MA35271B1 - Antagonistes de trpm8 et leur utilisation dans des traitements - Google Patents
Antagonistes de trpm8 et leur utilisation dans des traitementsInfo
- Publication number
- MA35271B1 MA35271B1 MA36692A MA36692A MA35271B1 MA 35271 B1 MA35271 B1 MA 35271B1 MA 36692 A MA36692 A MA 36692A MA 36692 A MA36692 A MA 36692A MA 35271 B1 MA35271 B1 MA 35271B1
- Authority
- MA
- Morocco
- Prior art keywords
- disorders
- trpm8
- compounds
- antagonists
- treatments
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title abstract 2
- 238000011282 treatment Methods 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 5
- 208000035475 disorder Diseases 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 208000019695 Migraine disease Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- 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
- A61P1/10—Laxatives
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P17/04—Antipruritics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- C07D401/14—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
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Otolaryngology (AREA)
- Communicable Diseases (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
Abstract
L'invention concerne des composés de formule (i) servant comme antagonistes de trpm8. De tels composés servent à traiter une pluralité de troubles et maladies à médiation par trpm8 et peuvent être utilisés pour préparer des médicaments et des compositions pharmaceutiques servant à traiter de tels troubles et maladies. De tels troubles peuvent être, de façon non exhaustive, les migraines et les douleurs neuropathiques. Les composés de formule (i) ont une structure dont les définitions des variables sont fournies ici.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161500843P | 2011-06-24 | 2011-06-24 | |
| PCT/US2012/043566 WO2012177893A2 (fr) | 2011-06-24 | 2012-06-21 | Antagonistes de trpm8 et leur utilisation dans des traitements |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35271B1 true MA35271B1 (fr) | 2014-07-03 |
Family
ID=46384521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA36692A MA35271B1 (fr) | 2011-06-24 | 2014-01-20 | Antagonistes de trpm8 et leur utilisation dans des traitements |
Country Status (23)
| Country | Link |
|---|---|
| US (3) | US8710043B2 (fr) |
| EP (1) | EP2723717A2 (fr) |
| JP (1) | JP2014527511A (fr) |
| KR (1) | KR20140045507A (fr) |
| CN (1) | CN103906733A (fr) |
| AP (1) | AP2013007331A0 (fr) |
| AR (1) | AR086750A1 (fr) |
| AU (1) | AU2012272895B2 (fr) |
| BR (1) | BR112013033316A2 (fr) |
| CA (1) | CA2839699A1 (fr) |
| CL (1) | CL2013003715A1 (fr) |
| CO (1) | CO6852073A2 (fr) |
| CR (1) | CR20140037A (fr) |
| EA (1) | EA201490152A1 (fr) |
| MA (1) | MA35271B1 (fr) |
| MX (1) | MX2013015274A (fr) |
| MY (1) | MY157429A (fr) |
| PE (1) | PE20140868A1 (fr) |
| PH (1) | PH12013502611A1 (fr) |
| TN (1) | TN2013000529A1 (fr) |
| TW (2) | TW201429948A (fr) |
| UY (1) | UY34160A (fr) |
| WO (1) | WO2012177893A2 (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8952009B2 (en) | 2012-08-06 | 2015-02-10 | Amgen Inc. | Chroman derivatives as TRPM8 inhibitors |
| CA2962922C (fr) * | 2014-09-29 | 2021-10-26 | The Scripps Research Institute | Modulateurs du recepteur de la sphingosine -1-phosphate pour le traitement de troubles cardio-pulmonaires |
