PE20081507A1 - Derivados de pirimidina como moduladores de jnk - Google Patents
Derivados de pirimidina como moduladores de jnkInfo
- Publication number
- PE20081507A1 PE20081507A1 PE2007001744A PE2007001744A PE20081507A1 PE 20081507 A1 PE20081507 A1 PE 20081507A1 PE 2007001744 A PE2007001744 A PE 2007001744A PE 2007001744 A PE2007001744 A PE 2007001744A PE 20081507 A1 PE20081507 A1 PE 20081507A1
- Authority
- PE
- Peru
- Prior art keywords
- pyrimidin
- alkyl
- ilamino
- indol
- halogen
- Prior art date
Links
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title abstract 2
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 title 1
- -1 CYCLOHEXYL Chemical class 0.000 abstract 2
- 108010055717 JNK Mitogen-Activated Protein Kinases Proteins 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical group O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Chemical group 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Chemical group 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000000565 sulfonamide group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61P11/06—Antiasthmatics
-
- 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
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- 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
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Emergency Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
REFERIDA A UN DERIVADO DE PIRIMIDINA DE FORMULA (I), DONDE X1 ES N, N-R3, CH3, C-R3, O; X2 ES N, NH, N-CH3, CH, CH2, ENTRE OTROS; X3 ES N, C O CH; X4 Y X5 SON C, CH O N; R ES -(CICLOHEXIL)-R2 O -(FENIL)-R8 SUSTITUIDOS OPCIONALMENTE CON METILO, FLUOR, CLORO O HIDROXI; R1 ES HALOGENO, NITRO, CN, OH, ENTRE OTROS; n ES UN ENTERO DE 0 A 2; R3 ES H O ALQUILO C1-C6; R2 ES H, OH, =O, CN, ENTRE OTROS; R8 ES H, ALQUILO C1-C6, OR3, SO2NH2, ENTRE OTROS; Z ES H, HALOGENO, ALQUILO C1-C12, NH2. SON COMPUESTOS PREFERIDOS: 4-[4-(4-BENCILOXI-INDOL-1-IL)-PIRIMIDIN-2-ILAMINO]-CICLOHEXA-NOL, 4-[4-(4-BROMOINDOL-1-IL)-PIRIMIDIN-2-ILAMINO]-CICLOHEXANOL, (2-METANOSULFONILETIL)AMIDA DEL ACIDO 4-(4-INDOL-1-IL)-PIRIMIDIN-2-ILAMINO]-CICLOHEXANOCARBOXILICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA Y A UN PROCESO DE PREPARACION. DICHOS COMPUESTOS SON MODULADORES DE QUINASAS C-JUN-N-TERMINALES (JNK) Y SON UTILES EN EL TRATAMIENTO DE TRASTORNOS INMUNES, INFLAMATORIOS, NEUROLOGICAS, ENTRE OTRAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87362506P | 2006-12-08 | 2006-12-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20081507A1 true PE20081507A1 (es) | 2008-11-12 |
Family
ID=39099641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007001744A PE20081507A1 (es) | 2006-12-08 | 2007-12-07 | Derivados de pirimidina como moduladores de jnk |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8399462B2 (es) |
| EP (1) | EP2102194A1 (es) |
| JP (1) | JP5179509B2 (es) |
| KR (1) | KR101152162B1 (es) |
| CN (1) | CN101547917A (es) |
| AR (1) | AR064133A1 (es) |
| AU (1) | AU2007328981B2 (es) |
| BR (1) | BRPI0720003A2 (es) |
| CA (1) | CA2670375A1 (es) |
| CL (1) | CL2007003502A1 (es) |
| IL (1) | IL198543A0 (es) |
| MX (1) | MX2009005508A (es) |
