JP5345842B2 - プロテインキナーゼモジュレーターとしてのピラゾール誘導体を含む医薬組み合わせ - Google Patents
プロテインキナーゼモジュレーターとしてのピラゾール誘導体を含む医薬組み合わせ Download PDFInfo
- Publication number
- JP5345842B2 JP5345842B2 JP2008517594A JP2008517594A JP5345842B2 JP 5345842 B2 JP5345842 B2 JP 5345842B2 JP 2008517594 A JP2008517594 A JP 2008517594A JP 2008517594 A JP2008517594 A JP 2008517594A JP 5345842 B2 JP5345842 B2 JP 5345842B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- pyrazol
- chloro
- group
- compound
- 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.)
- Expired - Fee Related
Links
- 0 *c1c(*CC#N)c(*)n[n]1* Chemical compound *c1c(*CC#N)c(*)n[n]1* 0.000 description 3
- GCPKPHGBTLLUHL-UHFFFAOYSA-N Cc(c(B(O)O)c1)n[n]1[Tl] Chemical compound Cc(c(B(O)O)c1)n[n]1[Tl] GCPKPHGBTLLUHL-UHFFFAOYSA-N 0.000 description 2
- AXGLVLCXHQPFTN-CBMCFHRWSA-N B[C@]1(C2)[C@H]2CC(CCNC)CC1 Chemical compound B[C@]1(C2)[C@H]2CC(CCNC)CC1 AXGLVLCXHQPFTN-CBMCFHRWSA-N 0.000 description 1
- AYRCQEYIRSRBFV-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(c(cc1)ccc1O)c(cc1)ccc1Br)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(c(cc1)ccc1O)c(cc1)ccc1Br)=O AYRCQEYIRSRBFV-UHFFFAOYSA-N 0.000 description 1
- FKSHHLBULFBFLH-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(c(cc1)ccc1OCCOC)c(cc1)ccc1Br)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(c(cc1)ccc1OCCOC)c(cc1)ccc1Br)=O FKSHHLBULFBFLH-UHFFFAOYSA-N 0.000 description 1
- UEOKBPJBPRZSFX-BKTKXEPCSA-N CC(CC(CCO)C(C/C(/C)=C/N)C=C)C(C1)C1/C=C(\C)/C(F)(F)F Chemical compound CC(CC(CCO)C(C/C(/C)=C/N)C=C)C(C1)C1/C=C(\C)/C(F)(F)F UEOKBPJBPRZSFX-BKTKXEPCSA-N 0.000 description 1
- SPHZQQHZVLQDHI-ZCUYZDGTSA-N CCCC(C[C@@H](C)CC)O[C@@H](CCC/C(/[C@@H]1[C@H](C)CNCC1)=C/C)CCNC Chemical compound CCCC(C[C@@H](C)CC)O[C@@H](CCC/C(/[C@@H]1[C@H](C)CNCC1)=C/C)CCNC SPHZQQHZVLQDHI-ZCUYZDGTSA-N 0.000 description 1
- SQQRSCFZYOKDGC-IKGGRYGDSA-N CCC[C@@H](CC(C)C)O[C@@H](CCC[C@@H](C)Br)CCNC Chemical compound CCC[C@@H](CC(C)C)O[C@@H](CCC[C@@H](C)Br)CCNC SQQRSCFZYOKDGC-IKGGRYGDSA-N 0.000 description 1
- KKXWIPGWXBNDIZ-HTYVYXPBSA-N CCC[C@@H](CC(COC)Cl)[C@H]([C@H](C)CC[C@@H](C)CC)O Chemical compound CCC[C@@H](CC(COC)Cl)[C@H]([C@H](C)CC[C@@H](C)CC)O KKXWIPGWXBNDIZ-HTYVYXPBSA-N 0.000 description 1
- YVKDRFRYNWXLSP-WCNVDHFSSA-N CCC[C@@H](CCCC(CC)OC)C(CC1)C=CC1C1[C@@H](C)NNC1 Chemical compound CCC[C@@H](CCCC(CC)OC)C(CC1)C=CC1C1[C@@H](C)NNC1 YVKDRFRYNWXLSP-WCNVDHFSSA-N 0.000 description 1
- LYXZQUGNMPVGRS-UHFFFAOYSA-N CN(C)C(C(c(cc1)ccc1Cl)c(cc1)ccc1Cl)=O Chemical compound CN(C)C(C(c(cc1)ccc1Cl)c(cc1)ccc1Cl)=O LYXZQUGNMPVGRS-UHFFFAOYSA-N 0.000 description 1
- PGXISSZYSCYEQD-UHFFFAOYSA-N CN(C)CC(c(cc1)ccc1Cl)c(cc1)ccc1Cl Chemical compound CN(C)CC(c(cc1)ccc1Cl)c(cc1)ccc1Cl PGXISSZYSCYEQD-UHFFFAOYSA-N 0.000 description 1