| US9765026B2 (en) * | 2015-08-28 | 2017-09-19 | Scinopharm Taiwan, Ltd. | Forms of apremilast and the process of making the same |
| ES2957232T3 (es) * | 2016-06-13 | 2024-01-15 | Mitsubishi Tanabe Pharma Corp | Composiciones para el tratamiento o la prevención de síntomas vasomotores |
| JP2020524717A (ja) * | 2017-06-22 | 2020-08-20 | キュラデブ・ファーマ・リミテッドCuradev Pharma Limited | ヒトstingの小分子調節因子 |
| WO2018234808A1 (fr) | 2017-06-22 | 2018-12-27 | Curadev Pharma Limited | Modulateurs à petites molécules de sting humain |
| WO2019124366A1 (fr) | 2017-12-19 | 2019-06-27 | Mitsubishi Tanabe Pharma Corporation | Compositions et méthodes de traitement ou de prévention de symptômes vasomoteurs |
| WO2019180627A1 (fr) * | 2018-03-21 | 2019-09-26 | Piramal Enterprises Limited | Synthèse asymétrique améliorée d'alpha-(diarylméthyl)alkylamines |
| WO2019202522A1 (fr) * | 2018-04-18 | 2019-10-24 | Piramal Enterprises Limited | Synthèse asymétrique améliorée d'amines chirales alpha-ramifiées |
| CN110981795B (zh) * | 2019-12-18 | 2021-02-12 | 武汉世纪久海检测技术有限公司 | 一种利用2-氰基异烟酸甲酯制备2-氨酰基异烟酸的方法 |
| KR20230026404A (ko) * | 2020-06-17 | 2023-02-24 | 머크 샤프 앤드 돔 엘엘씨 | Nav1.8 억제제로서의 2-옥소-옥사졸리딘-5-카르복스아미드 |
| WO2021257490A1 (fr) | 2020-06-17 | 2021-12-23 | Merck Sharp & Dohme Corp. | 2-oxoimidazolidine-4-carboxamides utilisés en tant qu'inhibiteurs de nav1.8 |
| CN115697327A (zh) * | 2020-06-17 | 2023-02-03 | 默沙东有限责任公司 | 作为nav1.8抑制剂的5-氧代-吡咯烷-3-甲酰胺 |
| CA3221549A1 (fr) * | 2021-06-08 | 2022-12-15 | Liqiang Fu | Composes d'isoindolinone et leurs utilisations |
| CN115108980B (zh) * | 2022-06-22 | 2023-06-16 | 济南大学 | 一种2-甲基喹啉类化合物的4号位酰基化衍生物的制备方法 |
| WO2025113520A1 (fr) * | 2023-11-28 | 2025-06-05 | 成都地奥制药集团有限公司 | Composé amide et son utilisation |
| CN119118901B (zh) * | 2024-09-09 | 2025-09-30 | 中国人民解放军北部战区总医院 | 一种氧吲哚类衍生物及其制备方法与在trpa1抑制剂方向的应用 |
Family Cites Families (178)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2483250A (en) | 1949-09-27 | Tt a it tt | ||
| DE2417763A1 (de) | 1974-04-11 | 1975-10-30 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE2428673A1 (de) | 1974-06-14 | 1976-01-02 | Bayer Ag | Carbonsaeureamide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| US5081131A (en) | 1986-01-13 | 1992-01-14 | American Cyanamid Company | Omega-((hetero)alkyl)benz(cd)-indol-2-amines |
| US5223499A (en) | 1989-05-30 | 1993-06-29 | Merck & Co., Inc. | 6-amino substituted imidazo[4,5-bipyridines as angiotensin II antagonists |
| ZA913730B (en) | 1990-05-30 | 1992-02-26 | Ici Plc | Anti-tumor compounds |
| US5380721A (en) | 1990-09-10 | 1995-01-10 | Sterling Winthrop Inc. | Aryl-fused and hetaryl-fused-2,4-diazepine and 2,4-diazocine antiarrhythmic agents |
| WO1992012973A1 (fr) | 1991-01-23 | 1992-08-06 | Nippon Kayaku Kabushiki Kaisha | Derive de chromane |
| ES2036926B1 (es) | 1991-08-08 | 1994-01-16 | Uriach & Cia Sa J | "procedimiento para la obtencion de derivados de la (2-alquil-3-piridil)metilpiperazina". |
| JP2600644B2 (ja) | 1991-08-16 | 1997-04-16 | 藤沢薬品工業株式会社 | チアゾリルベンゾフラン誘導体 |
| DE4135474A1 (de) | 1991-10-28 | 1993-04-29 | Bayer Ag | 2-aminomethyl-chromane |
| DE4138819A1 (de) | 1991-11-26 | 1993-05-27 | Basf Ag | Hydroxypyridoncarbonsaeureamide, deren herstellung und verwendung |
