KR20060089232A - 치환 벤자졸 및 raf 키나제의 억제제로서 그들의 사용 - Google Patents
치환 벤자졸 및 raf 키나제의 억제제로서 그들의 사용 Download PDFInfo
- Publication number
- KR20060089232A KR20060089232A KR1020067006470A KR20067006470A KR20060089232A KR 20060089232 A KR20060089232 A KR 20060089232A KR 1020067006470 A KR1020067006470 A KR 1020067006470A KR 20067006470 A KR20067006470 A KR 20067006470A KR 20060089232 A KR20060089232 A KR 20060089232A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- substituted
- methyl
- amino
- unsubstituted
- 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.)
- Ceased
Links
- 0 Bc1cc(NC(*2C)=Nc3c2ccc(Oc2cc(C(NC)=O)ncc2)c3)ccc1N Chemical compound Bc1cc(NC(*2C)=Nc3c2ccc(Oc2cc(C(NC)=O)ncc2)c3)ccc1N 0.000 description 5
- QLULGIRFKAWHOJ-UHFFFAOYSA-N OB(c1ccncc1)O Chemical compound OB(c1ccncc1)O QLULGIRFKAWHOJ-UHFFFAOYSA-N 0.000 description 2
- LGTOBOCIVPDCTA-UHFFFAOYSA-N Bc(c(C)c1)ccc1Nc1nc(C=C(C(C)C2)Oc3cc(CO)ncc3)c2[n]1C Chemical compound Bc(c(C)c1)ccc1Nc1nc(C=C(C(C)C2)Oc3cc(CO)ncc3)c2[n]1C LGTOBOCIVPDCTA-UHFFFAOYSA-N 0.000 description 1
- ODRLCTONCNSRBQ-UHFFFAOYSA-N CC(C)(C)OC(N(CC(N1C)=O)CC1=O)=O Chemical compound CC(C)(C)OC(N(CC(N1C)=O)CC1=O)=O ODRLCTONCNSRBQ-UHFFFAOYSA-N 0.000 description 1
- CJDYFMIDIQXELO-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(C)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(C)CC1)=O CJDYFMIDIQXELO-UHFFFAOYSA-N 0.000 description 1
- WMZHGAPKYJUAFH-UHFFFAOYSA-N CC(C)c1cc(Nc2nc(cc(cc3)Oc4ccnc(C(Nc5cc(C(C)(C)C)ccc5)=O)c4)c3[n]2C)ccc1 Chemical compound CC(C)c1cc(Nc2nc(cc(cc3)Oc4ccnc(C(Nc5cc(C(C)(C)C)ccc5)=O)c4)c3[n]2C)ccc1 WMZHGAPKYJUAFH-UHFFFAOYSA-N 0.000 description 1
- CLPZHEDSMNQBPP-UHFFFAOYSA-N CC1NC(C)CN(C)C1 Chemical compound CC1NC(C)CN(C)C1 CLPZHEDSMNQBPP-UHFFFAOYSA-N 0.000 description 1
- MIQPSMRKRPYFOB-UHFFFAOYSA-N CCN(CCO1)CC1/[O]=C1\N(C)CCCCC1 Chemical compound CCN(CCO1)CC1/[O]=C1\N(C)CCCCC1 MIQPSMRKRPYFOB-UHFFFAOYSA-N 0.000 description 1
- KWCVYUHZCVVARZ-UHFFFAOYSA-N CCc1cccc(NC(c2cc(Oc(cc3)cc4c3[n](C)c(Nc(cc3)ccc3Br)n4)ccn2)=O)c1 Chemical compound CCc1cccc(NC(c2cc(Oc(cc3)cc4c3[n](C)c(Nc(cc3)ccc3Br)n4)ccn2)=O)c1 KWCVYUHZCVVARZ-UHFFFAOYSA-N 0.000 description 1
- PREDVCVMQCMUDT-UHFFFAOYSA-N CN(C(CCC1N)=O)C1=O Chemical compound CN(C(CCC1N)=O)C1=O PREDVCVMQCMUDT-UHFFFAOYSA-N 0.000 description 1
- LAEXPJQUWCGDGC-UHFFFAOYSA-N CN(C(CNC1)=O)C1=O Chemical compound CN(C(CNC1)=O)C1=O LAEXPJQUWCGDGC-UHFFFAOYSA-N 0.000 description 1
- WRKUORHZZDCNMJ-UHFFFAOYSA-N CN(CC(N1CC(C(N2C)=O)OCC2=O)=O)CC1=O Chemical compound CN(CC(N1CC(C(N2C)=O)OCC2=O)=O)CC1=O WRKUORHZZDCNMJ-UHFFFAOYSA-N 0.000 description 1
- KOZRFVAOQYOQPI-UHFFFAOYSA-N CN(CC1)CCN1c(c(F)c1N)ccc1N Chemical compound CN(CC1)CCN1c(c(F)c1N)ccc1N KOZRFVAOQYOQPI-UHFFFAOYSA-N 0.000 description 1
- MJNGHBUJYPOPBE-UHFFFAOYSA-N CN1CC(CN2CCNCC2)OCC1 Chemical compound CN1CC(CN2CCNCC2)OCC1 MJNGHBUJYPOPBE-UHFFFAOYSA-N 0.000 description 1