- IGGFWLLVYRWCCO-UHFFFAOYSA-N CNC(C(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1-c1c[nH]nc1)=O Chemical compound CNC(C(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1-c1c[nH]nc1)=O IGGFWLLVYRWCCO-UHFFFAOYSA-N 0.000 description 1
- AXQWLYVOVYXKFB-UHFFFAOYSA-N CNC(C(c(cc1)ccc1Cl)c(cc1)ccc1Cl)=O Chemical compound CNC(C(c(cc1)ccc1Cl)c(cc1)ccc1Cl)=O AXQWLYVOVYXKFB-UHFFFAOYSA-N 0.000 description 1
- YCAFDYGANIWYNW-UHFFFAOYSA-N CNCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1N(C)C Chemical compound CNCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1N(C)C YCAFDYGANIWYNW-UHFFFAOYSA-N 0.000 description 1
- PAJNBJLDVKJXNX-UHFFFAOYSA-N CNCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1O Chemical compound CNCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1O PAJNBJLDVKJXNX-UHFFFAOYSA-N 0.000 description 1
- BLVZFJHSAUCMFX-UHFFFAOYSA-N CNCCC(c(cc1)ccc1-c1c[nH]nc1)c1cccc(Cl)c1 Chemical compound CNCCC(c(cc1)ccc1-c1c[nH]nc1)c1cccc(Cl)c1 BLVZFJHSAUCMFX-UHFFFAOYSA-N 0.000 description 1
- NZGWDNMCXFHPJD-UHFFFAOYSA-N CNS(c1cccc2c1ccnc2)(=O)=O Chemical compound CNS(c1cccc2c1ccnc2)(=O)=O NZGWDNMCXFHPJD-UHFFFAOYSA-N 0.000 description 1
- FGCYAZQVNZXMNP-UHFFFAOYSA-N COc(ccc(C(CCN)c(cc1)ccc1-c1c[nH]nc1)c1)c1Cl Chemical compound COc(ccc(C(CCN)c(cc1)ccc1-c1c[nH]nc1)c1)c1Cl FGCYAZQVNZXMNP-UHFFFAOYSA-N 0.000 description 1
- HPFUJWLGTWQWFZ-UHFFFAOYSA-N COc(ccc(C(c(cc1)ccc1Cl)N1CCNCC1)c1)c1Cl Chemical compound COc(ccc(C(c(cc1)ccc1Cl)N1CCNCC1)c1)c1Cl HPFUJWLGTWQWFZ-UHFFFAOYSA-N 0.000 description 1
- SYUVWZJEZRTOKR-UHFFFAOYSA-M Cc(c(-c1ccc(C(C(NC)=O)c(cc2)ccc2Cl)cc1)c1)n[n]1[Tl] Chemical compound Cc(c(-c1ccc(C(C(NC)=O)c(cc2)ccc2Cl)cc1)c1)n[n]1[Tl] SYUVWZJEZRTOKR-UHFFFAOYSA-M 0.000 description 1
- FCJYYASYFAJJRJ-UHFFFAOYSA-N Cc(c(-c1ccc(C2(CCNCC2)c(cc2)ccc2Cl)cc1)c1)n[n]1[Tl] Chemical compound Cc(c(-c1ccc(C2(CCNCC2)c(cc2)ccc2Cl)cc1)c1)n[n]1[Tl] FCJYYASYFAJJRJ-UHFFFAOYSA-N 0.000 description 1
- AAQFMGLCMDYAOZ-UHFFFAOYSA-N Cc1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1-c(nc1)ccc1C#N Chemical compound Cc1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1-c(nc1)ccc1C#N AAQFMGLCMDYAOZ-UHFFFAOYSA-N 0.000 description 1
- HBCQGNKMNRVLKJ-UHFFFAOYSA-N Cc1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1B(O)O Chemical compound Cc1n[n](C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1B(O)O HBCQGNKMNRVLKJ-UHFFFAOYSA-N 0.000 description 1
- HGJXGKHMXZTCMI-UHFFFAOYSA-N Clc1ccc(C(CNCC2CC2)c(cc2)ccc2-c2c[nH]nc2)cc1 Chemical compound Clc1ccc(C(CNCC2CC2)c(cc2)ccc2-c2c[nH]nc2)cc1 HGJXGKHMXZTCMI-UHFFFAOYSA-N 0.000 description 1
- HMEHLWUVHGJFIM-UHFFFAOYSA-N Clc1ccc(C2(CCNCC2)c(cc2)ccc2Br)cc1 Chemical compound Clc1ccc(C2(CCNCC2)c(cc2)ccc2Br)cc1 HMEHLWUVHGJFIM-UHFFFAOYSA-N 0.000 description 1
- HMEHLWUVHGJFIM-UHFFFAOYSA-O Clc1ccc(C2(CC[NH2+]CC2)c(cc2)ccc2Br)cc1 Chemical compound Clc1ccc(C2(CC[NH2+]CC2)c(cc2)ccc2Br)cc1 HMEHLWUVHGJFIM-UHFFFAOYSA-O 0.000 description 1
