CY1107433T1 - Παραγωγα 1-(2η-πυραζολ-3-υλο)-3-(4-[1-(βενζοϋλο)-πιπepιδιν-4-υλομεθυλο]-φαινυλο)-ουριας και συναφεις ενωσεις ως αναστολεις της ρ38 κινασης και/ή tnf-αναστολεις για την αντιμετωπιση φλεγμονων - Google Patents
Παραγωγα 1-(2η-πυραζολ-3-υλο)-3-(4-[1-(βενζοϋλο)-πιπepιδιν-4-υλομεθυλο]-φαινυλο)-ουριας και συναφεις ενωσεις ως αναστολεις της ρ38 κινασης και/ή tnf-αναστολεις για την αντιμετωπιση φλεγμονωνInfo
- Publication number
- CY1107433T1 CY1107433T1 CY20071100359T CY071100359T CY1107433T1 CY 1107433 T1 CY1107433 T1 CY 1107433T1 CY 20071100359 T CY20071100359 T CY 20071100359T CY 071100359 T CY071100359 T CY 071100359T CY 1107433 T1 CY1107433 T1 CY 1107433T1
- Authority
- CY
- Cyprus
- Prior art keywords
- treatment
- pipepidin
- benzoyloyl
- inflammations
- pyrazol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Η παρούσα εφεύρεση παρέχει ενώσεις του τύπου (I) όπου ( ) είναι προαιρετική γέφυρα αιθυλενίου· R1 είναι αλκύλιο, κυκλοαλκύλιο, αρύλιο ή αρύλιο υποκατεστημένο με έναν ή περισσότερους υποκατάστατες επιλεγόμενους από αλκύλιο, αλκοξυ ομάδα και αμινο ομάδα, ή R1 είναι πυριδύλιο ή πυριδύλιο υποκατεστημένο με έναν ή περισσότερους υποκατάστατες επιλεγόμενους από αλκύλιο, αλκοξυ ομάδα και αμινο ομάδα· R2 είναι προαιρετικά υποκατεστημένο αλκύλιο, αλκοξυαλκύλιο, προαιρετικά υποκατεστημένο κυκλοαλκυλαλκύλιο, αρυλαλκύλιο, ή R2 είναι αρυλαλκύλιο υποκατεστημένο με έναν ή περισσότερους υποκαταστάτες επιλεγόμενους από αλκύλιο, αλκοξυ ομάδα· Χ είναι -C(O)-, -C(Ο)-CH2-, -S(Ο)2-, ή NH-C(O)-· και Α είναι προαιρετικά υποκατεστημένο αλκύλιο ή άλλοι υποκατάστατες όπως ορίζονται στην αξίωση 1. Φαρμακευτικές συνθέσεις που περιλαμβάνουν τέτοιες ενώσεις, η παρασκευή αυτών, και η φαρμακευτική χρήση αυτών στην αντιμετώπιση παθολογικών καταστάσεων που μπορούν να ελεγχθούν μέσω της αναστολής της p38-κινάσης και/ή του παράγοντα νέκρωσης όγκων (TNF), όπως άσθματος ή φλεγμονής αρθρώσεων.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46828503P | 2003-05-06 | 2003-05-06 | |
EP04751319A EP1622610B1 (en) | 2003-05-06 | 2004-05-05 | 1-(2h-pyrazol-3-yl)-3-{4-[1-(benzoyl)-piperidin-4-ylmethyl]-phenyl}-urea derivatives and related compounds as inhibitors of p38 kinase and/or tnf inhibitors for the treatment of inflammations |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1107433T1 true CY1107433T1 (el) | 2012-12-19 |
Family
ID=28792177
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20071100359T CY1107433T1 (el) | 2003-05-06 | 2007-03-15 | Παραγωγα 1-(2η-πυραζολ-3-υλο)-3-(4-[1-(βενζοϋλο)-πιπepιδιν-4-υλομεθυλο]-φαινυλο)-ουριας και συναφεις ενωσεις ως αναστολεις της ρ38 κινασης και/ή tnf-αναστολεις για την αντιμετωπιση φλεγμονων |
Country Status (26)
Country | Link |
---|---|
US (1) | US7541368B2 (el) |
EP (1) | EP1622610B1 (el) |
JP (1) | JP4714150B2 (el) |
AT (1) | ATE348610T1 (el) |
AU (2) | AU2004238241A1 (el) |
BR (1) | BRPI0409991A (el) |
CA (1) | CA2524043C (el) |
CL (1) | CL2004000965A1 (el) |
CY (1) | CY1107433T1 (el) |
DE (1) | DE602004003806T2 (el) |
DK (1) | DK1622610T3 (el) |
ES (1) | ES2277271T3 (el) |
GB (1) | GB0320244D0 (el) |
HN (1) | HN2004000150A (el) |