| GB9127041D0 (en) | 1991-12-20 | 1992-02-19 | Fujisawa Pharmaceutical Co | New use |
| FR2692895A1 (fr) | 1992-06-26 | 1993-12-31 | Adir | Nouveaux 1-oxo 2,4,5,6-tétrahydro 2,3,7-triazaphénalènes leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent. |
| DE4304455A1 (de) | 1993-02-15 | 1994-08-18 | Bayer Ag | Heterocyclisch substituierte Phenyl-cyclohexan-carbonsäurederivate |
| EP0653434A1 (fr) | 1993-11-12 | 1995-05-17 | Tanabe Seiyaku Co., Ltd. | Dérivés de glucosamine, leur procédé de préparation et leur intermédiaires |
| CA2207618A1 (fr) | 1994-12-23 | 1996-07-04 | Helmut Pieper | Derives de piperazine, medicaments contenant ces composes, leur utilisation et leur procede de preparation |
| US5916906A (en) | 1995-03-14 | 1999-06-29 | Shaskan; Edward G. | Compositions comprising nicotinylalanine and an inhibitor of glycine conjugation or vitamin B6 |
| US5891872A (en) | 1995-04-07 | 1999-04-06 | Schering Corporation | Tricyclic compounds |
| IN186549B (fr) | 1995-04-19 | 2001-09-29 | Kumiai Chemical Co Ltd | |
| DE19518681A1 (de) | 1995-05-22 | 1996-11-28 | Bayer Ag | Verfahren zur Herstellung von 5,6-Dihydro-1,3-oxazinen |
| DE19523087A1 (de) | 1995-06-26 | 1997-01-02 | Bayer Ag | 1,3-Oxa(thia)zin-Derivate |
| IL118631A (en) | 1995-06-27 | 2002-05-23 | Tanabe Seiyaku Co | History of pyridazinone and processes for their preparation |
| GB9518552D0 (en) | 1995-09-11 | 1995-11-08 | Fujisawa Pharmaceutical Co | New heterocyclic compounds |
| EP0858457A1 (fr) | 1995-10-20 | 1998-08-19 | Dr. Karl Thomae GmbH | Heterocycles a 5 chainons, medicaments contenant ces composes, utilisation et procede de production correspondants |
| GB9525828D0 (en) | 1995-12-18 | 1996-02-21 | Bayer Ag | Use of hetarylacetic acid derivatives |
| US5977090A (en) | 1996-09-27 | 1999-11-02 | Guilford Pharmaceuticals Inc. | Pharmaceutical compositions and methods of treating compulsive disorders using NAALADase inhibitors |
| US6268384B1 (en) | 1997-08-29 | 2001-07-31 | Vertex Pharmaceuticals Incorporated | Compounds possessing neuronal activity |
| US6075029A (en) | 1998-01-02 | 2000-06-13 | Cell Therapeutics, Inc. | Xanthine modulators of metabolism of cellular P-450 |
| JP4432261B2 (ja) | 1998-01-21 | 2010-03-17 | 萬有製薬株式会社 | 複素芳香環縮合シクロペンテノピリジン誘導体 |
| EP1082095A1 (fr) | 1998-06-03 | 2001-03-14 | GPI NIL Holdings, Inc. | Compositions pour la croissance des cheveux a base de n-oxydes de ketones, de thioesters, d'amides ou d'esters heterocycliques, et utilisation de ces compositions |
| US5910595A (en) | 1998-06-26 | 1999-06-08 | Salsbury Chemicals, Inc. | Process for preparing oximidazoles |
| US6617351B1 (en) | 1998-07-31 | 2003-09-09 | Eli Lilly And Company | Amide, carbamate, and urea derivatives |
| US6166028A (en) | 1998-12-09 | 2000-12-26 | American Home Products Corporation | Diaminopuridine-containing thiourea inhibitors of herpes viruses |
| WO2000035889A1 (fr) | 1998-12-11 | 2000-06-22 | Sankyo Company, Limited | Benzylamines substituees |
| WO2000039102A1 (fr) | 1998-12-23 | 2000-07-06 | Du Pont Pharmaceuticals Company | INHIBITEURS DE LA THROMBINE OU DU FACTEUR Xa |
| US6200993B1 (en) | 1999-05-05 | 2001-03-13 | Merck Frosst Canada & Co. | Heterosubstituted pyridine derivatives as PDE4 inhibitors |
