MA38333A1 - Composés d'azabenzimidazole en tant qu'inhibiteurs d'isozymes pde4 pour le traitement de troubles du snc et d'autres affections - Google Patents
Composés d'azabenzimidazole en tant qu'inhibiteurs d'isozymes pde4 pour le traitement de troubles du snc et d'autres affectionsInfo
- Publication number
- MA38333A1 MA38333A1 MA38333A MA38333A MA38333A1 MA 38333 A1 MA38333 A1 MA 38333A1 MA 38333 A MA38333 A MA 38333A MA 38333 A MA38333 A MA 38333A MA 38333 A1 MA38333 A1 MA 38333A1
- Authority
- MA
- Morocco
- Prior art keywords
- snc
- disorders
- treatment
- conditions
- pde4 isozyme
- Prior art date
Links
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 208000035475 disorder Diseases 0.000 title abstract 2
- GAMYYCRTACQSBR-UHFFFAOYSA-N 4-azabenzimidazole Chemical class C1=CC=C2NC=NC2=N1 GAMYYCRTACQSBR-UHFFFAOYSA-N 0.000 title 1
- 101100296719 Caenorhabditis elegans pde-4 gene Proteins 0.000 title 1
- 108010044467 Isoenzymes Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 abstract 1
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 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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- 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
- 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
- A61P25/04—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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
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- 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
- A61P25/22—Anxiolytics
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- 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
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- 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
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- 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
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- 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
- A61P27/14—Decongestants or antiallergics
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- 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]
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Epidemiology (AREA)
Abstract
La présente invention concerne des composés représentés par la formule (i) : ou un sel pharmaceutiquement acceptable correspondant, les substituants étant tels que définis dans la description. Les composés représentés par la formule (i) sont utiles en tant qu'inhibiteurs de pde4 pour le traitement de troubles du snc et d'autres affections.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361766268P | 2013-02-19 | 2013-02-19 | |
| PCT/IB2014/058840 WO2014128585A1 (fr) | 2013-02-19 | 2014-02-06 | Composés d'azabenzimidazole en tant qu'inhibiteurs d'isozymes pde4 pour le traitement de troubles du snc et d'autres affections |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA38333A1 true MA38333A1 (fr) | 2017-02-28 |
Family
ID=50151342
