MA26697A1 - Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenant - Google Patents
Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenantInfo
- Publication number
- MA26697A1 MA26697A1 MA25810A MA25810A MA26697A1 MA 26697 A1 MA26697 A1 MA 26697A1 MA 25810 A MA25810 A MA 25810A MA 25810 A MA25810 A MA 25810A MA 26697 A1 MA26697 A1 MA 26697A1
- Authority
- MA
- Morocco
- Prior art keywords
- pharmaceutical compositions
- compositions containing
- gsk
- inhibitor compounds
- compounds
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 102000002254 Glycogen Synthase Kinase 3 Human genes 0.000 title abstract 3
- 108010014905 Glycogen Synthase Kinase 3 Proteins 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/456—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 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 other ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- 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
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyrrole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Composés nouveaux inhibiteurs de GSK-3, et compositions pharmaceutiques les contenant L'invention concerne des composés de formule (I) : dans laquelle R, R1, R2 et R3 représentent divers radicaux. Elle concerne également un procédé pour leur préparation et des compositions pharmaceutiques les contenant. Application : utilisation de ces composés et de ces composiLions, inhibiteurs de GSK-3, dans le traitement de diverses maladies.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9821974.4A GB9821974D0 (en) | 1998-10-08 | 1998-10-08 | Novel method and compounds |
| GBGB9827521.7A GB9827521D0 (en) | 1998-12-14 | 1998-12-14 | Novel method and compounds |
| GBGB9827883.1A GB9827883D0 (en) | 1998-12-17 | 1998-12-17 | Novel compounds |
| GBGB9905518.8A GB9905518D0 (en) | 1999-03-10 | 1999-03-10 | Novel method and compound |
| GBGB9907086.4A GB9907086D0 (en) | 1999-03-26 | 1999-03-26 | Novel compounds |
| GBGB9919362.5A GB9919362D0 (en) | 1999-08-16 | 1999-08-16 | Novel method and compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA26697A1 true MA26697A1 (fr) | 2004-12-20 |
Family
ID=27547324
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA25810A MA26697A1 (fr) | 1998-10-08 | 1999-10-06 | Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenant |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1119548B1 (fr) |
| JP (1) | JP2002527419A (fr) |
| AR (1) | AR020727A1 (fr) |
| AT (1) | ATE284387T1 (fr) |
| AU (1) | AU6111699A (fr) |
| DE (1) | DE69922526T2 (fr) |
| ES (1) | ES2234300T3 (fr) |
| HK (1) | HK1038564A1 (fr) |
| MA (1) | MA26697A1 (fr) |
| PE (1) | PE20001093A1 (fr) |
| WO (1) | WO2000021927A2 (fr) |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI263636B (en) * | 1999-09-16 | 2006-10-11 | Ciba Sc Holding Ag | Fluorescent maleimides and use thereof |
| DK1248604T4 (da) | 2000-01-21 | 2012-05-21 | Novartis Ag | Kombinationer indeholdende dipeptidylpeptidase-IV-inhibitorer og antidiabetiske midler |
| GB0008264D0 (en) * | 2000-04-04 | 2000-05-24 | Smithkline Beecham Plc | Novel method and compounds |
| ES2166328B1 (es) * | 2000-05-11 | 2003-09-16 | Consejo Superior Investigacion | Inhibidores heterociclicos del enzima gsk 3 utiles en el tratamiento de procesos neurodegenerativos e hiperproliferativos |
| CA2408747C (fr) * | 2000-05-11 | 2011-04-05 | Consejo Superior Investigaciones Cientificas | Inhibiteurs heterocycliques de la glycogene synthase kinase gsk-3 |
| IL153851A0 (en) * | 2000-07-27 | 2003-07-31 | Hoffmann La Roche | 3-indolyl-4-phenyl-1h-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3beta |
| SG159378A1 (en) * | 2000-11-07 | 2010-03-30 | Novartis Ag | Indolylmaleimide derivatives as protein kinase c inhibitors |
