MX2011012353A - Derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2, 3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de la cinasa janus. - Google Patents
Derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2, 3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de la cinasa janus.Info
- Publication number
- MX2011012353A MX2011012353A MX2011012353A MX2011012353A MX2011012353A MX 2011012353 A MX2011012353 A MX 2011012353A MX 2011012353 A MX2011012353 A MX 2011012353A MX 2011012353 A MX2011012353 A MX 2011012353A MX 2011012353 A MX2011012353 A MX 2011012353A
- Authority
- MX
- Mexico
- Prior art keywords
- pyrimidines
- pyrrolo
- hetero
- aryl
- pyrrol
- Prior art date
Links
- 229940122245 Janus kinase inhibitor Drugs 0.000 title abstract 2
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 102000042838 JAK family Human genes 0.000 abstract 1
- 108091082332 JAK family Proteins 0.000 abstract 1
- 229940116839 Janus kinase 1 inhibitor Drugs 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
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- 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
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- 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
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- C07D—HETEROCYCLIC COMPOUNDS
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- 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
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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Abstract
La presente invención se relaciona con derivados de N-(hetero)aril-pirrolidina de Fórmula I: (ver fórmula (I)) que son inhibidores de JAK, tal como inhibidores selectivos de JAK1 ¡ útiles en el tratamiento de enfermedades asociadas con JAK, entre las que se incluyen, por ejemplo, los trastornos inflamatorios y autoinmunes y también el cáncer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18062209P | 2009-05-22 | 2009-05-22 | |
| US22509209P | 2009-07-13 | 2009-07-13 | |
| PCT/US2010/035783 WO2010135650A1 (en) | 2009-05-22 | 2010-05-21 | N-(HETERO)ARYL-PYRROLIDINE DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AND PYRROL-3-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2011012353A true MX2011012353A (es) | 2011-12-14 |
Family
ID=42543342
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2011012353A MX2011012353A (es) | 2009-05-22 | 2010-05-21 | Derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2, 3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de la cinasa janus. |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US8716303B2 (es) |
| EP (1) | EP2432555B1 (es) |
| JP (1) | JP5775070B2 (es) |
| KR (1) | KR101771401B1 (es) |
| CN (1) | CN102458581B (es) |
| AR (1) | AR076794A1 (es) |
| AU (1) | AU2010249380B2 (es) |
| BR (1) | BRPI1012159B1 (es) |
| CA (1) | CA2762174C (es) |
| CL (1) | CL2011002956A1 (es) |
| CO (1) | CO6440524A2 (es) |
| CR (1) | CR20110620A (es) |
| EA (1) | EA025520B1 (es) |
| ES (1) | ES2487542T3 (es) |
| IL (1) | IL216463A (es) |
| MX (1) | MX2011012353A (es) |
| MY (1) | MY156727A (es) |
| NZ (1) | NZ596479A (es) |
| SG (1) | SG176130A1 (es) |
| TW (1) | TW201100429A (es) |
| WO (1) | WO2010135650A1 (es) |
| ZA (1) | ZA201108544B (es) |
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|---|---|---|---|---|
| EP2343298B9 (en) | 2005-12-13 | 2020-05-06 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
| CL2008001709A1 (es) | 2007-06-13 | 2008-11-03 | Incyte Corp | Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras. |
| RS53245B2 (sr) | 2007-06-13 | 2022-10-31 | Incyte Holdings Corp | Soli inhibitora janus kinaze (r)-3-(4-(7h-pirolo(2,3-d) pirimidin-4-il)-1h-pirazol-1-il)-3-ciklopentilpropan-nitrila |
