HRP20110962T1 - Derivati pirazolil-aminopiridina korisni kao inhibitori kinaze - Google Patents
Derivati pirazolil-aminopiridina korisni kao inhibitori kinaze Download PDFInfo
- Publication number
- HRP20110962T1 HRP20110962T1 HR20110962T HRP20110962T HRP20110962T1 HR P20110962 T1 HRP20110962 T1 HR P20110962T1 HR 20110962 T HR20110962 T HR 20110962T HR P20110962 T HRP20110962 T HR P20110962T HR P20110962 T1 HRP20110962 T1 HR P20110962T1
- Authority
- HR
- Croatia
- Prior art keywords
- 6alkyl
- formula
- compound
- cancer
- pharmaceutically acceptable
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- RSLYEFKTNVKNFJ-UHFFFAOYSA-N n-(1h-pyrazol-5-yl)pyridin-2-amine Chemical class C=1C=CC=NC=1NC=1C=CNN=1 RSLYEFKTNVKNFJ-UHFFFAOYSA-N 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- -1 nitro, cyano, hydroxy, trifluoromethoxy, amino, carboxy, carbamoyl Chemical group 0.000 claims abstract 40
- 150000001875 compounds Chemical class 0.000 claims abstract 34
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 27
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 19
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 18
- 239000001257 hydrogen Substances 0.000 claims abstract 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract 16
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 16
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract 14
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract 11
- 125000005843 halogen group Chemical group 0.000 claims abstract 11
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 10
- 229910052799 carbon Inorganic materials 0.000 claims abstract 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 9
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims abstract 8
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims abstract 8
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims abstract 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract 8
- 125000004452 carbocyclyl group Chemical group 0.000 claims abstract 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 3
- 125000001424 substituent group Chemical group 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 238000000034 method Methods 0.000 claims 7
- 206010028980 Neoplasm Diseases 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 201000011510 cancer Diseases 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 206010006187 Breast cancer Diseases 0.000 claims 4
- 208000026310 Breast neoplasm Diseases 0.000 claims 4
- 206010027406 Mesothelioma Diseases 0.000 claims 4
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 4
- 206010060862 Prostate cancer Diseases 0.000 claims 4
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 4
- 206010041067 Small cell lung cancer Diseases 0.000 claims 4
- 125000001589 carboacyl group Chemical group 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 201000001441 melanoma Diseases 0.000 claims 4
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 4
- 208000000587 small cell lung carcinoma Diseases 0.000 claims 4
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 4
- 150000001412 amines Chemical class 0.000 claims 3
- 229940079593 drug Drugs 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 238000011321 prophylaxis Methods 0.000 claims 3
- 238000011282 treatment Methods 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 2