- NZKIKXUXRVDQAK-UHFFFAOYSA-N NC(CC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1Cl)=O Chemical compound NC(CC(c(cc1)ccc1-c1c[nH]nc1)c(cc1)ccc1Cl)=O NZKIKXUXRVDQAK-UHFFFAOYSA-N 0.000 description 1
- PIJOWNYIEJSLJS-UHFFFAOYSA-N OC(CC[n]1cncc1)c(cc1)ccc1Br Chemical compound OC(CC[n]1cncc1)c(cc1)ccc1Br PIJOWNYIEJSLJS-UHFFFAOYSA-N 0.000 description 1
- QNLXJYQUWCNYBH-UHFFFAOYSA-N OC1(CCNCC1)c(cc1)ccc1Br Chemical compound OC1(CCNCC1)c(cc1)ccc1Br QNLXJYQUWCNYBH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69330905P | 2005-06-23 | 2005-06-23 | |
| US69349205P | 2005-06-23 | 2005-06-23 | |
| US69336705P | 2005-06-23 | 2005-06-23 | |
| US69331405P | 2005-06-23 | 2005-06-23 | |
| US69331505P | 2005-06-23 | 2005-06-23 | |
| US60/693,315 | 2005-06-23 | ||
| US60/693,492 | 2005-06-23 | ||
| US60/693,314 | 2005-06-23 | ||
| US60/693,367 | 2005-06-23 | ||
| US60/693,309 | 2005-06-23 | ||
| PCT/GB2006/002297 WO2006136837A2 (en) | 2005-06-23 | 2006-06-21 | Pharmaceutical combinations comprising pyrazole derivatives as protein kinase modulators |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008546754A JP2008546754A (ja) | 2008-12-25 |
| JP2008546754A5 JP2008546754A5 (enExample) | 2009-08-06 |
| JP5345842B2 true JP5345842B2 (ja) | 2013-11-20 |
Family
ID=37453306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008517594A Expired - Fee Related JP5345842B2 (ja) | 2005-06-23 | 2006-06-21 | プロテインキナーゼモジュレーターとしてのピラゾール誘導体を含む医薬組み合わせ |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8541461B2 (enExample) |
| EP (1) | EP1933832A2 (enExample) |
| JP (1) | JP5345842B2 (enExample) |
| WO (1) | WO2006136837A2 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE400551T1 (de) | 2002-01-04 | 2008-07-15 | Neurosearch As | Kaliumkanal-modulatoren |
| HRP20100675T1 (hr) | 2003-12-23 | 2011-01-31 | Astex Therapeutics Limited | Derivati pirazola kao modulatori protein kinaze |
| EP1902032A1 (en) | 2005-06-22 | 2008-03-26 | Astex Therapeutics Limited | Pharmaceutical compounds |
| US8541461B2 (en) | 2005-06-23 | 2013-09-24 | Astex Therapeutics Limited | Pharmaceutical combinations comprising pyrazole derivatives as protein kinase modulators |
| US9839667B2 (en) | 2005-10-14 | 2017-12-12 | Allergan, Inc. | Prevention and treatment of ocular side effects with a cyclosporin |
| US7745400B2 (en) * | 2005-10-14 | 2010-06-29 | Gregg Feinerman | Prevention and treatment of ocular side effects with a cyclosporin |
| UY30892A1 (es) * | 2007-02-07 | 2008-09-02 | Smithkline Beckman Corp | Inhibidores de la actividad akt |
| EP2114388B1 (en) * | 2007-02-07 | 2015-05-20 | GlaxoSmithKline LLC | Inhibitors of akt activity |
