JP5572388B2 - キナーゼ阻害剤としてのイミダゾトリアジンおよびイミダゾピリミジン - Google Patents
キナーゼ阻害剤としてのイミダゾトリアジンおよびイミダゾピリミジン Download PDFInfo
- Publication number
- JP5572388B2 JP5572388B2 JP2009538473A JP2009538473A JP5572388B2 JP 5572388 B2 JP5572388 B2 JP 5572388B2 JP 2009538473 A JP2009538473 A JP 2009538473A JP 2009538473 A JP2009538473 A JP 2009538473A JP 5572388 B2 JP5572388 B2 JP 5572388B2
- Authority
- JP
- Japan
- Prior art keywords
- imidazo
- quinolin
- ylcyclopropyl
- pyrimidin
- benzamide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 *c(nc1nc(*)c([I-][Cl+])n[n]11)c1IN Chemical compound *c(nc1nc(*)c([I-][Cl+])n[n]11)c1IN 0.000 description 8
- JGNATNBWFRQAKZ-RUZDIDTESA-N CC(C)C[C@H](C(NC)=O)NC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O Chemical compound CC(C)C[C@H](C(NC)=O)NC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O JGNATNBWFRQAKZ-RUZDIDTESA-N 0.000 description 1
- RDIILQOGOFSJPW-QPJJXVBHSA-N CC(C1C=C1)(/C(/C)=C/C)N Chemical compound CC(C1C=C1)(/C(/C)=C/C)N RDIILQOGOFSJPW-QPJJXVBHSA-N 0.000 description 1
- CZGAGJHZXZVLIV-UHFFFAOYSA-N CC(c1cnc2ncc(-c(cc3)cc(F)c3C(NC)=O)n[n]12)c(cc1)cc2c1nccc2 Chemical compound CC(c1cnc2ncc(-c(cc3)cc(F)c3C(NC)=O)n[n]12)c(cc1)cc2c1nccc2 CZGAGJHZXZVLIV-UHFFFAOYSA-N 0.000 description 1
- UOQMTZZNNVCSIE-UHFFFAOYSA-N CC(c1ncccc1)NC(c(cc1)ccc1-c(cn1)c[n]2c1ncc2C1(CC1)c1cc2cccnc2cc1)=O Chemical compound CC(c1ncccc1)NC(c(cc1)ccc1-c(cn1)c[n]2c1ncc2C1(CC1)c1cc2cccnc2cc1)=O UOQMTZZNNVCSIE-UHFFFAOYSA-N 0.000 description 1
- OAPWLSLSHAWBNJ-UHFFFAOYSA-N CN(C)CCNC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O Chemical compound CN(C)CCNC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O OAPWLSLSHAWBNJ-UHFFFAOYSA-N 0.000 description 1
- LKBVMWQVGLNHBP-UHFFFAOYSA-N CN(C1CC1)C(c(cc1)ccc1-c(cn1)n[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)=O Chemical compound CN(C1CC1)C(c(cc1)ccc1-c(cn1)n[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)=O LKBVMWQVGLNHBP-UHFFFAOYSA-N 0.000 description 1
- LIOLIMKSCNQPLV-UHFFFAOYSA-N CNC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O Chemical compound CNC(c(ccc(-c(cn1)n[n]2c1ncc2Cc(cc1)cc2c1nccc2)c1)c1F)=O LIOLIMKSCNQPLV-UHFFFAOYSA-N 0.000 description 1
- MBCPZGNJTNGMLV-UHFFFAOYSA-N CNS(c(ccc(-c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)c1)c1F)(=O)=O Chemical compound CNS(c(ccc(-c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)c1)c1F)(=O)=O MBCPZGNJTNGMLV-UHFFFAOYSA-N 0.000 description 1
- NCYXMOCIBILHPY-BYPYZUCNSA-N C[C@@H](CCI)C(N)=[ClH] Chemical compound C[C@@H](CCI)C(N)=[ClH] NCYXMOCIBILHPY-BYPYZUCNSA-N 0.000 description 1
- ILDUOLPTLPLSCS-SSDOTTSWSA-N C[C@@H]1CC=[IH](C)CC1 Chemical compound C[C@@H]1CC=[IH](C)CC1 ILDUOLPTLPLSCS-SSDOTTSWSA-N 0.000 description 1
- DSGWOZYJXUMLKK-UHFFFAOYSA-N C[n]1ncc(-c(cn2)c[n]3c2ncc3C2(CC2)c(cc2)cc3c2nccc3)c1 Chemical compound C[n]1ncc(-c(cn2)c[n]3c2ncc3C2(CC2)c(cc2)cc3c2nccc3)c1 DSGWOZYJXUMLKK-UHFFFAOYSA-N 0.000 description 1
- BJURGDWAIJKITD-UHFFFAOYSA-N N#CC[n]1ncc(-c(cn2)c[n]3c2ncc3C2(CC2)c(cc2)cc3c2nccc3)c1 Chemical compound N#CC[n]1ncc(-c(cn2)c[n]3c2ncc3C2(CC2)c(cc2)cc3c2nccc3)c1 BJURGDWAIJKITD-UHFFFAOYSA-N 0.000 description 1
