WO2004046118A3 - 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders - Google Patents
2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders Download PDFInfo
- Publication number
- WO2004046118A3 WO2004046118A3 PCT/US2003/014294 US0314294W WO2004046118A3 WO 2004046118 A3 WO2004046118 A3 WO 2004046118A3 US 0314294 W US0314294 W US 0314294W WO 2004046118 A3 WO2004046118 A3 WO 2004046118A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- amino
- phenyl
- proliferative disorders
- pyrimidine derivatives
- derivatives useful
- Prior art date
Links
Classifications
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003299474A AU2003299474A1 (en) | 2002-05-06 | 2003-05-06 | 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37832902P | 2002-05-06 | 2002-05-06 | |
US60/378,329 | 2002-05-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2004046118A2 WO2004046118A2 (en) | 2004-06-03 |
WO2004046118A3 true WO2004046118A3 (en) | 2004-08-12 |
Family
ID=29420382
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2003/013604 WO2003095448A1 (en) | 2002-05-06 | 2003-05-02 | Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders |
PCT/US2003/014294 WO2004046118A2 (en) | 2002-05-06 | 2003-05-06 | 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2003/013604 WO2003095448A1 (en) | 2002-05-06 | 2003-05-02 | Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders |
Country Status (2)
Country | Link |
---|---|
AU (2) | AU2003231231A1 (en) |
WO (2) | WO2003095448A1 (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7989448B2 (en) | 2005-01-19 | 2011-08-02 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US8557806B2 (en) | 2002-07-29 | 2013-10-15 | Rigel Pharmaceuticals, Inc. | Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds |
US8604042B2 (en) | 2005-11-01 | 2013-12-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
US8785692B2 (en) | 2007-03-12 | 2014-07-22 | Bayer Cropscience Ag | Substituted phenylamidines and the use thereof as fungicides |
US8835430B2 (en) | 2002-02-01 | 2014-09-16 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US8952027B2 (en) | 2008-04-16 | 2015-02-10 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
US9012462B2 (en) | 2008-05-21 | 2015-04-21 | Ariad Pharmaceuticals, Inc. | Phosphorous derivatives as kinase inhibitors |
US9248190B2 (en) | 2005-06-08 | 2016-02-02 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the JAK pathway |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
US9359308B2 (en) | 2011-11-23 | 2016-06-07 | Portola Pharmaceuticals, Inc. | Pyrazine kinase inhibitors |
JP7202315B2 (en) | 2017-05-26 | 2023-01-11 | キャンサー・リサーチ・テクノロジー・リミテッド | BCL6 inhibitors derived from benzimidazolones |
Families Citing this family (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0206215D0 (en) | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
US7109337B2 (en) | 2002-12-20 | 2006-09-19 | Pfizer Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
UA80767C2 (en) * | 2002-12-20 | 2007-10-25 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
GEP20084357B (en) | 2002-12-20 | 2008-04-29 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
PL1656372T3 (en) | 2003-07-30 | 2013-08-30 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases |
PT2287156E (en) * | 2003-08-15 | 2013-08-26 | Novartis Ag | 2,4-di(phenylamino)-pyrimidines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders |
EP1756090A1 (en) | 2004-05-14 | 2007-02-28 | Pfizer Products Incorporated | Pyrimidine derivatives for the treatment of abnormal cell growth |
EP1751142A1 (en) | 2004-05-14 | 2007-02-14 | Pfizer Products Incorporated | Pyrimidines derivatives for the treatment of abnormal cell growth |
