AR064133A1 - Moduladores de jnk - Google Patents
Moduladores de jnkInfo
- Publication number
- AR064133A1 AR064133A1 ARP070105424A ARP070105424A AR064133A1 AR 064133 A1 AR064133 A1 AR 064133A1 AR P070105424 A ARP070105424 A AR P070105424A AR P070105424 A ARP070105424 A AR P070105424A AR 064133 A1 AR064133 A1 AR 064133A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- nra
- halogen
- nrac
- phenyl
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 108010055717 JNK Mitogen-Activated Protein Kinases Proteins 0.000 abstract 2
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 abstract 1
- 101100097467 Arabidopsis thaliana SYD gene Proteins 0.000 abstract 1
- 125000006519 CCH3 Chemical group 0.000 abstract 1
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 229910017711 NHRa Inorganic materials 0.000 abstract 1
- 101100495925 Schizosaccharomyces pombe (strain 972 / ATCC 24843) chr3 gene Proteins 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 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
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 abstract 1
Classifications
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- 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)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Se refiere a compuestos moduladores de la JNK, (quinasa c-Jun-N-terminal), utiles para artritis reumatoidea, asma, diabetes tipo II, Alzheimer, Parkinson. Reivindicacion 1: Un compuesto de formula (1), en la que X1 es N, N-R3, CHR3, C-R3, u O; X2 es N, NH, N-CH3, CH, CH2, CHCH3 o C-CH3; X3 es N, C o CH, pero X1, X2, y X3 no son todos N al mismo tiempo; X4, X5 con independencia entre sí son C, CH o N; X6 es N o C-R1; en la que por lo menos dos, pero no más de cuatro de X1, X2, X3, X4, X5, y X6 son N; y en la que los enlaces entre X1 y X2, X2 y X3, X3 y X4, X4 y X5, X5 y X1, y X5 y X6 con independencia entre sí pueden ser sencillos o dobles o pueden formar un anillo aromático, con la condicion de que la estructura resultante sea químicamente estable; R es -(ciclohexil)-R2 o -(fenil)-R8, dichos ciclohexilo y fenilo están cada uno de ellos opcionalmente sustituidos por metilo, fluor, cloro o hidroxi; R1 es halogeno, nitro, -CN, -CH2CN, -OH, -NH2, -COOH o Y1R4; Y1 es -O-, -NH- , -S-, -SO-, -SO2-, -NHSO2-, -NHC(O)-, -C(O)NH-, -C(O)O-, o un enlace; R4 es alquilo C1-6, acilo, fenilo o bencilo, cada uno de ellos está sustituido por 0-3 hidroxi o halogeno; n es el numero 0, 1 o 2; R3 H o alquilo C1-6; R2 es H, -OH, -SO2NH2, =O, -CN, o -Y2-Y3-Y4-R5, en los que Y2 es -C(O)-, -C(O)NRa-, -SO2-, -O-, -NH-, o un enlace; Y3 es alquileno C1-6 o un enlace; Y4 es -O-, -NRa-, -S-, -SO2-, -C(O)-, -C(O)NRa-, -NRaC(O)-, -NRaC(O)O-, -NRaC(O)NRa-, -NHSO2-, -SO2-NH-, o un enlace; R5 es alquilo C1-6, cicloalquilo C3-10, heterociclilo, en el que R5 está opcionalmente sustituido por -OH o -NHRa; en el que cada Ra es con independencia H o alquilo C1-6; R8 es H, alquilo C1-6, -OR3, -SO2NH2, -NHSO2R3, -COOR3, -SO2R3, -NH2, -CONRaR3, - NHC(O)R3, -CF3, -NO2, halogeno, o -CN; Z es hidrogeno, halogeno, alquilo C1-12, o NH2; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87362506P | 2006-12-08 | 2006-12-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR064133A1 true AR064133A1 (es) | 2009-03-11 |
Family
ID=39099641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070105424A AR064133A1 (es) | 2006-12-08 | 2007-12-05 | 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 |
|---|---|---|---|---|
