JP2009506123A - 非受容体型チロシンキナーゼのtecファミリーの阻害剤として有用な3,5−二置換ピリド−2−オン - Google Patents
非受容体型チロシンキナーゼのtecファミリーの阻害剤として有用な3,5−二置換ピリド−2−オン Download PDFInfo
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- JP2009506123A JP2009506123A JP2008529213A JP2008529213A JP2009506123A JP 2009506123 A JP2009506123 A JP 2009506123A JP 2008529213 A JP2008529213 A JP 2008529213A JP 2008529213 A JP2008529213 A JP 2008529213A JP 2009506123 A JP2009506123 A JP 2009506123A
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- Prior art keywords
- alkyl
- aliphatic
- compound
- optionally substituted
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- 0 CN(*)*1=C(*)C(*)=C(*)NC1=O Chemical compound CN(*)*1=C(*)C(*)=C(*)NC1=O 0.000 description 3
- JDPUFBDGLAPBRV-UHFFFAOYSA-N O=C(C(Nc1ccccc1)=C1)NC=C1c1ccncc1 Chemical compound O=C(C(Nc1ccccc1)=C1)NC=C1c1ccncc1 JDPUFBDGLAPBRV-UHFFFAOYSA-N 0.000 description 2
- SARGYBHSRNDTIS-MMDYSHKOSA-N C/C=C/C(/C(C=C1Nc2nc3ccccc3cc2)=CNC1=O)=N\C(\NC)=C/C Chemical compound C/C=C/C(/C(C=C1Nc2nc3ccccc3cc2)=CNC1=O)=N\C(\NC)=C/C SARGYBHSRNDTIS-MMDYSHKOSA-N 0.000 description 1
- FNBQQRBAONNBBM-GORDUTHDSA-N C/C=C/c1nc(C(C=C2Nc3nc4ccccc4cc3)=CNC2=O)cnc1 Chemical compound C/C=C/c1nc(C(C=C2Nc3nc4ccccc4cc3)=CNC2=O)cnc1 FNBQQRBAONNBBM-GORDUTHDSA-N 0.000 description 1
- KKBZUNQUOWAUBA-UHFFFAOYSA-N C=C(C(Nc1ncccc1)=C1)NC=C1c1ccncc1 Chemical compound C=C(C(Nc1ncccc1)=C1)NC=C1c1ccncc1 KKBZUNQUOWAUBA-UHFFFAOYSA-N 0.000 description 1
- CGKBZUFBJPTIRK-UHFFFAOYSA-N CC(C)(C)OC(N(C)c1nc(-c(cn2)cc(Nc3nccc4c3cccc4)c2OC)cnc1)=O Chemical compound CC(C)(C)OC(N(C)c1nc(-c(cn2)cc(Nc3nccc4c3cccc4)c2OC)cnc1)=O CGKBZUFBJPTIRK-UHFFFAOYSA-N 0.000 description 1
- IIGCZBNZSHFOCO-UHFFFAOYSA-N CC1(C)OB(c(cc2NC)cnc2OC)OC1(C)C Chemical compound CC1(C)OB(c(cc2NC)cnc2OC)OC1(C)C IIGCZBNZSHFOCO-UHFFFAOYSA-N 0.000 description 1
- VHUNMPHJSAIBOF-UHFFFAOYSA-N CNc1nc(C(C=C2C=N)=CNC2=O)cnc1 Chemical compound CNc1nc(C(C=C2C=N)=CNC2=O)cnc1 VHUNMPHJSAIBOF-UHFFFAOYSA-N 0.000 description 1
- ASPCASJHFUNTQA-UHFFFAOYSA-N CNc1nc(C(C=C2Nc3n[s]c4ccccc34)=CNC2=O)cnc1 Chemical compound CNc1nc(C(C=C2Nc3n[s]c4ccccc34)=CNC2=O)cnc1 ASPCASJHFUNTQA-UHFFFAOYSA-N 0.000 description 1
- OWTZIFQVLLSJRL-UHFFFAOYSA-N CNc1nc(C(C=C2Nc3nccc4c3cccc4)=CNC2=O)cnc1 Chemical compound CNc1nc(C(C=C2Nc3nccc4c3cccc4)=CNC2=O)cnc1 OWTZIFQVLLSJRL-UHFFFAOYSA-N 0.000 description 1
- DAEGDNYLKMKZRG-UHFFFAOYSA-N Cc1n[s]c2ccccc12 Chemical compound Cc1n[s]c2ccccc12 DAEGDNYLKMKZRG-UHFFFAOYSA-N 0.000 description 1
- JDJAKKWRDBFAOK-UHFFFAOYSA-N O=C(C(Nc1nccc2ccccc12)=C1)NC=C1c1ccncc1 Chemical compound O=C(C(Nc1nccc2ccccc12)=C1)NC=C1c1ccncc1 JDJAKKWRDBFAOK-UHFFFAOYSA-N 0.000 description 1
- HCYUKBYNNQOSLE-UHFFFAOYSA-N O=C(C(Nc1ncccc1)=C1)NC=C1c1ccncc1 Chemical compound O=C(C(Nc1ncccc1)=C1)NC=C1c1ccncc1 HCYUKBYNNQOSLE-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07—ORGANIC CHEMISTRY
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Virology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71246005P | 2005-08-29 | 2005-08-29 | |
| PCT/US2006/033791 WO2007027729A1 (en) | 2005-08-29 | 2006-08-28 | 3, 5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-receptor tyrosine kinases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009506123A true JP2009506123A (ja) | 2009-02-12 |
| JP2009506123A5 JP2009506123A5 (https=) | 2009-10-08 |
Family