JP2007537238A (en) | 2004-05-14 | 2007-12-20 | ファイザー・プロダクツ・インク | Pyrimidine derivatives for the treatment of abnormal cell proliferation |
WO2006004776A1 (en) | 2004-06-29 | 2006-01-12 | Rigel Pharmaceuticals, Inc. | 4-pyrimidineamine compounds and their uses as anti-proliferative agents |
US20060051406A1 (en) * | 2004-07-23 | 2006-03-09 | Manjeet Parmar | Formulation of insoluble small molecule therapeutics in lipid-based carriers |
GB0419160D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
GB0419161D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
WO2006037117A1 (en) * | 2004-09-27 | 2006-04-06 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
EP1814878B1 (en) | 2004-11-24 | 2012-01-04 | Rigel Pharmaceuticals, Inc. | Spiro-2, 4-pyrimidinediamine compounds and their uses |
US20060247263A1 (en) * | 2005-04-19 | 2006-11-02 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
KR100602320B1 (en) * | 2005-05-03 | 2006-07-18 | 주식회사 하이닉스반도체 | Non-volatile memory device having uniform programming speed |
US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
US8246984B2 (en) | 2005-12-06 | 2012-08-21 | Rigel Pharmaceuticals, Inc. | Formulation of insoluble small molecule therapeutics in lipid-based carriers |
UA89123C2 (en) | 2005-12-21 | 2009-12-25 | Пфайзер Продактс Инк. | Pyrimidine derivatives for the treatment of abnormal cell growth |
TW200736232A (en) * | 2006-01-26 | 2007-10-01 | Astrazeneca Ab | Pyrimidine derivatives |
JP2009528295A (en) | 2006-02-24 | 2009-08-06 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Compositions and methods for inhibition of the JAK pathway |
GB2451594A (en) * | 2006-03-15 | 2009-02-04 | Csir | Modulation of phosphoryl transferase activity of glutamine synthetase |
WO2007105023A1 (en) * | 2006-03-15 | 2007-09-20 | Csir | Modulation of phosphoryl transferase activity of glutamine synthetase |
DK2089369T3 (en) | 2006-10-19 | 2011-05-09 | Rigel Pharmaceuticals Inc | 2,4-Pyrimidinediamine Derivatives as Inhibitors of JAK Kinases for the Treatment of Autoimmune Diseases |
CL2007003049A1 (en) | 2006-10-23 | 2008-05-16 | Cephalon Inc Pharmacopeia Drug | COMPOUNDS DERIVED FROM 2,4-DIAMINOPIRIMIDINE; PHARMACEUTICAL COMPOSITION, USEFUL TO TREAT PROLIFERATIVE DISORDERS. |
GEP20125691B (en) | 2006-12-08 | 2012-11-26 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
EP1939185A1 (en) * | 2006-12-20 | 2008-07-02 | Bayer Schering Pharma Aktiengesellschaft | New types of hetaryl-phenylendiamin-pyrimidines as protein kinase inhibitors for the treatment of cancer |
EP2535329A3 (en) | 2006-12-22 | 2013-03-27 | F. Hoffmann-La Roche AG | Spiro-piperidine derivatives |
FR2911137B1 (en) * | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | NOVEL 2,4-DIANILINOPYRIMIDE DERIVATIVES, THEIR PREPARATION AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND IN PARTICULAR AS INHIBITORS OF IKK |
MX2009009117A (en) * | 2007-03-01 | 2009-09-03 | Supergen Inc | Pyrimidine-2,4-diamine derivatives and their use as jak2 kinase inhibitors. |
AU2014201847B2 (en) * | 2007-04-18 | 2015-12-24 | Pfizer Products Inc. | Sulfonyl amide derivatives for the treatment of abnormal cell growth |
CN101678215B (en) | 2007-04-18 | 2014-10-01 | 辉瑞产品公司 | Sulfonyl amide derivatives for the treatment of abnormal cell growth |
AU2016201820B2 (en) * | 2007-04-18 | 2018-03-08 | Pfizer Products Inc. | Sulfonyl amide derivatives for the treatment of abnormal cell growth |
CA2707653A1 (en) * | 2007-12-03 | 2009-06-11 | Boehringer Ingelheim International Gmbh | Diaminopyridines for the treatment of diseases which are characterised by excessive or anomal cell proliferation |