- SGDSKMVBYKVJMR-UHFFFAOYSA-N O=C(c(cc1)ccc1-c(cn1)n[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)NC1CCC1 Chemical compound O=C(c(cc1)ccc1-c(cn1)n[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)NC1CCC1 SGDSKMVBYKVJMR-UHFFFAOYSA-N 0.000 description 1
- QQVINJKZCRCARD-UHFFFAOYSA-N O=C(c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)NCC1OCCC1 Chemical compound O=C(c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)NCC1OCCC1 QQVINJKZCRCARD-UHFFFAOYSA-N 0.000 description 1
- DYUSDUFIQGBLDZ-UHFFFAOYSA-N OC(CC1)CCC1NC(c(c(F)c1)cc(F)c1-c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)=O Chemical compound OC(CC1)CCC1NC(c(c(F)c1)cc(F)c1-c(cn1)c[n]2c1ncc2C1(CC1)c(cc1)cc2c1nccc2)=O DYUSDUFIQGBLDZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
-
- 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/495—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
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- 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
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
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- 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
- A61P37/02—Immunomodulators
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- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurosurgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Neurology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86084006P | 2006-11-22 | 2006-11-22 | |
| US60/860,840 | 2006-11-22 | ||
| US86145906P | 2006-11-29 | 2006-11-29 | |
| US60/861,459 | 2006-11-29 | ||
| US95723607P | 2007-08-22 | 2007-08-22 | |
| US60/957,236 | 2007-08-22 | ||
| PCT/US2007/085100 WO2008064157A1 (en) | 2006-11-22 | 2007-11-19 | Imidazotriazines and imidazopyrimidines as kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010510319A JP2010510319A (ja) | 2010-04-02 |
| JP2010510319A5 JP2010510319A5 (enExample) | 2011-01-13 |
| JP5572388B2 true JP5572388B2 (ja) | 2014-08-13 |
Family
ID=39166437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009538473A Active JP5572388B2 (ja) | 2006-11-22 | 2007-11-19 | キナーゼ阻害剤としてのイミダゾトリアジンおよびイミダゾピリミジン |
Country Status (37)
Families Citing this family (144)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS55634B1 (sr) | 2005-12-13 | 2017-06-30 | Incyte Holdings Corp | Heteroaril substituisani pirolo[2,3-b]piridini i pirolo[2,3-b]pirimidini kao inhibitori janus kinaze |
| RU2008144571A (ru) | 2006-04-12 | 2010-05-20 | Мерк энд Ко., Инк. (US) | Пиридиламидные антагонисты кальциевых каналов т-типа |
| EP2057164A1 (en) * | 2006-08-07 | 2009-05-13 | Incyte Corporation | Triazolotriazines as kinase inhibitors |
| PL3034075T3 (pl) | 2006-11-22 | 2019-03-29 | Incyte Holdings Corporation | Imidazotriazyny i imidazopirymidyny jako inhibitory kinaz |
| HUE043732T2 (hu) | 2007-06-13 | 2019-09-30 | Incyte Holdings Corp | Januskináz gátló hatású (R)-3-(4-(7H pirrolo[2,3-d]pirimidin-4-il)-1H-pirazol-1-il)-3-ciklopentilpropánnitril sók alkalmazása |
