TN2009000138A1 - Biaryl-ether-urees - Google Patents
Biaryl-ether-ureesInfo
- Publication number
- TN2009000138A1 TN2009000138A1 TNP2009000138A TN2009000138A TN2009000138A1 TN 2009000138 A1 TN2009000138 A1 TN 2009000138A1 TN P2009000138 A TNP2009000138 A TN P2009000138A TN 2009000138 A TN2009000138 A TN 2009000138A TN 2009000138 A1 TN2009000138 A1 TN 2009000138A1
- Authority
- TN
- Tunisia
- Prior art keywords
- compounds
- biaryl
- urea
- ether
- preparation
- Prior art date
Links
- 239000004202 carbamide Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- 102100029111 Fatty-acid amide hydrolase 1 Human genes 0.000 abstract 2
- 108010046094 fatty-acid amide hydrolase Proteins 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture 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
- 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
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- 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
- A61P17/06—Antipsoriatics
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- 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
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- 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
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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
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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
- A61P25/04—Centrally acting analgesics, e.g. opioids
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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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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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
- A61P25/20—Hypnotics; Sedatives
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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
- A61P27/06—Antiglaucoma agents or miotics
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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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
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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
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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
- A61P9/12—Antihypertensives
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- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
-
- 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
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Psychiatry (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Otolaryngology (AREA)
- Anesthesiology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La présente invention concerne les composés de formule (I) ou un de leurs sels pharmaceutiquement acceptables, des procédés pour la préparation des composés, les intermédiaires utilisés dans la préparation des composés ; des compositions contenant les composés et des utilisations des composés dans le traitement de maladies ou d'affections associées à une activité d' hydrolase d'amide d'acide gras (FAAH).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82996606P | 2006-10-18 | 2006-10-18 | |
| US96521007P | 2007-08-17 | 2007-08-17 | |