BRPI0906799A2 (en) | 2008-01-11 | 2015-07-14 | Hoffmann La Roche | Beta Amyloid Modulators |
CA2713716A1 (en) * | 2008-02-22 | 2009-08-27 | F. Hoffmann-La Roche Ag | Modulators for amyloid beta |
VN29259A1 (en) | 2008-04-16 | 2012-04-25 | Portola Pharm Inc | 2, 6-diamino- pyrimidin- 5-yl-carboxamides as syk or JAK kinases inhibitors |
US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
AU2009238590A1 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
DE102008049323A1 (en) * | 2008-09-29 | 2010-04-01 | Henkel Ag & Co. Kgaa | New developer components |
WO2010040661A1 (en) | 2008-10-09 | 2010-04-15 | F. Hoffmann-La Roche Ag | Modulators for amyloid beta |
EP2355817A1 (en) | 2008-11-10 | 2011-08-17 | F. Hoffmann-La Roche AG | Heterocyclic gamma secretase modulators |
CN102292333B (en) * | 2009-01-15 | 2015-05-13 | 里格尔药品股份有限公司 | Protein kinase c inhibitors and uses thereof |
US8933227B2 (en) | 2009-08-14 | 2015-01-13 | Boehringer Ingelheim International Gmbh | Selective synthesis of functionalized pyrimidines |
WO2011018517A1 (en) | 2009-08-14 | 2011-02-17 | Boehringer Ingelheim International Gmbh | Regioselective preparation of 2-amino-5-trifluoromethylpyrimidine derivatives |
EP2519517B1 (en) | 2009-12-29 | 2015-03-25 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
US8486967B2 (en) | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
JP5607241B2 (en) | 2010-05-21 | 2014-10-15 | ケミリア・エービー | New pyrimidine derivatives |
WO2012061428A2 (en) | 2010-11-01 | 2012-05-10 | Portola Pharmaceuticals, Inc. | Nicotinamides as jak kinase modulators |
US20130317029A1 (en) | 2010-11-01 | 2013-11-28 | Portola Pharmaceuticals, Inc. | Oxypyrimidines as syk modulators |
EP3176154B1 (en) | 2010-11-01 | 2019-02-20 | Portola Pharmaceuticals, Inc. | Benzamides and nicotinamides as syk modulators |
CA2816957A1 (en) | 2010-11-07 | 2012-05-10 | Targegen, Inc. | Compositions and methods for treating myelofibrosis |
US9006241B2 (en) | 2011-03-24 | 2015-04-14 | Noviga Research Ab | Pyrimidine derivatives |
US9249124B2 (en) | 2011-03-30 | 2016-02-02 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Aurora kinase inhibitors and methods of making and using thereof |
CN103501612B (en) | 2011-05-04 | 2017-03-29 | 阿里亚德医药股份有限公司 | The compound that cell is bred in cancer caused by suppression EGF-R ELISA |
WO2013013188A1 (en) | 2011-07-21 | 2013-01-24 | Tolero Pharmaceuticals, Inc. | Heterocyclic protein kinase inhibitors |
US9382239B2 (en) * | 2011-11-17 | 2016-07-05 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-Jun-N-terminal kinase (JNK) |
EP2606884A1 (en) * | 2011-12-21 | 2013-06-26 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Inhibitors of notch signaling pathway and use thereof in treatment of cancers |
US20150166591A1 (en) | 2012-05-05 | 2015-06-18 | Ariad Pharmaceuticals, Inc. | Methods and compositions for raf kinase mediated diseases |
KR101446742B1 (en) * | 2012-08-10 | 2014-10-01 | 한국화학연구원 | N2,N4-bis(4-(piperazin-1-yl)phenyl)pyrimidine-2,4-diamine derivatives or pharmaceutically acceptable salt thereof, and pharmaceutical composition for the prevention or treatment of cancer containing the same as an active ingredient |
US9676756B2 (en) | 2012-10-08 | 2017-06-13 | Portola Pharmaceuticals, Inc. | Substituted pyrimidinyl kinase inhibitors |
US9758522B2 (en) | 2012-10-19 | 2017-09-12 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
CN105308033B (en) | 2013-03-14 | 2018-08-24 | 特雷罗药物股份有限公司 | JAK2 and ALK2 inhibitor and its application method |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