| GB0704932D0 (en) * | 2007-03-14 | 2007-04-25 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| WO2009158374A2 (en) * | 2008-06-26 | 2009-12-30 | Smithkline Beecham Corporation | Inhibitors of akt activity |
| US8389731B2 (en) * | 2009-05-15 | 2013-03-05 | Northwestern University | Chiral pyrrolidine core compounds en route to inhibitors of nitric oxide synthase |
| US8809372B2 (en) | 2011-09-30 | 2014-08-19 | Asana Biosciences, Llc | Pyridine derivatives |
| US9199975B2 (en) | 2011-09-30 | 2015-12-01 | Asana Biosciences, Llc | Biaryl imidazole derivatives for regulating CYP17 |
| WO2015008221A1 (en) * | 2013-07-16 | 2015-01-22 | Dr. Reddy’S Laboratories Limited | Novel crystalline forms of pemetrexed tromethamine salts |
| LT3902547T (lt) | 2018-12-28 | 2024-01-25 | Deciphera Pharmaceuticals, Llc | Csf1r inhibitoriai, skirti panaudoti vėžio gydymui |
| WO2025122952A1 (en) | 2023-12-08 | 2025-06-12 | Deciphera Pharmaceuticals, Llc | Formulations of vimseltinib |
Family Cites Families (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2046628A1 (en) | 1989-02-08 | 1990-08-09 | Dee W. Brooks | 4-hydroxythiazoles as 5-lipoxygenase inhibitors |
| US5049570A (en) | 1990-01-23 | 1991-09-17 | Du Pont Merck Pharmaceutical Company | Pyridylphenyl nitrogen heterocycle-substituted carbinols and derivatives thereof with anti-inflammatory activity |
| FR2707295A1 (fr) | 1993-06-07 | 1995-01-13 | Rhone Poulenc Agrochimie | Fongicides pyrazoles substitués en position 3 par un hétérocycle. |
| US6756388B1 (en) | 1993-10-12 | 2004-06-29 | Pfizer Inc. | Benzothiophenes and related compounds as estrogen agonists |
| US5532356A (en) | 1995-06-06 | 1996-07-02 | The Dupont Merck Pharmaceutical Company | Method for preparing N,N'-disubstituted cyclic ureas |
| GB9512961D0 (en) | 1995-06-26 | 1995-08-30 | Pfizer Ltd | Antifungal agents |
| CA2249645A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| GB2314327B (en) | 1996-04-30 | 2000-07-12 | Kodak Ltd | Pyrazolone image dye-forming couplers |
| AR008789A1 (es) | 1996-07-31 | 2000-02-23 | Bayer Corp | Piridinas y bifenilos substituidos |
| WO1998025617A1 (en) | 1996-12-13 | 1998-06-18 | Merck & Co., Inc. | Substituted aryl piperazines as modulators of chemokine receptor activity |
| US6020357A (en) | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
| GB9700555D0 (en) | 1997-01-13 | 1997-03-05 | Merck Sharp & Dohme | Therapeutic agents |
| US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
| AU751139B2 (en) | 1997-10-13 | 2002-08-08 | Astellas Pharma Inc. | Amide derivative |
| CA2319465C (en) | 1998-01-29 | 2013-03-19 | Viropharma Incorporated | Compounds, compositions and methods for treating or preventing pneumovirus infection and associated diseases |
| GB9804734D0 (en) | 1998-03-05 | 1998-04-29 | Pfizer Ltd | Compounds |
