ECSP11010945A - Aminotriazolopiridinas y su uso como inhibidores de cinasa - Google Patents
Aminotriazolopiridinas y su uso como inhibidores de cinasaInfo
- Publication number
- ECSP11010945A ECSP11010945A EC2011010945A ECSP11010945A ECSP11010945A EC SP11010945 A ECSP11010945 A EC SP11010945A EC 2011010945 A EC2011010945 A EC 2011010945A EC SP11010945 A ECSP11010945 A EC SP11010945A EC SP11010945 A ECSP11010945 A EC SP11010945A
- Authority
- EC
- Ecuador
- Prior art keywords
- aminotriazolopiridinas
- effective amount
- cinase
- inhibitors
- heteroaryl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- -1 Heteroaryl Compound Chemical class 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 2
- 102000020233 phosphotransferase Human genes 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 230000004968 inflammatory condition Effects 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000037361 pathway Effects 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
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/04—Dimeric indole alkaloids, e.g. vincaleucoblastine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/06—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00 containing at least one condensed beta-lactam ring system, provided for by groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00, e.g. a penem or a cepham system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Child & Adolescent Psychology (AREA)
- Virology (AREA)
Abstract
Se proporcionan en la presente Compuestos de Heteroarilo de la fórmula (I): donde R1 y R2 son como se definen en la presente, composiciones que comprenden una cantidad efectiva de un Compuesto de Heteroarilo y métodos para tratar o prevenir condiciones inflamatorias o cáncer, y condiciones tratables o prevenibles por la inhibición de una cinasa o ruta de cinasa que comprende administrar una cantidad efectiva de un Compuesto de Heteroarilo a un sujeto en necesidad del mismo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9521708P | 2008-09-08 | 2008-09-08 | |
| US23047909P | 2009-07-31 | 2009-07-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP11010945A true ECSP11010945A (es) | 2011-05-31 |
Family
ID=41228355
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2011010945A ECSP11010945A (es) | 2008-09-08 | 2011-04-01 | Aminotriazolopiridinas y su uso como inhibidores de cinasa |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US8299056B2 (es) |
| EP (1) | EP2344494B1 (es) |
| JP (1) | JP5689060B2 (es) |
| KR (1) | KR20110053266A (es) |
| CN (2) | CN102203093B (es) |
| AU (1) | AU2009288618B2 (es) |
| BR (1) | BRPI0918854A2 (es) |
| CA (1) | CA2735806A1 (es) |
| CL (1) | CL2011000480A1 (es) |
| CO (1) | CO6531502A2 (es) |
| CR (1) | CR20110132A (es) |
| EC (1) | ECSP11010945A (es) |
| ES (1) | ES2581565T3 (es) |
| IL (1) | IL211549A (es) |
| MX (1) | MX2011002536A (es) |
| NI (1) | NI201100048A (es) |
| NZ (1) | NZ591551A (es) |
| PE (1) | PE20110387A1 (es) |
| RU (1) | RU2552642C2 (es) |
| TW (1) | TWI453207B (es) |
| WO (1) | WO2010027500A1 (es) |
| ZA (1) | ZA201101586B (es) |
Families Citing this family (149)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60100852A (ja) * | 1984-09-28 | 1985-06-04 | Hitachi Ltd | 情報伝送方法 |
| KR101389246B1 (ko) | 2004-07-15 | 2014-04-24 | 브리스톨-마이어스스퀴브컴파니 | 아릴- 및 헤테로아릴-치환된 테트라히드로이소퀴놀린, 및 이것의 노르에피네프린, 도파민 및 세로토닌의 재흡수를 차단하기 위한 용도 |
| EP2252617A1 (en) | 2008-02-13 | 2010-11-24 | CGI Pharmaceuticals, Inc. | 6-aryl-imidaz0[l, 2-a]pyrazine derivatives, method of making, and method of use thereof |
| KR101247840B1 (ko) | 2008-02-22 | 2013-03-26 | 에프. 호프만-라 로슈 아게 | 아밀로이드 베타 조절제 |
| 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 |
| AU2009259867A1 (en) * | 2008-06-20 | 2009-12-23 | Genentech, Inc. | Triazolopyridine JAK inhibitor compounds and methods |