AU2014337122B2 (en) | 2013-10-18 | 2019-01-03 | Dana-Farber Cancer Institute, Inc. | Heteroaromatic compounds useful for the treatment of proliferative diseases |
EP3057956B1 (en) | 2013-10-18 | 2021-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
WO2016022460A1 (en) | 2014-08-03 | 2016-02-11 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Potent dual brd4-kinase inhibitors as cancer therapeutics |
CA2972239A1 (en) | 2014-12-23 | 2016-06-30 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
JP6861166B2 (en) | 2015-03-27 | 2021-04-21 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | Inhibitor of cyclin-dependent kinase |
WO2017044858A2 (en) | 2015-09-09 | 2017-03-16 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
WO2017066428A1 (en) | 2015-10-13 | 2017-04-20 | H. Lee Moffitt Cancer Center & Research Institute, Inc. | Brd4-kinase inhibitors as cancer therapeutics |
WO2019000682A1 (en) | 2017-06-30 | 2019-01-03 | 北京泰德制药股份有限公司 | Rho-associated protein kinase inhibitor, pharmaceutical composition containing rho-associated protein kinase inhibitor, preparation method and use of the pharmaceutical composition |
US10323023B2 (en) | 2017-06-30 | 2019-06-18 | Beijing Tide Pharmaceutical Co., Ltd. | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof |
CN117343049A (en) | 2017-06-30 | 2024-01-05 | 北京泰德制药股份有限公司 | Rho-related protein kinase inhibitor, pharmaceutical composition containing Rho-related protein kinase inhibitor, and preparation method and application of Rho-related protein kinase inhibitor |
CN109776522B (en) * | 2017-10-30 | 2020-12-29 | 广东东阳光药业有限公司 | Substituted heteroaryl compounds, compositions and uses thereof |
CN112533602A (en) | 2018-04-05 | 2021-03-19 | 大日本住友制药肿瘤公司 | AXL kinase inhibitors and uses thereof |
AU2019252793A1 (en) | 2018-04-13 | 2020-10-15 | Sumitomo Pharma Oncology, Inc. | PIM kinase inhibitors for treatment of myeloproliferative neoplasms and fibrosis associated with cancer |
WO2020006724A1 (en) * | 2018-07-05 | 2020-01-09 | 清华大学 | Compound for targeted degradation of fak protein and use thereof |
CN112512597A (en) | 2018-07-26 | 2021-03-16 | 大日本住友制药肿瘤公司 | Methods for treating diseases associated with aberrant ACVR1 expression and ACVR1 inhibitors useful therefor |
CN111362922A (en) * | 2018-12-26 | 2020-07-03 | 上海喆邺生物科技有限公司 | 2, 4-diaminopyrimidine derivatives and their use |
WO2020167990A1 (en) | 2019-02-12 | 2020-08-20 | Tolero Pharmaceuticals, Inc. | Formulations comprising heterocyclic protein kinase inhibitors |
CN114105887B (en) * | 2021-09-16 | 2023-12-01 | 沈阳药科大学 | Aminopyrimidine derivative and preparation method and application thereof |
WO2024097653A1 (en) | 2022-10-31 | 2024-05-10 | Sumitomo Pharma America, Inc. | Pim1 inhibitor for treating myeloproliferative neoplasms |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997019065A1 (en) * | 1995-11-20 | 1997-05-29 | Celltech Therapeutics Limited | Substituted 2-anilinopyrimidines useful as protein kinase inhibitors |
WO2000039101A1 (en) * | 1998-12-24 | 2000-07-06 | Astrazeneca Ab | Pyrimidine compounds |
WO2001064656A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | 2,4,di(hetero-)arylamino(-oxy)-5-substituted pyrimidines as antineoplastic agents |
WO2001064655A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | 2, 4-di(hetero-)arylamino (-oxy)-5-substituted pyrimidines as antineoplastic agents |
WO2001064654A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | Pyrimidine compounds |
WO2003031406A2 (en) * | 2001-10-12 | 2003-04-17 | Irm Llc | Kinase inhibitor scaffolds and methods for their preparation |
WO2003032997A1 (en) * | 2001-10-17 | 2003-04-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Pyrimidine derivatives, pharmaceutical agent containing said compounds, use and method for making same |
