DE602004024572D1 - Zusammensetzungen, die sich als inhibitoren von proteinkinasen eignen - Google Patents
Zusammensetzungen, die sich als inhibitoren von proteinkinasen eignenInfo
- Publication number
- DE602004024572D1 DE602004024572D1 DE602004024572T DE602004024572T DE602004024572D1 DE 602004024572 D1 DE602004024572 D1 DE 602004024572D1 DE 602004024572 T DE602004024572 T DE 602004024572T DE 602004024572 T DE602004024572 T DE 602004024572T DE 602004024572 D1 DE602004024572 D1 DE 602004024572D1
- Authority
- DE
- Germany
- Prior art keywords
- inhibitors
- protein kinases
- compounds
- compositions suited
- compositions
- 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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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
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- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
- C07D333/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D333/70—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
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- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D495/14—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51088103P | 2003-10-14 | 2003-10-14 | |
PCT/US2004/033749 WO2005037843A1 (en) | 2003-10-14 | 2004-10-14 | Compositions useful as inhibitors of protein kinases |
Publications (1)
Publication Number | Publication Date |
---|---|
DE602004024572D1 true DE602004024572D1 (de) | 2010-01-21 |
Family
ID=36585960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE602004024572T Active DE602004024572D1 (de) | 2003-10-14 | 2004-10-14 | Zusammensetzungen, die sich als inhibitoren von proteinkinasen eignen |
Country Status (12)
Country | Link |
---|---|
US (3) | US7700609B2 (de) |
EP (1) | EP1692140B1 (de) |
JP (2) | JP2007509848A (de) |
CN (3) | CN1897950A (de) |
AT (1) | ATE451376T1 (de) |
AU (1) | AU2004282172B2 (de) |
CA (1) | CA2542113A1 (de) |
DE (1) | DE602004024572D1 (de) |
ES (1) | ES2338234T3 (de) |
HK (1) | HK1096673A1 (de) |
TW (1) | TW200530251A (de) |
WO (1) | WO2005037843A1 (de) |
Families Citing this family (177)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1897950A (zh) | 2003-10-14 | 2007-01-17 | 惠氏公司 | 稠合芳基和杂芳基衍生物及其使用方法 |
PL1718283T3 (pl) | 2004-01-22 | 2013-08-30 | Univ Miami | Miejscowe preparaty koenzymu Q10 i sposoby ich zastosowania |
US7772232B2 (en) * | 2004-04-15 | 2010-08-10 | Bristol-Myers Squibb Company | Quinazolinyl compounds as inhibitors of potassium channel function |
US8057815B2 (en) | 2004-04-19 | 2011-11-15 | Portola Pharmaceuticals, Inc. | Methods of treatment with Syk inhibitors |
EP2719698B1 (de) | 2004-05-14 | 2016-10-05 | Millennium Pharmaceuticals, Inc. | Verfahren zur Herstellung von Inhibitoren der Aurorakinase |
MY147767A (en) * | 2004-06-16 | 2013-01-31 | Janssen Pharmaceutica Nv | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders |
US20060276528A1 (en) * | 2004-08-24 | 2006-12-07 | Abdel-Magid Ahmed F | Novel benzo-fused heteroaryl sulfamide derivatives useful as anticonvulsant agents |
PE20060500A1 (es) * | 2004-08-24 | 2006-07-13 | Janssen Pharmaceutica Nv | Derivados de heteroaril sulfamida benzo-fusionada como anticonvulsivantes |
JP5002460B2 (ja) | 2004-10-04 | 2012-08-15 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | タンパク質キナーゼインヒビターとして有用なラクタム化合物 |
DE602005023333D1 (de) | 2004-10-15 | 2010-10-14 | Takeda Pharmaceutical | Kinaseinhibitoren |
WO2006127184A1 (en) * | 2005-05-20 | 2006-11-30 | Janssen Pharmaceutica N.V. | Process for preparation of sulfamide derivatives |
EP1935977A4 (de) * | 2005-09-20 | 2009-05-06 | Univ Nihon | Transkriptionale regulation der hochaffinen ige-rezeptor-kette |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
US8716231B2 (en) * | 2005-12-19 | 2014-05-06 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain |
US20070155823A1 (en) * | 2005-12-19 | 2007-07-05 | Smith-Swintosky Virginia L | Use of benzo-fused heterocycle sulfamide derivatives as neuroprotective agents |
US8691867B2 (en) * | 2005-12-19 | 2014-04-08 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for the treatment of substance abuse and addiction |
US8497298B2 (en) * | 2005-12-19 | 2013-07-30 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for lowering lipids and lowering blood glucose levels |
US20070155824A1 (en) * | 2005-12-19 | 2007-07-05 | Smith-Swintosky Virginia L | Use of benzo-fused heterocycle sulfamide derivatives for disease modification / epileptogenesis |
US8937096B2 (en) | 2005-12-19 | 2015-01-20 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocyle sulfamide derivatives for the treatment of mania and bipolar disorder |
AR058389A1 (es) * | 2005-12-19 | 2008-01-30 | Janssen Pharmaceutica Nv | Uso de derivados heterociclicos benzo-fusionados de sulfamida para el tratamiento de la obesidad |
WO2007087068A2 (en) * | 2006-01-13 | 2007-08-02 | Pharmacyclics, Inc. | Inhibitors of tyrosine kinases and uses thereof |
TW201412738A (zh) | 2006-01-17 | 2014-04-01 | Vertex Pharma | 適合作為傑納斯激酶(janus kinase)抑制劑之氮雜吲哚 |
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US20100280026A1 (en) | 2010-11-04 |
JP2011241231A (ja) | 2011-12-01 |
US20050148603A1 (en) | 2005-07-07 |
CN101824043A (zh) | 2010-09-08 |
EP1692140A1 (de) | 2006-08-23 |
EP1692140B1 (de) | 2009-12-09 |
CN1894258A (zh) | 2007-01-10 |
TW200530251A (en) | 2005-09-16 |
US8288400B2 (en) | 2012-10-16 |
CN1894258B (zh) | 2010-06-16 |
US8017619B2 (en) | 2011-09-13 |
AU2004282172B2 (en) | 2011-03-10 |
WO2005037843A1 (en) | 2005-04-28 |
JP2007509848A (ja) | 2007-04-19 |
AU2004282172A1 (en) | 2005-04-28 |
CA2542113A1 (en) | 2005-04-28 |
CN1897950A (zh) | 2007-01-17 |
ES2338234T3 (es) | 2010-05-05 |
US7700609B2 (en) | 2010-04-20 |
ATE451376T1 (de) | 2009-12-15 |
US20120183577A1 (en) | 2012-07-19 |
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