| US8309718B2 (en) * | 2007-11-16 | 2012-11-13 | Incyte Corporation | 4-pyrazolyl-N-arylpyrimidin-2-amines and 4-pyrazolyl-N-heteroarylpyrimidin-2-amines as janus kinase inhibitors |
| 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. |
| JOP20190230A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
| HRP20192203T1 (hr) | 2009-05-22 | 2020-03-06 | Incyte Holdings Corporation | 3-[4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il]oktan- ili heptan-nitril kao jak inhibitori |
| WO2010135650A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | N-(HETERO)ARYL-PYRROLIDINE DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AND PYRROL-3-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS |
| CA2766100C (en) | 2009-06-29 | 2018-05-22 | Incyte Corporation | Pyrimidinones as pi3k inhibitors |
| TWI466885B (zh) | 2009-07-31 | 2015-01-01 | Japan Tobacco Inc | 含氮螺環化合物及其醫藥用途 |
| TW201113285A (en) | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| BR112012008267B1 (pt) | 2009-10-09 | 2022-10-04 | Incyte Holdings Corporation | Derivados hidroxila, ceto e glucuronida de 3-(4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1- il)-3-ciclopentilpropanonitrila |
| JP5858434B2 (ja) * | 2010-02-18 | 2016-02-10 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Janusキナーゼ阻害薬としてのシクロブタンおよびメチルシクロブタン誘導体 |
| SI3354652T1 (sl) | 2010-03-10 | 2020-08-31 | Incyte Holdings Corporation | Derivati piperidin-4-il azetidina kot inhibitorji JAK1 |
| MY161078A (en) | 2010-05-21 | 2017-04-14 | Incyte Holdings Corp | Topical formulation for a jak inhibitor |
| WO2012068440A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
| JP5917545B2 (ja) | 2010-11-19 | 2016-05-18 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Jak阻害剤としてのシクロブチル置換ピロロピリジンおよびピロロピリミジン誘導体 |
| CN103237793B (zh) * | 2010-12-01 | 2015-06-10 | 日产化学工业株式会社 | 具有多发性骨髓瘤的治疗效果的吡唑化合物 |
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| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| US9394282B2 (en) | 2011-09-22 | 2016-07-19 | Merck Sharp & Dohme Corp. | Pyrazole carboxamides as Janus kinase inhibitors |
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| US20130129675A1 (en) | 2009-12-04 | 2013-05-23 | Board Of Regents, The University Of Texas System | Interferon therapies in combination with blockade of stat3 activation |
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| NZ596479A (en) | 2014-01-31 |
| US8716303B2 (en) | 2014-05-06 |
| ZA201108544B (en) | 2013-04-24 |
| BRPI1012159B1 (pt) | 2022-01-25 |
| CN102458581A (zh) | 2012-05-16 |
| KR101771401B1 (ko) | 2017-08-25 |
| EA201171454A1 (ru) | 2012-06-29 |
| CL2011002956A1 (es) | 2012-05-25 |
| SG176130A1 (en) | 2011-12-29 |
| US20100298334A1 (en) | 2010-11-25 |
| AU2010249380B2 (en) | 2015-08-20 |
| AU2010249380A1 (en) | 2011-12-08 |
| WO2010135650A1 (en) | 2010-11-25 |
| MY156727A (en) | 2016-03-15 |
| ES2487542T3 (es) | 2014-08-21 |
| EA025520B1 (ru) | 2017-01-30 |
| AR076794A1 (es) | 2011-07-06 |
| KR20120034665A (ko) | 2012-04-12 |
| EP2432555B1 (en) | 2014-04-30 |
| US20140221379A1 (en) | 2014-08-07 |
| US9334274B2 (en) | 2016-05-10 |
| JP2012527483A (ja) | 2012-11-08 |
| CO6440524A2 (es) | 2012-05-15 |
| EP2432555A1 (en) | 2012-03-28 |
| CA2762174C (en) | 2018-02-20 |
| CR20110620A (es) | 2012-02-02 |
| CA2762174A1 (en) | 2010-11-25 |
| IL216463A (en) | 2017-09-28 |
| BRPI1012159A2 (pt) | 2020-09-15 |
| CN102458581B (zh) | 2016-03-30 |
| JP5775070B2 (ja) | 2015-09-09 |
| IL216463A0 (en) | 2012-02-29 |
| TW201100429A (en) | 2011-01-01 |
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