| DE69935335T2 (de) | 1998-08-07 | 2007-11-22 | Novartis Vaccines and Diagnostics, Inc., Emeryville | Pyrazole als modulatoren des östrogenrezeptors |
| HN1999000149A (es) | 1998-09-09 | 2000-01-12 | Pfizer Prod Inc | Derivados de 4,4-biarilpiperidina |
| US6503905B1 (en) | 1998-12-29 | 2003-01-07 | Pfizer Inc | 3,3-biarylpiperidine and 2,2-biarylmorpholine derivatives |
| AU4308300A (en) | 1999-05-03 | 2000-11-17 | Dr. Reddy's Research Foundation | Pyrazoles having antiinflammatory activity |
| MXPA01011634A (es) | 1999-05-14 | 2002-07-30 | Neurocrine Biosciences Inc | Imidazo- y pirrolo [1,2-a]pirimid-4-onas como antagonistas receptores de la hormona liberadora de gonadotropina. |
| US6632815B2 (en) | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| DE60040676D1 (de) | 1999-09-17 | 2008-12-11 | Millennium Pharm Inc | BENZAMIDE UND ÄHNLICHE INHIBITOREN VON FAKTOR Xa |
| NZ517828A (en) | 1999-09-17 | 2003-10-31 | Millennium Pharm Inc | Inhibitors having activity against mammalian factor Xa |
| US7393842B2 (en) | 2001-08-31 | 2008-07-01 | University Of Connecticut | Pyrazole analogs acting on cannabinoid receptors |
| US6455525B1 (en) | 1999-11-04 | 2002-09-24 | Cephalon, Inc. | Heterocyclic substituted pyrazolones |
| CA2401778C (en) | 2000-02-29 | 2010-12-21 | Cor Therapeutics, Inc. | Benzamides and related inhibitors of factor xa |
| IL136458A0 (en) | 2000-05-30 | 2001-06-14 | Peptor Ltd | Protein kinase inhibitors |
| US6511994B2 (en) | 2000-10-11 | 2003-01-28 | Merck & Co., Inc. | Modulators of CCR5 chemokine receptor activity |
| WO2002088090A2 (en) | 2001-04-27 | 2002-11-07 | Vertex Pharmaceuticals Incorporated | Pyrazole derived kinase inhibitors |
| WO2003011855A2 (en) | 2001-08-03 | 2003-02-13 | Vertex Pharmaceuticals Incorporated | Pyrazole-derived kinase inhibitors and uses thereof |
| FR2830192B1 (fr) | 2001-09-28 | 2004-08-20 | Oreal | Composition tinctoriale comprenant une base d'oxydation du type diaminopyrazole et un coupleur pyrazolo-azole |
| WO2003048081A2 (en) | 2001-12-04 | 2003-06-12 | Bristol-Myers Squibb Company | Glycinamides as factor xa inhibitors |
| EP1465869B1 (en) | 2001-12-21 | 2013-05-15 | Exelixis Patent Company LLC | Modulators of lxr |
| PL218749B1 (pl) | 2002-02-14 | 2015-01-30 | Pharmacia Corp | Pochodna pirydynonu oraz jej zastosowanie do wytwarzania leku |
| US7078421B2 (en) | 2002-03-20 | 2006-07-18 | Metabolex, Inc. | Substituted phenylacetic acids |
| EP1492477B1 (en) | 2002-04-08 | 2016-04-13 | Boston Scientific Scimed, Inc. | Satiation devices and methods |
| US20050026929A1 (en) | 2002-04-23 | 2005-02-03 | Axys Pharmaceuticals, Inc. | Novel phenyl derivatives as inducers of apoptosis |
| JP4468810B2 (ja) | 2002-07-24 | 2010-05-26 | キューエルティー インコーポレーティッド | ピラゾリルベンゾチアゾール誘導体および治療薬としてのそれらの使用法 |