WO2003040141A1 (en) * | 2001-09-28 | 2003-05-15 | Bayer Pharmaceuticals Corporation | Oxazolyl-phenyl-2,4-diamino-pyrimidine compounds and methods for treating hyperproliferative disorders |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW225528B (en) * | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
US5543520A (en) * | 1993-10-01 | 1996-08-06 | Ciba-Geigy Corporation | Pyrimidine derivatives |
-
2003
- 2003-05-02 WO PCT/US2003/013604 patent/WO2003095448A1/en not_active Application Discontinuation
- 2003-05-02 AU AU2003231231A patent/AU2003231231A1/en not_active Abandoned
- 2003-05-06 AU AU2003299474A patent/AU2003299474A1/en not_active Abandoned
- 2003-05-06 WO PCT/US2003/014294 patent/WO2004046118A2/en not_active Application Discontinuation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997019065A1 (en) * | 1995-11-20 | 1997-05-29 | Celltech Therapeutics Limited | Substituted 2-anilinopyrimidines useful as protein kinase inhibitors |
WO2000039101A1 (en) * | 1998-12-24 | 2000-07-06 | Astrazeneca Ab | Pyrimidine compounds |
WO2001064656A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | 2,4,di(hetero-)arylamino(-oxy)-5-substituted pyrimidines as antineoplastic agents |
WO2001064655A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | 2, 4-di(hetero-)arylamino (-oxy)-5-substituted pyrimidines as antineoplastic agents |
WO2001064654A1 (en) * | 2000-03-01 | 2001-09-07 | Astrazeneca Ab | Pyrimidine compounds |
WO2003040141A1 (en) * | 2001-09-28 | 2003-05-15 | Bayer Pharmaceuticals Corporation | Oxazolyl-phenyl-2,4-diamino-pyrimidine compounds and methods for treating hyperproliferative disorders |
WO2003031406A2 (en) * | 2001-10-12 | 2003-04-17 | Irm Llc | Kinase inhibitor scaffolds and methods for their preparation |
WO2003032997A1 (en) * | 2001-10-17 | 2003-04-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Pyrimidine derivatives, pharmaceutical agent containing said compounds, use and method for making same |
Non-Patent Citations (3)
Title |
---|
DING ET AL: "A Combinatorial Scaffold Approach toward Kinase-Directed Heterocycle Libraries", 2 February 2002, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, PAGE(S) 1594-1596, ISSN: 0002-7863, XP002210160 * |
GHOSH D: "2,4-BIS(ARYLAMINO)-6-METHYL PYRIMIDINES AS ANTIMICROBIAL AGENTS", JOURNAL OF THE INDIAN CHEMICAL SOCIETY, THE INDIAN CHEMICAL SOCIETY, CALCUTTA, IN, vol. 58, no. 5, May 1981 (1981-05-01), pages 512 - 513, XP000918018, ISSN: 0019-4522 * |
GHOSH, D.; MUKHERJEE,M.: "2,4-Bis(arylamino)-5-methylpyrimidines as Antimicrobial Agents", J. MED. CHEM., vol. 10, 1967, pages 974 - 975, XP002281234 * |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9913842B2 (en) | 2002-02-01 | 2018-03-13 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US9018204B1 (en) | 2002-02-01 | 2015-04-28 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US9416112B2 (en) | 2002-02-01 | 2016-08-16 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US9346765B2 (en) | 2002-02-01 | 2016-05-24 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US8835430B2 (en) | 2002-02-01 | 2014-09-16 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
US8557806B2 (en) | 2002-07-29 | 2013-10-15 | Rigel Pharmaceuticals, Inc. | Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds |
US8476263B2 (en) | 2005-01-19 | 2013-07-02 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US8785437B2 (en) | 2005-01-19 | 2014-07-22 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US7989448B2 (en) | 2005-01-19 | 2011-08-02 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US9532998B2 (en) | 2005-01-19 | 2017-01-03 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US8211889B2 (en) | 2005-01-19 | 2012-07-03 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US8211888B2 (en) | 2005-01-19 | 2012-07-03 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US9266912B2 (en) | 2005-01-19 | 2016-02-23 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
US9248190B2 (en) | 2005-06-08 | 2016-02-02 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the JAK pathway |
US8604042B2 (en) | 2005-11-01 | 2013-12-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
US8785692B2 (en) | 2007-03-12 | 2014-07-22 | Bayer Cropscience Ag | Substituted phenylamidines and the use thereof as fungicides |
US8952027B2 (en) | 2008-04-16 | 2015-02-10 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
US9579320B2 (en) | 2008-04-16 | 2017-02-28 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
US9012462B2 (en) | 2008-05-21 | 2015-04-21 | Ariad Pharmaceuticals, Inc. | Phosphorous derivatives as kinase inhibitors |
US9359308B2 (en) | 2011-11-23 | 2016-06-07 | Portola Pharmaceuticals, Inc. | Pyrazine kinase inhibitors |
JP7202315B2 (en) | 2017-05-26 | 2023-01-11 | キャンサー・リサーチ・テクノロジー・リミテッド | BCL6 inhibitors derived from benzimidazolones |
Also Published As
Publication number | Publication date |
---|---|
WO2003095448A1 (en) | 2003-11-20 |
WO2004046118A2 (en) | 2004-06-03 |
AU2003231231A1 (en) | 2003-11-11 |
AU2003299474A8 (en) | 2004-06-15 |
AU2003299474A1 (en) | 2004-06-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2004046118A3 (en) | 2-4-(di-phenyl-amino)-pyrimidine derivatives useful for treating hyper-proliferative disorders | |
WO2003097614A3 (en) | Process for the preparation of rosuvastatin | |
WO2005033072A3 (en) | Heterocyclic amides and sulfonamides | |
WO2004018457A8 (en) | Pyrrolidinedione substituted piperidine-phthalazones as pde4 inhibitors | |
WO2004013120A8 (en) | Novel benzodioxoles | |
WO2004018449A8 (en) | Piperidine-derivatives as pde4 inhibitors | |
WO2004035569A3 (en) | Novel compounds with antibacterial activity | |
WO2001019828A3 (en) | Kinase inhibitors as therapeutic agents | |
WO2006013095A3 (en) | Condensed pyridines as kinase inhibitors | |
WO2005074603A3 (en) | Aminobenzoxazoles as therapeutic agents | |
BR0308461A (en) | Pyrimidine Derivatives | |
CA2506441A1 (en) | 5-substituted-pyrazine or pyridine glucokinase activators | |
NO20054404L (en) | 5,7-Diaminopyrazolo [4,3-D] Pyrimidines Useful in the Treatment of Hypertension | |
BR0210030A (en) | Phenylpyridinecarbonylpiperazine derivative | |
WO2001023390A3 (en) | Azepinoindole derivatives, the production and use thereof | |
IS6902A (en) | Non-aryl N-substituted heterocyclic NMDA / NR2B antagonists | |
NO20071642L (en) | N-Benzenesulfonyl-substituted anilino-pyrimidine analogs | |
WO2004013131A3 (en) | Pyridines and pyrimidines substituted by 4-trifluoromethylpyrazolyl | |
NZ594385A (en) | Aminopyrimidines useful as kinase inhibitors | |
IL174217A0 (en) | 2,4 di (hetero)- arylamino-pyrimidine derivatives as zap-70 and/or syk inhibitors | |
AUPS019702A0 (en) | Condensed heterocyclic compounds | |
WO2005009345A3 (en) | 2-desmethyl ansamycin compounds | |
WO2004022540A3 (en) | Pyridazinone and pyridone derivatives as adenosine antagonists | |
DE60207104D1 (en) | 2-AMINO-4-HETEROARYLETHYL-THIAZOLINE DERIVATIVES AND THEIR USE AS INDUCIBLE NO-SYNTHASE INHIBITORS | |
ZA200306121B (en) | Crystal of pyrimidine nucleoside derivative |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
122 | Ep: pct application non-entry in european phase | ||
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |