PE20091158A1 - 5-anilinoimidazopiridinas y metodos de uso - Google Patents
5-anilinoimidazopiridinas y metodos de usoInfo
- Publication number
- PE20091158A1 PE20091158A1 PE2008002130A PE2008002130A PE20091158A1 PE 20091158 A1 PE20091158 A1 PE 20091158A1 PE 2008002130 A PE2008002130 A PE 2008002130A PE 2008002130 A PE2008002130 A PE 2008002130A PE 20091158 A1 PE20091158 A1 PE 20091158A1
- Authority
- PE
- Peru
- Prior art keywords
- halo
- alkyl
- fluor
- imidazo
- pyridin
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 4
- CUMTUBVTKOYYOU-UHFFFAOYSA-N 2-fluoro-4-iodoaniline Chemical compound NC1=CC=C(I)C=C1F CUMTUBVTKOYYOU-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 208000032839 leukemia Diseases 0.000 abstract 1
- 201000005202 lung cancer Diseases 0.000 abstract 1
- 208000020816 lung neoplasm Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
-
- 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
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 5-ANILINOIMIDAZOPIRIDINAS DE FORMULA (I) DONDE Z1 ES CR1 O N; R1 Y R1' SON CADA UNO H, HALO, ALQUILO(C1-C3), CF3, ENTRE OTROS; Z2 ES CR2 O N; Z3 ES CR3 O N, SIEMPRE QUE SOLO UNO DE Z1, Z2 Y Z3 SEA N; R2 Y R3 SON CADA UNO H, HALO, CN, CF3, OCF3, ENTRE OTROS; R4 ES H, ALQUILO(C1-C6) O CARBOCICLILO(C3-C4); Y ES W-C(O)- O W', DONDE W ES X1-N(R5)- O R11'-O-, EN DONDE R5 ES H O ALQUILO(C1-C12); X1 ES R11' O -OR11'; R11' ES H, ALQUILO(C1-C12), ALQUENILO(C2-C8), ENTRE OTROS; W' ES UN COMPUESTO DE FORMULA (i), (ii), ENTRE OTROS, DONDE R7 ES HALO, CN, CF3, ENTRE OTROS; R8 ES ALQUILO(C1-C12), ARILO, ENTRE OTROS; Het ES HETEROARILO; X4 ES (a), EN DONDE R6 ES H, HALO, -OCF3, ENTRE OTROS; R6' ES H, HALO, NO2, ENTRE OTROS; p ES DE 0 A 3. SON COMPUESTOS PREFERIDOS: (2-HIDROXIETOXI)-AMIDA DEL ACIDO 5-(2-FLUOR-4-YODOFENILAMINO)-IMIDAZO[1,5-a]PIRIDIN-6-CARBOXILICO, ((R)-2,3-DIHIDROXI-PROPOXI)-AMIDA DEL ACIDO 5-(2-FLUOR-4-YODO-FENILAMINO)-IMIDAZO[1,5-a]PIRIDIN-6-CARBOXILICO, ((S)-2-HIDROXI-PROPOXI)-AMIDA DEL ACIDO 5-(2-FLUOR-4-YODO-FENILAMINO)-IMIDAZO[1,5-a]PIRIDIN-6-CARBOXILICO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ACTIVIDAD DE MEK QUINASA SIENDO UTILES EN EL TRATAMIENTO DE CANCER AL PULMON, LEUCEMIA, ARTRITIS REUMATOIDEA
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1512907P | 2007-12-19 | 2007-12-19 | |
| US5401408P | 2008-05-16 | 2008-05-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20091158A1 true PE20091158A1 (es) | 2009-08-28 |
Family
ID=40350172
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008002130A PE20091158A1 (es) | 2007-12-19 | 2008-12-18 | 5-anilinoimidazopiridinas y metodos de uso |
| PE2013000381A PE20131210A1 (es) | 2007-12-19 | 2008-12-18 | Derivados de 5-anilinoimidazopiridina como inhibidores de mek |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2013000381A PE20131210A1 (es) | 2007-12-19 | 2008-12-18 | Derivados de 5-anilinoimidazopiridina como inhibidores de mek |
Country Status (27)
| Country | Link |
|---|---|
| US (4) | US7923456B2 (es) |
| EP (2) | EP2222675B1 (es) |
| JP (1) | JP5421925B2 (es) |
| KR (1) | KR101195329B1 (es) |
| CN (1) | CN101945870B (es) |
| AR (1) | AR069803A1 (es) |
| AU (1) | AU2008343065B2 (es) |
| BR (1) | BRPI0819529A2 (es) |
| CA (1) | CA2706571C (es) |
| CL (1) | CL2008003810A1 (es) |
| CY (2) | CY1114663T1 (es) |
| DK (2) | DK2690101T3 (es) |
| ES (2) | ES2546171T3 (es) |
| HR (1) | HRP20151002T1 (es) |
| HU (1) | HUE025192T2 (es) |
| IL (1) | IL205977A (es) |
| MX (1) | MX2010006800A (es) |
| MY (1) | MY158829A (es) |
| NZ (1) | NZ586802A (es) |
| PE (2) | PE20091158A1 (es) |
| PL (2) | PL2222675T3 (es) |
| PT (2) | PT2690101E (es) |
| RU (1) | RU2441004C1 (es) |
| SI (2) | SI2690101T1 (es) |
| TW (1) | TWI441820B (es) |
| WO (1) | WO2009085983A1 (es) |
| ZA (1) | ZA201003625B (es) |
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| US8343977B2 (en) | 2009-12-30 | 2013-01-01 | Arqule, Inc. | Substituted triazolo-pyrimidine compounds |
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| CN102020651B (zh) | 2010-11-02 | 2012-07-18 | 北京赛林泰医药技术有限公司 | 6-芳基氨基吡啶酮甲酰胺mek抑制剂 |
| AU2012290121B2 (en) | 2011-08-01 | 2015-11-26 | Genentech, Inc. | Methods of treating cancer using PD-1 axis binding antagonists and MEK inhibitors |
| WO2013082511A1 (en) | 2011-12-02 | 2013-06-06 | Genentech, Inc. | Methods for overcoming tumor resistance to vegf antagonists |
| KR101689946B1 (ko) | 2012-06-08 | 2016-12-26 | 에프. 호프만-라 로슈 아게 | 암의 치료를 위한 포스포이노시타이드 3 키나제 억제제 화합물 및 화학치료제의 돌연변이체 선택성 및 조합물 |
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| CN108358939A (zh) * | 2014-07-29 | 2018-08-03 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环化合物及其制备方法和用途 |
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| CN117321418A (zh) | 2021-03-18 | 2023-12-29 | 诺华股份有限公司 | 癌症生物标志物及其使用方法 |
| TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗ＴＧＦβ抗體及其他治療劑用於治療增殖性疾病之用途 |
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| KR20250027281A (ko) | 2022-05-20 | 2025-02-25 | 노파르티스 아게 | Epha2 bcl-xl 억제제 항체-약물 접합체 및 그의 사용 방법 |
| CN119562832A (zh) | 2022-05-20 | 2025-03-04 | 诺华股份有限公司 | Met bcl-xl抑制剂抗体-药物缀合物及其使用方法 |
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