| NO (1) | NO20091942L (es) |
| PE (1) | PE20081507A1 (es) |
| RU (1) | RU2493155C2 (es) |
| TW (1) | TW200831101A (es) |
| WO (1) | WO2008068171A1 (es) |
| ZA (1) | ZA200903495B (es) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2158182A2 (en) | 2007-06-15 | 2010-03-03 | F. Hoffmann-Roche AG | A novel process for the preparation of 3-amino-pentan-1,5-diol |
| EP2205564B1 (en) * | 2007-10-23 | 2014-07-30 | F. Hoffmann-La Roche AG | Novel kinase inhibitors |
| CA2722158A1 (en) | 2008-05-16 | 2009-11-19 | F. Hoffmann-La Roche Ag | Inhibitors of jnk |
| EP2379527A1 (en) * | 2008-12-19 | 2011-10-26 | F. Hoffmann-La Roche AG | Pyrimidin- 2 -ylamino derivatives and their use to treat inflammation |
| SG173792A1 (en) | 2009-02-24 | 2011-10-28 | Hoffmann La Roche | Imidazo [1, 2 -a] pyridines as jnk modulators |
| JP6073677B2 (ja) | 2009-06-12 | 2017-02-01 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | 縮合複素環式化合物およびそれらの使用 |
| WO2011018417A1 (en) * | 2009-08-10 | 2011-02-17 | F. Hoffmann-La Roche Ag | Inhibitors of jnk |
| NZ599041A (en) * | 2009-11-13 | 2014-05-30 | Genosco | Kinase inhibitors |
| CA2784807C (en) | 2009-12-29 | 2021-12-14 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
| EP2576559B1 (en) * | 2010-06-04 | 2015-03-04 | F.Hoffmann-La Roche Ag | Inhibitors of jnk |
| MX2012013589A (es) * | 2010-06-04 | 2012-12-17 | Hoffmann La Roche | Derivados de 2-amino pirimidina utiles como inhibidores de cinasas del extremo n-terminal de c-jun (jnk). |
| CA2826295C (en) | 2011-02-04 | 2020-10-20 | Duquesne University Of The Holy Spirit | Bicyclic and tricyclic pyrimidine tyrosine kinase inhibitors with antitubulin activity and methods of treating a patient |
| SG10201601802YA (en) | 2011-03-10 | 2016-04-28 | Daiichi Sankyo Co Ltd | Dispiropyrrolidine derivatives |
| EP2822935B1 (en) | 2011-11-17 | 2019-05-15 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-jun-n-terminal kinase (jnk) |
| DK2903440T3 (en) | 2012-10-02 | 2017-12-11 | Bayer Cropscience Ag | THETEROCYCLIC COMPOUNDS AS PESTICIDES |
| WO2014063068A1 (en) | 2012-10-18 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| WO2014063061A1 (en) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
| US10000483B2 (en) | 2012-10-19 | 2018-06-19 | Dana-Farber Cancer Institute, Inc. | Bone marrow on X chromosome kinase (BMX) inhibitors and uses thereof |
| EP2964221B1 (en) | 2013-03-04 | 2017-12-06 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2014134776A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2014134772A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| WO2014134774A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| CA2927917C (en) | 2013-10-18 | 2022-08-09 | Syros Pharmaceuticals, Inc. | Heteroaromatic compounds useful for the treatment of proliferative diseases |
| JP6491202B2 (ja) | 2013-10-18 | 2019-03-27 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | サイクリン依存性キナーゼ7(cdk7)の多環阻害剤 |
| WO2015073344A1 (en) * | 2013-11-14 | 2015-05-21 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| RS58175B1 (sr) | 2014-04-04 | 2019-03-29 | Syros Pharmaceuticals Inc | Inhibitori ciklin-zavisne kinaze 7 (cdk7) |
