AR070224A1 - Inhibidores de proteina quinasa y uso de los mismos - Google Patents
Inhibidores de proteina quinasa y uso de los mismosInfo
- Publication number
- AR070224A1 AR070224A1 ARP090100188A ARP090100188A AR070224A1 AR 070224 A1 AR070224 A1 AR 070224A1 AR P090100188 A ARP090100188 A AR P090100188A AR P090100188 A ARP090100188 A AR P090100188A AR 070224 A1 AR070224 A1 AR 070224A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- independently
- nr5c
- nr5r6
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 102000004169 proteins and genes Human genes 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 abstract 2
- 125000000464 thioxo group Chemical group S=* 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Una composicion farmacéutica que los comprende y el uso de los mismos para la preparacion de un medicamento para el tratamiento de enfermedades hiperproliferativas o inflamatorias. Reivindicacion 1: Un compuesto de la formula (1) en la que: W1 es CR8 o N, y W2 es -C-C:::C-Ar; o W1 es -C-C:::C-Ar, y W2 es CR8 o N; Y es -S-, -O-, -NH-, o -NHCH2-; X es N o N+ -O-; -------- representa un enlace sencillo o un doble enlace; Ar es arilo, carbociclilo, heteroarilo o heterociclilo; donde el arilo y heteroarilo están opcional e independientemente sustituidos con hasta 4 grupos representados por R3, y donde el carbociclilo y heterociclilo están opcional e independientemente sustituidos con hasta 4 grupos representados por R4; R1 y R2 se seleccionan independientemente entre H, halogeno, ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, cicloalquilo C3-8, heterocicloalquilo de 5-10 miembros, -C(O)OR5, -C(O)R5, -OC(O)R5, -C(O)NR5R6, -NR5C(O)NR5R6, -NR5C(O)OR5, -NR5C(O)R5, -NR5C(S)NR5R6, -S(O)pNR5R6, -NR5R6, -S(O)pR5, -NR5S(O)pR5, donde cada uno de dichos alquilo, alquenilo, alquinilo, alcoxi, cicloalquilo y heterocicloalquilo está sustituido o sin sustituir; o R1 y R2 pueden tomarse junto con los átomos intermedios para formar un anillo cicloalquilo C5-6 que está sustituido o sin sustituir; y p es un numero entero de 0 a 2; cada R3 es independientemente: i) halogeno, -X1-OH, -X1-CN, -X1-OR10, X1-CO2R10, -X1-NR10C(O)N(R10)2, -X1-NR10C(S)N(R10)2, -X1-NR10CO2R10, -X1-COR10, -X1-N(R10)2, -X1-N+(R10)3, -X1- OCOR10, -X1-SO2N(R10)2, -X1-S(O)nR10, -X1-NR10S(O)nR10, -X1-NR10COR10, -X1- OC(O)N(R10)2, -X1-CON(R10)2 o -X1-NR10CO2R10; o ii) alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o iii) arilo, aralquilo, ariloxi, heteroarilo, heteroaralquilo o heteroariloxi, cada uno opcional e independientemente sustituido con hasta 3 grupos seleccionados entre halogeno, -CN, -OH, -NH2, -NH-alquilo C1-6, -N-(alquilo C1-6)2, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alcoxicarbonilo C1-6, -CONH2, -CONH-alquilo C1-6, -CON-(aIquilo C1-6)2, -CO-alquilo C1-6 o -CO2H;o iv) carbociclilo o heterociclilo, cada uno opcional e independientemente sustituido con hasta 3 grupos seleccionados entre halogeno, -CN, -OH, -NH2, -NH-alquilo C1-6, -N-(alquilo C1-6)2, alquil C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alcoxicarbonilo C1-6, -CONH2, -CONH-alquilo C1-6, -CON-(alquilo C1-6)2, -CO-alquilo C1-6, -CO2H, arilo, heteroarilo, oxo y tioxo; cada X1 es independientemente un enlace covalente, un alquileno C1-6, alquenileno C1-6 o alquinileno C1-6; cada R4 es