CN101600718B - 咪唑并[1,2-b]哒嗪和吡唑并[1,5-a]嘧啶衍生物及其作为蛋白激酶抑制剂的用途 - Google Patents
咪唑并[1,2-b]哒嗪和吡唑并[1,5-a]嘧啶衍生物及其作为蛋白激酶抑制剂的用途 Download PDFInfo
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- CN101600718B CN101600718B CN2007800412832A CN200780041283A CN101600718B CN 101600718 B CN101600718 B CN 101600718B CN 2007800412832 A CN2007800412832 A CN 2007800412832A CN 200780041283 A CN200780041283 A CN 200780041283A CN 101600718 B CN101600718 B CN 101600718B
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- 0 CCCC1CCC(CC*C)CC1 Chemical compound CCCC1CCC(CC*C)CC1 0.000 description 6
- QUMFENBLHSNPNH-UHFFFAOYSA-N CCC(CNc(cc1)n[n]2c1ncc2-c1cc(OC(F)(F)F)ccc1)N1CCN(C)CC1 Chemical compound CCC(CNc(cc1)n[n]2c1ncc2-c1cc(OC(F)(F)F)ccc1)N1CCN(C)CC1 QUMFENBLHSNPNH-UHFFFAOYSA-N 0.000 description 1
- HZOZGTVOMTVWDK-UHFFFAOYSA-N CCN1CCC(CNC(C=C2)=NN3C2=NCC3(C)c2cc(OC(F)(F)F)ccc2)CC1 Chemical compound CCN1CCC(CNC(C=C2)=NN3C2=NCC3(C)c2cc(OC(F)(F)F)ccc2)CC1 HZOZGTVOMTVWDK-UHFFFAOYSA-N 0.000 description 1
- IKJWCJBQADONGF-UHFFFAOYSA-N CN1CCC(CNc(cc2)n[n]3c2ncc3-c(cc(cc2)OC(F)(F)F)c2O)CC1 Chemical compound CN1CCC(CNc(cc2)n[n]3c2ncc3-c(cc(cc2)OC(F)(F)F)c2O)CC1 IKJWCJBQADONGF-UHFFFAOYSA-N 0.000 description 1
- MHXGEROHKGDZGO-UHFFFAOYSA-N CN1CCC(CNc(cc2)n[n]3c2ncc3-c2cccc(OC(F)(F)F)c2)CC1 Chemical compound CN1CCC(CNc(cc2)n[n]3c2ncc3-c2cccc(OC(F)(F)F)c2)CC1 MHXGEROHKGDZGO-UHFFFAOYSA-N 0.000 description 1
- SQZQTKQCWIKGPB-UHFFFAOYSA-N COc(ccc(C(F)(F)F)c1)c1-c1cnc(cc2)[n]1nc2Cl Chemical compound COc(ccc(C(F)(F)F)c1)c1-c1cnc(cc2)[n]1nc2Cl SQZQTKQCWIKGPB-UHFFFAOYSA-N 0.000 description 1
- UWDLNRUFHRYMSE-UHFFFAOYSA-N Cc1cc(N)nnc1Cl Chemical compound Cc1cc(N)nnc1Cl UWDLNRUFHRYMSE-UHFFFAOYSA-N 0.000 description 1
- VVYQQZDXZWTXIU-UHFFFAOYSA-N Cc1cc2[n]cc(-c3cc(OC(F)(F)F)ccc3)[n]2nc1NCC1CCN(C)CC1 Chemical compound Cc1cc2[n]cc(-c3cc(OC(F)(F)F)ccc3)[n]2nc1NCC1CCN(C)CC1 VVYQQZDXZWTXIU-UHFFFAOYSA-N 0.000 description 1
- VFPVLQQNCLDGTI-UHFFFAOYSA-N Cc1cc2ncc[n]2nc1Cl Chemical compound Cc1cc2ncc[n]2nc1Cl VFPVLQQNCLDGTI-UHFFFAOYSA-N 0.000 description 1
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- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61P35/04—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
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86456606P | 2006-11-06 | 2006-11-06 | |
| US60/864,566 | 2006-11-06 | ||
| US89252307P | 2007-03-01 | 2007-03-01 | |
| US60/892,523 | 2007-03-01 | ||
| US95798807P | 2007-08-24 | 2007-08-24 | |
| US60/957,988 | 2007-08-24 | ||
| PCT/US2007/083773 WO2008058126A2 (en) | 2006-11-06 | 2007-11-06 | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101600718A CN101600718A (zh) | 2009-12-09 |
| CN101600718B true CN101600718B (zh) | 2013-07-03 |
Family
ID=39277096
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2007800412832A Active CN101600718B (zh) | 2006-11-06 | 2007-11-06 | 咪唑并[1,2-b]哒嗪和吡唑并[1,5-a]嘧啶衍生物及其作为蛋白激酶抑制剂的用途 |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US7750007B2 (https=) |
| EP (1) | EP2086979B1 (https=) |
| JP (1) | JP5357763B2 (https=) |
| KR (1) | KR101546493B1 (https=) |
| CN (1) | CN101600718B (https=) |
| AU (1) | AU2007316417B2 (https=) |
| BR (1) | BRPI0718029A2 (https=) |
| CA (1) | CA2667487C (https=) |
| MX (1) | MX2009004700A (https=) |
| MY (1) | MY146474A (https=) |
| NZ (1) | NZ576234A (https=) |
| RU (1) | RU2487875C2 (https=) |
| SG (1) | SG176461A1 (https=) |
| WO (1) | WO2008058126A2 (https=) |
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| CN101395155A (zh) * | 2005-10-07 | 2009-03-25 | 埃克塞里艾克西斯公司 | PI3Kα的吡啶并嘧啶酮抑制剂 |
| EP2455382B1 (en) | 2005-12-13 | 2016-10-26 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
| US7683060B2 (en) | 2006-08-07 | 2010-03-23 | Incyte Corporation | Triazolotriazines as kinase inhibitors |
| CA2663091A1 (en) * | 2006-09-07 | 2008-03-13 | Biogen Idec Ma Inc. | Modulators of interleukin-1 receptor-associated kinase |
