EA200901505A1 - 3,6-дизамещенные имидазо[1,2-b]пиридазины и 3,5-дизамещенные пиразоло[1,5-a]пиримидины в качестве ингибиторов фосфатидилинозитол-3-киназы - Google Patents
3,6-дизамещенные имидазо[1,2-b]пиридазины и 3,5-дизамещенные пиразоло[1,5-a]пиримидины в качестве ингибиторов фосфатидилинозитол-3-киназыInfo
- Publication number
- EA200901505A1 EA200901505A1 EA200901505A EA200901505A EA200901505A1 EA 200901505 A1 EA200901505 A1 EA 200901505A1 EA 200901505 A EA200901505 A EA 200901505A EA 200901505 A EA200901505 A EA 200901505A EA 200901505 A1 EA200901505 A1 EA 200901505A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- designed
- piridazines
- phosphatidylinositol
- pyrazolo
- pyrimidines
- Prior art date
Links
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- 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
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- 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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Otolaryngology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Настоящее изобретение относится к соединениям формулы I, способам их получения, более конкретно к этим соединениям для применения для лечения человека или животного, для лечения воспалительного или обструктивного заболевания дыхательных путей, нарушений, обычно встречающихся при трансплантации, или пролиферативного заболевания, которое связано с ингибированием киназ связанного с PI3-киназой семейства протеинкиназ.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US91734807P | 2007-05-11 | 2007-05-11 | |
PCT/EP2008/055751 WO2008138889A2 (en) | 2007-05-11 | 2008-05-09 | 3, 6-disubstituted-imidazo [1, 2-b] pyridazines and 3, 5-disubstituted pyrazolo[1, 5-a] pyrimidines as phosphatidylinositol-3-kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
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EA200901505A1 true EA200901505A1 (ru) | 2010-06-30 |
Family
ID=39769090
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200901505A EA200901505A1 (ru) | 2007-05-11 | 2008-05-09 | 3,6-дизамещенные имидазо[1,2-b]пиридазины и 3,5-дизамещенные пиразоло[1,5-a]пиримидины в качестве ингибиторов фосфатидилинозитол-3-киназы |
Country Status (17)
Country | Link |
---|---|
US (1) | US20100311729A1 (ru) |
EP (1) | EP2155202A2 (ru) |
JP (1) | JP2010526795A (ru) |
KR (1) | KR20100016460A (ru) |
CN (1) | CN101678026A (ru) |
AR (1) | AR067326A1 (ru) |
AU (1) | AU2008250293A1 (ru) |
BR (1) | BRPI0811600A2 (ru) |
CA (1) | CA2686903A1 (ru) |
CL (1) | CL2008001364A1 (ru) |
EA (1) | EA200901505A1 (ru) |
MX (1) | MX2009012127A (ru) |
PA (1) | PA8780101A1 (ru) |
PE (1) | PE20090714A1 (ru) |
TW (1) | TW200911810A (ru) |
UY (1) | UY31076A1 (ru) |
WO (1) | WO2008138889A2 (ru) |
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UA111382C2 (uk) | 2011-10-10 | 2016-04-25 | Оріон Корпорейшн | Інгібітори протеїнкінази |
GB201205669D0 (en) | 2012-03-30 | 2012-05-16 | Agency Science Tech & Res | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
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CA2483306A1 (en) * | 2002-04-23 | 2003-11-06 | Shionogi & Co., Ltd. | Pyrazolo[1,5-a]pyrimidine derivative and nad(p)h oxidase inhibitor containing the same |
US7550470B2 (en) * | 2002-12-11 | 2009-06-23 | Merck & Co. Inc. | Substituted pyrazolo[1,5-A]pyrimidines as tyrosine kinase inhibitors |
US20100216798A1 (en) * | 2005-07-29 | 2010-08-26 | Astellas Pharma Inc | Fused heterocycles as lck inhibitors |
