WO2007076460A3 - Substituted thiazole ureas useful as inhibitors of protein kinases - Google Patents
Substituted thiazole ureas useful as inhibitors of protein kinases Download PDFInfo
- Publication number
- WO2007076460A3 WO2007076460A3 PCT/US2006/062524 US2006062524W WO2007076460A3 WO 2007076460 A3 WO2007076460 A3 WO 2007076460A3 US 2006062524 W US2006062524 W US 2006062524W WO 2007076460 A3 WO2007076460 A3 WO 2007076460A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitors
- protein kinases
- substituted thiazole
- ureas useful
- present
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- 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
- C07D417/02—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 two hetero rings
- C07D417/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
- C07D413/02—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
-
- 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
- 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
Abstract
The present invention relates to compounds and methods useful as inhibitors of protein kinases, including B-Raf and several receptor tyrosine and cytoplasmic tyrosine kinases. The present invention is directed to new substituted pyrimidinyloxy urea compounds of Formula (I) and compositions and their application as pharmaceuticals for the treatment of disease. Methods of modulating of protein kinase activity in a human or animal subject are also provided for the treatment diseases such as cancers.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75348805P | 2005-12-23 | 2005-12-23 | |
US60/753,488 | 2005-12-23 | ||
US85150406P | 2006-10-13 | 2006-10-13 | |
US60/851,504 | 2006-10-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007076460A2 WO2007076460A2 (en) | 2007-07-05 |
WO2007076460A3 true WO2007076460A3 (en) | 2007-08-16 |
Family
ID=38042636
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/062524 WO2007076460A2 (en) | 2005-12-23 | 2006-12-21 | Substituted thiazole ureas useful as inhibitors of protein kinases |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2007076460A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9278962B2 (en) | 2011-04-22 | 2016-03-08 | Cytokinetics, Inc. | Certain heterocycles, compositions thereof, and methods for their use |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CL2009000447A1 (en) | 2008-02-29 | 2010-01-04 | Array Biopharma Inc Y Genentech Inc | Compounds derived from (1h-pyrrolo {2,3-b} pyridin-5-yl) -sulfonamido-substituted benzamide; preparation procedure; pharmaceutical composition; and its use in the treatment of cancer, through the inhibition of raf. |
MX2010009411A (en) | 2008-02-29 | 2010-11-30 | Array Biopharma Inc | Pyrazole [3, 4-b] pyridine raf inhibitors. |
AR081331A1 (en) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | AMINO- PYRIMIDINES COMPOSITIONS OF THE SAME AND METHODS FOR THE USE OF THE SAME |
AR081626A1 (en) | 2010-04-23 | 2012-10-10 | Cytokinetics Inc | AMINO-PYRIDAZINIC COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE OF THE SAME TO TREAT CARDIAC AND SKELETIC MUSCULAR DISORDERS |
EP2560488B1 (en) | 2010-04-23 | 2015-10-28 | Cytokinetics, Inc. | Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use |
CN103965182A (en) * | 2014-05-22 | 2014-08-06 | 遵义医学院 | Medicament of 1,3,4-oxadiazole containing pyrazole compound prepared for treating tumor |
CN109060764B (en) * | 2018-08-23 | 2020-12-29 | 安徽中科赛飞尔科技有限公司 | Preparation method of functionalized SERS platform and application of functionalized SERS platform in ATP detection |
CN109134451A (en) * | 2018-09-10 | 2019-01-04 | 遵义医学院 | 1,3- 2-substituted carbamide class and thiourea derivatives and its application |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4135312A1 (en) * | 1990-10-25 | 1992-04-30 | Fuji Photo Film Co Ltd | COLOR PHOTOGRAPHIC SILVER HALOGENIDE MATERIAL |
WO1999032111A1 (en) * | 1997-12-22 | 1999-07-01 | Bayer Corporation | INHIBITION OF p38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS |
WO1999032106A1 (en) * | 1997-12-22 | 1999-07-01 | Bayer Corporation | Inhibition of raf kinase using substituted heterocyclic ureas |
WO2004014903A1 (en) * | 2002-08-02 | 2004-02-19 | Ab Science | 2-(3-aminoaryl)amino-4-aryl-thiazoles and their use as c-kit inhibitors |
WO2005000298A2 (en) * | 2003-06-03 | 2005-01-06 | Novartis Ag | 5-membered heterocycle-based p-38 inhibitors |
WO2005040139A2 (en) * | 2003-10-23 | 2005-05-06 | Ab Science | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
WO2006064375A2 (en) * | 2004-12-16 | 2006-06-22 | Ab Science | Aminoaryl substituted five-membered ring heterocyclic compounds for the treatment of diseases |
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2006
- 2006-12-21 WO PCT/US2006/062524 patent/WO2007076460A2/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4135312A1 (en) * | 1990-10-25 | 1992-04-30 | Fuji Photo Film Co Ltd | COLOR PHOTOGRAPHIC SILVER HALOGENIDE MATERIAL |
WO1999032111A1 (en) * | 1997-12-22 | 1999-07-01 | Bayer Corporation | INHIBITION OF p38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS |
WO1999032106A1 (en) * | 1997-12-22 | 1999-07-01 | Bayer Corporation | Inhibition of raf kinase using substituted heterocyclic ureas |
WO2004014903A1 (en) * | 2002-08-02 | 2004-02-19 | Ab Science | 2-(3-aminoaryl)amino-4-aryl-thiazoles and their use as c-kit inhibitors |
WO2005000298A2 (en) * | 2003-06-03 | 2005-01-06 | Novartis Ag | 5-membered heterocycle-based p-38 inhibitors |
WO2005040139A2 (en) * | 2003-10-23 | 2005-05-06 | Ab Science | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
WO2006064375A2 (en) * | 2004-12-16 | 2006-06-22 | Ab Science | Aminoaryl substituted five-membered ring heterocyclic compounds for the treatment of diseases |
Non-Patent Citations (5)
Title |
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"Interchim Intermediates", 18 January 2005, INTERCHIM, 211 BIS J.F. KENNEDY, BP 1140, MONTLUCON, 03103, FRANCE * |
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 1940, FISCHER, HANS ET AL: "Bile pigments. XXVII. Synthesis of 4,4'-dimethyl-3,3'-diethyl-5,5'- diaminopyrromethenes", XP002434967, retrieved from STN Database accession no. 1940:10545 * |
DATABASE CHEMCATS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 18 January 2005 (2005-01-18), XP002434966, retrieved from STN Database accession no. 2005:1023349 * |
DATABASE REGISTRY [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 21 December 1991 (1991-12-21), XP002434965, retrieved from STN Database accession no. 138050-39-2 * |
Z. PHYSIOL. CHEM. , 262, 37-46, 1939 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9278962B2 (en) | 2011-04-22 | 2016-03-08 | Cytokinetics, Inc. | Certain heterocycles, compositions thereof, and methods for their use |
Also Published As
Publication number | Publication date |
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WO2007076460A2 (en) | 2007-07-05 |
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