HR (1) | HRP20070020T3 (el) |
JO (1) | JO2473B1 (el) |
MX (1) | MXPA05011400A (el) |
MY (1) | MY140830A (el) |
PA (1) | PA8601901A1 (el) |
PE (1) | PE20050523A1 (el) |
PL (1) | PL1622610T3 (el) |
PT (1) | PT1622610E (el) |
SI (1) | SI1622610T1 (el) |
TW (1) | TWI335223B (el) |
UY (1) | UY28310A1 (el) |
WO (1) | WO2004100946A1 (el) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7135575B2 (en) | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
EP1761520B1 (en) | 2004-06-23 | 2008-07-09 | Eli Lilly And Company | Kinase inhibitors |
EP1778686B9 (en) | 2004-08-12 | 2009-07-08 | Pfizer Limited | Triazolopyridinylsulfanyl derivatives as p38 map kinase inhibitors |
DE102004039789A1 (de) | 2004-08-16 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
WO2007089646A1 (en) | 2006-01-31 | 2007-08-09 | Array Biopharma Inc. | Kinase inhibitors and methods of use thereof |
US20090270350A1 (en) * | 2006-02-10 | 2009-10-29 | Pfizer Inc. | Pyridinone Pyrazole Urea and Pyrimidinone Pyrazole Urea Derivatives |
WO2007113005A2 (en) * | 2006-04-03 | 2007-10-11 | European Molecular Biology Laboratory (Embl) | 2-substituted 3-aminosulfonyl-thiophene derivatives as aurora kinase inhibitors |
US7666888B2 (en) | 2006-07-20 | 2010-02-23 | Amgen Inc. | Substituted azole aromatic heterocycles as inhibitors of 11β-HSD-1 |
MX2009002019A (es) | 2006-08-24 | 2009-03-09 | Novartis Ag | Derivados de 2-(pirazin-2-il)-tiazol y 2-(1h-pirazol-3-il)-tiazol asi como compuestos relacionados como inhibidores de la estearoil-coa-desaturasa (scd) para el tratamiento de trastornos metabolicos, cardiovasculares, y otros. |
CN101516877B (zh) | 2006-09-22 | 2013-09-11 | 诺瓦提斯公司 | 杂环有机化合物 |
US8258160B2 (en) | 2006-12-20 | 2012-09-04 | Novartis Ag | SCD1 inhibitors triazole and tetrazole compounds |
DE102007047737A1 (de) * | 2007-10-05 | 2009-04-30 | Merck Patent Gmbh | Piperidin- und Piperazinderivate |
EA020641B1 (ru) | 2008-10-02 | 2014-12-30 | Респайверт Лимитед | Производные n-(1-фенил-3-алкилпиразол-5-ил)-n'-арилмочевины |
GB0818033D0 (en) | 2008-10-02 | 2008-11-05 | Respivert Ltd | Novel compound |
MX2011006219A (es) * | 2008-12-11 | 2011-06-28 | Respivert Ltd | Inhibidores de la proteina cinasa activada por el mitogeno p38. |
GB0905955D0 (en) | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
EP2236505A1 (de) | 2009-04-03 | 2010-10-06 | Bayer CropScience AG | Acylierte Aminopyridine und - pyridazine als Insektizide |
WO2011021645A1 (ja) * | 2009-08-19 | 2011-02-24 | 大日本住友製薬株式会社 | 2環性ウレア誘導体、またはその薬学的に許容される塩 |
EP2503887B1 (en) | 2009-11-24 | 2016-01-06 | Merck Sharp & Dohme Corp. | Substituted biaryl derivatives and methods of use thereof |
JP5787977B2 (ja) * | 2010-04-08 | 2015-09-30 | レスピバート・リミテツド | P38mapキナーゼ阻害剤 |
KR101332830B1 (ko) | 2012-07-05 | 2013-11-27 | 한국화학연구원 | 페닐우레아 유도체 또는 이의 약학적으로 허용가능한 염을 포함하는 항암감작제 |
TWI648282B (zh) * | 2014-03-27 | 2019-01-21 | 印度商托仁特生技有限公司 | 新熔合咪唑苯并噻唑化合物 |
WO2017151409A1 (en) | 2016-02-29 | 2017-09-08 | University Of Florida Research Foundation, Incorporated | Chemotherapeutic methods |
AU2017228398A1 (en) | 2016-03-03 | 2018-10-18 | Cornell University | Small molecule IRE1-alpha inhibitors |
KR20200067170A (ko) | 2017-10-05 | 2020-06-11 | 풀크럼 쎄러퓨틱스, 인코포레이티드 | FSHD의 치료를 위하여 DUX4 및 하류 유전자 발현을 저감시키는 p38 키나제 저해제 |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
CA3142097A1 (en) | 2018-05-30 | 2019-12-05 | Washington University | Mitogen-activated protein kinase inhibitors, methods of making, and methods of use thereof |
CA3120514A1 (en) * | 2018-11-20 | 2020-05-28 | Sironax Ltd | Cyclic ureas |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1043995T1 (de) * | 1997-12-22 | 2001-06-07 | Bayer Corp., Pittsburgh | INHIBIERUNG DER p38 KINASE-AKTIVITÄT DURCH DIE VERWENDUNG VON ARYL- UND HETEROARYLSUBSTITUIERTEN HARNSTOFFEN |
US6316466B1 (en) * | 1998-05-05 | 2001-11-13 | Syntex (U.S.A.) Llc | Pyrazole derivatives P-38 MAP kinase inhibitors |
UA73492C2 (en) * | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents |
-
2003
- 2003-08-29 GB GBGB0320244.7A patent/GB0320244D0/en not_active Ceased
-
2004
- 2004-04-25 JO JO200448A patent/JO2473B1/en active
- 2004-05-03 PE PE2004000447A patent/PE20050523A1/es not_active Application Discontinuation
- 2004-05-04 HN HN2004000150A patent/HN2004000150A/es unknown
- 2004-05-05 PL PL04751319T patent/PL1622610T3/pl unknown
- 2004-05-05 SI SI200430166T patent/SI1622610T1/sl unknown
- 2004-05-05 AT AT04751319T patent/ATE348610T1/de active
- 2004-05-05 MX MXPA05011400A patent/MXPA05011400A/es active IP Right Grant
- 2004-05-05 CL CL200400965A patent/CL2004000965A1/es unknown
- 2004-05-05 ES ES04751319T patent/ES2277271T3/es not_active Expired - Lifetime
- 2004-05-05 DK DK04751319T patent/DK1622610T3/da active
- 2004-05-05 PT PT04751319T patent/PT1622610E/pt unknown
- 2004-05-05 EP EP04751319A patent/EP1622610B1/en not_active Expired - Lifetime
- 2004-05-05 BR BRPI0409991-5A patent/BRPI0409991A/pt not_active IP Right Cessation
- 2004-05-05 CA CA002524043A patent/CA2524043C/en not_active Expired - Fee Related
- 2004-05-05 WO PCT/US2004/013875 patent/WO2004100946A1/en active IP Right Grant
- 2004-05-05 DE DE602004003806T patent/DE602004003806T2/de not_active Expired - Lifetime
- 2004-05-05 AU AU2004238241A patent/AU2004238241A1/en not_active Abandoned
- 2004-05-05 JP JP2006532565A patent/JP4714150B2/ja not_active Expired - Fee Related
- 2004-05-06 MY MYPI20041681A patent/MY140830A/en unknown
- 2004-05-06 TW TW093112701A patent/TWI335223B/zh not_active IP Right Cessation
- 2004-05-06 PA PA20048601901A patent/PA8601901A1/es unknown
- 2004-05-06 UY UY28310A patent/UY28310A1/es not_active Application Discontinuation
-
2005
- 2005-11-01 US US11/264,063 patent/US7541368B2/en not_active Expired - Fee Related
-
2007
- 2007-01-19 HR HR20070020T patent/HRP20070020T3/xx unknown
- 2007-03-15 CY CY20071100359T patent/CY1107433T1/el unknown
-
2010
- 2010-10-26 AU AU2010236021A patent/AU2010236021A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
HRP20070020T3 (en) | 2007-04-30 |
ATE348610T1 (de) | 2007-01-15 |
HN2004000150A (es) | 2008-03-03 |
CA2524043A1 (en) | 2004-11-25 |
BRPI0409991A (pt) | 2006-05-09 |
MY140830A (en) | 2010-01-29 |
EP1622610A1 (en) | 2006-02-08 |
WO2004100946A1 (en) | 2004-11-25 |