| PCT/IB2007/003202 WO2008047229A2 (fr) | 2006-10-18 | 2007-10-05 | Composés d'urée de bisaryle éther |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2009000138A1 true TN2009000138A1 (fr) | 2010-10-18 |
Family
ID=39314409
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2009000138A TN2009000138A1 (fr) | 2006-10-18 | 2009-04-14 | Biaryl-ether-urees |
Country Status (38)
| Country | Link |
|---|---|
| US (1) | US8044052B2 (fr) |
| EP (1) | EP2076508B1 (fr) |
| JP (1) | JP4434313B2 (fr) |
| KR (1) | KR101181194B1 (fr) |
| CN (1) | CN101595102B (fr) |
| AP (1) | AP2780A (fr) |
| AR (1) | AR063331A1 (fr) |
| AT (1) | ATE493984T1 (fr) |
| AU (1) | AU2007311591B2 (fr) |
| BR (1) | BRPI0717596B8 (fr) |
| CA (1) | CA2663984C (fr) |
| CL (1) | CL2007003000A1 (fr) |
| CR (2) | CR10701A (fr) |
| CY (1) | CY1111170T1 (fr) |
| DE (1) | DE602007011793D1 (fr) |
| DK (1) | DK2076508T3 (fr) |
| EA (1) | EA015488B1 (fr) |
| ES (1) | ES2357340T3 (fr) |
| GE (1) | GEP20125425B (fr) |
| HN (1) | HN2007000407A (fr) |
| HR (1) | HRP20110158T1 (fr) |
| IL (1) | IL197664A (fr) |
| MA (1) | MA30801B1 (fr) |
| ME (1) | ME01308B (fr) |
| MX (1) | MX2009004233A (fr) |
| MY (1) | MY145460A (fr) |
| NO (1) | NO342266B1 (fr) |
| NZ (1) | NZ575624A (fr) |
| PE (1) | PE20081265A1 (fr) |
| PL (1) | PL2076508T3 (fr) |
| PT (1) | PT2076508E (fr) |
| RS (2) | RS20090154A (fr) |
| SI (1) | SI2076508T1 (fr) |
| TN (1) | TN2009000138A1 (fr) |
| TW (1) | TWI404715B (fr) |
| UY (1) | UY30649A1 (fr) |
| WO (1) | WO2008047229A2 (fr) |
| ZA (1) | ZA200902548B (fr) |
Families Citing this family (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UY29321A1 (es) | 2004-12-30 | 2006-03-31 | Janssen Pharmaceutica Nv | Piperazinilureas y piperidinilureas como moduladores de hidrolasa de amida de ácidos grasos |
| JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| SI2076508T1 (sl) | 2006-10-18 | 2011-04-29 | Pfizer Prod Inc | Spojine biaril eter sečnine |
| CN102046179B (zh) | 2008-04-09 | 2015-01-14 | 英菲尼提制药公司 | 脂肪酸酰胺水解酶抑制剂 |
| JP2011518143A (ja) * | 2008-04-17 | 2011-06-23 | ファイザー・インク | Faah阻害剤として有用なエーテルベンジリデンピペリジンアリールカルボキサミド化合物 |
| CA2717087A1 (fr) * | 2008-04-17 | 2009-10-22 | Pfizer Inc. | Carboxamides d'aryle a 5 atomes de type 4-[3-(aryloxy)benzylidene]-3-methylpiperidine |
| WO2009127946A1 (fr) * | 2008-04-17 | 2009-10-22 | Pfizer Inc. | Composés de 4-benzylidène-3-méthylpipéridine-aryl-carboxamide utiles comme inhibiteurs de faah |
| JP2011518142A (ja) * | 2008-04-17 | 2011-06-23 | ファイザー・インク | Faah阻害剤として有用なエーテルベンジリデンピペリジン5員アリールカルボキサミド化合物 |
| EP2276737A1 (fr) * | 2008-04-17 | 2011-01-26 | Pfizer Inc. | Composés aryl carboxamides de 4-[3-(aryloxy)benzylidène]-3-méthyl pipéridine utiles comme inhibiteurs de la faah |
| WO2010068453A1 (fr) | 2008-11-25 | 2010-06-17 | Janssen Pharmaceutica Nv | Modulateurs d'urée substitués par hétéroaryle d'amide d'acide gras hydrolase |
| US8598356B2 (en) | 2008-11-25 | 2013-12-03 | Janssen Pharmaceutica Nv | Heteroaryl-substituted urea modulators of fatty acid amide hydrolase |
| WO2010064597A1 (fr) * | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | Dérivé de pipéridine |
| CA2747419C (fr) | 2009-01-12 | 2014-07-08 | Icagen, Inc. | Derives sulfonamides |
| US8546564B2 (en) | 2009-04-07 | 2013-10-01 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| US8541581B2 (en) | 2009-04-07 | 2013-09-24 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| US9062116B2 (en) | 2009-04-23 | 2015-06-23 | Infinity Pharmaceuticals, Inc. | Anti-fatty acid amide hydrolase-2 antibodies and uses thereof |