| US9862688B2 (en) | 2014-04-23 | 2018-01-09 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged janus kinase inhibitors and uses thereof |
| WO2015164614A1 (en) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Janus kinase inhibitors and uses thereof |
| WO2016036586A1 (en) | 2014-09-03 | 2016-03-10 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| BR112017012272A2 (pt) * | 2014-12-11 | 2018-01-30 | Beta Pharma, Inc. | derivados de 2-anilinopirimidina como moduladores de egfr |
| HK1245260A1 (zh) | 2014-12-23 | 2018-08-24 | Dana-Farber Cancer Institute, Inc. | 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂 |
| CN107427521B (zh) | 2015-03-27 | 2021-08-03 | 达纳-法伯癌症研究所股份有限公司 | 细胞周期蛋白依赖性激酶的抑制剂 |
| CA2986441A1 (en) | 2015-06-12 | 2016-12-15 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| EP4019515A1 (en) | 2015-09-09 | 2022-06-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| WO2017133664A1 (en) * | 2016-02-05 | 2017-08-10 | Savira Pharmaceuticals Gmbh | Bicyclic pyridine and pyrimidine derivatives and their use in the treatment, amelioration or prevention of influenza |
| WO2017133658A1 (en) * | 2016-02-05 | 2017-08-10 | Savira Pharmaceuticals Gmbh | 4, 7-diazaindole and 4, 7-diazaindazole derivatives and their use in the treatment, amelioration or prevention of influenza |
| AU2018283289B2 (en) | 2017-06-16 | 2021-03-25 | Beta Pharma, Inc. | Pharmaceutical formulations of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide and salts thereof |
| JOP20180094A1 (ar) | 2017-10-18 | 2019-04-18 | Hk Inno N Corp | مركب حلقي غير متجانس كمثبط بروتين كيناز |
| JP7590185B2 (ja) | 2018-06-25 | 2024-11-26 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | Taireファミリーキナーゼインヒビターおよびそれらの使用 |
| KR102195348B1 (ko) * | 2018-11-15 | 2020-12-24 | 에이치케이이노엔 주식회사 | 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물 |
| EP3902542A4 (en) | 2018-12-28 | 2022-09-07 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 and uses thereof |
| MX2023000630A (es) * | 2020-07-14 | 2023-03-15 | Wuhan Ll Science & Technology Development Co Ltd | Inhibidor de rock, y método de preparacion para el mismo y uso del mismo. |
| CN113563310B (zh) * | 2021-06-25 | 2022-10-11 | 浙江工业大学 | 一种4-(1-甲基吲哚-3-基)嘧啶类衍生物及其应用 |
| WO2023107705A1 (en) | 2021-12-10 | 2023-06-15 | Incyte Corporation | Bicyclic amines as cdk12 inhibitors |
| CN114790174B (zh) * | 2022-04-14 | 2023-09-29 | 淮阴工学院 | 一种连续合成1h-吲唑类化合物的方法 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4788195A (en) * | 1986-01-13 | 1988-11-29 | American Cyanamid Company | 4,5,6-substituted-N-(substituted-phenyl)-2-pyrimidinamines |
| JP2003523942A (ja) | 1999-06-30 | 2003-08-12 | メルク エンド カムパニー インコーポレーテッド | Srcキナーゼ阻害剤化合物 |
| GB9919778D0 (en) | 1999-08-21 | 1999-10-27 | Zeneca Ltd | Chemical compounds |
| US20030004174A9 (en) * | 2000-02-17 | 2003-01-02 | Armistead David M. | Kinase inhibitors |
| WO2001062233A2 (en) * | 2000-02-25 | 2001-08-30 | F. Hoffmann La Roche Ag | Adenosine receptor modulators |
| GB0103926D0 (en) * | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
| IL156784A0 (en) | 2001-02-20 | 2004-02-08 | Astrazeneca Ab | 2-arylamino-pyrimidines for the treatment of gsk3-related disorders |