DE102005042742A1 (de) * | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
US20070078136A1 (en) * | 2005-09-22 | 2007-04-05 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
WO2007039439A1 (en) * | 2005-09-27 | 2007-04-12 | F.Hoffmann-La Roche Ag | Oxadiazolyl pyrazolo-pyrimidines as mglur2 antagonists |
JP5600004B2 (ja) * | 2006-09-05 | 2014-10-01 | エモリー ユニバーシティー | 感染の予防または治療のためのチロシンキナーゼ阻害剤 |
CN101594909A (zh) * | 2006-09-07 | 2009-12-02 | 比奥根艾迪克Ma公司 | 用于治疗炎性病症、细胞增殖性失调、免疫失调的irak调节剂 |
ATE502943T1 (de) * | 2006-09-29 | 2011-04-15 | Novartis Ag | Pyrazolopyrimidine als pi3k-lipidkinasehemmer |
BRPI0717928A2 (pt) * | 2006-10-30 | 2013-11-05 | Novartis Ag | Imidazopiridazinas como inibidores da cinase de lipídio pi3k |
EP2089393A1 (en) * | 2006-10-30 | 2009-08-19 | Novartis AG | Heterocyclic compounds as antiinflammatory agents |
CA2667487C (en) * | 2006-11-06 | 2017-04-04 | Supergen, Inc. | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
AR064420A1 (es) * | 2006-12-21 | 2009-04-01 | Alcon Mfg Ltd | Composiciones farmaceuticas oftalmicas que comprenden una cantidad efectiva de analogos de 6-aminoimidazo[1,2b]piridazinas, utiles para el tratamiento del glaucoma y/o controlar la presion intraocular normal o elevada(iop). |
MX2009012066A (es) * | 2007-05-09 | 2009-11-19 | Novartis Ag | Imidazopirinas sustituidas como inhibidoras de cinasa de lipido p13k. |
-
2008
- 2008-05-08 AR ARP080101956A patent/AR067326A1/es not_active Application Discontinuation
- 2008-05-09 AU AU2008250293A patent/AU2008250293A1/en not_active Abandoned
- 2008-05-09 MX MX2009012127A patent/MX2009012127A/es not_active Application Discontinuation
- 2008-05-09 KR KR1020097023565A patent/KR20100016460A/ko not_active Application Discontinuation
- 2008-05-09 CN CN200880015653A patent/CN101678026A/zh active Pending
- 2008-05-09 EP EP08759487A patent/EP2155202A2/en not_active Withdrawn
- 2008-05-09 JP JP2010506947A patent/JP2010526795A/ja active Pending
- 2008-05-09 TW TW097117328A patent/TW200911810A/zh unknown
- 2008-05-09 CL CL2008001364A patent/CL2008001364A1/es unknown
- 2008-05-09 BR BRPI0811600A patent/BRPI0811600A2/pt not_active Application Discontinuation
- 2008-05-09 PE PE2008000821A patent/PE20090714A1/es not_active Application Discontinuation
- 2008-05-09 EA EA200901505A patent/EA200901505A1/ru unknown
- 2008-05-09 PA PA20088780101A patent/PA8780101A1/es unknown
- 2008-05-09 US US12/599,143 patent/US20100311729A1/en not_active Abandoned
- 2008-05-09 CA CA002686903A patent/CA2686903A1/en not_active Abandoned
- 2008-05-09 WO PCT/EP2008/055751 patent/WO2008138889A2/en active Application Filing
- 2008-05-09 UY UY31076A patent/UY31076A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO2008138889A8 (en) | 2009-07-09 |
WO2008138889A3 (en) | 2009-04-30 |
PE20090714A1 (es) | 2009-07-17 |
WO2008138889A2 (en) | 2008-11-20 |
UY31076A1 (es) | 2009-01-05 |
PA8780101A1 (es) | 2008-12-18 |
CL2008001364A1 (es) | 2008-12-19 |
US20100311729A1 (en) | 2010-12-09 |
KR20100016460A (ko) | 2010-02-12 |
MX2009012127A (es) | 2009-11-19 |
BRPI0811600A2 (pt) | 2019-09-10 |
CA2686903A1 (en) | 2008-11-20 |
CN101678026A (zh) | 2010-03-24 |
TW200911810A (en) | 2009-03-16 |
AU2008250293A1 (en) | 2008-11-20 |
AR067326A1 (es) | 2009-10-07 |
EP2155202A2 (en) | 2010-02-24 |
JP2010526795A (ja) | 2010-08-05 |
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