| US9149465B2 (en) | 2009-05-18 | 2015-10-06 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
| US8765735B2 (en) | 2009-05-18 | 2014-07-01 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
| US8927551B2 (en) | 2009-05-18 | 2015-01-06 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
| WO2010141809A1 (fr) | 2009-06-05 | 2010-12-09 | Janssen Pharmaceutica Nv | Modulateurs heterocycliques a base d'uree a substitution aryle de l'hydrolase des amides d'acides gras (faah) |
| WO2010141817A1 (fr) | 2009-06-05 | 2010-12-09 | Janssen Pharmaceutica Nv | Modulateurs d'amide d'acide gras hydrolase de type diamine urée spirocyclique substituée par un groupe hétéroaryle |
| JP5738766B2 (ja) | 2009-09-09 | 2015-06-24 | 大日本住友製薬株式会社 | 8−オキソジヒドロプリン誘導体 |
| WO2011077313A1 (fr) | 2009-12-22 | 2011-06-30 | Pfizer Inc. | Pipéridinecarboxamides en tant qu'inhibiteurs de mpges - 1 |
| WO2011085216A2 (fr) | 2010-01-08 | 2011-07-14 | Ironwood Pharmaceuticals, Inc. | Utilisation d'inhibiteurs de faah pour traiter la maladie de parkinson et le syndrome des jambes sans repos |
| EP2531511A1 (fr) | 2010-02-03 | 2012-12-12 | Infinity Pharmaceuticals, Inc. | Inhibiteurs de l'hydrolase d'amides d'acides gras |
| CA2789606A1 (fr) | 2010-02-25 | 2011-09-01 | Pfizer Limited | Analogues peptidiques en tant qu'agonistes des recepteurs opioides |
| WO2011123719A2 (fr) | 2010-03-31 | 2011-10-06 | Ironwood Pharmaceuticals, Inc. | Utilisation d'inhibiteurs de faah pour le traitement des douleurs abdominales, viscérales et pelviennes |
| UA108233C2 (uk) | 2010-05-03 | 2015-04-10 | Модулятори активності гідролази амідів жирних кислот | |
| ES2526675T3 (es) | 2010-07-09 | 2015-01-14 | Pfizer Limited | N-sulfonilbenzamidas como inhibidores de los canales de sodio dependientes de voltaje |
| WO2012004743A1 (fr) | 2010-07-09 | 2012-01-12 | Pfizer Limited | Benzènesulfonamides utiles en tant qu'inhibiteurs des canaux sodiques |
| WO2012007883A1 (fr) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Composés chimiques |
| WO2012007869A2 (fr) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Composés chimiques |
| WO2012007861A1 (fr) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Dérivés de n-sulfonylbenzamide utiles comme inhibiteurs du canal sodique voltage-dépendant |
| US9096500B2 (en) | 2010-07-12 | 2015-08-04 | Pfizer Limited | Acyl sulfonamide compounds |
| JP2013532186A (ja) | 2010-07-12 | 2013-08-15 | ファイザー・リミテッド | 化合物 |
| WO2012095781A1 (fr) | 2011-01-13 | 2012-07-19 | Pfizer Limited | Dérivés d'indazole comme inhibiteurs des canaux sodiques |
| PE20141050A1 (es) | 2011-04-05 | 2014-08-30 | Pfizer Ltd | Inhibidores de quinasa relacionados con pirrolo (2,3-d) pirimidina tropomiosina |
| US8957025B2 (en) | 2011-07-13 | 2015-02-17 | Pfizer Inc. | Enkephalin analogues |
| EP2758375A1 (fr) * | 2011-09-23 | 2014-07-30 | Advinus Therapeutics Limited | Composés amides, compositions et applications de ceux-ci |
| WO2013054185A1 (fr) | 2011-10-13 | 2013-04-18 | Pfizer, Inc. | Dérivés de pyrimidine et de pyridine utiles en thérapie |
| JP5946538B2 (ja) | 2011-10-26 | 2016-07-06 | ファイザー・リミテッドPfizer Limited | ナトリウムチャネルモジュレーターとして有用な(4−フェニルイミダゾール−2−イル)エチルアミン誘導体 |