TW200509912A (en) | 2005-03-16 |
JO2473B1 (en) | 2009-01-20 |
CA2524043C (en) | 2009-12-29 |
JP4714150B2 (ja) | 2011-06-29 |
DE602004003806T2 (de) | 2007-11-22 |
AU2010236021A1 (en) | 2010-11-18 |
JP2007502324A (ja) | 2007-02-08 |
PE20050523A1 (es) | 2005-07-07 |
DE602004003806D1 (de) | 2007-02-01 |
US20060063796A1 (en) | 2006-03-23 |
UY28310A1 (es) | 2004-11-30 |
SI1622610T1 (sl) | 2007-04-30 |
MXPA05011400A (es) | 2005-12-12 |
DK1622610T3 (da) | 2007-04-23 |
ES2277271T3 (es) | 2007-07-01 |
TWI335223B (en) | 2011-01-01 |
CL2004000965A1 (es) | 2005-04-22 |
PA8601901A1 (es) | 2004-11-26 |
EP1622610B1 (en) | 2006-12-20 |
PL1622610T3 (pl) | 2007-05-31 |
AU2004238241A1 (en) | 2004-11-25 |
GB0320244D0 (en) | 2003-10-01 |
US7541368B2 (en) | 2009-06-02 |
PT1622610E (pt) | 2007-02-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY1107433T1 (el) | Παραγωγα 1-(2η-πυραζολ-3-υλο)-3-(4-[1-(βενζοϋλο)-πιπepιδιν-4-υλομεθυλο]-φαινυλο)-ουριας και συναφεις ενωσεις ως αναστολεις της ρ38 κινασης και/ή tnf-αναστολεις για την αντιμετωπιση φλεγμονων | |
CY1114803T1 (el) | Παραγωγα πυριμιδινο σουλφοναμιδιου ως ρυθμιστες υποδοχεων χημειοκινης | |
CY1114037T1 (el) | 2-(μορφολιν-4-υλ) πυριμιδινες ως αναστολεις της κινασης της φωσφατιδυλο-ινοσιτολης (ρι) 3 και η χρηση τους στη θεραπεια του καρκινου | |
EA200700902A1 (ru) | 3-ариламинопиридиновые производные | |
SE0402762D0 (sv) | Indazole sulphonamide derivatives | |
GEP20053600B (en) | 3-(4-Amidopyrrol-2-Ylmethlidene)-2- Indolinone Derivatives as Protein Kinase Inhibitors | |
SE0202463D0 (sv) | Novel compounds | |
WO2002057261A3 (en) | Diaminothiazoles and their use as inhibitors of cyclin-dependent kinase | |
MY141220A (en) | Pyrazole derivatives as inhibitors of receptor tyrosine kinases | |
ATE371656T1 (de) | Heteroaryl-pyrimidinderivate als jak-inhibitoren | |
DE60206911D1 (de) | Imidazol-2-carbonsäureamid derivate als raf-kinase-inhibitoren | |
IL175716A (en) | 2- (4-Bromo- or 4-Methyl-Phenylamino) -6-Oxo-1,6-Dihydropyridines and their use in drug preparation | |
DE60333387D1 (de) | Triazolopyridazine als proteinkinase-inhibitoren | |
UA88012C2 (uk) | Похідні хіназоліндіону як інгібітори parp | |
MX2007009372A (es) | Nuevos compuestos ii derivados de 2-piridina como inhibidores de elastasa neutrofila. | |
DE602005002562D1 (de) | Pyrrolylsubstituierte pyridoä2,3-düpyrimidin-7-one und derivate davon als therapeutische mittel | |
SG147450A1 (en) | Sustained release pharmaceutical compositions comprising aplindore and derivatives thereof | |
DK1458713T3 (da) | Indolinonderivater anvendelige som proteinkinaseinhibitorer | |
ATE359791T1 (de) | Pyrimidin-2,4-dion-derivate als matrix- metalloproteinase-hemmer | |
DK1641454T3 (da) | Pyrazolo[3,4-B]pyridin-6-oner som GSK-3-hæmmere | |
BRPI0508107A (pt) | derivados de indazol e composições farmacêuticas contendo os mesmos | |
ATE279410T1 (de) | 3-aminopyrazole als inhibitoren von cyclinabhängigen kinasen | |
EA200501233A1 (ru) | 4-аминопиримидин-5-он | |
SE0302570D0 (sv) | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof | |
SE0104326D0 (sv) | Therapeutic heterocycles |