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38333A MA38333A1 (fr) | 2013-02-19 | 2014-02-06 | Composés d'azabenzimidazole en tant qu'inhibiteurs d'isozymes pde4 pour le traitement de troubles du snc et d'autres affections |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US9120788B2 (fr) |
| EP (1) | EP2958915B1 (fr) |
| JP (2) | JP6505023B2 (fr) |
| KR (1) | KR20150119370A (fr) |
| CN (1) | CN105121439A (fr) |
| AP (1) | AP2015008663A0 (fr) |
| AR (1) | AR094702A1 (fr) |
| AU (1) | AU2014220351A1 (fr) |
| BR (1) | BR112015019276A2 (fr) |
| CA (1) | CA2900302C (fr) |
| CL (1) | CL2015002222A1 (fr) |
| CR (1) | CR20150425A (fr) |
| CU (1) | CU20150082A7 (fr) |
| DO (1) | DOP2015000201A (fr) |
| EA (1) | EA201591360A1 (fr) |
| EC (1) | ECSP15035278A (fr) |
| ES (1) | ES2638850T3 (fr) |
| HK (1) | HK1217945A1 (fr) |
| IL (1) | IL240672A0 (fr) |
| MA (1) | MA38333A1 (fr) |
| MD (1) | MD20150071A2 (fr) |
| MX (1) | MX2015010714A (fr) |
| NI (1) | NI201500112A (fr) |
| PE (1) | PE20151332A1 (fr) |
| PH (1) | PH12015501755A1 (fr) |
| SG (1) | SG11201505878UA (fr) |
| TN (1) | TN2015000347A1 (fr) |
| TW (1) | TW201443048A (fr) |
| UY (1) | UY35333A (fr) |
| WO (1) | WO2014128585A1 (fr) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AP2015008663A0 (en) * | 2013-02-19 | 2015-08-31 | Pfizer | Azabenzimidazole compounds as inhibitors of PDE4 isozymes for the treatment of cns and other disorders |
| EP3172210B1 (fr) | 2014-07-24 | 2020-01-15 | Pfizer Inc | Composés de pyrazolopyrimidine |
| SG11201700243YA (en) * | 2014-08-06 | 2017-02-27 | Pfizer | Imidazopyridazine compounds |
| HRP20210403T1 (hr) | 2015-04-29 | 2021-10-29 | Janssen Pharmaceutica Nv | Azabenzimidazoli i njihova uporaba kao modulatora ampa receptora |
| WO2016176449A1 (fr) | 2015-04-29 | 2016-11-03 | Janssen Pharmaceutica Nv | Composés de benzimidazolone et de benzothiazolone et leur utilisation comme modulateurs des récepteurs ampa |
| ES2767707T3 (es) | 2015-04-29 | 2020-06-18 | Janssen Pharmaceutica Nv | Compuestos de indolona y su uso como moduladores de receptor AMPA |
| AU2016255431B2 (en) | 2015-04-29 | 2020-05-07 | Janssen Pharmaceutica Nv | Imidazopyrazines and pyrazolopyrimidines and their use as AMPA receptor modulators |
| ES2832893T3 (es) | 2015-06-17 | 2021-06-11 | Pfizer | Compuestos tricíclicos y su uso como inhibidores de la fosfodiesterasa |
| AR107099A1 (es) * | 2015-12-22 | 2018-03-21 | Gruenenthal Gmbh | Compuestos espiro-[indolin heterocicloalcano] como inhibidores de la fosfodiesterasa |
| PL3419979T3 (pl) | 2016-02-23 | 2020-06-29 | Pfizer Inc. | Związki 6,7-dihydro-5h-pirazolo[5,1-b][1,3]oksazyno-2- karboksyamidowe |
| JP7050054B2 (ja) * | 2016-08-22 | 2022-04-07 | メッドシャイン ディスカバリー インコーポレイテッド | Pde4阻害剤としての縮合環系化合物 |
| WO2018234354A1 (fr) | 2017-06-20 | 2018-12-27 | Grünenthal GmbH | Nouveaux composés 3-indole et 3-indazole substitués utilisées en tant qu'inhibiteurs de phosphodiestérase |
| WO2018234353A1 (fr) | 2017-06-20 | 2018-12-27 | Grünenthal GmbH | Nouveaux composés indole et indazole substitués utilisés en tant qu'inhibiteurs de la phosphodiestérase |