| US9273011B2 (en) | 2011-10-28 | 2016-03-01 | Inhibitaxin Limited | Substituted pyridazines for the treatment of pain |
| ES2593533T3 (es) | 2011-12-15 | 2016-12-09 | Pfizer Limited | Derivados de sulfonamida |
| WO2013093688A1 (fr) | 2011-12-19 | 2013-06-27 | Pfizer Limited | Dérivés sulfonamides et leur utilisation en tant qu'inhibiteurs de vgsc |
| EP2800740A1 (fr) | 2012-01-04 | 2014-11-12 | Pfizer Limited | N-aminosulfonylbenzamides |
| ES2548228T3 (es) | 2012-02-03 | 2015-10-15 | Pfizer Inc | Derivados de bencimidazol e imidazopiridina como moduladores de canal de sodio |
| US9163021B2 (en) | 2012-10-04 | 2015-10-20 | Pfizer Limited | Pyrrolo[3,2-c]pyridine tropomyosin-related kinase inhibitors |
| CA2885247A1 (fr) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Inhibiteurs de kinases apparentes a la tropomyosine |
| CA2885253A1 (fr) | 2012-10-04 | 2014-04-10 | Pfizer Limited | Inhibiteurs de kinase associee a la tropomyosine pyrrolo[2,3-d]pyrimidine |
| US9630896B2 (en) | 2013-11-22 | 2017-04-25 | Tansna Therapeutics, Inc. | 2,5-dialkyl-4-H/halo/ether-phenol compounds |
| US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
| PL3319959T3 (pl) | 2015-07-06 | 2022-02-14 | Alkermes, Inc. | Hetero-haloinhibitory deacetylazy histonowej |
| EP3566055B1 (fr) | 2017-01-06 | 2025-03-12 | Janssen Pharmaceutica NV | Inhibiteurs de la scd pour le traitement de troubles neurologiques |
| CA3049443A1 (fr) | 2017-01-11 | 2018-07-19 | Rodin Therapeutics, Inc. | Inhibiteurs bicycliques d'histone desacetylase |
| LT3645518T (lt) * | 2017-06-30 | 2021-10-11 | Amgen Inc. | Omekamitivo mekarbilo sintezė |
| AU2018313094A1 (en) | 2017-08-07 | 2020-02-20 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
| EA039850B1 (ru) * | 2018-04-30 | 2022-03-21 | Эмджен Инк. | Синтез омекамтива мекарбила |
| CN110437205B (zh) * | 2018-08-24 | 2022-07-08 | 广东东阳光药业有限公司 | 吡啶烯基哌啶衍生物及其用途 |
| EA202192047A1 (ru) * | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
| EP4380571A1 (fr) * | 2021-08-04 | 2024-06-12 | Jazz Pharmaceuticals Ireland Ltd. | Méthode de traitement d'un trouble de stress post-traumatique |
| WO2024167423A1 (fr) | 2023-02-07 | 2024-08-15 | Captor Therapeutics S.A. | Composés de dégradation de gspt1 |
| US12410137B2 (en) | 2023-07-17 | 2025-09-09 | Apogee Pharmaceuticals, Inc. | Fatty acid amide hydrolase modulators, compositions comprising the same and uses thereof |
Family Cites Families (100)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB138405A (en) | 1919-01-16 | 1920-02-12 | Thomas Thompson | Improvements in or relating to suction or delivery valves for pumps |
| GB1138405A (en) | 1966-12-28 | 1969-01-01 | Ici Ltd | Morpholine derivatives |
| US3576810A (en) * | 1968-06-20 | 1971-04-27 | Robins Co Inc A H | 1-substituted-3-(-4)-aroylpiperidines |
| GB1260886A (en) | 1969-06-20 | 1972-01-19 | Ici Ltd | Process for aryloxymethylmorpholine derivatives |
| BE759013R (fr) | 1969-11-17 | 1971-05-17 | Ici Ltd | Derives de la |
| BE758766A (fr) | 1969-11-17 | 1971-05-10 | Ici Ltd | Nouveaux derives de la morpholine et de la |
| US4116665A (en) * | 1976-04-02 | 1978-09-26 | Eli Lilly And Company | Method of regulating the growth of aquatic weeds with pyridine derivatives |