independientemente un grupo representado por R3, oxo o tioxo; n es un numero entero de 0 a 2; cada R5 y R6 se seleccionan independientemente entre H, alquilo C1-4, cicloalquilo C3-8 o fenilo; donde dichos alquilo, cicloalquilo y fenilo están opcional e independientemente sustituidos con halogeno, -CN, -OH, -NH2, -OCF3, -OMe o alquilo C1-3; R7 y R8 son independientemente H, halogeno, ciano, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, -OR5, cicloalquilo C3-8, heterocicloalquilo de 5-10 miembros, -C(O)OR5, -C(O)R5, -OC(O)R5, -C(O)NR5R6, -NR5C(O)NR5R6, -NR5C(O)OR5, -NR5C(O)R5, -NR5C(S)NR5R6, -S(O)pNR5R6, -NR5R6, -SR5, -NR5S(O)pR5, donde cada uno de dichos alquilo, alquenilo, alquinilo, cicloalquilo y heterocicloalquilo está sustituido o sin sustituir; y cada R10 es independientemente H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, heterocicloalquilo de 5-10 miembros, arilo, aralquilo, heteroarilo o heteroaralquilo; donde dichos alquilo, alquenilo, alquinilo, alcoxi, cicloalquilo, heterocicloalquilo, arilo, aralquilo, heteroarilo y heteroaralquilo están opcional e independientemente sustituidos con halogeno, -CN, -OH, -NH2, - NH-alquilo C1-3, -N-(alquilo C1-3)2, -CONH2, -CONH-alquilo C1-3, -CON-(alquilo C1-3)2, -CO-alquilo C1-3, -CO2H, alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1-3, alquiloxicarbonilo C1-3, cicloalquilo C3-7 o fenilo; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1187208P | 2008-01-22 | 2008-01-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR070224A1 true AR070224A1 (es) | 2010-03-25 |
Family
ID=40474950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090100188A AR070224A1 (es) | 2008-01-22 | 2009-01-22 | Inhibidores de proteina quinasa y uso de los mismos |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20110282056A1 (es) |
| EP (1) | EP2231282A1 (es) |
| JP (1) | JP2011510004A (es) |
| KR (1) | KR20100102651A (es) |
| CN (1) | CN101918079A (es) |
| AR (1) | AR070224A1 (es) |
| AU (1) | AU2009206775A1 (es) |
| BR (1) | BRPI0907236A2 (es) |
| CA (1) | CA2709806A1 (es) |
| EA (1) | EA020885B1 (es) |
| IL (1) | IL206690A0 (es) |
| MX (1) | MX2010007584A (es) |
| WO (1) | WO2009094123A1 (es) |
| ZA (1) | ZA201003420B (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2356116A1 (en) | 2008-11-20 | 2011-08-17 | OSI Pharmaceuticals, Inc. | Substituted pyrroloý2,3-b¨-pyridines and-pyrazines |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| US20130072495A1 (en) | 2010-05-14 | 2013-03-21 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
| US8835472B2 (en) * | 2010-09-02 | 2014-09-16 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| US8877754B2 (en) * | 2010-09-06 | 2014-11-04 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| DE102011111400A1 (de) | 2011-08-23 | 2013-02-28 | Merck Patent Gmbh | Bicyclische heteroaromatische Verbindungen |
| JP2016507537A (ja) | 2013-02-07 | 2016-03-10 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 置換アセチレン誘導体およびmGluR4の正のアロステリックモジュレーターとしてのそれらの使用 |
| WO2014194245A2 (en) * | 2013-05-31 | 2014-12-04 | Nimbus Iris, Inc. | Cdk8 inhibitors and uses thereof |
| WO2014194242A2 (en) * | 2013-05-31 | 2014-12-04 | Nimbus Iris, Inc. | Flt3 inhibitors and uses thereof |
| US10195188B2 (en) | 2016-06-13 | 2019-02-05 | Chemocentryx, Inc. | Method of treating pancreatic cancer |