| RU2010120671A (ru) * | 2007-10-24 | 2011-11-27 | Мерк Шарп Энд Домэ Корп. (Us) | Гетероциклические фениламидные антагонисты кальциевых каналов т-типа |
| WO2009106577A1 (en) | 2008-02-28 | 2009-09-03 | Novartis Ag | Imidazo [1,2-b] pyridazine derivatives for the treatment of c-met tyrosine kinase mediated disease |
| MX393622B (es) | 2008-05-21 | 2025-03-24 | Incyte Corp | Sales de 2-fluoro-n-metil-4-[7-(quinolin-6-il-metil)-imidazo[1,2-b][1,2,4]triazin-2-il]benzamida y procesos relacionados con la preparacion de las mismas. |
| WO2010002472A1 (en) * | 2008-07-02 | 2010-01-07 | Ambit Biosciences Corporation | Jak kinase modulating compounds and methods of use thereof |
| FR2933982A1 (fr) * | 2008-07-18 | 2010-01-22 | Sanofi Aventis | Nouveaux derives imidazo°1,2-a!pyrimidine, leur procede de preparation, leur application a titre de medicaments, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de met |
| UY32049A (es) * | 2008-08-14 | 2010-03-26 | Takeda Pharmaceutical | Inhibidores de cmet |
| JOP20190231A1 (ar) * | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
| MA33032B1 (fr) * | 2009-02-13 | 2012-02-01 | Bayer Schering Pharma Ag | Pyrimidines condensees |
| EP2432555B1 (en) | 2009-05-22 | 2014-04-30 | 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 |
| KR20120030447A (ko) | 2009-05-22 | 2012-03-28 | 인사이트 코포레이션 | Jak 저해물질로서 3-[4-(7h-피롤로[2,3-d]피리미딘-4-일)-1h-피라졸-1-일]옥탄- 또는 헵탄-니트릴 |
| MX2011013816A (es) | 2009-06-29 | 2012-04-11 | Incyte Corp | Pirimidinonas como inhibidores de pi3k. |
| BR112012003262A8 (pt) | 2009-08-12 | 2016-05-17 | Novartis Ag | compostos de hidrazona heterocíclica e seus usos para tratar câncer e inflamação |
| EA201200318A1 (ru) | 2009-08-20 | 2012-09-28 | Новартис Аг | Гетероциклические оксимы |
| WO2011028685A1 (en) | 2009-09-01 | 2011-03-10 | Incyte Corporation | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| SI3511330T1 (sl) | 2009-12-31 | 2021-01-29 | Hutchison Medipharma Limited | Sintetična umetna spojina uporabna v pripravi triazolopiridinskih zaviralcev c-Met |
| CN102812027B (zh) | 2010-02-03 | 2015-01-07 | 因西特公司 | 作为C-MET抑制剂的咪唑并[1,2-b][1,2,4]三嗪 |
| TWI531572B (zh) | 2010-03-10 | 2016-05-01 | 英塞特公司 | 作為jak1抑制劑之哌啶-4-基三亞甲亞胺衍生物 |
| US8518945B2 (en) * | 2010-03-22 | 2013-08-27 | Hoffmann-La Roche Inc. | Pyrrolopyrazine kinase inhibitors |
| US8410117B2 (en) * | 2010-03-26 | 2013-04-02 | Hoffmann-La Roche Inc. | Imidazopyrimidine derivatives |
| EP2558463A1 (en) | 2010-04-14 | 2013-02-20 | Incyte Corporation | Fused derivatives as i3 inhibitors |
| MX2012011941A (es) * | 2010-04-14 | 2013-08-27 | Array Biopharma Inc | Imidazo [1, 2-c] pirimidinas 5, 7-substituidas como inhibidores de jak cinasas. |
| AU2011254242B2 (en) * | 2010-05-17 | 2015-10-29 | Incozen Therapeutics Pvt. Ltd. | Novel 3,5-disubstitued-3H-imidazo[4,5-b]pyridine and 3,5- disubstitued -3H-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of protein kinases |
| US20110288107A1 (en) | 2010-05-21 | 2011-11-24 | Bhavnish Parikh | Topical formulation for a jak inhibitor |
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