| IL56369A (en) | 1978-01-20 | 1984-05-31 | Erba Farmitalia | Alpha-phenoxybenzyl propanolamine derivatives,their preparation and pharmaceutical compositions comprising them |
| GB8424979D0 (en) * | 1984-10-03 | 1984-11-07 | Wyeth John & Brother Ltd | Benzenesulphonamide derivatives |
| GB2167407B (en) | 1984-11-22 | 1988-05-11 | Erba Farmitalia | Enantiomers of phenoxy derivatives of benzyl morpholine and salts thereof |
| KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
| US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
| ATE140223T1 (de) | 1991-12-18 | 1996-07-15 | Schering Corp | Imidolylalkyl-derivate substituiert mit einem stickstoffenthaltende-6 gliedrigen ring |
| DE4326344A1 (de) | 1993-08-05 | 1995-02-09 | Thomae Gmbh Dr K | Carbonamide, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| AU7823894A (en) | 1993-08-27 | 1995-03-21 | Vrije Universiteit | New imidazole derivatives having agonistic or antagonistic activity on the histamine h3 receptor |
| EP0749425A1 (fr) | 1995-01-11 | 1996-12-27 | Samjin Pharm. Co., Ltd. | Nouveaux derives piperazines, leurs procedes de preparation, et compositions les contenant |
| US6271015B1 (en) * | 1995-06-12 | 2001-08-07 | The Scripps Research Institute | Fatty-acid amide hydrolase |
| GB9526560D0 (en) | 1995-12-27 | 1996-02-28 | Bayer Ag | Use of 2-Amino-Heterocycles |
| FR2744449B1 (fr) | 1996-02-02 | 1998-04-24 | Pf Medicament | Nouvelles piperazines aromatiques derivees de cycloazanes substitues, ainsi que leur procede de preparation, les compositions pharmaceutiques et leur utilisation comme medicaments |
| GB9711643D0 (en) | 1997-06-05 | 1997-07-30 | Janssen Pharmaceutica Nv | Glass thermoplastic systems |
| US6207665B1 (en) | 1997-06-12 | 2001-03-27 | Schering Aktiengesellschaft | Piperazine derivatives and their use as anti-inflammatory agents |
| US6184242B1 (en) * | 1997-09-04 | 2001-02-06 | Syntex Usa (Llc) | 2-(substituted-phenyl)amino-imidazoline derivatives |
| CZ298747B6 (cs) | 1998-04-01 | 2008-01-16 | Janssen Pharmaceutica N. V. | Derivát pyridinu, způsob jeho výroby a použití a farmaceutická kompozice s jeho obsahem |
| HUP0202144A3 (en) | 1998-12-29 | 2003-10-28 | Pharmacia And Upjohn Co Kalama | Method for the preparation of aryl ethers and their intermediates and the novel intermediates |
| PE20001566A1 (es) | 1999-03-26 | 2001-02-05 | Ucb Sa | Piperazinas 1,4-sustituidas, piperidinas 1,4-sustituidas y 4-alquilidenilpiperidinas 1-sustituidas |
| EP1169024B1 (fr) | 1999-03-31 | 2005-12-21 | Janssen Pharmaceutica N.V. | Amidon pregelatinise dans une formulation a liberation regulee |
| US6632815B2 (en) * | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| CA2386517A1 (fr) | 1999-10-07 | 2001-04-12 | Takeda Chemical Industries, Ltd. | Derives d'amines |
| US6476041B1 (en) | 1999-10-29 | 2002-11-05 | Merck & Co., Inc. | 1,4 substituted piperidinyl NMDA/NR2B antagonists |
| YU54402A (sh) | 2000-01-18 | 2005-11-28 | Pfizer Products Inc. | Antagonisti faktora otpuštanja kortikotropina |
| HRP20020737A2 (en) | 2000-02-11 | 2005-10-31 | Vertex Pharmaceuticals Incorporated | Piperazine and piperidine derivatives for treatment or prevention of nruronal damage |
| GB0004297D0 (en) * | 2000-02-23 | 2000-04-12 | Ucb Sa | 2-oxo-1 pyrrolidine derivatives process for preparing them and their uses |