| CN101679211A (zh) * | 2007-06-15 | 2010-03-24 | 霍夫曼-拉罗奇有限公司 | 用于制备3-氨基-戊-1,5-二醇的新方法 |
| CA2701275C (en) * | 2007-10-23 | 2016-06-21 | F. Hoffmann-La Roche Ag | Kinase inhibitors |
| EP2283009B1 (en) * | 2008-05-16 | 2012-08-29 | 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 |
| CN102480966B (zh) | 2009-06-12 | 2015-09-16 | 达娜-法勃肿瘤研究所公司 | 融合的杂环化合物及其用途 |
| 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 |
| AU2010343102B2 (en) | 2009-12-29 | 2016-03-24 | Dana-Farber Cancer Institute, Inc. | Type II Raf kinase inhibitors |
| WO2011151358A1 (en) * | 2010-06-04 | 2011-12-08 | F. Hoffmann-La Roche Ag | 2 -amino- pyrimidine derivatives useful as inhibitors of jnk |
| WO2011151357A1 (en) * | 2010-06-04 | 2011-12-08 | F. Hoffmann-La Roche Ag | Inhibitors of jnk |
| US9139590B2 (en) | 2011-02-04 | 2015-09-22 | Duquesne University Of The Holy Spirit | Bicyclic and tricyclic pyrimidine tyrosine kinase inhibitors with antitubulin activity and methods of treating a patient |
| HUE038714T2 (hu) | 2011-03-10 | 2018-11-28 | Daiichi Sankyo Co Ltd | Dispiropirrolidin származék |
| EP2822935B1 (en) | 2011-11-17 | 2019-05-15 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-jun-n-terminal kinase (jnk) |
| JP6313312B2 (ja) | 2012-10-02 | 2018-04-18 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 農薬としての複素環化合物 |
| US10112927B2 (en) | 2012-10-18 | 2018-10-30 | 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 |
| WO2014134774A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| EP2964221B1 (en) | 2013-03-04 | 2017-12-06 | 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 |
| WO2014134776A1 (en) | 2013-03-04 | 2014-09-12 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| EP3057956B1 (en) | 2013-10-18 | 2021-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
| ES2676734T3 (es) | 2013-10-18 | 2018-07-24 | Syros Pharmaceuticals, Inc. | Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas |
| US9809568B2 (en) * | 2013-11-14 | 2017-11-07 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| CA2944669A1 (en) | 2014-04-04 | 2015-10-08 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| WO2015164604A1 (en) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged janus kinase inhibitors and uses thereof |
| US10017477B2 (en) | 2014-04-23 | 2018-07-10 | Dana-Farber Cancer Institute, Inc. | Janus kinase inhibitors and uses thereof |
| US10954240B2 (en) | 2014-09-03 | 2021-03-23 | Merck Sharp & Dohme Corp. | Compounds inhibiting leucine-rich repeat kinase enzyme activity |
| SG11201704685TA (en) * | 2014-12-11 | 2017-07-28 | Beta Pharma Inc | Substituted 2-anilinopyrimidine derivatives as egfr modulators |
| US10870651B2 (en) | 2014-12-23 | 2020-12-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
| AU2016243529B2 (en) | 2015-03-27 | 2021-03-25 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| US10702527B2 (en) | 2015-06-12 | 2020-07-07 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| JP7028766B2 (ja) | 2015-09-09 | 2022-03-02 | 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 | サイクリン依存性キナーゼの阻害剤 |
| 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 |
| 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 |
| TW201904577A (zh) | 2017-06-16 | 2019-02-01 | 美商貝達醫藥公司 | N-(2-(2-二甲胺基)乙氧基)-4-甲氧基-5-((4-(1-甲基-1h-吲哚-3-基)嘧啶-2-基)胺基)苯基)丙烯醯胺及其鹽之醫藥調配物 |
| JOP20180094A1 (ar) | 2017-10-18 | 2019-04-18 | Hk Inno N Corp | مركب حلقي غير متجانس كمثبط بروتين كيناز |
| AU2019295632B2 (en) | 2018-06-25 | 2025-03-06 | Dana-Farber Cancer Institute, Inc. | Taire family kinase inhibitors and uses thereof |