- RXYPXQSKLGGKOL-UHFFFAOYSA-N CN1CCN(C)CC1 Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N CN1CCNCC1 Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- CDXLSMUOLYXICF-UHFFFAOYSA-N CNC(C(C1)[N+]([O-])=O)=CCC1Oc1ccnc(CO)c1 Chemical compound CNC(C(C1)[N+]([O-])=O)=CCC1Oc1ccnc(CO)c1 CDXLSMUOLYXICF-UHFFFAOYSA-N 0.000 description 1
- VTLQTHDJUGLYOA-UHFFFAOYSA-N CNC(c1cc(Oc(cc2)cc3c2[n](C)c(Nc2cc(-c4ccncc4)cc(F)c2OC)n3)ccn1)=O Chemical compound CNC(c1cc(Oc(cc2)cc3c2[n](C)c(Nc2cc(-c4ccncc4)cc(F)c2OC)n3)ccn1)=O VTLQTHDJUGLYOA-UHFFFAOYSA-N 0.000 description 1
- OJENAJAPLBHEKF-UHFFFAOYSA-N CNC(c1nccc(Oc(cc2)cc3c2[n](C)c(Nc2ccccc2I)n3)c1)=O Chemical compound CNC(c1nccc(Oc(cc2)cc3c2[n](C)c(Nc2ccccc2I)n3)c1)=O OJENAJAPLBHEKF-UHFFFAOYSA-N 0.000 description 1
- JOVTVEXJZXHXMT-UHFFFAOYSA-N CNC(c1nccc(Oc(cc2)cc3c2[n](C)c(Nc2ccccc2Sc2ccccc2)n3)c1)=O Chemical compound CNC(c1nccc(Oc(cc2)cc3c2[n](C)c(Nc2ccccc2Sc2ccccc2)n3)c1)=O JOVTVEXJZXHXMT-UHFFFAOYSA-N 0.000 description 1
- WDGQHUSWMGRXAC-NVMNQCDNSA-N CNc(c(N)c1)ccc1Oc1ccnc(/C=N\OC)c1 Chemical compound CNc(c(N)c1)ccc1Oc1ccnc(/C=N\OC)c1 WDGQHUSWMGRXAC-NVMNQCDNSA-N 0.000 description 1
- XQAZZUSVBUUVDS-UHFFFAOYSA-N CNc(c(N)c1)ccc1Oc1ccnc(CO)c1 Chemical compound CNc(c(N)c1)ccc1Oc1ccnc(CO)c1 XQAZZUSVBUUVDS-UHFFFAOYSA-N 0.000 description 1
- FEOLZZVRQKERDR-PXNMLYILSA-N CNc(ccc(Oc1cc(/C=N\O)ncc1)c1)c1[N+]([O-])=O Chemical compound CNc(ccc(Oc1cc(/C=N\O)ncc1)c1)c1[N+]([O-])=O FEOLZZVRQKERDR-PXNMLYILSA-N 0.000 description 1
- WTWNAWPQCMHEGE-UHFFFAOYSA-N CNc(ccc(Oc1cc(C=O)ncc1)c1)c1[N+]([O-])=O Chemical compound CNc(ccc(Oc1cc(C=O)ncc1)c1)c1[N+]([O-])=O WTWNAWPQCMHEGE-UHFFFAOYSA-N 0.000 description 1
- IRAJTRFSBJFFGT-UHFFFAOYSA-N COc(c(N)cc(Br)c1)c1F Chemical compound COc(c(N)cc(Br)c1)c1F IRAJTRFSBJFFGT-UHFFFAOYSA-N 0.000 description 1
- OZTHAIFCHYWJBM-UHFFFAOYSA-N C[O](c(c([N+]([O-])=O)cc(Br)c1)c1F)I Chemical compound C[O](c(c([N+]([O-])=O)cc(Br)c1)c1F)I OZTHAIFCHYWJBM-UHFFFAOYSA-N 0.000 description 1
- MIJTWRNGPSSNPA-UHFFFAOYSA-N C[n]1c(Nc(cc2)ccc2SC(F)(F)F)nc2cc(Oc3cc(C(NCCCN(CCC4)C4=O)=O)ncc3)ccc12 Chemical compound C[n]1c(Nc(cc2)ccc2SC(F)(F)F)nc2cc(Oc3cc(C(NCCCN(CCC4)C4=O)=O)ncc3)ccc12 MIJTWRNGPSSNPA-UHFFFAOYSA-N 0.000 description 1
- YZZQVNCYKMPCPO-ZRGSRPPYSA-N C[n]1c(Nc2ccc(C(F)(F)F)cc2)nc2c1ccc(Oc1cc(/C=N\O)ncc1)c2 Chemical compound C[n]1c(Nc2ccc(C(F)(F)F)cc2)nc2c1ccc(Oc1cc(/C=N\O)ncc1)c2 YZZQVNCYKMPCPO-ZRGSRPPYSA-N 0.000 description 1
- NMXMFJJNQWLAQV-UHFFFAOYSA-N C[n]1c(Nc2cccc(I)c2)nc2c1ccc(O)c2 Chemical compound C[n]1c(Nc2cccc(I)c2)nc2c1ccc(O)c2 NMXMFJJNQWLAQV-UHFFFAOYSA-N 0.000 description 1
- TUVXPFIKWFDPQB-UHFFFAOYSA-N Cc(c(-c1c[o]cc1)c1)ccc1[N+]([O-])=O Chemical compound Cc(c(-c1c[o]cc1)c1)ccc1[N+]([O-])=O TUVXPFIKWFDPQB-UHFFFAOYSA-N 0.000 description 1
- XFZFJQHXWJIBQV-UHFFFAOYSA-N Cc(c(Br)c1)ccc1[N+]([O-])=O Chemical compound Cc(c(Br)c1)ccc1[N+]([O-])=O XFZFJQHXWJIBQV-UHFFFAOYSA-N 0.000 description 1
- DIPGYZSCGXBTEU-UHFFFAOYSA-N Nc(c(F)c(cc1)F)c1[N+]([O-])=O Chemical compound Nc(c(F)c(cc1)F)c1[N+]([O-])=O DIPGYZSCGXBTEU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
-
- 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
-
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Ceramic Engineering (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/675,927 | 2003-09-29 | ||
| US10/675,927 US8299108B2 (en) | 2002-03-29 | 2003-09-29 | Substituted benzazoles and methods of their use as inhibitors of raf kinase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20060089232A true KR20060089232A (ko) | 2006-08-08 |
Family
ID=34422104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020067006470A Ceased KR20060089232A (ko) | 2003-09-29 | 2004-09-29 | 치환 벤자졸 및 raf 키나제의 억제제로서 그들의 사용 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US8299108B2 (https=) |
| EP (1) | EP1675584A1 (https=) |
| JP (1) | JP2007507428A (https=) |
| KR (1) | KR20060089232A (https=) |
| CN (1) | CN1913884A (https=) |
| AU (1) | AU2004277405A1 (https=) |
| BR (1) | BRPI0414908A (https=) |
| CA (1) | CA2539748A1 (https=) |
| EA (1) | EA011890B1 (https=) |
| IL (1) | IL174431A0 (https=) |
| MX (1) | MXPA06003435A (https=) |
| WO (1) | WO2005032548A1 (https=) |
| ZA (1) | ZA200603418B (https=) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1158985B1 (en) | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| ME00275B (me) | 1999-01-13 | 2011-02-10 | Bayer Corp | ω-KARBOKSIARIL SUPSTITUISANI DIFENIL KARBAMIDI KAO INHIBITORI RAF KINAZE |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| WO2003068229A1 (en) | 2002-02-11 | 2003-08-21 | Bayer Pharmaceuticals Corporation | Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors |
| SI1478358T1 (sl) | 2002-02-11 | 2013-09-30 | Bayer Healthcare Llc | Sorafenib tozilat za zdravljenje bolezni, značilnih po abnormalni angiogenezi |
| WO2003082272A1 (en) * | 2002-03-29 | 2003-10-09 | Chiron Corporation | Substituted benzazoles and use thereof as raf kinase inhibitors |
| US7557129B2 (en) | 2003-02-28 | 2009-07-07 | Bayer Healthcare Llc | Cyanopyridine derivatives useful in the treatment of cancer and other disorders |
| CA2526285A1 (en) | 2003-05-15 | 2004-12-23 | Arqule, Inc. | Inhibitors of p38 and methods of using the same |
| EP1636585B2 (en) | 2003-05-20 | 2012-06-13 | Bayer HealthCare LLC | Diaryl ureas with kinase inhibiting activity |
| EP1663978B1 (en) | 2003-07-23 | 2007-11-28 | Bayer Pharmaceuticals Corporation | Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
| KR20060118472A (ko) * | 2003-10-16 | 2006-11-23 | 카이론 코포레이션 | 치환 벤자졸 및 raf 키나아제의 저해제로서 그것의 사용 |
| WO2006010082A1 (en) * | 2004-07-08 | 2006-01-26 | Arqule, Inc. | 1,4-disubstituted naphtalenes as inhibitors of p38 map kinase |
| EP2258704A1 (en) * | 2004-10-19 | 2010-12-08 | ArQule, Inc. | Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase |
| US7429608B2 (en) * | 2005-01-20 | 2008-09-30 | Amgen Inc. | Benzo[d]imidazol analogs as vanilloid receptor ligands and their use in treatments |
| TWI370820B (en) * | 2005-04-27 | 2012-08-21 | Takeda Pharmaceutical | Fused heterocyclic compounds |