| JP2006502190A (ja) * | 2002-09-18 | 2006-01-19 | ザ キュレイターズ オブ ザ ユニバーシティー オブ ミズーリ | デルタ−オピオイド受容体に選択的なオピエート類似物 |
| US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
| WO2004110350A2 (en) | 2003-05-14 | 2004-12-23 | Torreypines Therapeutics, Inc. | Compouds and uses thereof in modulating amyloid beta |
| JP2007516196A (ja) | 2003-07-02 | 2007-06-21 | ガラパゴス エヌブイ | Rhoキナーゼ阻害剤としてのピラジン及びピラリジン誘導体 |
| CA2532965C (en) | 2003-07-22 | 2013-05-14 | Astex Therapeutics Limited | 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
| WO2005035506A1 (ja) | 2003-10-15 | 2005-04-21 | Ube Industries, Ltd. | 新規インダゾール誘導体 |
| US20050165031A1 (en) | 2003-11-13 | 2005-07-28 | Ambit Biosciences Corporation | Urea derivatives as ABL modulators |
| HRP20100675T1 (hr) * | 2003-12-23 | 2011-01-31 | Astex Therapeutics Limited | Derivati pirazola kao modulatori protein kinaze |
| JP5213229B2 (ja) | 2004-04-23 | 2013-06-19 | エグゼリクシス, インコーポレイテッド | キナーゼ調節因子および使用方法 |
| UY29177A1 (es) | 2004-10-25 | 2006-05-31 | Astex Therapeutics Ltd | Derivados sustituidos de purina, purinona y deazapurina, composiciones que los contienen métodos para su preparación y sus usos |
| US7994172B2 (en) | 2004-12-28 | 2011-08-09 | Exelixis, Inc. | [1H-pyrazolo[3, 4-D]pyrimidin-4-yl]-piperidine or -piperazine compounds as serine-theoronine kinase modulators (P70s6k, Atk1 and Atk2) for the treatment of immunological, inflammatory and proliferative diseases |
| US7423043B2 (en) | 2005-02-18 | 2008-09-09 | Lexicon Pharmaceuticals, Inc. | 4-Piperidin-1-yl-7H-pyrrolo[2,3-d]pyrimidine compounds |
| WO2006136823A1 (en) | 2005-06-21 | 2006-12-28 | Astex Therapeutics Limited | Heterocyclic containing amines as kinase b inhibitors |
| WO2006136829A2 (en) | 2005-06-21 | 2006-12-28 | Astex Therapeutics Limited | Pyrazole derivatives and their use as pka and pkb modulators |
| UY29610A1 (es) | 2005-06-21 | 2007-01-31 | Cancer Rec Tech Ltd | Aril-alquilaminas y heteroaril-alquilaminas como inhibidores de la quinasa proteínica |
| GB2427406A (en) | 2005-06-21 | 2006-12-27 | Astex Technology Ltd | Silicon-containing PKB/PKA kinase inhibitors |
| EP1902032A1 (en) | 2005-06-22 | 2008-03-26 | Astex Therapeutics Limited | Pharmaceutical compounds |
| US8541461B2 (en) | 2005-06-23 | 2013-09-24 | Astex Therapeutics Limited | Pharmaceutical combinations comprising pyrazole derivatives as protein kinase modulators |
| GB0704932D0 (en) * | 2007-03-14 | 2007-04-25 | Astex Therapeutics Ltd | Pharmaceutical compounds |
-
2006
- 2006-06-21 US US11/993,823 patent/US8541461B2/en not_active Expired - Fee Related
- 2006-06-21 WO PCT/GB2006/002297 patent/WO2006136837A2/en not_active Ceased
- 2006-06-21 JP JP2008517594A patent/JP5345842B2/ja not_active Expired - Fee Related
- 2006-06-21 EP EP06755597A patent/EP1933832A2/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| JP2008546754A (ja) | 2008-12-25 |