| EP3643711A1 (fr) | 2018-10-24 | 2020-04-29 | Bayer Animal Health GmbH | Nouveaux composés anthelminthiques |
| EP3870292A4 (fr) | 2018-10-26 | 2022-11-09 | The Research Foundation for The State University of New York | Combinaison d'un inhibiteur de réabsorption spécifique de la sérotonine et d'un agoniste partiel du récepteur de la sérotonine 1a pour réduire la dyskinésie induite par l-dopa |
| US12528813B2 (en) | 2019-11-13 | 2026-01-20 | Nippon Shinyaku Co., Ltd. | Substituted imidazo[4,5-b]pyridines as M3 receptor PAMs |
| JP7601425B2 (ja) * | 2020-03-31 | 2024-12-17 | エルジー・ケム・リミテッド | 膵島移植保護用組成物 |
| CN112390750B (zh) * | 2020-11-11 | 2022-03-01 | 常州大学 | 作为选择性磷酸二酯酶2抑制剂的喹啉酮类化合物及其制备方法 |
Family Cites Families (138)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5814651A (en) | 1992-12-02 | 1998-09-29 | Pfizer Inc. | Catechol diethers as selective PDEIV inhibitors |
| EP0683234B2 (fr) | 1993-01-25 | 2007-06-06 | Takeda Chemical Industries, Ltd. | Anticorps dirige contre le beta-amyloide ou un derive de ce dernier et son utilisation |
| JPH08295667A (ja) * | 1995-04-27 | 1996-11-12 | Takeda Chem Ind Ltd | 複素環化合物、その製造法および剤 |
| JPH08295687A (ja) * | 1995-04-28 | 1996-11-12 | Ube Ind Ltd | 無水シトラコン酸の製造法 |
| DE19709877A1 (de) | 1997-03-11 | 1998-09-17 | Bayer Ag | 1,5-Dihydro-pyrazolo[3,4-d]-pyrimidinon-derivate |
| US8173127B2 (en) | 1997-04-09 | 2012-05-08 | Intellect Neurosciences, Inc. | Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof |
| WO1998044955A1 (fr) | 1997-04-09 | 1998-10-15 | Mindset Ltd. | Anticorps recombines specifiques contre les terminaisons beta-amyloide, codage par molecule d'adn, et leurs procedes d'utilisation |
| GB9722520D0 (en) | 1997-10-24 | 1997-12-24 | Pfizer Ltd | Compounds |
| TWI239847B (en) | 1997-12-02 | 2005-09-21 | Elan Pharm Inc | N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease |
| US6905686B1 (en) | 1997-12-02 | 2005-06-14 | Neuralab Limited | Active immunization for treatment of alzheimer's disease |
| CZ27399A3 (cs) | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
| JP2004509059A (ja) * | 1999-06-03 | 2004-03-25 | アボット・ラボラトリーズ | 細胞接着抑制性抗炎症化合物 |
| EP1418175A1 (fr) | 1999-06-28 | 2004-05-12 | Janssen Pharmaceutica N.V. | Inhibiteurs de réplication du virus respiratoire syncytial |
| DE60118521T2 (de) | 2000-01-07 | 2006-10-12 | Universitaire Instelling Antwerpen | Purin derivate, ihre herstellung und verwendung |
| IL151378A0 (en) | 2000-02-24 | 2003-04-10 | Univ Washington | Humanized antibodies that sequester amyloid beta peptide |
| AU2001252609A1 (en) | 2000-04-27 | 2001-11-12 | Imperial Cancer Research Technology Ltd. | Imidazopyridine derivatives |
| DE10045112A1 (de) | 2000-09-11 | 2002-03-21 | Merck Patent Gmbh | Verwendung von Indolderivaten zur Behandlung von Erkrankungen des zentralen Nervensystems |
| WO2002042429A2 (fr) | 2000-11-03 | 2002-05-30 | Proteotech, Inc. | Procedes d'isolement de composes inhibiteurs d'amyloide, et utilisation de composes utilises a partir d'uncaria tomentosa et de plantes parentes |
| GB0115181D0 (en) | 2001-06-20 | 2001-08-15 | Glaxo Group Ltd | Novel use |