- CNVPBZZBCDUDPL-NSHDSACASA-N 5-fluoro-2-[[(1s)-1-(5-fluoropyridin-2-yl)ethyl]amino]-6-[(3-propan-2-yloxy-1h-pyrazol-5-yl)amino]pyridine-3-carbonitrile Chemical compound N1C(OC(C)C)=CC(NC=2C(=CC(=C(N[C@@H](C)C=3N=CC(F)=CC=3)N=2)C#N)F)=N1 CNVPBZZBCDUDPL-NSHDSACASA-N 0.000 claims 2
- 208000024893 Acute lymphoblastic leukemia Diseases 0.000 claims 2
- 208000014697 Acute lymphocytic leukaemia Diseases 0.000 claims 2
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 2
- 206010005003 Bladder cancer Diseases 0.000 claims 2
- 206010008342 Cervix carcinoma Diseases 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 2
- 206010065859 Congenital fibrosarcoma Diseases 0.000 claims 2
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 2
- 208000007766 Kaposi sarcoma Diseases 0.000 claims 2
- 208000008839 Kidney Neoplasms Diseases 0.000 claims 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 2
- 206010025323 Lymphomas Diseases 0.000 claims 2
- 206010070665 Mesoblastic nephroma Diseases 0.000 claims 2
- 208000034578 Multiple myelomas Diseases 0.000 claims 2
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 2
- 206010029260 Neuroblastoma Diseases 0.000 claims 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims 2
- 206010033128 Ovarian cancer Diseases 0.000 claims 2
- 206010061535 Ovarian neoplasm Diseases 0.000 claims 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 2
- 206010033701 Papillary thyroid cancer Diseases 0.000 claims 2
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 2
- 208000024770 Thyroid neoplasm Diseases 0.000 claims 2
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 2
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims 2
- 230000001028 anti-proliverative effect Effects 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 2
- 201000010881 cervical cancer Diseases 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 201000004101 esophageal cancer Diseases 0.000 claims 2
- 206010017758 gastric cancer Diseases 0.000 claims 2
- 201000010536 head and neck cancer Diseases 0.000 claims 2
- 208000014829 head and neck neoplasm Diseases 0.000 claims 2
- 206010073071 hepatocellular carcinoma Diseases 0.000 claims 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 2
- 201000010982 kidney cancer Diseases 0.000 claims 2
- 208000032839 leukemia Diseases 0.000 claims 2
- 208000014018 liver neoplasm Diseases 0.000 claims 2
- 201000005202 lung cancer Diseases 0.000 claims 2
- 208000020816 lung neoplasm Diseases 0.000 claims 2
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 201000000050 myeloid neoplasm Diseases 0.000 claims 2
- 201000002528 pancreatic cancer Diseases 0.000 claims 2
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 2
- 230000003248 secreting effect Effects 0.000 claims 2
- 201000011549 stomach cancer Diseases 0.000 claims 2
- 201000002510 thyroid cancer Diseases 0.000 claims 2
- 208000030045 thyroid gland papillary carcinoma Diseases 0.000 claims 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- XRJMPARQQIMFNL-INIZCTEOSA-N 5-fluoro-2-[[(1r)-1-(4-fluorophenyl)-2-hydroxyethyl]amino]-6-[(3-propan-2-yloxy-1h-pyrazol-5-yl)amino]pyridine-3-carbonitrile Chemical compound N1C(OC(C)C)=CC(NC=2C(=CC(=C(N[C@@H](CO)C=3C=CC(F)=CC=3)N=2)C#N)F)=N1 XRJMPARQQIMFNL-INIZCTEOSA-N 0.000 claims 1