| KR102195348B1 (ko) * | 2018-11-15 | 2020-12-24 | 에이치케이이노엔 주식회사 | 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물 |
| JP7660063B2 (ja) | 2018-12-28 | 2025-04-10 | 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 | サイクリン依存性キナーゼ7のインヒビターおよびそれらの使用 |
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| 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 |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | 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 |
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| US7361665B2 (en) * | 2002-07-09 | 2008-04-22 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases |
| TW200528101A (en) | 2004-02-03 | 2005-09-01 | Astrazeneca Ab | Chemical compounds |
| WO2006050076A1 (en) * | 2004-10-29 | 2006-05-11 | Janssen Pharmaceutica, N.V. | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
| CN101218241B (zh) * | 2005-05-16 | 2011-02-16 | Irm责任有限公司 | 用作蛋白激酶抑制剂的吡咯并吡啶衍生物 |
| DE102006012617A1 (de) * | 2006-03-20 | 2007-09-27 | Merck Patent Gmbh | 4-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
| MX2009002229A (es) | 2006-09-08 | 2009-03-16 | Hoffmann La Roche | Benzotriazoles como moduladores de cinasas. |
| MX2009003456A (es) | 2006-10-02 | 2009-04-14 | Irm Llc | Compuestos y composiciones como inhibidores de proteina cinasa. |
| EP2079728B1 (en) | 2006-10-10 | 2013-09-25 | Amgen Inc. | N-aryl pyrazole compounds for use against diabetes |
| 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 WO PCT/EP2007/062920 patent/WO2008068171A1/en not_active Ceased
- 2007-11-28 MX MX2009005508A patent/MX2009005508A/es not_active Application Discontinuation
- 2007-11-28 KR KR1020097011056A patent/KR101152162B1/ko not_active Expired - Fee Related
- 2007-11-28 CN CNA2007800450228A patent/CN101547917A/zh active Pending
- 2007-11-28 JP JP2009539701A patent/JP5179509B2/ja not_active Expired - Fee Related
- 2007-11-28 EP EP07847445A patent/EP2102194A1/en not_active Withdrawn
- 2007-11-28 BR BRPI0720003A patent/BRPI0720003A2/pt not_active IP Right Cessation
- 2007-11-28 CA CA002670375A patent/CA2670375A1/en not_active Abandoned
- 2007-11-28 AU AU2007328981A patent/AU2007328981B2/en not_active Expired - Fee Related
- 2007-11-28 RU RU2009125672/04A patent/RU2493155C2/ru not_active IP Right Cessation
- 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 US US12/001,021 patent/US8399462B2/en not_active Expired - Fee Related
- 2007-12-07 PE PE2007001744A patent/PE20081507A1/es not_active Application Discontinuation
-
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 |
|---|---|
| JP5179509B2 (ja) | 2013-04-10 |
| WO2008068171A9 (en) | 2009-07-16 |
| EP2102194A1 (en) | 2009-09-23 |
| TW200831101A (en) | 2008-08-01 |
| MX2009005508A (es) | 2009-06-03 |
| CL2007003502A1 (es) | 2008-06-27 |
| BRPI0720003A2 (pt) | 2018-09-18 |
| RU2009125672A (ru) | 2011-01-20 |
| AU2007328981B2 (en) | 2013-07-11 |
| NO20091942L (no) | 2009-07-07 |
| CN101547917A (zh) | 2009-09-30 |
| PE20081507A1 (es) | 2008-11-12 |
| WO2008068171A1 (en) | 2008-06-12 |
| RU2493155C2 (ru) | 2013-09-20 |
| US20080146565A1 (en) | 2008-06-19 |
| KR20090075877A (ko) | 2009-07-09 |
| KR101152162B1 (ko) | 2012-07-10 |
| AU2007328981A1 (en) | 2008-06-12 |
| ZA200903495B (en) | 2010-04-28 |
| JP2010511655A (ja) | 2010-04-15 |
| US8399462B2 (en) | 2013-03-19 |
| CA2670375A1 (en) | 2008-06-12 |
| IL198543A0 (en) | 2010-02-17 |
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