| UA75392C2 (en) * | 2001-02-23 | 2006-04-17 | Merck & Co Inc | N-substituted non-aryl heterocyclic antagonists nmda/nr2b |
| US20040171630A1 (en) * | 2001-06-19 | 2004-09-02 | Yuntae Kim | Tyrosine kinase inhibitors |
| EP1463730B1 (en) * | 2001-12-17 | 2006-04-19 | SmithKline Beecham Corporation | Pyrazolopyridazine derivatives |
| TW200302722A (en) | 2002-02-13 | 2003-08-16 | Astrazeneca Ab | Therapeutic agents |
| WO2004005283A1 (en) * | 2002-07-09 | 2004-01-15 | Vertex Pharmaceuticals Incorporated | Imidazoles, oxazoles and thiazoles with protein kinase inhibiting activities |
| TW200528101A (en) | 2004-02-03 | 2005-09-01 | Astrazeneca Ab | Chemical compounds |
| US7855205B2 (en) * | 2004-10-29 | 2010-12-21 | Janssen Pharmaceutica Nv | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
| WO2006124863A2 (en) * | 2005-05-16 | 2006-11-23 | Irm Llc | Pyrrolopyridine derivatives as protein kinase inhibitors |
| DE102006012617A1 (de) * | 2006-03-20 | 2007-09-27 | Merck Patent Gmbh | 4-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
| WO2008028860A1 (en) | 2006-09-08 | 2008-03-13 | F. Hoffmann-La Roche Ag | Benzotriazole kinase modulators |
| KR101101675B1 (ko) | 2006-10-02 | 2011-12-30 | 노파르티스 아게 | 단백질 키나제 억제제로서의 화합물 및 조성물 |
| CL2007002904A1 (es) | 2006-10-10 | 2008-06-06 | Amgen Inc Soc Organizada Bajo | Compuestos derivados de pirazolopirimidina; composicion farmaceutica; y uso para tratar una enfermedad seleccionada de diabetes, obesidad, asma y artritis entre otras. |
| EP2379527A1 (en) * | 2008-12-19 | 2011-10-26 | F. Hoffmann-La Roche AG | Pyrimidin- 2 -ylamino derivatives and their use to treat inflammation |
-
2007
- 2007-11-28 AU AU2007328981A patent/AU2007328981B2/en not_active Expired - Fee Related
- 2007-11-28 CA CA002670375A patent/CA2670375A1/en not_active Abandoned
- 2007-11-28 MX MX2009005508A patent/MX2009005508A/es not_active Application Discontinuation
- 2007-11-28 BR BRPI0720003A patent/BRPI0720003A2/pt not_active IP Right Cessation
- 2007-11-28 KR KR1020097011056A patent/KR101152162B1/ko not_active Expired - Fee Related
- 2007-11-28 EP EP07847445A patent/EP2102194A1/en not_active Withdrawn
- 2007-11-28 WO PCT/EP2007/062920 patent/WO2008068171A1/en not_active Ceased
- 2007-11-28 RU RU2009125672/04A patent/RU2493155C2/ru not_active IP Right Cessation
- 2007-11-28 JP JP2009539701A patent/JP5179509B2/ja not_active Expired - Fee Related
- 2007-11-28 CN CNA2007800450228A patent/CN101547917A/zh active Pending
- 2007-12-05 AR ARP070105424A patent/AR064133A1/es not_active Application Discontinuation
- 2007-12-05 CL CL200703502A patent/CL2007003502A1/es unknown
- 2007-12-06 TW TW096146549A patent/TW200831101A/zh unknown
- 2007-12-07 PE PE2007001744A patent/PE20081507A1/es not_active Application Discontinuation
- 2007-12-07 US US12/001,021 patent/US8399462B2/en not_active Expired - Fee Related
-
2009
- 2009-05-04 IL IL198543A patent/IL198543A0/en unknown
- 2009-05-19 NO NO20091942A patent/NO20091942L/no not_active Application Discontinuation
- 2009-05-20 ZA ZA200903495A patent/ZA200903495B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010511655A (ja) | 2010-04-15 |