| AU2001241676A1 (en) | 2000-03-03 | 2001-09-17 | Ortho-Mcneil Pharmaceutical, Inc. | 3-(diarylmethylene)-8-azabicyclo(3.2.1)octane derivatives |
| JP2001303987A (ja) * | 2000-04-21 | 2001-10-31 | Toyota Motor Corp | 筒内噴射式内燃機関のスロットル制御装置 |
| WO2001095856A2 (fr) | 2000-06-15 | 2001-12-20 | Chaconne Nsi Co., Ltd. | Derive d'uree en tant qu'agent anticancereux et son procede de preparation |
| US20020183316A1 (en) | 2000-10-27 | 2002-12-05 | Kevin Pan | Amidoalkyl-piperidine and amidoalkyl-piperazine derivatives useful for the treatment of nervous system disorders |
| AU2002243920A1 (en) | 2001-02-08 | 2002-08-19 | Nps Pharmaceuticals, Inc. | Methods and compounds for treating neurologic or neuropsychiatric disorders and identifying compounds to treat the same |
| US20040204477A1 (en) * | 2001-07-09 | 2004-10-14 | Juergen Moll | Interaction inhibitors of tcf-4 with beta-catenin |
| AU2002363236A1 (en) | 2001-10-30 | 2003-05-12 | Millennium Pharmaceuticals, Inc. | Compounds, pharmaceutical compositions and methods of use therefor |
| US20040034101A1 (en) * | 2001-11-05 | 2004-02-19 | Cypress Bioscience, Inc. | Treatment and prevention of depression secondary to pain (DSP) |
| JP3865626B2 (ja) * | 2001-11-08 | 2007-01-10 | 株式会社ベステックスキョーエイ | パイプ部材 |
| FR2833261B1 (fr) * | 2001-12-06 | 2004-07-02 | Yang Ji Chemical Company Ltd | Nouveaux composes inhibiteurs specifiques de la phospholipase a2 secretee non pancreatique humaine du groupe ii |
| US20040063726A1 (en) * | 2002-02-08 | 2004-04-01 | Artman Linda D | Methods and compounds for treating neurologic or neuropsychiatric disorders and identifying compounds to treat the same |
| CA2475764C (fr) | 2002-03-13 | 2011-05-31 | Janssen Pharmaceutica N.V. | Nouveaux inhibiteurs de l'histone deacetylase |
| US6995144B2 (en) | 2002-03-14 | 2006-02-07 | Eisai Co., Ltd. | Nitrogen containing heterocyclic compounds and medicines containing the same |
| WO2003080060A1 (fr) | 2002-03-20 | 2003-10-02 | Schering Aktiengesellschaft | Inhibiteurs antithrombotiques de pai-1, a base de piperazine substituee |
| TWI283241B (en) | 2002-05-29 | 2007-07-01 | Tanabe Seiyaku Co | Novel piperidine compound |
| CA2503078A1 (fr) | 2002-10-21 | 2004-05-06 | Janssen Pharmaceutica N.V. | Analyse destinee a determiner l'activite de l'hydrolase des amides d'acides gras |
| AR043633A1 (es) * | 2003-03-20 | 2005-08-03 | Schering Corp | Ligandos de receptores de canabinoides |
| NZ543366A (en) | 2003-04-03 | 2008-11-28 | Merck Patent Gmbh | Carbonyl compounds |
| SE0301442D0 (sv) | 2003-05-16 | 2003-05-16 | Astrazeneca Ab | Diarylmethylidene piperidine derivatives, preparations therof and uses thereof |
| SE0301443D0 (sv) | 2003-05-16 | 2003-05-16 | Astrazeneca Ab | Diarylmethylidene piperidine derivatives, preparations thereof and uses thereof |
| AR045047A1 (es) | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
| GB0325287D0 (en) | 2003-10-29 | 2003-12-03 | Merck Sharp & Dohme | Therapeutic agents |
| GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
| NZ545694A (en) * | 2003-12-03 | 2010-04-30 | Ym Bioscience Australia Pty Lt | Azole-based kinase inhibitors |
| WO2005075472A1 (fr) * | 2004-02-03 | 2005-08-18 | Janssen Pharmaceutica, N.V. | Derives de 3-(diheteroarylnethylene)-8-azabicyclo[3.2.1]octane et de 3-(aryl)(heteroaryl)methylene)-8-azabicyclo[3.2.1]octane |