| WO2003000697A1 (fr) | 2001-06-22 | 2003-01-03 | Takeda Chemical Industries, Ltd. | Derive de furo-isoquinoline, procede de production de ce compose et utilisation de ce compose |
| ATE296630T1 (de) | 2001-06-27 | 2005-06-15 | Merck Frosst Canada Inc | Substituierte 8-arylchinoline als pde4-hemmer |
| KR20040017246A (ko) | 2001-06-29 | 2004-02-26 | 니켄 가가쿠 가부시키가이샤 | 사이클로알케논 유도체 |
| WO2003008396A1 (fr) | 2001-07-16 | 2003-01-30 | Nikken Chemicals Co., Ltd. | Derive d'oxazine actif sur le plan optique |
| DE50207119D1 (de) | 2001-07-18 | 2006-07-20 | Merck Patent Gmbh | 4-(benzyliden-amino)-3-(methylsulfanyl) -4h-(1, 2, 4) triazin-5-on derivate mit pde -iv hemmender und tnf-antagonistischer wirkung zur behandlung von herzkrankheiten und allergien |
| WO2003008373A1 (fr) | 2001-07-19 | 2003-01-30 | Merck Patent Gmbh | Hydrazides de tyrosine |
| FR2827599A1 (fr) | 2001-07-20 | 2003-01-24 | Neuro3D | Composes derives de quinoleine et quinoxaline,preparation et utilisations |
| GB0118373D0 (en) | 2001-07-27 | 2001-09-19 | Glaxo Group Ltd | Novel therapeutic method |
| TWI221838B (en) | 2001-08-09 | 2004-10-11 | Tanabe Seiyaku Co | Pyrazinoisoquinoline compound or naphthalene compound |
| EP1285922A1 (fr) | 2001-08-13 | 2003-02-26 | Warner-Lambert Company | 1-alkyl ou 1-cycloalkyltriazolo[4,3-a]quinazolin-5-ones comme inhibiteurs de phosphodiestérase |
| FR2828693B1 (fr) | 2001-08-14 | 2004-06-18 | Exonhit Therapeutics Sa | Nouvelle cible moleculaire de la neurotoxicite |
| AU2002333193A1 (en) | 2001-08-15 | 2003-03-03 | Leo Pharma A/S | A pharmaceutical composition for dermal application |
| CA2456985A1 (fr) | 2001-08-15 | 2003-02-27 | Icos Corporation | 2h-phtalazine-1-ones et procedes d'utilisation de celles-ci |
| CA2451998A1 (fr) | 2001-08-17 | 2003-02-27 | Eli Lilly And Company | Anticorps anti-$g(a)$g(b) |
| JO2311B1 (en) | 2001-08-29 | 2005-09-12 | ميرك فروست كندا ليمتد | Alkyl inhibitors Ariel phosphodiesterase-4 |
| GB0122031D0 (en) | 2001-09-12 | 2001-10-31 | Pfizer Ltd | Use of pde4 inhibitors in a dry powder inhaler |
| MXPA04002562A (es) | 2001-09-19 | 2004-05-31 | Altana Pharma Ag | Combinacion de un pde-4 y nsaid. |
| US20050014762A1 (en) | 2001-09-19 | 2005-01-20 | Rolf Beume | Combination |
| WO2003035650A1 (fr) | 2001-09-25 | 2003-05-01 | Takeda Chemical Industries, Ltd. | Inhibiteur d'entree |
| EP1432707B1 (fr) | 2001-10-02 | 2012-03-28 | Pharmacia & Upjohn Company LLC | Composes d'heteoraryle fusionne substitues par azabicyclo utiles pour le traitement de maladies |
| GB0123951D0 (en) | 2001-10-05 | 2001-11-28 | Glaxo Group Ltd | Therapies for treating respiratory diseases |
| DE10150517A1 (de) | 2001-10-12 | 2003-04-17 | Merck Patent Gmbh | Verwendung von Phosphodiesterase IV-Inhibitoren |
| CA2463469A1 (fr) | 2001-10-16 | 2003-04-24 | Memory Pharmaceuticals Corporation | Derives 4-(4-alcoky-3-hydroxyphenyle)-2-pyrrolidone utilises en tant qu'inhibiteurs de la pde4 pour le traitement de syndromes neurologiques |
| EP1440072A4 (fr) | 2001-10-30 | 2005-02-02 | Conforma Therapeutic Corp | Analogues de purine presentant une activite inhibitrice de hsp90 |
| US20040259863A1 (en) | 2001-10-31 | 2004-12-23 | Hans-Michael Eggenweiler | Type 4 phosphodiesterase inhibitors and uses thereof |
| US6833371B2 (en) | 2001-11-01 | 2004-12-21 | Icagen, Inc. | Pyrazolopyrimidines |
| US20030195205A1 (en) | 2001-11-02 | 2003-10-16 | Pfizer Inc. | PDE9 inhibitors for treating cardiovascular disorders |
| AR037517A1 (es) | 2001-11-05 | 2004-11-17 | Novartis Ag | Derivados de naftiridinas, un proceso para su preparacion, composicion farmaceutica y el uso de los mismos para la preparacion de un medicamento para el tratamiento de una enfermedad inflamatoria |
| KR100898894B1 (ko) | 2001-11-05 | 2009-05-21 | 메르크 파텐트 게엠베하 | 히드라조노-말로니트릴 |
| US20030092706A1 (en) | 2001-11-09 | 2003-05-15 | Johannes Barsig | Combination |
| IS7221A (is) | 2001-11-15 | 2004-04-15 | Memory Pharmaceuticals Corporation | Hringlaga adenosínmónófosfat fosfódíesterasa 4D7 ísóform og aðferðir til notkunar þeirra |
| FR2832711B1 (fr) | 2001-11-26 | 2004-01-30 | Warner Lambert Co | Derives de triazolo [4,3-a] pyrido [2,3-d] pyrimidin-5-ones, compositions les contenant, procede de preparation et utilisation |
| US20050101000A1 (en) | 2002-12-11 | 2005-05-12 | Isis Pharmaceuticals Inc. | Modulation of phosphodiesterase 4B expression |
| DE10238723A1 (de) | 2002-08-23 | 2004-03-11 | Bayer Ag | Phenyl-substituierte Pyrazolyprimidine |
| DE10238724A1 (de) | 2002-08-23 | 2004-03-04 | Bayer Ag | Alkyl-substituierte Pyrazolpyrimidine |
| EP1633786A4 (fr) | 2002-10-09 | 2007-07-25 | Rinat Neuroscience Corp | Methodes de traitement de la maladie d'alzheimer au moyen d'anticorps diriges contre le peptide g(b)-amyloide et compositions les comprenant |
| WO2004042390A2 (fr) | 2002-11-08 | 2004-05-21 | Bayer Healthcare Ag | Diagnostic et therapeutique de maladies associees a la phosphodiesterase 4b (pde4b) humaine |
| AU2003299651A1 (en) | 2002-12-11 | 2004-06-30 | Merck And Co., Inc. | Tyrosine kinase inhibitors |
| JP2006522747A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | 縮合1,2,4−トリアゾールの薬学的使用 |
| WO2004089471A2 (fr) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Utilisation pharmaceutique de pyrazolo[1,5-a]pyrimidines substituees |
| US20040220186A1 (en) | 2003-04-30 | 2004-11-04 | Pfizer Inc. | PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease |
| US7741341B2 (en) | 2003-05-19 | 2010-06-22 | Sanofi-Aventis Deutschland Gmbh | Benzimidazole-derivatives as factor Xa inhibitors |
| EP1638935A1 (fr) | 2003-06-19 | 2006-03-29 | Pfizer Products Inc. | Antagoniste de nk1 |
| CN1816530A (zh) | 2003-07-01 | 2006-08-09 | 麦克公司 | 用于治疗高眼压症的眼用组合物 |
| FR2857966A1 (fr) | 2003-07-24 | 2005-01-28 | Aventis Pharma Sa | Produits aryl-heteroaromatiques, compositions les contenant et utilisation |
| US20050020587A1 (en) | 2003-07-25 | 2005-01-27 | Pfizer Inc | Nicotinamide derivatives useful as PDE4 inhibitors |
| WO2005025616A1 (fr) | 2003-09-09 | 2005-03-24 | Takeda Pharmaceutical Company Limited | Utilisation d'un anticorps |