| EP2102194A1 (en) | 2009-09-23 |
| NO20091942L (no) | 2009-07-07 |
| US8399462B2 (en) | 2013-03-19 |
| CA2670375A1 (en) | 2008-06-12 |
| RU2493155C2 (ru) | 2013-09-20 |
| RU2009125672A (ru) | 2011-01-20 |
| AU2007328981B2 (en) | 2013-07-11 |
| IL198543A0 (en) | 2010-02-17 |
| US20080146565A1 (en) | 2008-06-19 |
| AU2007328981A1 (en) | 2008-06-12 |
| TW200831101A (en) | 2008-08-01 |
| WO2008068171A1 (en) | 2008-06-12 |
| BRPI0720003A2 (pt) | 2018-09-18 |
| KR20090075877A (ko) | 2009-07-09 |
| MX2009005508A (es) | 2009-06-03 |
| AR064133A1 (es) | 2009-03-11 |
| WO2008068171A9 (en) | 2009-07-16 |
| KR101152162B1 (ko) | 2012-07-10 |
| ZA200903495B (en) | 2010-04-28 |
| CN101547917A (zh) | 2009-09-30 |
| CL2007003502A1 (es) | 2008-06-27 |
| JP5179509B2 (ja) | 2013-04-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20081507A1 (es) | Derivados de pirimidina como moduladores de jnk | |
| PE20091236A1 (es) | Derivados de pirimidina como immunomoduladores de tlr7 | |
| PE20081262A1 (es) | Derivados de fenilo como moduladores de cinasas y composiciones | |
| PE20110150A1 (es) | Amidofenoxiindazoles como inhibidores de c-met | |
| PE20091734A1 (es) | Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso | |
| PE20091033A1 (es) | Derivados de nicotinamida como agentes anticancerosos y su preparacion | |
| PE20090694A1 (es) | Compuestos moduladores de sirtuinas | |
| PE20110547A1 (es) | Compuestos de isoindolina con actividad anticancerigena | |
| PE20110285A1 (es) | Derivados de sulfonamidofenil propionamida como ligandos del receptor vaniloide del subtipo 1 | |
| PE20090552A1 (es) | Compuestos de pirimidina hidrazida como inhibidores de pgds | |
| PE20130405A1 (es) | Compuestos de pirazol-4-il-heterociclil-carboxamida y metodos de uso | |
| PE20080074A1 (es) | Derivados de amida como agentes inhibidores de la quinasa c-fms | |
| PL2240150T3 (pl) | Kompozycje oftalmiczne z amfoterycznym środkiem powierzchniowo czynnym i kwasem hialuronowym | |
| PE20071236A1 (es) | Derivados de piperidinilo como moduladores de la actividad del receptor de quimiocina | |
| PE20070136A1 (es) | COMPUESTOS DERIVADOS DE N-(PIRIDIN-2-IL)-SULFONAMIDA COMO INHIBIDORES DE LA ENZIMA 11-beta-HIDROXIESTEROIDE DESHIDROGENASA HUMANA TIPO 1 | |
| PE20121335A1 (es) | Compuestos derivados de amida como inhibidores de raf cinasas | |
| AR072904A1 (es) | Compuestos de fenilamino-isonicotinamida y composiciones farmaceuticas que los contienen | |
| PE20140408A1 (es) | Derivados espiro-oxindol como antagonistas de mdm2 | |
| PE20091065A1 (es) | Derivados bis-(sulfonilamino) en terapia 066 | |
| PE20091816A1 (es) | Inhibidores de bace | |
| CR10682A (es) | Compuestos de tiazol pirazolopirimidina | |
| PE20091436A1 (es) | Derivados de sulfonamidas sustituidas como moduladores b1r | |
| HRP20180285T1 (hr) | Novi 4,6-disupstituirani derivati aminopirimidina | |
| PE20080856A1 (es) | Inhibidores de metaloproteasas de matriz | |
| PE20091092A1 (es) | Compuestos heterociclicos como inhibidores de la via hedgehog |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration | ||
| FD | Application declared void or lapsed |