| CN1942470A (zh) * | 2004-04-09 | 2007-04-04 | 默克公司 | Akt活性抑制剂 |
| EP1742626A2 (fr) | 2004-04-23 | 2007-01-17 | The Regents of The University of California | Composes et procedes de traitement de la douleur non inflammatoire au moyen d'agonistes de pparalpha |
| SE0401343D0 (sv) | 2004-05-25 | 2004-05-25 | Astrazeneca Ab | Therapeutic compounds: Pyridine N oxide as scaffold |
| ATE415397T1 (de) | 2004-06-04 | 2008-12-15 | Arena Pharm Inc | Substituierte aryl- und heteroarylderivate als modulatoren des stoffwechsels und für die prophylaxe und behandlung von damit in zusammenhang stehenden erkrankungen |
| DE102004039789A1 (de) | 2004-08-16 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP1814551A2 (fr) | 2004-09-20 | 2007-08-08 | Xenon Pharmaceuticals Inc. | Derives de pyridazine destines a l'inhibition du desaturase-coa-stearoyl de l'humain |
| DE102004045796A1 (de) | 2004-09-22 | 2006-03-23 | Merck Patent Gmbh | Arzneimittel enthaltend Carbonylverbindungen sowie deren Verwendung |
| EP1797040A1 (fr) | 2004-09-29 | 2007-06-20 | Ranbaxy Laboratories Limited | Antagonistes de recepteurs muscariniques |
| US7491720B2 (en) * | 2004-10-29 | 2009-02-17 | Banyu Pharmaceutical Co., Ltd. | Aminopyridine derivatives having Aurora A selective inhibitory action |
| EP1657241A1 (fr) | 2004-11-03 | 2006-05-17 | Schering Aktiengesellschaft | Nouveaux urées d' anthranylamide pyridine ayant une activité inhibitrice de kinase du récepteur de VEGF |
| EP1655297A1 (fr) | 2004-11-03 | 2006-05-10 | Schering Aktiengesellschaft | Pyridineurées de nicotinamide commes inhibiteurs du recepteur kinase du facteur de croissance endothéliale vasculaire (VEGF) |
| TW200633990A (en) | 2004-11-18 | 2006-10-01 | Takeda Pharmaceuticals Co | Amide compound |
| US20060167044A1 (en) * | 2004-12-20 | 2006-07-27 | Arnaiz Damian O | Piperidine derivatives and their use as anti-inflammatory agents |
| CA2589748C (fr) | 2004-12-24 | 2013-08-13 | Astrazeneca Ab | Composes heterocycliques en tant qu'antagonistes de ccr2b |
| EP1838311A1 (fr) | 2004-12-24 | 2007-10-03 | Prosidion Limited | Agonistes du récepteur couplé aux protéines g (gpr116) et leur emploi dans le traitement de l'obésité et du diabète |
| UY29321A1 (es) * | 2004-12-30 | 2006-03-31 | Janssen Pharmaceutica Nv | Piperazinilureas y piperidinilureas como moduladores de hidrolasa de amida de ácidos grasos |
| JP2008529519A (ja) | 2005-02-10 | 2008-08-07 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | 脂肪酸アミドヒドロラーゼ分析 |
| JP2008530171A (ja) * | 2005-02-16 | 2008-08-07 | ノイロサーチ アクティーゼルスカブ | 新規なジアザ二環系アリール誘導体及びそれらの医療上の使用 |
| TW200640864A (en) | 2005-02-17 | 2006-12-01 | Astellas Pharma Inc | Pyridyl non-aromatic nitrogenated heterocyclic-1-carboxylate ester derivative |
| US20090082435A1 (en) | 2005-04-28 | 2009-03-26 | The Regents Of The University Of California | Methods, Compositions, And Compounds For Modulation Of Monoacylglycerol Lipase, Pain, And Stress-Related Disorders |
| GB0510139D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B1 |
| WO2006129842A1 (fr) | 2005-06-01 | 2006-12-07 | Banyu Pharmaceutical Co., Ltd. | Nouveau derive aminopyridine ayant une activite d’inhibition selective de l’aurora-a |
| JPWO2006137465A1 (ja) | 2005-06-24 | 2009-01-22 | 塩野義製薬株式会社 | 含窒素複素環誘導体 |
| US20100063081A1 (en) | 2005-06-30 | 2010-03-11 | Stuart Edward Bradly | CPCR Agonists |