| KR20040016828A (ko) | 2000-12-08 | 2004-02-25 | 오르토-맥네일 파마슈티칼, 인코퍼레이티드 | 키나제 저해제로서 인다졸릴-치환된 피롤린 화합물 |
| AUPR213700A0 (en) | 2000-12-18 | 2001-01-25 | Biota Scientific Management Pty Ltd | Antiviral agents |
| GB0103031D0 (en) * | 2001-02-07 | 2001-03-21 | Smithkline Beecham Plc | Novel treatment |
| ATE318596T1 (de) * | 2001-03-29 | 2006-03-15 | Topotarget As | Succinimid- und maleimidderivate und ihre verwendung als katalytische inhibitoren der topoisomerase ii |
| US7132445B2 (en) | 2001-04-16 | 2006-11-07 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| US20040106794A1 (en) | 2001-04-16 | 2004-06-03 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| MXPA04000906A (es) * | 2001-08-03 | 2004-11-22 | Novo Nordisk As | Nuevos derivados de 2,4-diaminotiazol. |
| TWI335221B (en) * | 2001-09-27 | 2011-01-01 | Alcon Inc | Inhibtors of glycogen synthase kinase-3 (gsk-3) for treating glaucoma |
| MXPA04003439A (es) | 2001-10-12 | 2004-07-08 | Schering Corp | Compuestos de maleimida 3,4 disustituidos como antagonistas de receptor de quimiocina cxc. |
| US6878709B2 (en) | 2002-01-04 | 2005-04-12 | Schering Corporation | 3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists |
| AU2003235798A1 (en) * | 2002-01-10 | 2003-07-24 | F. Hoffmann-La Roche Ag | Use of a gsk-3beta inhibitor in the manufacture of a medicament for increasing bone formation |
| AU2003220026A1 (en) * | 2002-03-01 | 2003-09-16 | Chiron Corporation | Methods and compositions for the treatment of ischemia |
| PL371366A1 (en) | 2002-03-01 | 2005-06-13 | Takeda Pharmaceutical Company Limited | Antidepressant |
| EP1485089B1 (fr) | 2002-03-18 | 2013-04-17 | Merck Sharp & Dohme Corp. | Traitements combines pour maladies induites par la chimiokine |
| ATE447404T1 (de) * | 2002-03-29 | 2009-11-15 | Novartis Vaccines & Diagnostic | Substituierte benzazole und ihre verwendung als raf-kinase-hemmer |
| CA2485527A1 (fr) | 2002-05-08 | 2003-11-20 | Janssen Pharmaceutica N.V. | Inhibiteurs substitues de la pyrroline kinase |
| JP2005531607A (ja) | 2002-06-05 | 2005-10-20 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | キナーゼ阻害剤として置換ピロリン |
| RU2004135382A (ru) | 2002-06-05 | 2005-06-27 | Янссен Фармацевтика Н.В. (Be) | Замещенные пирролины в качестве ингибиторов киназы |
| ES2273043T3 (es) * | 2002-08-02 | 2007-05-01 | Vertex Pharmaceuticals Incorporated | Composiciones de pirazol utiles como inhibidores de gsk-3. |
| PE20040570A1 (es) | 2002-10-09 | 2004-08-30 | Pharmacopeia Drug Discovery | Tiadiazoldioxidos y tiadiazoloxidos como ligandos del receptor de cxc- y cc-quimiocina |
| GB0224830D0 (en) | 2002-10-24 | 2002-12-04 | Sterix Ltd | Compound |
| PL376301A1 (en) * | 2002-10-24 | 2005-12-27 | Sterix Limited | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1 and type 2 |
| WO2005024755A2 (fr) * | 2002-12-31 | 2005-03-17 | Deciphera Pharmaceuticals, Llc. | Medicaments destines au traitement de troubles neurodegeneratifs ou de diabetes |
| US7279576B2 (en) | 2002-12-31 | 2007-10-09 | Deciphera Pharmaceuticals, Llc | Anti-cancer medicaments |
| US7202257B2 (en) | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
| US7144911B2 (en) | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
| GB0303319D0 (en) | 2003-02-13 | 2003-03-19 | Novartis Ag | Organic compounds |
| WO2004094422A1 (fr) | 2003-03-27 | 2004-11-04 | Janssen Pharmaceutica N.V. | Pyrrolines substitues inhibiteurs de kinase |
| BRPI0411366A (pt) | 2003-06-13 | 2006-07-25 | Janssen Pharmaceutica Nv | derivados de indazolil (indolil) maleimida substituìdos como inibidores de cinase |
| GB0316232D0 (en) * | 2003-07-11 | 2003-08-13 | Astrazeneca Ab | Therapeutic agents |
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| EP1694659B8 (fr) | 2003-12-19 | 2008-10-08 | Schering Corporation | Utilisation de thiadiazoles comme ligands des recepteurs aux chimiokines cxc et cc |