- QRAQXWWNHQMCBH-LBPRGKRZSA-N 5-fluoro-2-[[(1s)-1-(4-fluorophenyl)ethyl]amino]-6-[(3-propan-2-yloxy-1h-pyrazol-5-yl)amino]pyridine-3-carbonitrile Chemical compound N1C(OC(C)C)=CC(NC=2C(=CC(=C(N[C@@H](C)C=3C=CC(F)=CC=3)N=2)C#N)F)=N1 QRAQXWWNHQMCBH-LBPRGKRZSA-N 0.000 claims 1
- MCYKNGQWXNQVMX-VIFPVBQESA-N 6-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]-2-[[(1s)-1-(3,5-difluoropyridin-2-yl)ethyl]amino]-5-fluoropyridine-3-carbonitrile Chemical compound N([C@@H](C)C=1C(=CC(F)=CN=1)F)C(C(=CC=1F)C#N)=NC=1NC(=NN1)C=C1C1CC1 MCYKNGQWXNQVMX-VIFPVBQESA-N 0.000 claims 1
- LHQVKNUTINLXOZ-KRWDZBQOSA-N 6-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]-5-fluoro-2-[[(1r)-1-(4-fluorophenyl)-2-hydroxyethyl]amino]pyridine-3-carbonitrile Chemical compound N([C@@H](CO)C=1C=CC(F)=CC=1)C(C(=CC=1F)C#N)=NC=1NC(=NN1)C=C1C1CC1 LHQVKNUTINLXOZ-KRWDZBQOSA-N 0.000 claims 1
- RIJRDASGHLOWRC-NSHDSACASA-N 6-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]-5-fluoro-2-[[(1s)-1-(4-fluorophenyl)ethyl]amino]pyridine-3-carbonitrile Chemical compound N([C@@H](C)C=1C=CC(F)=CC=1)C(C(=CC=1F)C#N)=NC=1NC(=NN1)C=C1C1CC1 RIJRDASGHLOWRC-NSHDSACASA-N 0.000 claims 1
- UQIYWYOAEAUPCY-JTQLQIEISA-N 6-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]-5-fluoro-2-[[(1s)-1-(5-fluoropyridin-2-yl)ethyl]amino]pyridine-3-carbonitrile Chemical compound N([C@@H](C)C=1N=CC(F)=CC=1)C(C(=CC=1F)C#N)=NC=1NC(=NN1)C=C1C1CC1 UQIYWYOAEAUPCY-JTQLQIEISA-N 0.000 claims 1
- 208000006168 Ewing Sarcoma Diseases 0.000 claims 1
- 206010039491 Sarcoma Diseases 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
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
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D405/14—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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65005305P | 2005-02-04 | 2005-02-04 | |
| US65332905P | 2005-02-16 | 2005-02-16 | |
| US72163305P | 2005-09-29 | 2005-09-29 | |
| PCT/GB2006/000334 WO2006082392A1 (en) | 2005-02-04 | 2006-02-01 | Pyrazolylaminopyridine derivatives useful as kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20110962T1 true HRP20110962T1 (hr) | 2012-01-31 |
Family
ID=36177856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20110962T HRP20110962T1 (hr) | 2005-02-04 | 2011-12-21 | Derivati pirazolil-aminopiridina korisni kao inhibitori kinaze |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US8324252B2 (ko) |
| EP (2) | EP1846394B1 (ko) |
| JP (1) | JP5139084B2 (ko) |
| KR (1) | KR101302945B1 (ko) |
| CN (1) | CN101155800B (ko) |
| AR (1) | AR056184A1 (ko) |
| AT (1) | ATE530545T1 (ko) |
| AU (1) | AU2006210710B2 (ko) |
| BR (1) | BRPI0606793A8 (ko) |
| CA (1) | CA2595834C (ko) |
| CY (2) | CY1115078T1 (ko) |
| DK (2) | DK1846394T3 (ko) |
| ES (2) | ES2555063T3 (ko) |
| HK (2) | HK1114374A1 (ko) |
| HR (1) | HRP20110962T1 (ko) |
| HU (1) | HUE025671T2 (ko) |
| IL (1) | IL184674A (ko) |
| ME (1) | ME02645B (ko) |
| MX (1) | MX2007009437A (ko) |
| MY (1) | MY149512A (ko) |
| NO (1) | NO341112B1 (ko) |
| NZ (1) | NZ561145A (ko) |
| PL (2) | PL2383268T3 (ko) |
| PT (2) | PT1846394E (ko) |
| RS (1) | RS52061B (ko) |
| SA (1) | SA06270007B1 (ko) |
| SI (2) | SI2383268T1 (ko) |
| TW (1) | TWI370127B (ko) |
| UY (1) | UY29360A1 (ko) |
| WO (1) | WO2006082392A1 (ko) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2308731T3 (es) | 2005-02-16 | 2008-12-01 | Astrazeneca Ab | Compuestos quimicos. |