| PE20070099A1 (es) | 2005-06-30 | 2007-02-06 | Janssen Pharmaceutica Nv | N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso |
| CN101296914B (zh) | 2005-08-26 | 2012-07-18 | 盐野义制药株式会社 | 具有ppar激动活性的衍生物 |
| US7131609B1 (en) | 2005-08-31 | 2006-11-07 | Kimberly-Clark Worldwide, Inc. | Dispenser for sheet material |
| CA2635232A1 (fr) | 2005-12-29 | 2007-07-12 | N.V. Organon | Inhibiteurs de l'amide hydrolase d'acides gras |
| US20070155707A1 (en) | 2005-12-29 | 2007-07-05 | Kadmus Pharmaceuticals, Inc. | Ionizable inhibitors of fatty acid amide hydrolase |
| US20070259879A1 (en) | 2006-03-06 | 2007-11-08 | Trimeris, Inc. | Piperazine and piperidine biaryl derivatives |
| TW200811157A (en) * | 2006-05-05 | 2008-03-01 | Astrazeneca Ab | mGluR5 modulators I |
| US20080076924A1 (en) | 2006-06-30 | 2008-03-27 | Patrick Betschmann | Piperazines as P2X7 antagonists |
| EP2054055A2 (fr) | 2006-08-18 | 2009-05-06 | N.V. Organon | Inhibiteur de faah et agent analgésique, anti-inflammatoire ou anti-pyrétique combinés |
| WO2008024139A2 (fr) | 2006-08-18 | 2008-02-28 | N.V. Organon | Inhibiteurs d'hydrolase des amides d'acides gras |
| US7888394B2 (en) | 2006-08-21 | 2011-02-15 | N.V. Organon | Synthesis, polymorphs, and pharmaceutical formulation of FAAH inhibitors |
| JPWO2008023720A1 (ja) | 2006-08-23 | 2010-01-14 | アステラス製薬株式会社 | ウレア化合物又はその塩 |
| WO2008030752A2 (fr) | 2006-09-07 | 2008-03-13 | N.V. Organon | Procédés de détermination des doses efficaces des inhibiteurs de l'amide d'acide gras-hydrolase in vivo |
| US20090099240A1 (en) | 2006-10-02 | 2009-04-16 | N.V. Organon | Methods for treating energy metabolism disorders by inhibiting fatty acid amide hydrolase activity |
| JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| SI2076508T1 (sl) | 2006-10-18 | 2011-04-29 | Pfizer Prod Inc | Spojine biaril eter sečnine |
| CA2674359A1 (fr) | 2006-11-20 | 2008-05-29 | N.V. Organon | Inhibiteurs stabilises metaboliquement d'hydrolase d'amides d'acide gras |
| NZ552238A (en) | 2006-12-20 | 2009-07-31 | Seperex Nutritionals Ltd | An extract |
| MX2009012765A (es) | 2007-05-25 | 2009-12-16 | Janssen Pharmaceutica Nv | Moduladores de urea con heteroarilo sustituido de acido graso amida hidrolasa. |
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| MA32009B1 (fr) | Nouveaux derives de pyrazolo [3,4-d]pyrimidine en tant qu'agents anticancereux | |
| TNSN04156A1 (fr) | Pyridinones substituees servant de modulateurs de la map-kinase p38 | |
| TNSN08270A1 (fr) | Dérivés pyrimidiques destinés à traiter une croissance cellulaire anormale | |
| TNSN99031A1 (fr) | Composes heterocycliques nouveaux inhibiteurs de romatases, procede pour leur preparation et compositions pharmaceutiques les contenant | |
| MA33178B1 (fr) | Pipéridines substituées comme antagonistes de ccr3 | |
| TNSN05073A1 (fr) | Quinazolinones spirocondensees nouvelles et leur utilisation comme inhibiteurs de phosphodiesterase | |
| MA31919B1 (fr) | Composés inhibiteurs de la dipeptidyl peptidase-iv, leurs procédés de préparation, et compositions pharmaceutiques contenant ces composés comme agent actif | |
| MA30313B1 (fr) | Amines secondaires en tant qu'inhibiteurs de la renine | |
| MA29411B1 (fr) | 1h-quinazoline -2,4-diones et leur utilisation en tant que ligands du recepteur ampa |