| SG10202012434QA (en) * | 2016-06-13 | 2021-01-28 | Chemocentryx Inc | Methods of treating pancreatic cancer |
| CN109843294A (zh) * | 2016-08-15 | 2019-06-04 | 普渡研究基金会 | 4-取代的氨基异喹啉衍生物 |
| US10449186B2 (en) * | 2017-06-21 | 2019-10-22 | University Of Kentucky Research Foundation | Phenylethynyl-substituted benzenes and heterocycles for the treatment of cancer |
| KR20190043437A (ko) | 2017-10-18 | 2019-04-26 | 씨제이헬스케어 주식회사 | 단백질 키나제 억제제로서의 헤테로고리 화합물 |
| KR102195348B1 (ko) | 2018-11-15 | 2020-12-24 | 에이치케이이노엔 주식회사 | 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE139232T1 (de) * | 1989-10-11 | 1996-06-15 | Teijin Ltd | Bizyklische pyrimidinderivate, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammensetzung |
| DE4218978A1 (de) * | 1992-06-10 | 1993-12-16 | Merck Patent Gmbh | 2,3-Dihydro-furo(2,3-b)pyridine |
| US7338957B2 (en) * | 2003-08-28 | 2008-03-04 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| TWI339206B (en) * | 2003-09-04 | 2011-03-21 | Vertex Pharma | Compositions useful as inhibitors of protein kinases |
| US7776869B2 (en) * | 2004-10-18 | 2010-08-17 | Amgen Inc. | Heteroaryl-substituted alkyne compounds and method of use |
| DE602006014540D1 (en) * | 2005-05-16 | 2010-07-08 | Irm Llc | Pyrrolopyridinderivate als proteinkinaseinhibitoren |
| NZ565255A (en) * | 2005-06-22 | 2010-04-30 | Plexxikon Inc | Pyrrolo[2,3-b] pyridine derivatives as protein kinase inhibitors |
| CA2635899A1 (en) * | 2006-01-19 | 2007-07-26 | Osi Pharmaceuticals, Inc. | Fused heterobicyclic kinase inhibitors |
| WO2009055674A1 (en) * | 2007-10-26 | 2009-04-30 | Targegen Inc. | Pyrrolopyrimidine alkynyl compounds and methods of making and using same |
-
2009
- 2009-01-20 KR KR1020107015260A patent/KR20100102651A/ko not_active Ceased
- 2009-01-20 CN CN2009801021159A patent/CN101918079A/zh active Pending
- 2009-01-20 MX MX2010007584A patent/MX2010007584A/es not_active Application Discontinuation
- 2009-01-20 EA EA201000848A patent/EA020885B1/ru not_active IP Right Cessation
- 2009-01-20 US US12/811,053 patent/US20110282056A1/en not_active Abandoned
- 2009-01-20 WO PCT/US2009/000291 patent/WO2009094123A1/en not_active Ceased
- 2009-01-20 JP JP2010543142A patent/JP2011510004A/ja not_active Withdrawn
- 2009-01-20 EP EP09703781A patent/EP2231282A1/en not_active Withdrawn
- 2009-01-20 AU AU2009206775A patent/AU2009206775A1/en not_active Abandoned
- 2009-01-20 CA CA2709806A patent/CA2709806A1/en not_active Abandoned
- 2009-01-20 BR BRPI0907236A patent/BRPI0907236A2/pt not_active IP Right Cessation
- 2009-01-22 AR ARP090100188A patent/AR070224A1/es unknown
-
2010
- 2010-05-14 ZA ZA2010/03420A patent/ZA201003420B/en unknown
- 2010-06-29 IL IL206690A patent/IL206690A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL206690A0 (en) | 2010-12-30 |
| BRPI0907236A2 (pt) | 2017-06-06 |
| JP2011510004A (ja) | 2011-03-31 |
| CN101918079A (zh) | 2010-12-15 |
| KR20100102651A (ko) | 2010-09-24 |
| EA020885B1 (ru) | 2015-02-27 |
| EP2231282A1 (en) | 2010-09-29 |
| EA201000848A1 (ru) | 2010-12-30 |
| WO2009094123A1 (en) | 2009-07-30 |
| CA2709806A1 (en) | 2009-07-30 |
| US20110282056A1 (en) | 2011-11-17 |
| MX2010007584A (es) | 2010-08-03 |
| AU2009206775A1 (en) | 2009-07-30 |
| ZA201003420B (en) | 2011-08-31 |
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