| NZ564317A (en) * | 2005-05-16 | 2011-01-28 | Astrazeneca Ab | Pyrazolylaminopyrimidine derivatives useful as tyrosine kinase inhibitors |
| ES2391783T3 (es) | 2005-10-28 | 2012-11-29 | Astrazeneca Ab | Derivados de 4-(3-aminopirazol)pirimidina para su uso como agentes inhibidores de las tirosina cinasas en el tratamiento del cáncer |
| US20090275515A1 (en) * | 2006-10-18 | 2009-11-05 | Yuntae Kim | 2-hydroxy-2-phenylthiophenylpropionamides as androgen receptor modulators |
| WO2008053812A1 (fr) * | 2006-10-27 | 2008-05-08 | Mitsubishi Tanabe Pharma Corporation | Dérivé de cyanopyridine et son utilisation médicale |
| TW200826937A (en) * | 2006-11-01 | 2008-07-01 | Astrazeneca Ab | New use |
| WO2008117050A1 (en) * | 2007-03-27 | 2008-10-02 | Astrazeneca Ab | Pyrazolyl-amino-substituted pyrazines and their use for the treatment of cancer |
| UA99459C2 (en) * | 2007-05-04 | 2012-08-27 | Астразенека Аб | 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer |
| JP5524491B2 (ja) * | 2008-03-04 | 2014-06-18 | 石原産業株式会社 | ３−アミノ−２−クロロ−６−トリフルオロメチルピリジンの製造方法 |
| WO2010020810A1 (en) * | 2008-08-19 | 2010-02-25 | Astrazeneca Ab | 2-(imidaz0lylamin0)-pyridine derivatives and their use as jak kinase inhibitors |
| EP2338888A1 (en) | 2009-12-24 | 2011-06-29 | Almirall, S.A. | Imidazopyridine derivatives as JAK inhibitors |
| UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
| SG186877A1 (en) | 2010-06-30 | 2013-02-28 | Fujifilm Corp | Novel nicotinamide derivatives or salts thereof |
| UY33517A (es) | 2010-07-19 | 2012-02-29 | Astrazeneca Ab | Depósito farmacéutico para 5-fluoro-2-[[(1S)-1-(5-fluoro-2-piridil)etil]amino]-6-[(5-isopropoxi-1H-pirazol-3-il)amino]piridin-3-carbonitrilo?. |
| EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
| PL2799431T3 (pl) | 2011-12-28 | 2018-07-31 | Fujifilm Corporation | Nowa pochodna nikotynamidu lub jej sól |
| CA2867469A1 (en) | 2012-03-16 | 2013-09-19 | Axikin Pharmaceuticals, Inc. | 3,5-diaminopyrazole kinase inhibitors |
| TWI585088B (zh) | 2012-06-04 | 2017-06-01 | 第一三共股份有限公司 | 作爲激酶抑制劑之咪唑并［１，２－ｂ］嗒衍生物 |
| ES2823237T3 (es) * | 2012-11-05 | 2021-05-06 | Univ Emory | Derivados de 7,8-dihidroxiflavona y de flavona 7,8-sustituida, composiciones y métodos relacionados con los mismos |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| PL3179992T3 (pl) | 2014-08-11 | 2022-08-16 | Acerta Pharma B.V. | Kombinacje terapeutyczne inhibitora BTK, inhibitora PD-1 i/lub inhibitora PD-L1 |
| HUE056329T2 (hu) | 2014-08-11 | 2022-02-28 | Acerta Pharma Bv | BTK-inhibitor és BCL-2-inhibitor terápiás kombinációi |
| SG11201705088VA (en) | 2014-12-23 | 2017-07-28 | Axikin Pharmaceuticals Inc | 3,5-diaminopyrazole kinase inhibitors |
| WO2017157885A1 (de) | 2016-03-16 | 2017-09-21 | Bayer Cropscience Aktiengesellschaft | N-(cyanbenzyl)-6-(cyclopropylcarbonylamino)-4-(phenyl)-pyridin-2-carboxamid-derivate und verwandte verbindungen als pestizide pflanzenschutzmittel |
| WO2018172250A1 (en) | 2017-03-21 | 2018-09-27 | Bayer Pharma Aktiengesellschaft | 2-methyl-quinazolines |
| WO2019201848A1 (en) | 2018-04-18 | 2019-10-24 | Bayer Pharma Aktiengesellschaft | 2-methyl-aza-quinazolines |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| EP3974434A4 (en) | 2019-05-21 | 2023-11-08 | Zhejiang Hisun Pharmaceutical Co., Ltd. | MACROLIDE DERIVATIVES, PRODUCTION PROCESS AND USE THEREOF |