| WO2006136837A2 (en) | 2006-12-28 |
| US8541461B2 (en) | 2013-09-24 |
| EP1933832A2 (en) | 2008-06-25 |
| WO2006136837A3 (en) | 2007-02-15 |
| US20100166699A1 (en) | 2010-07-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5345842B2 (ja) | プロテインキナーゼモジュレーターとしてのピラゾール誘導体を含む医薬組み合わせ | |
| KR101346886B1 (ko) | 제약 화합물 | |
| KR101164258B1 (ko) | 단백질 키나아제 조절제로서의 피라졸 유도체 | |
| JP2009536186A (ja) | 癌処置のためのジアゾール誘導体の医薬組合せ | |
| US8435970B2 (en) | Pharmaceutical combinations of 1-cyclopropyl-3-[3-(5-morpholin-4-ylmethyl-1H-benzoimidazol-2-yl)-1H-pyrazol-4-yl]-urea | |
| AU783992B2 (en) | Method of using a cyclooxygenase-2 inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia | |
| JP5721949B2 (ja) | 複合薬剤 | |
| US20100021420A1 (en) | Combinations of pyrazole derivatives for the inhibition of cdks and gsk's | |
| US20110159111A1 (en) | Pharmaceutical combinations | |
| US20090263398A1 (en) | Pharmaceutical combinations | |
| US20090082370A1 (en) | Pharmaceutical Combinations of PK Inhibitors and Other Active Agents | |
| KR20070107707A (ko) | 피라졸 키나제 억제제와 추가 항종양제의 조합물 | |
| JP2010505931A (ja) | 複合薬剤 | |
| CN114846003A (zh) | 用于治疗癌症的氘代化合物 | |
| CZ20032783A3 (cs) | Antiangiogenní kombinovaná terapie pro léčbu rakoviny | |
| US20190000850A1 (en) | Combination cancer therapy | |
| US20240360135A1 (en) | Imidazo[1,2-b]pyridazinyl compounds and uses thereof | |
| WO2021141538A1 (en) | Combination therapy | |
| CN101484173A (zh) | Pk抑制剂与其他活性药的药物组合 | |
| HK1068563A (en) | Antiangiogenic combination therapy for the treatment of cancer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090619 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090619 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100528 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120228 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120522 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120529 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120620 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120627 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120726 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120802 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120822 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20121023 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130206 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20130206 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20130306 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130402 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130617 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130723 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130815 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |