MA28798B1 - Dérivés de triazolopyridinylsufanyle servant d'inhibiteurs de kinase MAP P38 - Google Patents
Dérivés de triazolopyridinylsufanyle servant d'inhibiteurs de kinase MAP P38Info
- Publication number
- MA28798B1 MA28798B1 MA29676A MA29676A MA28798B1 MA 28798 B1 MA28798 B1 MA 28798B1 MA 29676 A MA29676 A MA 29676A MA 29676 A MA29676 A MA 29676A MA 28798 B1 MA28798 B1 MA 28798B1
- Authority
- MA
- Morocco
- Prior art keywords
- triazolopyridinylsufanyl
- map
- derivatives
- kinase inhibitors
- kinase
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 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
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Reproductive Health (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0418015A GB0418015D0 (en) | 2004-08-12 | 2004-08-12 | New compounds |
| US69155905P | 2005-06-17 | 2005-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA28798B1 true MA28798B1 (fr) | 2007-08-01 |
Family
ID=35783420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA29676A MA28798B1 (fr) | 2004-08-12 | 2007-02-12 | Dérivés de triazolopyridinylsufanyle servant d'inhibiteurs de kinase MAP P38 |
Country Status (34)
| Country | Link |
|---|---|
| US (2) | US7511057B2 (fr) |
| EP (1) | EP1778686B9 (fr) |
| JP (1) | JP4084836B2 (fr) |
| AP (1) | AP2326A (fr) |
| AR (1) | AR050692A1 (fr) |
| AT (1) | ATE412652T1 (fr) |
| AU (1) | AU2005273612B2 (fr) |
| BR (1) | BRPI0514255A (fr) |
| CA (1) | CA2576297C (fr) |
| CR (1) | CR8918A (fr) |
| CU (1) | CU23497A3 (fr) |
| CY (1) | CY1108788T1 (fr) |
| DE (1) | DE602005010714D1 (fr) |
| DK (1) | DK1778686T3 (fr) |
| EA (1) | EA012119B1 (fr) |
| EC (1) | ECSP077232A (fr) |
| ES (1) | ES2314690T3 (fr) |
| GE (1) | GEP20104973B (fr) |
| GT (1) | GT200500218A (fr) |
| HN (1) | HN2005000418A (fr) |
| HR (1) | HRP20080608T3 (fr) |
| IL (1) | IL181047A (fr) |
| MA (1) | MA28798B1 (fr) |
| MX (1) | MX2007001759A (fr) |
| MY (1) | MY140021A (fr) |
| NL (1) | NL1029726C2 (fr) |
| NO (1) | NO339320B1 (fr) |
| NZ (1) | NZ552868A (fr) |
| PL (1) | PL1778686T3 (fr) |
| PT (1) | PT1778686E (fr) |
| SI (1) | SI1778686T1 (fr) |
| SV (1) | SV2006002193A (fr) |
| TN (1) | TNSN07050A1 (fr) |
| WO (1) | WO2006018718A2 (fr) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7572807B2 (en) * | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
| US7579360B2 (en) * | 2005-06-09 | 2009-08-25 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| US20090012079A1 (en) * | 2006-02-09 | 2009-01-08 | Russell Andrew Lewthwaite | Triazolopyridine Compounds |
| JP5244369B2 (ja) * | 2006-11-10 | 2013-07-24 | 富士フイルム株式会社 | 5−アミノピラゾール誘導体の製造方法、アゾ色素 |
| EP1992344A1 (fr) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha comme cible therapeutique pour les maladies associées á une mutation de FGFR3 |
| US8119658B2 (en) * | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| CA2712574C (fr) | 2008-02-04 | 2014-01-07 | Pfizer Limited | Forme polymorphe |
| US8498729B2 (en) | 2008-08-29 | 2013-07-30 | Smp Logic Systems Llc | Manufacturing execution system for use in manufacturing baby formula |
| CA2736913A1 (fr) * | 2008-09-12 | 2010-03-18 | Dorothee Viemann | Moyens et procedes pour evaluer une therapie avec un inhibiteur de map-kinase p38 |
| CA2752693A1 (fr) | 2009-02-17 | 2010-08-26 | Chiesi Farmaceutici S.P.A. | Derives de triazolopyridine utilises comme inhibiteurs de la p38 map kinase |
| GB0905955D0 (en) | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
| EP2438066A2 (fr) | 2009-06-05 | 2012-04-11 | Cephalon, Inc. | Préparation et utilisation de dérivés de 1,2,4-triazolo[1,5a]pyridine |
| GB201005589D0 (en) | 2010-04-01 | 2010-05-19 | Respivert Ltd | Novel compounds |
| US9024041B2 (en) | 2010-04-08 | 2015-05-05 | Respivert Ltd. | P38 MAP kinase inhibitors |
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