| EP4054579A1 (en) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
Family Cites Families (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| DE69720965T2 (de) | 1996-02-13 | 2004-02-05 | Astrazeneca Ab | Chinazolinderivate und deren verwendung als vegf hemmer |
| WO1997032856A1 (en) | 1996-03-05 | 1997-09-12 | Zeneca Limited | 4-anilinoquinazoline derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| ATE245641T1 (de) | 1998-02-17 | 2003-08-15 | Tularik Inc | Antivirale pyrimidinderivate |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| DE19917785A1 (de) | 1999-04-20 | 2000-10-26 | Bayer Ag | 2,4-Diamino-pyrimidin-Derivate |
| US6399780B1 (en) | 1999-08-20 | 2002-06-04 | Cephalon, Inc. | Isomeric fused pyrrolocarbazoles and isoindolones |
| JP3892296B2 (ja) | 1999-09-10 | 2007-03-14 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼ阻害薬 |
| DE60043397D1 (de) | 1999-12-28 | 2010-01-07 | Pharmacopeia Inc | Cytokine, insbesondere tnf-alpha, hemmer |
| AU2001237041B9 (en) | 2000-02-17 | 2005-07-28 | Amgen Inc. | Kinase inhibitors |
| DK1282607T3 (en) | 2000-05-08 | 2016-02-01 | Janssen Pharmaceutica Nv | Prodrugs of HIV replication inhibiting pyrimidines |
| KR20030013433A (ko) | 2000-05-31 | 2003-02-14 | 아스트라제네카 아베 | 혈관 손상 활성을 가진 인돌 유도체 |
| CA2411160A1 (en) | 2000-07-07 | 2002-01-17 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as vascular damaging agents |
| JP2004504391A (ja) | 2000-07-07 | 2004-02-12 | アンギオジェン・ファーマシューティカルズ・リミテッド | 血管新生阻害剤としてのコルキノール誘導体 |
| CN1518543A (zh) | 2000-08-31 | 2004-08-04 | �Ʒ� | 吡唑衍生物和它们作为蛋白激酶抑制剂的用途 |
| US7071217B2 (en) | 2000-09-01 | 2006-07-04 | Smithkline Beecham Corporation | Substituted oxindole derivatives as tyrosine kinase inhibitors |
| JP2004508366A (ja) | 2000-09-01 | 2004-03-18 | グラクソ グループ リミテッド | オキシインドール誘導体 |
| JP4105949B2 (ja) | 2000-09-15 | 2008-06-25 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
| PT1355905E (pt) | 2000-12-21 | 2007-05-31 | Vertex Pharma | Compostos de pirazole úteis como inibidores de proteínaquinase |
| EP1347971B1 (en) | 2000-12-21 | 2006-03-01 | Bristol-Myers Squibb Company | Thiazolyl inhibitors of tec family tyrosine kinases |
| US20030130264A1 (en) | 2001-02-16 | 2003-07-10 | Tularik Inc. | Methods of using pyrimidine-based antiviral agents |
| DE60215682T2 (de) | 2001-09-27 | 2007-09-06 | Smithkline Beecham Corp. | AZAOXOINDOL DERIVATE ALS Trk PROTEIN KINASE HEMMSTOFFE ZUR BEHANDLUNG VON KREBS UND CHRONISCHEM SCHMERZ |
| SE0104140D0 (sv) | 2001-12-07 | 2001-12-07 | Astrazeneca Ab | Novel Compounds |
| JP2003231687A (ja) | 2002-02-04 | 2003-08-19 | Japan Tobacco Inc | ピラゾリル縮合環化合物及びその医薬用途 |
| AU2003286711A1 (en) | 2002-10-25 | 2004-05-13 | Vertex Pharmaceuticals Incorporated | Indazolinone compositions useful as kinase inhibitors |
| NZ545270A (en) | 2003-07-30 | 2010-04-30 | Rigel Pharmaceuticals Inc | 2,4-Pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases |
| MY141220A (en) | 2003-11-17 | 2010-03-31 | Astrazeneca Ab | Pyrazole derivatives as inhibitors of receptor tyrosine kinases |
| EP1742921A2 (en) * | 2004-04-21 | 2007-01-17 | AstraZeneca AB | Pyrazole derivatives useful for the treatment of cancer |
| AU2005289426A1 (en) | 2004-09-27 | 2006-04-06 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
