFFFAOYSA-N 0.000 description 1
- VTDPQCSGILMTQN-UHFFFAOYSA-N C[n]1c2c(cc(-c3cc(C#N)ccc3)[nH]3)c3ncc2nc1 Chemical compound C[n]1c2c(cc(-c3cc(C#N)ccc3)[nH]3)c3ncc2nc1 VTDPQCSGILMTQN-UHFFFAOYSA-N 0.000 description 1
- HNEBPTAKURBYRM-UHFFFAOYSA-N N#Cc1cccc(Br)n1 Chemical compound N#Cc1cccc(Br)n1 HNEBPTAKURBYRM-UHFFFAOYSA-N 0.000 description 1
- CKISHVSXTZSISU-UHFFFAOYSA-N Nc(c(NN)c(c(Cl)n1)N)c1Cl Chemical compound Nc(c(NN)c(c(Cl)n1)N)c1Cl CKISHVSXTZSISU-UHFFFAOYSA-N 0.000 description 1
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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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- 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
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- 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
- A61P17/06—Antipsoriatics
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- 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
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- 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
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- A—HUMAN NECESSITIES
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- 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]
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- A—HUMAN NECESSITIES
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- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- 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
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67969205P | 2005-05-10 | 2005-05-10 | |
| US60/679,692 | 2005-05-10 | ||
| US11/430,215 US7737279B2 (en) | 2005-05-10 | 2006-05-08 | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
| US11/430,215 | 2006-05-08 | ||
| PCT/US2006/017950 WO2006122137A1 (en) | 2005-05-10 | 2006-05-09 | 1, 6 -dihydro- 1,3, 5, 6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same as inhibitors of ikk enzyme activity |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008540547A JP2008540547A (ja) | 2008-11-20 |
| JP2008540547A5 JP2008540547A5 (enExample) | 2009-06-04 |
| JP5047164B2 true JP5047164B2 (ja) | 2012-10-10 |
Family
ID=36808856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008511281A Expired - Fee Related JP5047164B2 (ja) | 2005-05-10 | 2006-05-09 | IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US7737279B2 (enExample) |
| EP (1) | EP1888584B1 (enExample) |
| JP (1) | JP5047164B2 (enExample) |
| AR (1) | AR053725A1 (enExample) |
| AT (1) | ATE465162T1 (enExample) |
| CY (1) | CY1110419T1 (enExample) |
| DE (1) | DE602006013816D1 (enExample) |
| DK (1) | DK1888584T3 (enExample) |
| ES (1) | ES2342976T3 (enExample) |
| PE (1) | PE20061424A1 (enExample) |
| PL (1) | PL1888584T3 (enExample) |
| PT (1) | PT1888584E (enExample) |
| SI (1) | SI1888584T1 (enExample) |
| TW (1) | TW200718422A (enExample) |
| WO (1) | WO2006122137A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7737279B2 (en) * | 2005-05-10 | 2010-06-15 | Bristol-Myers Squibb Company | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
| UY31881A (es) | 2008-06-10 | 2010-01-29 | Abbott Lab | Derivados sustituidos de imidazo[1,5-a]pirrolo[2,3-e]pirazinas e imidazo[1,2-a]pirrolo[2,3-e]pirazinas, sus sales, prodrogas, metabolitos biológicalmente activos, estereoisómeros e isómeros farmacéuticamente aceptables. |
| AU2010289497B2 (en) | 2009-09-03 | 2016-04-14 | Bristol-Myers Squibb Company | JAK2 inhibitors and their use for the treatment of myeloproliferative diseases and cancer |
| CA2991896A1 (en) * | 2009-12-01 | 2011-06-09 | Abbvie Inc. | Novel tricyclic compounds as protein kinase inhibitors |
| KR20120102724A (ko) | 2009-12-01 | 2012-09-18 | 아보트 러보러터리즈 | 신규한 트리사이클릭 화합물 |
| CN102712640A (zh) * | 2010-01-12 | 2012-10-03 | 弗·哈夫曼-拉罗切有限公司 | 三环杂环化合物、其组合物和应用方法 |
| WO2011112687A2 (en) * | 2010-03-10 | 2011-09-15 | Kalypsys, Inc. | Heterocyclic inhibitors of histamine receptors for the treatment of disease |
| TWI633087B (zh) | 2012-06-13 | 2018-08-21 | 赫孚孟拉羅股份公司 | 新穎二氮雜螺環烷及氮雜螺環烷 |
| RS59512B1 (sr) * | 2012-09-25 | 2019-12-31 | Hoffmann La Roche | Derivati heksahidropirolo[3,4−c]pirola i srodna jedinjenja kao inhibitori autotaksina (atx) i kao inhibitori proizvodnje lizofosfatidne kiseline (lpa) za lečenje npr. bubrežnih bolesti |
| AR095079A1 (es) | 2013-03-12 | 2015-09-16 | Hoffmann La Roche | Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo |
| US9518058B2 (en) | 2013-08-29 | 2016-12-13 | Bristol-Myers Squibb Company | Process for the preparation of N,N-dicyclopropyl-4-(1,5-dimethyl-1H-pyrazol-3-ylamino)-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide |
| JPWO2015060368A1 (ja) | 2013-10-23 | 2017-03-09 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2015078803A1 (en) | 2013-11-26 | 2015-06-04 | F. Hoffmann-La Roche Ag | NEW OCTAHYDRO-CYCLOBUTA [1,2-c;3,4-c']DIPYRROL-2-YL |
| CN106103446B (zh) | 2014-03-26 | 2019-07-30 | 豪夫迈·罗氏有限公司 | 作为自分泌运动因子(atx)和溶血磷脂酸(lpa)生产抑制剂的二环化合物 |
| KR20160128428A (ko) | 2014-03-26 | 2016-11-07 | 에프. 호프만-라 로슈 아게 | 오토탁신(atx) 및 리소포스파티드산(lpa) 생성 억제제로서의 축합형 [1,4]다이아제핀 화합물 |
| MA41898A (fr) | 2015-04-10 | 2018-02-13 | Hoffmann La Roche | Dérivés de quinazolinone bicyclique |
| CN108026077B (zh) | 2015-09-04 | 2021-11-05 | 豪夫迈·罗氏有限公司 | 苯氧基甲基衍生物 |
| EP3353178B1 (en) | 2015-09-24 | 2021-07-14 | F. Hoffmann-La Roche AG | Bicyclic compounds as dual atx/ca inhibitors |
| KR20180054635A (ko) | 2015-09-24 | 2018-05-24 | 에프. 호프만-라 로슈 아게 | 오토탁신(atx) 억제제로서 이환형 화합물 |
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| US11512092B2 (en) | 2015-10-16 | 2022-11-29 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
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| CA2420967A1 (en) | 2000-08-07 | 2002-02-14 | Neurogen Corporation | Heterocyclic compounds as ligands of the gabaa receptor |
| EP1490371B1 (en) * | 2002-04-03 | 2007-08-15 | Bristol-Myers Squibb Company | Thiophene-based tricyclic compounds and pharmaceutical compositions comprising same |
| US7329668B2 (en) * | 2003-02-25 | 2008-02-12 | Bristol-Myers Squibb Company | Pyrazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same |
| US7176214B2 (en) | 2003-05-21 | 2007-02-13 | Bristol-Myers Squibb Company | Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same |
| US7071333B2 (en) * | 2003-07-30 | 2006-07-04 | Bristol-Myers Squibb Company | Triazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same |
| PL1653959T3 (pl) * | 2003-08-14 | 2015-10-30 | 3M Innovative Properties Co | Modyfikatory odpowiedzi immunologicznej modyfikowane lipidami |
| GB0403635D0 (en) | 2004-02-18 | 2004-03-24 | Devgen Nv | Pyridinocarboxamides with improved activity as kinase inhibitors |
| US20050250829A1 (en) | 2004-04-23 | 2005-11-10 | Takeda San Diego, Inc. | Kinase inhibitors |
| WO2006053166A1 (en) * | 2004-11-12 | 2006-05-18 | Bristol-Myers Squibb Company | 8h-imidazo[4,5-d]thiazolo[4,5-b]pyridine based tricyclic compounds and pharmaceutical compositions comprising same |
| US7456194B2 (en) * | 2004-11-12 | 2008-11-25 | Bristol-Myers Squibb Company | Imidazo-fused oxazolo [4,5-b]pyridine and imidazo-fused thiazolo[4,5-b]pyridine based tricyclic compounds and pharmaceutical compositions comprising same |
| US7737279B2 (en) * | 2005-05-10 | 2010-06-15 | Bristol-Myers Squibb Company | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
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- 2006-05-09 DK DK06759417.6T patent/DK1888584T3/da active
- 2006-05-09 SI SI200630671T patent/SI1888584T1/sl unknown
- 2006-05-09 ES ES06759417T patent/ES2342976T3/es active Active
- 2006-05-09 WO PCT/US2006/017950 patent/WO2006122137A1/en not_active Ceased
- 2006-05-09 EP EP06759417A patent/EP1888584B1/en not_active Not-in-force
- 2006-05-09 AT AT06759417T patent/ATE465162T1/de active
- 2006-05-09 DE DE602006013816T patent/DE602006013816D1/de active Active
- 2006-05-09 PT PT06759417T patent/PT1888584E/pt unknown
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| JP2008540547A (ja) | 2008-11-20 |
| DE602006013816D1 (de) | 2010-06-02 |
| PT1888584E (pt) | 2010-06-22 |
| US20060270654A1 (en) | 2006-11-30 |
| US8268855B2 (en) | 2012-09-18 |
| WO2006122137A1 (en) | 2006-11-16 |
| PL1888584T3 (pl) | 2010-09-30 |
| US7737279B2 (en) | 2010-06-15 |
| US20100210629A1 (en) | 2010-08-19 |
| ES2342976T3 (es) | 2010-07-20 |
| EP1888584A1 (en) | 2008-02-20 |
| SI1888584T1 (sl) | 2010-07-30 |
| TW200718422A (en) | 2007-05-16 |
| EP1888584B1 (en) | 2010-04-21 |
| ATE465162T1 (de) | 2010-05-15 |
| PE20061424A1 (es) | 2006-12-17 |
| DK1888584T3 (da) | 2010-08-09 |
| AR053725A1 (es) | 2007-05-16 |
| CY1110419T1 (el) | 2015-04-29 |
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