| GB0322722D0 (en) | 2003-09-27 | 2003-10-29 | Glaxo Group Ltd | Compounds |
| GB0322726D0 (en) | 2003-09-27 | 2003-10-29 | Glaxo Group Ltd | Compounds |
| CN1918175A (zh) | 2003-09-29 | 2007-02-21 | 托皮根药品公司 | 治疗包括炎症状况的疾病的寡核苷酸组合物和方法 |
| GB0327319D0 (en) | 2003-11-24 | 2003-12-24 | Pfizer Ltd | Novel pharmaceuticals |
| WO2005066151A2 (fr) | 2003-12-19 | 2005-07-21 | Takeda San Diego, Inc. | Inhibiteurs d'histone desacetylase |
| BRPI0507374A (pt) | 2004-02-02 | 2007-07-10 | Pfizer Prod Inc | moduladores do receptor de histamina-3 |
| JP2008503446A (ja) | 2004-05-06 | 2008-02-07 | プレキシコン,インコーポレーテッド | Pde4b阻害剤及びその使用 |
| US7456164B2 (en) | 2004-05-07 | 2008-11-25 | Pfizer, Inc | 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands |
| EP1595881A1 (fr) | 2004-05-12 | 2005-11-16 | Pfizer Limited | Dérivés de tetrahydronaphthyridine en tant que ligands de récepteur H3 d'histamine |
| GEP20115195B (en) | 2004-07-30 | 2011-04-11 | Rinat Neuroscience Corp | Antibodies directed against amyloid-beta peptide and use thereof |
| EP1786813A2 (fr) | 2004-09-03 | 2007-05-23 | Plexxikon, Inc. | Inhibiteurs de la phosphodiesterase 4b (pde4b) |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| US7547698B2 (en) | 2004-09-20 | 2009-06-16 | Xenon Pharmaceuticals Inc. | Bicyclic heterocyclic derivatives and their use as inhibitors of stearoyl-coadesaturase (SCD) |
| CN101083985A (zh) | 2004-09-21 | 2007-12-05 | 幸讬制药公司 | 用于炎症及免疫相关用途的化合物 |
| FR2877015B1 (fr) | 2004-10-21 | 2007-10-26 | Commissariat Energie Atomique | Revetement nanostructure et procede de revetement. |
| DE102004054634A1 (de) * | 2004-11-12 | 2006-05-18 | Schwarz Pharma Ag | Azaindolcarboxamide |
| WO2006069081A2 (fr) | 2004-12-22 | 2006-06-29 | Washington University In St. Louis | Utilisation d'anticorps anti-a$g(b) pour le traitement d'un traumatisme cerebral |
| JPWO2006088246A1 (ja) | 2005-02-18 | 2008-07-10 | 武田薬品工業株式会社 | Gpr34受容体機能調節剤 |
| GB0503955D0 (en) | 2005-02-25 | 2005-04-06 | Glaxo Group Ltd | Novel compounds |
| PE20061323A1 (es) | 2005-04-29 | 2007-02-09 | Rinat Neuroscience Corp | Anticuerpos dirigidos contra el peptido amiloide beta y metodos que utilizan los mismos |
| CA2608018C (fr) | 2005-05-12 | 2010-07-13 | Pfizer Inc. | Formes cristallines anhydres de n-[1-(2-ethoxyethyl)-5-(n-ethyl-n-methylamino)-7-(4-methylpyridin-2-yl-amino)-1h-pyrazolo[4,3-d]pyrimidine-3-carbonyl]methanesulfonamide |
| WO2006126082A2 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Pyridine [3,4-b] pyrazinones |
| WO2006126083A1 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Composes de pyridine [3 , 4-b] pyrazinones utilises comme inhibiteurs de pde-5 |
| CA2603830A1 (fr) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Co Llc | Pyridine [2,3-b] pyrazinones |
| DE602006018301D1 (de) | 2005-06-22 | 2010-12-30 | Pfizer Prod Inc | Histamin-3-rezeptorantagonisten |
| US8158673B2 (en) | 2005-10-27 | 2012-04-17 | Pfizer Inc. | Histamine-3 receptor antagonists |
| EP1945639A1 (fr) | 2005-11-04 | 2008-07-23 | Pfizer Limited | Dérivé de tétrahydronaphtyridine |
| WO2007063385A2 (fr) | 2005-12-01 | 2007-06-07 | Pfizer Products Inc. | Antagonistes des recepteurs de l'histamine 3 pour des amines spirocycliques |
| WO2007069053A1 (fr) | 2005-12-14 | 2007-06-21 | Pfizer Products Inc. | Antagonistes benzimidazoliques du récepteur h-3 |
| WO2007088462A1 (fr) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Antagonistes du récepteur du h-3 à base de spirochromane |
| WO2007088450A2 (fr) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Chromane antagoniste du récepteur h-3 |
| WO2007099423A1 (fr) | 2006-03-02 | 2007-09-07 | Pfizer Products Inc. | Dérivés de 1-pyrrolidine indane en tant qu'antagonistes du récepteur d'histamine 3 |
| US20090163482A1 (en) | 2006-03-13 | 2009-06-25 | Mchardy Stanton Furst | Tetralines antagonists of the h-3 receptor |
| GB0605462D0 (en) | 2006-03-17 | 2006-04-26 | Glaxo Group Ltd | Novel compounds |
| NZ571540A (en) | 2006-04-21 | 2010-10-29 | Pfizer Prod Inc | Pyridine[3,4-b]pyrazinones for inhibiting PDE-5 |
| WO2007138431A2 (fr) | 2006-05-30 | 2007-12-06 | Pfizer Products Inc. | Antagonistes de l'éther histamine-3 azabicyclique |
| US20080090834A1 (en) | 2006-07-06 | 2008-04-17 | Pfizer Inc | Selective azole pde10a inhibitor compounds |
| WO2008006050A2 (fr) | 2006-07-07 | 2008-01-10 | Govek Steven P | Inhibiteurs de pde4 à base de composés d'hétéroaryle bicyclique |
| US8138205B2 (en) | 2006-07-07 | 2012-03-20 | Kalypsys, Inc. | Heteroarylalkoxy-substituted quinolone inhibitors of PDE4 |
| US7985753B2 (en) | 2006-08-04 | 2011-07-26 | Merz Pharma Gmbh & Co. Kgaa | Substituted pyrazolo[1,5-A]pyrimidines as metabotropic glutamate receptor modulators |
| EP1900739A1 (fr) | 2006-08-30 | 2008-03-19 | Cellzome Ag | Dérivés de diazolodiazine comme inhibiteurs de kinases |
| WO2008033739A2 (fr) * | 2006-09-12 | 2008-03-20 | Neurogen Corporation | Dérivés de benzimidazolecarboxamide |
| US20100105729A1 (en) | 2006-10-06 | 2010-04-29 | Kalypsys, Inc. | Aryl-substituted heterocyclic pde4 inhibitors as anti-inflammatory agents |
| WO2008045664A2 (fr) | 2006-10-06 | 2008-04-17 | Kalypsys, Inc. | Inhibiteurs hétérocycliques de pde4 |
| US20080102475A1 (en) | 2006-10-13 | 2008-05-01 | Zhengyan Kan | Alternatively spliced isoform of phosphodiesterase 4B (PDE4B) |
| CL2007002994A1 (es) | 2006-10-19 | 2008-02-08 | Wyeth Corp | Compuestos derivados heterociclicos que contienen sulfamoilo, inhibidores de hsp90; composicion farmaceutica; y uso para el tratamiento del cancer, tal como cancer de mama, de colon y prostata, entre otros. |
| WO2008056176A1 (fr) | 2006-11-10 | 2008-05-15 | Scottish Biomedical Limited | Pyrazolopyrimidines utiles comme inhibiteurs de la phosphodiestérase |
| AU2008208653B2 (en) | 2007-01-22 | 2012-11-22 | Pfizer Products Inc. | Tosylate salt of a therapeutic compound and pharmaceutical compositions thereof |
| US20120121540A1 (en) | 2007-08-10 | 2012-05-17 | Franz Ulrich Schmitz | Certain Nitrogen Containing Bicyclic Chemical Entities For Treating Viral Infections |