| JP2008525422A (ja) | 2004-12-23 | 2008-07-17 | ファイザー・プロダクツ・インク | 抗癌剤として有用な複素芳香族誘導体 |
| EP1841760B1 (en) | 2004-12-30 | 2011-08-10 | Exelixis, Inc. | Pyrimidine derivatives as kinase modulators and method of use |
| ES2308731T3 (es) | 2005-02-16 | 2008-12-01 | Astrazeneca Ab | Compuestos quimicos. |
| DK1853602T3 (da) | 2005-02-16 | 2010-09-20 | Astrazeneca Ab | Kemiske forbindelser |
| JP2008540335A (ja) | 2005-04-27 | 2008-11-20 | アストラゼネカ・アクチエボラーグ | ピラゾリル・ピリミジン誘導体の疼痛治療における使用 |
| JP5075624B2 (ja) | 2005-04-28 | 2012-11-21 | 田辺三菱製薬株式会社 | シアノピリジン誘導体及びその医薬としての用途 |
| WO2006117560A1 (en) | 2005-05-05 | 2006-11-09 | Astrazeneca Ab | Pyrazolyl-amino- substituted pyrimidines and their use in the treatment of cancer |
| NZ564317A (en) | 2005-05-16 | 2011-01-28 | Astrazeneca Ab | Pyrazolylaminopyrimidine derivatives useful as tyrosine kinase inhibitors |
| ES2391783T3 (es) | 2005-10-28 | 2012-11-29 | Astrazeneca Ab | Derivados de 4-(3-aminopirazol)pirimidina para su uso como agentes inhibidores de las tirosina cinasas en el tratamiento del cáncer |
| US7572809B2 (en) | 2005-12-19 | 2009-08-11 | Hoffmann-La Roche Inc. | Isoquinoline aminopyrazole derivatives |
| AU2007263655A1 (en) | 2006-06-30 | 2008-01-03 | Astrazeneca Ab | Pyrimidine derivatives useful in the treatment of cancer |
| TW200826937A (en) | 2006-11-01 | 2008-07-01 | Astrazeneca Ab | New use |
| TW200823196A (en) | 2006-11-01 | 2008-06-01 | Astrazeneca Ab | New use |
-
2006
- 2006-02-01 AT AT06701619T patent/ATE530545T1/de active
- 2006-02-01 DK DK06701619.6T patent/DK1846394T3/da active
- 2006-02-01 HU HUE11167362A patent/HUE025671T2/en unknown
- 2006-02-01 SI SI200631992T patent/SI2383268T1/sl unknown
- 2006-02-01 BR BRPI0606793A patent/BRPI0606793A8/pt not_active IP Right Cessation
- 2006-02-01 SI SI200631240T patent/SI1846394T1/sl unknown
- 2006-02-01 WO PCT/GB2006/000334 patent/WO2006082392A1/en active Application Filing
- 2006-02-01 RS RS20110563A patent/RS52061B/en unknown
- 2006-02-01 CN CN2006800101082A patent/CN101155800B/zh not_active Expired - Fee Related
- 2006-02-01 AU AU2006210710A patent/AU2006210710B2/en not_active Ceased
- 2006-02-01 DK DK11167362.0T patent/DK2383268T3/en active
- 2006-02-01 PL PL11167362T patent/PL2383268T3/pl unknown
- 2006-02-01 PT PT06701619T patent/PT1846394E/pt unknown
- 2006-02-01 JP JP2007553688A patent/JP5139084B2/ja not_active Expired - Fee Related
- 2006-02-01 PT PT111673620T patent/PT2383268E/pt unknown
- 2006-02-01 KR KR1020077020258A patent/KR101302945B1/ko not_active IP Right Cessation
- 2006-02-01 MX MX2007009437A patent/MX2007009437A/es active IP Right Grant
- 2006-02-01 NZ NZ561145A patent/NZ561145A/en not_active IP Right Cessation
- 2006-02-01 ES ES11167362.0T patent/ES2555063T3/es active Active
- 2006-02-01 CA CA2595834A patent/CA2595834C/en not_active Expired - Fee Related
- 2006-02-01 US US11/815,140 patent/US8324252B2/en not_active Expired - Fee Related
- 2006-02-01 EP EP06701619A patent/EP1846394B1/en active Active
- 2006-02-01 ME MEP-2011-563A patent/ME02645B/me unknown
- 2006-02-01 PL PL06701619T patent/PL1846394T3/pl unknown
- 2006-02-01 ES ES06701619T patent/ES2375735T3/es active Active
- 2006-02-01 EP EP11167362.0A patent/EP2383268B1/en active Active
- 2006-02-02 AR ARP060100376A patent/AR056184A1/es not_active Application Discontinuation
- 2006-02-03 MY MYPI20060475A patent/MY149512A/en unknown