| TWI387592B (zh) * | 2005-08-30 | 2013-03-01 | Novartis Ag | 經取代之苯并咪唑及其作為與腫瘤形成相關激酶之抑制劑之方法 |
| WO2007047397A2 (en) * | 2005-10-13 | 2007-04-26 | Smithkline Beecham Corporation | Phenol ethers as modulators of the opioid receptors |
| CN101379060B (zh) * | 2006-02-10 | 2012-05-23 | 转化技术制药公司 | 作为Aurora激酶抑制剂的苯并唑系衍生物、组合物和使用方法 |
| CA2649288C (en) | 2006-04-19 | 2015-11-24 | Novartis Ag | 6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling |
| PT2046292E (pt) | 2006-07-21 | 2010-04-26 | Novartis Ag | Formulações de éteres benzimidazolil-piridílicos |
| PE20130814A1 (es) | 2006-08-30 | 2013-08-08 | Novartis Ag | Sales de benzimidazolil piridil eteres y formulaciones que las contienen |
| JP5294419B2 (ja) * | 2007-04-05 | 2013-09-18 | 第一三共株式会社 | 縮合二環式ヘテロアリール誘導体 |
| CL2008001626A1 (es) | 2007-06-05 | 2009-06-05 | Takeda Pharmaceuticals Co | Compuestos derivados de heterociclos fusionados, agente farmaceutico que los comprende y su uso en la profilaxis y tratamiento del cancer. |
| EP2181987B9 (en) | 2007-08-23 | 2014-09-03 | Takeda Pharmaceutical Company Limited | 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer |
| JP5350247B2 (ja) * | 2007-08-29 | 2013-11-27 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| EP2573087A1 (en) | 2007-09-21 | 2013-03-27 | Array Biopharma, Inc. | Pyridin-2-yl-amino-1,2,4-thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus |
| BRPI0818003A2 (pt) * | 2007-10-18 | 2019-09-24 | Novartis Ag | inibidores de csf-1r, composições e métodos de uso |
| US8697874B2 (en) * | 2008-12-01 | 2014-04-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| JO3101B1 (ar) | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | مشتقات بنزوثيازول كعوامل مضادة للسرطان |
| EP2361254A1 (en) * | 2008-12-05 | 2011-08-31 | ArQule, Inc. | Raf inhibitors and their uses |
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- 2004-09-29 WO PCT/US2004/032161 patent/WO2005032548A1/en not_active Ceased
- 2004-09-29 JP JP2006528331A patent/JP2007507428A/ja not_active Withdrawn
- 2004-09-29 EP EP04789345A patent/EP1675584A1/en not_active Withdrawn
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- 2004-09-29 CN CNA2004800326778A patent/CN1913884A/zh active Pending
- 2004-09-29 MX MXPA06003435A patent/MXPA06003435A/es not_active Application Discontinuation
- 2004-09-29 KR KR1020067006470A patent/KR20060089232A/ko not_active Ceased
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| EA011890B1 (ru) | 2009-06-30 |
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| US20040122237A1 (en) | 2004-06-24 |
| IL174431A0 (en) | 2006-08-01 |
| MXPA06003435A (es) | 2006-06-20 |
| CN1913884A (zh) | 2007-02-14 |
| JP2007507428A (ja) | 2007-03-29 |
| AU2004277405A1 (en) | 2005-04-14 |
| US8299108B2 (en) | 2012-10-30 |
| EA200600689A1 (ru) | 2006-08-25 |
| BRPI0414908A (pt) | 2006-11-07 |
| ZA200603418B (en) | 2007-07-25 |
| US20120288501A1 (en) | 2012-11-15 |
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