| SG183699A1 (en) | 2007-08-10 | 2012-09-27 | Lundbeck & Co As H | Heteroaryl amide analogues |
| EP2085398A1 (fr) | 2008-02-01 | 2009-08-05 | Merz Pharma GmbH & Co. KGaA | Pyrazolopyrimidines, leur procédé de préparation et leur utilisation en tant que médicament |
| WO2009108551A2 (fr) | 2008-02-25 | 2009-09-03 | H. Lundbeck A/S | Analogues d’hétéroarylamide |
| GB2461702A (en) | 2008-07-08 | 2010-01-13 | Dyson Technology Ltd | Hand drying apparatus |
| US9643922B2 (en) | 2008-08-18 | 2017-05-09 | Yale University | MIF modulators |
| WO2010034738A2 (fr) | 2008-09-24 | 2010-04-01 | Basf Se | Composés pyrazoliques utilisables dans la lutte contre les invertébrés nuisibles |
| WO2010059836A1 (fr) | 2008-11-20 | 2010-05-27 | Decode Genetics Ehf | Composés bicycliques substitués à pont aza pour maladie cardiovasculaire et du système nerveux central |
| US20100204265A1 (en) | 2009-02-09 | 2010-08-12 | Genelabs Technologies, Inc. | Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections |
| WO2010106494A1 (fr) | 2009-03-20 | 2010-09-23 | H.L. Hall & Sons Limited | Utilisation de compositions pharmaceutiques contenant du mésembrénone |
| CA2778949C (fr) | 2009-10-30 | 2018-02-27 | Janssen Pharmaceutica Nv | Derives d'imidazo[1,2-b]pyridazine et leur utilisation comme inhibiteurs de pde10 |
| AU2010323209A1 (en) | 2009-11-25 | 2012-06-14 | Merz Pharma Gmbh & Co. Kgaa | Crystalline forms of substituted pyrazolopyrimidines |
| AR079451A1 (es) | 2009-12-18 | 2012-01-25 | Nycomed Gmbh | Compuestos 3,4,4a,10b-tetrahidro-1h-tiopirano[4,3-c]isoquinolina |
| EP2549874A4 (fr) | 2010-03-23 | 2013-10-02 | High Point Pharmaceuticals Llc | Dérivés d'imidazole[1,2-b]pyridazine substitués, compositions pharmaceutiques et procédés d'utilisation en tant qu'inhibiteurs de bêta-sécrétase |
| WO2011143106A1 (fr) | 2010-05-10 | 2011-11-17 | Gilead Sciences, Inc. | Composés pyrazolopyridiniques bifonctionnels |
| NZ603136A (en) | 2010-05-10 | 2014-11-28 | Gilead Sciences Inc | Bifunctional quinoline derivatives |
| WO2012067822A1 (fr) | 2010-11-16 | 2012-05-24 | Abbott Laboratories | Modulateurs des canaux potassiques à base de pyrazolo[1,5-a]pyrimidine |
| US9096605B2 (en) | 2011-08-24 | 2015-08-04 | Glaxosmithkline Llc | Pyrazolopyrimidine derivatives as PI3 kinase inhibitors |
| AP2015008663A0 (en) * | 2013-02-19 | 2015-08-31 | Pfizer | Azabenzimidazole compounds as inhibitors of PDE4 isozymes for the treatment of cns and other disorders |
| WO2014200882A1 (fr) | 2013-06-11 | 2014-12-18 | Janssen Pharmaceutica Nv | Inhibiteurs de pde10a pour le traitement du diabète de type ii |
| GB201321734D0 (en) | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic Agents |
| WO2015140614A1 (fr) | 2014-03-21 | 2015-09-24 | Align Technology, Inc. | Appareil orthodontique segmenté doté d'élastiques |
| EP3172210B1 (fr) | 2014-07-24 | 2020-01-15 | Pfizer Inc | Composés de pyrazolopyrimidine |
| SG11201700243YA (en) | 2014-08-06 | 2017-02-27 | Pfizer | Imidazopyridazine compounds |
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