| EA200900573A1 (ru) * | 2006-10-20 | 2009-10-30 | АйАрЭм ЭлЭлСи | Композиции и способы для модуляции рецепторов c-kit и pdgfr |
| ME02372B (me) | 2006-11-22 | 2016-06-20 | Incyte Holdings Corp | Imidazotriazini i imidazopiramidini kao inhibitori kinaze |
| AR067326A1 (es) * | 2007-05-11 | 2009-10-07 | Novartis Ag | Imidazopiridinas y pirrolo -pirimidinas sustituidas como inhibidores de cinasa de lipido |
| EP3070090B1 (en) | 2007-06-13 | 2018-12-12 | Incyte Holdings Corporation | Use of salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h- pyrazol-1-yl)-3- cyclopentylpropanenitrile |
| FR2918061B1 (fr) * | 2007-06-28 | 2010-10-22 | Sanofi Aventis | Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique. |
| CA2724842A1 (en) * | 2008-05-19 | 2009-11-26 | Sunovion Pharmaceuticals Inc. | Imidazo[1,2-a]pyridine compounds |
| WO2009143211A2 (en) | 2008-05-21 | 2009-11-26 | Incyte Corporation | Salts of 2-fluoro-n-methyl-4-[7-(quinolin-6-yl-methyl)- imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide and processes related to preparing the same |
| US9156812B2 (en) | 2008-06-04 | 2015-10-13 | Bristol-Myers Squibb Company | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
| AR071997A1 (es) * | 2008-06-04 | 2010-07-28 | Bristol Myers Squibb Co | Forma cristalina de 6-((4s)-2-metil-4-(2-naftil)-1,2,3,4-tetrahidroisoquinolin-7-il)piridazin-3-amina |
| WO2010022081A1 (en) * | 2008-08-19 | 2010-02-25 | Array Biopharma Inc. | Triazolopyridine compounds as pim kinase inhibitors |
| US8987251B2 (en) | 2008-08-19 | 2015-03-24 | Array Biopharma Inc. | Triazolopyridine compounds as PIM kinase inhibitors |
| US8895550B2 (en) | 2008-08-19 | 2014-11-25 | Array Biopharma Inc. | Triazolopyridine compounds as PIM kinase inhibitors |
| TWI496779B (zh) * | 2008-08-19 | 2015-08-21 | Array Biopharma Inc | 作為pim激酶抑制劑之三唑吡啶化合物 |
| PT2350075E (pt) | 2008-09-22 | 2014-06-09 | Array Biopharma Inc | Compostos imidazo[1,2b]piridazina substituídos como inibidores da trk cinase |
| CL2009001884A1 (es) * | 2008-10-02 | 2010-05-14 | Incyte Holdings Corp | Uso de 3-ciclopentil-3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)propanonitrilo, inhibidor de janus quinasa, y uso de una composición que lo comprende para el tratamiento del ojo seco. |
| AR074052A1 (es) | 2008-10-22 | 2010-12-22 | Array Biopharma Inc | Compuestos pirazolo{1,5-a}pirimidina sustituida como inhibidores de trk cinasa |
| EP2429295B1 (en) | 2009-05-12 | 2013-12-25 | Albany Molecular Research, Inc. | Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof |
| BRPI1011066A2 (pt) | 2009-05-20 | 2017-03-21 | Cylene Pharmaceuticals Inc | "pirazolopirimidinas e heterociclos relacionados como inibidores de quinase |
| JP5775070B2 (ja) * | 2009-05-22 | 2015-09-09 | インサイト・コーポレイションIncyte Corporation | ヤヌスキナーゼ阻害剤としてのピラゾール−4−イル−ピロロ[2,3−d]ピリミジンおよびピロール−3−イル−ピロロ[2,3−d]ピリミジンのN−(ヘテロ)アリール−ピロリジン誘導体 |
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| US9227971B2 (en) | 2010-01-19 | 2016-01-05 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyrimidine compounds as mTOR inhibitors |
| EA025304B1 (ru) | 2010-02-03 | 2016-12-30 | Инсайт Холдингс Корпорейшн | ИМИДАЗО[1,2-b][1,2,4]ТРИАЗИНЫ В КАЧЕСТВЕ c-Met ИНГИБИТОРОВ |
| UY33221A (es) | 2010-02-09 | 2011-09-30 | Univ California | MÉTODOS PARA TRATAR CÁNCER USANDO INHIBIDORES DE PI3K Y mTOR EN COMBINACIÓN CON INHIBIDORES DE AUTOFAGIA |
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| CN1798747A (zh) * | 2000-08-22 | 2006-07-05 | 葛兰素集团有限公司 | 为蛋白激酶抑制剂的稠合的吡唑衍生物 |
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| CA2667487C (en) | 2017-04-04 |
| CN101600718A (zh) | 2009-12-09 |
| KR101546493B1 (ko) | 2015-08-21 |
| RU2487875C2 (ru) | 2013-07-20 |
| US8710057B2 (en) | 2014-04-29 |
| US20110281863A1 (en) | 2011-11-17 |
| WO2008058126A3 (en) | 2008-06-26 |
| CA2667487A1 (en) | 2008-05-15 |
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