- 2006-02-03 TW TW095103831A patent/TWI370127B/zh not_active IP Right Cessation
- 2006-02-03 UY UY29360A patent/UY29360A1/es not_active Application Discontinuation
- 2006-02-04 SA SA06270007A patent/SA06270007B1/ar unknown
-
2007
- 2007-07-17 IL IL184674A patent/IL184674A/en not_active IP Right Cessation
- 2007-07-20 NO NO20073791A patent/NO341112B1/no not_active IP Right Cessation
-
2008
- 2008-02-13 HK HK08101578.0A patent/HK1114374A1/xx not_active IP Right Cessation
-
2011
- 2011-12-21 HR HR20110962T patent/HRP20110962T1/hr unknown
-
2012
- 2012-01-11 CY CY20121100025T patent/CY1115078T1/el unknown
- 2012-05-02 HK HK12104298.7A patent/HK1163677A1/zh not_active IP Right Cessation
- 2012-11-29 US US13/688,790 patent/US8835465B2/en not_active Expired - Fee Related
-
2015
- 2015-11-26 CY CY20151101071T patent/CY1119077T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HRP20110962T1 (hr) | Derivati pirazolil-aminopiridina korisni kao inhibitori kinaze | |
| HRP20100477T1 (hr) | Kemijski spojevi | |
| RU2007134396A (ru) | Химические соединения | |
| AR046779A1 (es) | Derivados de pirazol, metodos para su preparacion y usos de los mismos en la fabricacion de composiciones farmaceuticas y medicamentos que los contienen con actividad inhibitoria de trk para el tratamiento o profilaxis del cancer. | |
| RU2007134380A (ru) | Антибактериальные производные пиперидина | |
| JP2012509263A5 (ko) | ||
| CY1106788T1 (el) | Πυριμιδινες και τριαζινες αναστολης της αντιγραφης του hiv | |
| DK1537104T3 (da) | Azabicycloalkylethere og deres anvendelse som alfa7-nAChR-agonister | |
| ME01488B (me) | Derivati oksadiazola i njihovo korišćenje kao potencijatora metabotropnih glutamatnih receptora-842 | |
| AR049662A1 (es) | Derivados de 1,3-fenilendiamina con efecto inhibitorio de b-raf; un metodo para su preparacion, composiciones farmaceuticas que los contienen y su utilizacion en la fabricacion de medicamentos para el tratamiento del cancer | |
| HRP20110156T1 (hr) | Monociklički heterocikli kao inhibitori kinaze | |
| NO20060082L (no) | Indol azaindol og relaterte heterosykliske N-substituerte piperazinderivater | |
| HK1077571A1 (en) | Biaryl diazabicycloalkane amides as nicotinic acetylcholine agonists | |
| GEP20125502B (en) | Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors | |
| MX2009011208A (es) | Derivados de acido nicotinico como moduladores del receptor de glutamato metabotropico-5. | |
| AR063643A1 (es) | Compuestos quimicos derivados de quinolina, un metodo de preparacion y composiciones farmaceuticas | |
| GEP20084391B (en) | Pyrazoles and methods of making and using the same | |
| DE602004024375D1 (de) | Carboxamidderivate | |
| NZ547615A (en) | Quinoline derivatives and use thereof as mycobacterial inhibitors | |
| GEP20125379B (en) | 2 -pyridine carboxamide derivatives as sodium channel modulators | |
| WO2009080836A3 (en) | Macrocyclic indoles as hepatitis c virus inhibitors | |
| BRPI0606313A2 (pt) | derivados de 4-(1h-indol-3-il)-pirimidin-2-ilamina, processo para sua preparação e seu uso em terapia | |
| UA84712C2 (en) | N-substituted pyrazolyl-amidyl-benzimidazolyl c-kit inhibitors | |
| NO20051695L (no) | Nye spirokondenserte kinazolinoner og deres anvendelse som fosfodiestereaseinbibitorer | |
| HK1133012A1 (en) | Pyrimidinones as casein kinase ii (ck2) modulators |