ID=37564011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008529213A Pending JP2009506123A (ja) | 2005-08-29 | 2006-08-28 | 非受容体型チロシンキナーゼのtecファミリーの阻害剤として有用な3,5−二置換ピリド−2−オン |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7786130B2 (https=) |
| EP (1) | EP1919906B1 (https=) |
| JP (1) | JP2009506123A (https=) |
| AT (1) | ATE528302T1 (https=) |
| AU (1) | AU2006284900A1 (https=) |
| CA (1) | CA2620352A1 (https=) |
| WO (1) | WO2007027729A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010504287A (ja) * | 2006-09-11 | 2010-02-12 | シージーアイ ファーマシューティカルズ,インコーポレイティド | ある種の置換アミド、その製造方法および使用方法 |
| JP2012501313A (ja) * | 2008-09-02 | 2012-01-19 | ノバルティス アーゲー | ヘテロ環pimキナーゼ阻害剤 |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007027594A1 (en) * | 2005-08-29 | 2007-03-08 | Vertex Pharmaceuticals Incorporated | 3,5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-receptor tyrosine kinases |
| EP1919905B1 (en) | 2005-08-29 | 2011-02-23 | Vertex Pharmaceuticals Incorporated | 3,5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-recptor tyrosine kinases |
| WO2009053269A1 (en) | 2007-10-23 | 2009-04-30 | F. Hoffmann-La Roche Ag | Novel kinase inhibitors |
| US7683064B2 (en) | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
| ES2552320T3 (es) | 2008-06-24 | 2015-11-27 | F. Hoffmann-La Roche Ag | Nuevas piridín-2-onas y piridazín-3-onas sustituidas |
| BRPI0913879A2 (pt) | 2008-07-02 | 2019-09-24 | Hoffmann La Roche | fenilpirazinonas como inibidores de quinase |
| AR082590A1 (es) | 2010-08-12 | 2012-12-19 | Hoffmann La Roche | Inhibidores de la tirosina-quinasa de bruton |
| WO2013153539A1 (en) | 2012-04-13 | 2013-10-17 | Glenmark Pharmaceuticals S.A. | Tricyclic compounds as tec kinase inhibitors |
| AU2013250726B2 (en) | 2012-04-20 | 2017-01-05 | Advinus Therapeutics Limited | Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof |
| WO2013157021A1 (en) | 2012-04-20 | 2013-10-24 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
| HRP20170217T1 (hr) | 2013-04-25 | 2017-04-21 | Beigene, Ltd. | Fuzinirani heterociklički spojevi kao inhibitori protein kinaze |
| EA034666B1 (ru) | 2013-09-13 | 2020-03-04 | Бейджин Свитзерланд Гмбх | Антитело против pd-1 и его применение для лечения рака или вирусной инфекции и фрагмент антитела |
| WO2015112847A1 (en) * | 2014-01-24 | 2015-07-30 | Confluence Life Sciences, Inc. | Arylpyridinone itk inhibitors for treating inflammation and cancer |
| TWI726608B (zh) | 2014-07-03 | 2021-05-01 | 英屬開曼群島商百濟神州有限公司 | 抗pd-l1抗體及其作為治療及診斷之用途 |
| EP3042903B1 (en) | 2015-01-06 | 2019-08-14 | Impetis Biosciences Ltd. | Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof |
| CA2973597A1 (en) | 2015-01-23 | 2016-07-28 | Confluence Life Sciences, Inc. | Heterocyclic itk inhibitors for treating inflammation and cancer |
| US10864203B2 (en) | 2016-07-05 | 2020-12-15 | Beigene, Ltd. | Combination of a PD-1 antagonist and a RAF inhibitor for treating cancer |
| CA3033827A1 (en) | 2016-08-16 | 2018-02-22 | Beigene, Ltd. | Crystalline form of (s)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl )-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide,preparation, and uses thereof |
| PT3500299T (pt) | 2016-08-19 | 2024-02-21 | Beigene Switzerland Gmbh | Combinação de zanubrutinib com um anticorpo anti-cd20 ou anti-pd-1 para utilização no tratamento do cancro |
| CN109982687A (zh) | 2016-09-19 | 2019-07-05 | 梅制药公司 | 联合疗法 |
| WO2018140648A1 (en) | 2017-01-25 | 2018-08-02 | Eric Jon Jacobsen | Pyrrolopyrimidine itk inhibitors for treating inflammation and cancer |
| EP3573989A4 (en) | 2017-01-25 | 2020-11-18 | Beigene, Ltd. | CRYSTALLINE FORMS OF (S) -7- (1- (BUT-2-YNOYL) PIPERIDIN-4-YL) -2- (4-PHENOXYPHENYL) -4, 5, 6, 7-TETRAHY DROPYRAZOLO [1, 5-A ] PYRIMIDINE-3-CARBOXAMIDE, PREPARATION AND ASSOCIATED USES |
| TW202515616A (zh) | 2017-06-26 | 2025-04-16 | 英屬開曼群島商百濟神州有限公司 | 抗pd-1抗體或其抗原結合片段在製備治療用於患有肝細胞癌(hcc)之藥物的用途 |
| WO2019034009A1 (en) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY |
| CN111801334B (zh) | 2017-11-29 | 2023-06-09 | 百济神州瑞士有限责任公司 | 使用包含btk抑制剂的组合治疗惰性或侵袭性b-细胞淋巴瘤 |
| WO2020249001A1 (zh) | 2019-06-10 | 2020-12-17 | 百济神州瑞士有限责任公司 | 一种含有布鲁顿氏酪氨酸激酶抑制剂的口服固体片剂及其制备方法 |
| US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004532241A (ja) * | 2001-05-04 | 2004-10-21 | ノバルティス アクチエンゲゼルシャフト | 血管形成阻害活性を有するフタラジン誘導体 |
| JP2004534010A (ja) * | 2001-03-28 | 2004-11-11 | ブリストル−マイヤーズ スクイブ カンパニー | 新規なチロシンキナーゼ阻害剤 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5308854A (en) | 1990-06-18 | 1994-05-03 | Merck & Co., Inc. | Inhibitors of HIV reverse transcriptase |
| IL98526A0 (en) | 1990-06-18 | 1992-07-15 | Merck & Co Inc | Pyridones,processes for their preparation and pharmaceutical compositions containing them |
| CN1034934C (zh) | 1990-06-19 | 1997-05-21 | 明治制果株式会社 | 血管紧张素ii拮抗性吡啶衍生物的制备方法 |
| IL99731A0 (en) | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
| DE4221583A1 (de) | 1991-11-12 | 1993-05-13 | Bayer Ag | Substituierte biphenylpyridone |
| US5290941A (en) | 1992-10-14 | 1994-03-01 | Merck & Co., Inc. | Facile condensation of methylbenzoxazoles with aromatic aldehydes |
| DE4314963A1 (de) | 1993-05-06 | 1994-11-10 | Bayer Ag | Substituierte Pyridine und 2-Oxo-1,2-dihydropyridine |
| DE4314964A1 (de) | 1993-05-06 | 1994-11-10 | Bayer Ag | Pyridinylmethyl-substiutierte Pyridine und Pyridone |
| DE4316077A1 (de) | 1993-05-13 | 1994-11-17 | Bayer Ag | Substituierte Mono- und Bihydridylmethylpyridone |
| US6979695B2 (en) | 1996-04-23 | 2005-12-27 | Targacept, Inc. | Compounds capable of activating cholinergic receptors |
| BR9909976A (pt) | 1998-04-27 | 2000-12-26 | Centre Nat Rech Scient | Composto, processo para a obtenção de compostos, derivado litiado, composições farmacêuticas, e, processos de tratamento de doenças relacionadas com hiv e de tratamento de infecção de hiv |
| US6774138B2 (en) | 1999-08-31 | 2004-08-10 | Merck & Co., Inc. | Thiazolyl(pyridyl)ethyne compounds |
| IL150650A0 (en) | 2000-01-20 | 2003-02-12 | Eisai Co Ltd | Piperidine derivatives and pharmaceutical compositions containing the same |
| IL152848A0 (en) | 2000-06-12 | 2003-06-24 | Eisai Co Ltd | 1,2-dihydropyridine derivatives, pharmaceutical compositions containing the same and methods for the production thereof |
| US6670380B2 (en) | 2000-11-20 | 2003-12-30 | Bristol-Myers Squibb Co. | Pyridone inhibitors of fatty acid binding protein and method |
| ES2330719T3 (es) | 2000-12-28 | 2009-12-15 | SHIONOGI & CO., LTD. | Derivados de 2-piridona con afinidad para el receptor cannabinoide de tipo 2. |
| GB0129260D0 (en) | 2001-12-06 | 2002-01-23 | Eisai London Res Lab Ltd | Pharmaceutical compositions and their uses |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| RS52392B (sr) | 2002-02-14 | 2013-02-28 | Pharmacia Corporation | Supstituisani piridinoni kao modulatori p38 map kinaze |
| JP4208512B2 (ja) | 2002-07-23 | 2009-01-14 | 株式会社クラレ | 5−(2’−ピリジル)−2−ピリドン誘導体の製造方法 |
| AU2003274025A1 (en) | 2002-10-17 | 2004-05-04 | Syngenta Participations Ag | Pyridine derivatives useful as herbicides |
| WO2004035563A1 (en) | 2002-10-17 | 2004-04-29 | Syngenta Participations Ag | 3-heterocyclylpyridine derivatives useful as herbicides |
| WO2004050657A2 (en) | 2002-11-27 | 2004-06-17 | Artesian Therapeutics, Inc. | COMPOUNDS WITH MIXED PDE-INHIBITORY AND β-ADRENERGIC ANTAGONIST OR PARTIAL AGONIST ACTIVITY FOR TREATMENT OF HEART FAILURE |
| US20070117978A1 (en) | 2002-12-23 | 2007-05-24 | Artesian Therapecutics, Inc | Cardiotonic compounds with inhibitory activity against beta-adrenergic receptors and phosphodiesterase |
| US20070010541A1 (en) | 2003-07-14 | 2007-01-11 | The General Hospital Corporation | Methods for treating vascular diseases |
| PE20060285A1 (es) | 2004-03-30 | 2006-05-08 | Aventis Pharma Inc | Piridonas sustituidas como inhibidores de pol(adp-ribosa)-polimerasa (parp) |
| BRPI0514094A (pt) * | 2004-08-02 | 2008-05-27 | Osi Pharm Inc | composto, composição, e, método de tratamento de distúrbio hiperproliferativo |
| CA2591413A1 (en) | 2004-12-16 | 2006-06-22 | Vertex Pharmaceuticals Incorporated | Pyrid-2-ones useful as inhibitors of tec family protein kinases for the treatment of inflammatory, proliferative and immunologically-mediated diseases |
| CA2601628C (en) | 2005-03-10 | 2014-05-13 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
| WO2007027594A1 (en) | 2005-08-29 | 2007-03-08 | Vertex Pharmaceuticals Incorporated | 3,5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-receptor tyrosine kinases |
| EP1919905B1 (en) | 2005-08-29 | 2011-02-23 | Vertex Pharmaceuticals Incorporated | 3,5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-recptor tyrosine kinases |
-
2006
- 2006-08-28 JP JP2008529213A patent/JP2009506123A/ja active Pending
- 2006-08-28 AT AT06813936T patent/ATE528302T1/de not_active IP Right Cessation
- 2006-08-28 CA CA002620352A patent/CA2620352A1/en not_active Abandoned
- 2006-08-28 AU AU2006284900A patent/AU2006284900A1/en not_active Abandoned
- 2006-08-28 WO PCT/US2006/033791 patent/WO2007027729A1/en not_active Ceased
- 2006-08-28 US US11/511,086 patent/US7786130B2/en not_active Expired - Fee Related
- 2006-08-28 EP EP06813936A patent/EP1919906B1/en not_active Not-in-force
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004534010A (ja) * | 2001-03-28 | 2004-11-11 | ブリストル−マイヤーズ スクイブ カンパニー | 新規なチロシンキナーゼ阻害剤 |
| JP2004532241A (ja) * | 2001-05-04 | 2004-10-21 | ノバルティス アクチエンゲゼルシャフト | 血管形成阻害活性を有するフタラジン誘導体 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010504287A (ja) * | 2006-09-11 | 2010-02-12 | シージーアイ ファーマシューティカルズ,インコーポレイティド | ある種の置換アミド、その製造方法および使用方法 |
| JP2012501313A (ja) * | 2008-09-02 | 2012-01-19 | ノバルティス アーゲー | ヘテロ環pimキナーゼ阻害剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007027729A1 (en) | 2007-03-08 |
| EP1919906A1 (en) | 2008-05-14 |
| US20070179156A1 (en) | 2007-08-02 |
| CA2620352A1 (en) | 2007-03-08 |
| ATE528302T1 (de) | 2011-10-15 |
| US7786130B2 (en) | 2010-08-31 |
| EP1919906B1 (en) | 2011-10-12 |
| AU2006284900A1 (en) | 2007-03-08 |
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