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| WO2005087710A1 (fr) * | 2004-03-15 | 2005-09-22 | Takeda Pharmaceutical Company Limited | Dérivé de l'acide aminophénylpropanoïque |
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| BRPI0510954A (pt) * | 2004-05-12 | 2007-11-20 | Bayer Cropscience Gmbh | regulação do crescimento de uma planta |
| CA2589127C (fr) | 2004-12-08 | 2013-02-05 | Johannes Gutenberg-Universitat Mainz | Derives de 3-(indolyl)-4-arylmaleimide et utilisation comme inhibiteurs de l'angiogenese |
| WO2006073364A1 (fr) * | 2005-01-10 | 2006-07-13 | Astrazeneca Ab | Derives non aniliques d'isothiazol-3(2h)-thione 1,1-dioxides servant de modulateurs de recepteurs nucleaires hepatiques |
| SE0500058D0 (sv) * | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 5 |
| SE0500056D0 (sv) * | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 4 |
| SE0500055D0 (sv) * | 2005-01-10 | 2005-01-10 | Astrazeneca Ab | Therapeutic agents 3 |
| KR20070094963A (ko) * | 2005-01-10 | 2007-09-27 | 아스트라제네카 아베 | 간 x 수용체 조절제로서 이소티아졸-3(2h)-온1,1-디옥사이드 유도체 |
| WO2007005403A1 (fr) | 2005-06-29 | 2007-01-11 | Schering Corporation | Oxadiazolopyrazines 5,6-di-substituées et thiadiazolopyrazines comme ligands récepteurs de cxc-chimiokine |
| MX2008000366A (es) | 2005-06-29 | 2008-03-07 | Schering Corp | Oxadiazoles di-sustituidos como ligandos del receptor cxc-quimiocina. |
| EP2258359A3 (fr) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline |
| JP2009506069A (ja) | 2005-08-26 | 2009-02-12 | ブレインセルス,インコーポレイティド | ムスカリン性受容体調節による神経発生 |
| PL1931350T5 (pl) | 2005-09-14 | 2021-11-15 | Takeda Pharmaceutical Company Limited | Podanie inhibitorów dipeptydylo-peptydazy |
| US7985756B2 (en) | 2005-10-21 | 2011-07-26 | Braincells Inc. | Modulation of neurogenesis by PDE inhibition |
| WO2007053596A1 (fr) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Modulation de la neurogenese dont la mediation est assuree par recepteur gaba |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| WO2007134136A2 (fr) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenèse par modulation de l'angiotensine |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| WO2010099217A1 (fr) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine |
| WO2011041293A1 (fr) | 2009-09-30 | 2011-04-07 | Takeda Pharmaceutical Company Limited | Dérivés pyrazolo [1, 5a] pyrimidines comme inhibiteurs de kinase 1 régulatrice de signal d'apoptose |
| EP2343291A1 (fr) | 2009-12-18 | 2011-07-13 | Johannes Gutenberg-Universität Mainz | Composés de 3-(indolyl)- ou 3-(azaindolyl)-4-arylmaléimide et leur utilisation dans le traitement de tumeurs |
| WO2011097079A1 (fr) | 2010-02-03 | 2011-08-11 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinase 1 régulant le signal d'apoptose |
| KR101643721B1 (ko) * | 2010-11-09 | 2016-07-28 | 후지안 하이시 파머수티클스, 인코포레이티드 | 키나아제 활성을 증진시키기 위한 화합물 및 이의 응용 |
| EP2474541A1 (fr) | 2010-12-23 | 2012-07-11 | Johannes- Gutenberg-Universität Mainz | Composés conjugués de 3-(indolyl)- et 3-(azaindolyl)-4-arylmaléimide et leur utilisation dans le traitement de tumeurs |
| US8461179B1 (en) | 2012-06-07 | 2013-06-11 | Deciphera Pharmaceuticals, Llc | Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
| WO2014204585A1 (fr) * | 2013-05-03 | 2014-12-24 | The Brigham And Women's Hospital, Inc. | Méthodes de traitement d'une cardiomyopathie |
| EP3741375A1 (fr) | 2014-07-17 | 2020-11-25 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Procédés de traitement de maladies associées aux jonctions neuromusculaires |
| WO2016207366A1 (fr) | 2015-06-26 | 2016-12-29 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Méthodes et compositions pharmaceutiques de traitement d'infections virales |
| US20180256623A1 (en) * | 2015-09-16 | 2018-09-13 | University Of Virginia Patent Foundation | Compositions and method for regulating adipose tissue lipolysis, insulin-resistance, and hyperglycemia |
| CN108368049A (zh) | 2015-09-24 | 2018-08-03 | 葛兰素史克知识产权开发有限公司 | 吲哚胺2,3-双加氧酶的调节剂 |
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| CN106188007B (zh) * | 2016-06-29 | 2018-08-14 | 东华大学 | 一种3-哌啶基-4-吲哚马来酰亚胺类化合物及其制备和应用 |
| AU2019216351B2 (en) | 2018-01-31 | 2024-07-25 | Deciphera Pharmaceuticals, Llc | Combination therapy for the treatment of mastocytosis |
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| AU2020419197B2 (en) | 2019-12-30 | 2023-08-31 | Deciphera Pharmaceuticals, Llc | Amorphous kinase inhibitor formulations and methods of use thereof |
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| US11779572B1 (en) | 2022-09-02 | 2023-10-10 | Deciphera Pharmaceuticals, Llc | Methods of treating gastrointestinal stromal tumors |
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|---|---|---|---|---|
| US3335147A (en) * | 1965-04-29 | 1967-08-08 | Us Vitamin Pharm Corp | Anilino-pyridinium-maleimides |
| SK75289A3 (en) * | 1988-02-10 | 1998-05-06 | Hoffmann La Roche | Substituted pyrroles, their use for producing a drug, and the drug on their base |
| DE4005969A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte pyrrole, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
| DE4005970A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte maleinimide, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
| WO1997041854A1 (fr) * | 1996-05-07 | 1997-11-13 | The Trustees Of The University Of Pennsylvania | Inhibiteurs de glycogene synthetase kinase-3 et procedes d'identification et d'utilisation de ces inhibiteurs |
| DE19637042A1 (de) * | 1996-09-12 | 1998-03-19 | Boehringer Mannheim Gmbh | Heterocyclische Verbindungen und deren Verwendung in der Detektion von Nucleinsäuren |
| WO1998016528A1 (fr) * | 1996-10-11 | 1998-04-23 | Chiron Corporation | Inhibiteurs puriques de glycogene synthase kinase 3 (gsk3) |
| ES2190221T3 (es) * | 1998-05-04 | 2003-07-16 | Zentaris Ag | Derivados de indol y su uso para el tratamiento de enfermedades malignas y otras, que se basan en proliferaciones celulares patologicas. |
| AU4929999A (en) * | 1998-07-30 | 2000-02-21 | Japan Tobacco Inc. | Disubstituted maleimide compounds and medicinal utilization thereof |
-
1999
- 1999-10-05 JP JP2000575836A patent/JP2002527419A/ja active Pending
- 1999-10-05 AT AT99947744T patent/ATE284387T1/de not_active IP Right Cessation
- 1999-10-05 AU AU61116/99A patent/AU6111699A/en not_active Abandoned
- 1999-10-05 DE DE69922526T patent/DE69922526T2/de not_active Expired - Fee Related
- 1999-10-05 WO PCT/GB1999/003280 patent/WO2000021927A2/fr not_active Ceased
- 1999-10-05 EP EP99947744A patent/EP1119548B1/fr not_active Expired - Lifetime
- 1999-10-05 HK HK02100210.2A patent/HK1038564A1/zh unknown
- 1999-10-05 ES ES99947744T patent/ES2234300T3/es not_active Expired - Lifetime
- 1999-10-06 PE PE1999001014A patent/PE20001093A1/es not_active Application Discontinuation
- 1999-10-06 MA MA25810A patent/MA26697A1/fr unknown
- 1999-10-06 AR ARP990105056A patent/AR020727A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1119548B1 (fr) | 2004-12-08 |
| WO2000021927A3 (fr) | 2000-07-13 |
| HK1038564A1 (zh) | 2002-03-22 |
| EP1119548A1 (fr) | 2001-08-01 |
| ES2234300T3 (es) | 2005-06-16 |
| DE69922526D1 (de) | 2005-01-13 |
| AU6111699A (en) | 2000-05-01 |
| AR020727A1 (es) | 2002-05-29 |
| JP2002527419A (ja) | 2002-08-27 |
| DE69922526T2 (de) | 2005-06-02 |
| WO2000021927A2 (fr) | 2000-04-20 |
| PE20001093A1 (es) | 2000-12-22 |
| ATE284387T1 (de) | 2004-12-15 |
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