| GB0817207D0 (en) | 2008-09-19 | 2008-10-29 | Pimco 2664 Ltd | therapeutic apsac compounds and their use |
| JP5502089B2 (ja) | 2008-10-09 | 2014-05-28 | エフ.ホフマン−ラ ロシュ アーゲー | アミロイドβのモジュレーター |
| WO2010052199A1 (en) | 2008-11-10 | 2010-05-14 | F. Hoffmann-La Roche Ag | Heterocyclic gamma secretase modulators |
| EA021293B1 (ru) | 2008-12-08 | 2015-05-29 | Джилид Коннектикут, Инк. | ИМИДАЗОПИРАЗИНОВЫЕ ИНГИБИТОРЫ Syk, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СОДЕРЖАЩАЯ ИМИДАЗОПИРАЗИНОВЫЕ ИНГИБИТОРЫ Syk, И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
| SG171991A1 (en) | 2008-12-08 | 2011-07-28 | Gilead Connecticut Inc | Imidazopyrazine syk inhibitors |
| US8450321B2 (en) | 2008-12-08 | 2013-05-28 | Gilead Connecticut, Inc. | 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor |
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| CN113583110B (zh) * | 2021-08-19 | 2023-07-21 | 华南农业大学 | 一种苯并三唑半抗原、人工抗原和抗体及其制备方法与应用 |
| CN113801152B (zh) * | 2021-08-30 | 2023-08-11 | 上海日异生物科技有限公司 | 3-羧基-5-羟基苯硼酸的合成方法 |
| CN115819425A (zh) * | 2022-12-22 | 2023-03-21 | 五邑大学 | 一种三唑并六元氮杂环-2-胺类化合物及其制备方法和应用 |
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2009
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- 2009-09-08 RU RU2011113540/04A patent/RU2552642C2/ru not_active IP Right Cessation
- 2009-09-08 CN CN200980144169.1A patent/CN102203093B/zh not_active Expired - Fee Related
- 2009-09-08 KR KR1020117007996A patent/KR20110053266A/ko not_active Ceased
- 2009-09-08 NZ NZ591551A patent/NZ591551A/en not_active IP Right Cessation
- 2009-09-08 JP JP2011526054A patent/JP5689060B2/ja not_active Expired - Fee Related
- 2009-09-08 EP EP09789271.5A patent/EP2344494B1/en active Active
- 2009-09-08 AU AU2009288618A patent/AU2009288618B2/en not_active Ceased
- 2009-09-08 WO PCT/US2009/005020 patent/WO2010027500A1/en not_active Ceased
- 2009-09-08 BR BRPI0918854-1A patent/BRPI0918854A2/pt not_active IP Right Cessation
- 2009-09-08 US US12/555,018 patent/US8299056B2/en active Active
- 2009-09-08 PE PE2011000599A patent/PE20110387A1/es not_active Application Discontinuation
- 2009-09-08 ES ES09789271.5T patent/ES2581565T3/es active Active
- 2009-09-08 CA CA2735806A patent/CA2735806A1/en not_active Abandoned
- 2009-09-08 MX MX2011002536A patent/MX2011002536A/es active IP Right Grant
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2011
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- 2011-03-11 CR CR20110132A patent/CR20110132A/es unknown
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2012
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| Publication number | Publication date |
|---|---|
| CO6531502A2 (es) | 2012-09-28 |
| CN104910148B (zh) | 2017-06-27 |
| US8299056B2 (en) | 2012-10-30 |
| ZA201101586B (en) | 2012-05-30 |
| CR20110132A (es) | 2011-06-20 |
| AU2009288618B2 (en) | 2014-10-02 |
| US20130005707A1 (en) | 2013-01-03 |
| CN102203093A (zh) | 2011-09-28 |
| CL2011000480A1 (es) | 2011-09-16 |
| ES2581565T3 (es) | 2016-09-06 |
| JP5689060B2 (ja) | 2015-03-25 |
| AU2009288618A1 (en) | 2010-03-11 |
| JP2012502029A (ja) | 2012-01-26 |
| BRPI0918854A2 (pt) | 2019-02-26 |
| RU2552642C2 (ru) | 2015-06-10 |
| NI201100048A (es) | 2011-11-17 |
| TW201024293A (en) | 2010-07-01 |
| RU2011113540A (ru) | 2012-10-20 |
| US20100093698A1 (en) | 2010-04-15 |
| EP2344494B1 (en) | 2016-04-20 |
| CN102203093B (zh) | 2015-05-13 |
| CN104910148A (zh) | 2015-09-16 |
| WO2010027500A1 (en) | 2010-03-11 |
| IL211549A0 (en) | 2011-05-31 |
| KR20110053266A (ko) | 2011-05-19 |
| PE20110387A1 (es) | 2011-06-22 |
| IL211549A (en) | 2017-04-30 |
| NZ591551A (en) | 2011-10-28 |
| CA2735806A1 (en) | 2010-03-11 |
| MX2011002536A (es) | 2011-04-04 |
| EP2344494A1 (en) | 2011-07-20 |
| TWI453207B (zh) | 2014-09-21 |
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