| TR200002099A2 (tr) | 1999-07-22 | 2001-06-21 | Sankyo Company Limited | Siklobüten türevleri, bunların hazırlanması ve terapötik kullanımları |
| GB9919588D0 (en) | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| BR0013593A (pt) | 1999-09-01 | 2002-05-07 | Unilever Nv | Método para alvejar manchas de tecido |
| BR0013592A (pt) | 1999-09-01 | 2002-05-07 | Unilever Nv | Embalagem comercial para alvejar manchas de tecido em um licor de lavagem aquoso, e, uso da mesma |
| EP1208188A1 (fr) | 1999-09-01 | 2002-05-29 | Unilever Plc | Composition et procede de blanchiment d'un substrat |
| US7291641B2 (en) | 1999-10-11 | 2007-11-06 | Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) | Derivatives of heterocycles with 5 members, their preparation and their use as medicaments |
| CA2325358C (fr) | 1999-11-10 | 2005-08-02 | Pfizer Products Inc. | Amides de l'acide 7-¬(4'-trifluoromethylbiphenyl-2-carbonyl)amino|-quinoleine-3-carboxylique et methodes pour inhiber la secretion d'apolipoproteine b |
| CN1260227C (zh) | 1999-11-10 | 2006-06-21 | 武田药品工业株式会社 | 含氮的五元杂环化合物 |
| IL139450A0 (en) | 1999-11-10 | 2001-11-25 | Pfizer Prod Inc | Methods of administering apo b-secretion/mtp inhibitors |
| TW574193B (en) | 1999-12-03 | 2004-02-01 | Astrazeneca Ab | Novel phenalkyloxy-phenyl derivatives, pharmaceutical composition containing the same and their uses |
| JP2003519697A (ja) | 1999-12-28 | 2003-06-24 | ファイザー・プロダクツ・インク | 炎症性疾患、自己免疫疾患および呼吸器疾患の処置に有用な非ペプチド系のvla−4依存性細胞結合阻害薬 |
| EP1254114A2 (fr) | 2000-01-28 | 2002-11-06 | Melacure Therapeutics AB | Nouveaux agonistes et antagonistes de recepteurs des melanocortines |
| CA2399791A1 (fr) | 2000-02-11 | 2001-08-16 | Bristol-Myers Squibb Company | Modulateurs de recepteurs aux cannabinoides, leurs procedes de preparation et utilisations de modulateurs de recepteurs aux cannabinoides pour le traitement de maladies respiratoires et non respiratoires |
| US20020019527A1 (en) | 2000-04-27 | 2002-02-14 | Wei-Bo Wang | Substituted phenyl farnesyltransferase inhibitors |
| JP2004509064A (ja) | 2000-04-27 | 2004-03-25 | アボット・ラボラトリーズ | 置換フェニルファルネシルトランスフェラーゼ阻害剤 |
| US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
| US6417367B1 (en) | 2000-08-11 | 2002-07-09 | Pfizer Inc. | Methods of making quinoline amides |
| US20030050211A1 (en) | 2000-12-14 | 2003-03-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Enzymatic detergent compositions |
| WO2002051396A1 (fr) | 2000-12-26 | 2002-07-04 | Sankyo Company, Limited | Compositions pharmaceutiques contenant des derives de cyclobutene |
| US20040106635A1 (en) | 2001-03-29 | 2004-06-03 | Iwao Takamuro | Spiroisoquinoline compound, a method for preparing the same and an intermediate thereof |
| DE10121003A1 (de) | 2001-04-28 | 2002-12-19 | Aventis Pharma Gmbh | Anthranilsäureamide, Verfahren zur Herstellung, ihrer Verwendung als Medikament sowie sie enthaltende pharmazeutische Zubereitungen |
| MY130373A (en) | 2001-10-29 | 2007-06-29 | Malesci Sas | Linear basic compounds having nk-2 antagonist activity and formulations thereof |
| RU2293083C2 (ru) | 2001-11-27 | 2007-02-10 | Ф.Хоффманн-Ля Рош Аг | Производные бензотиазола и лекарственное средство на их основе |
| JP2005510564A (ja) | 2001-11-28 | 2005-04-21 | 藤沢薬品工業株式会社 | アポリポタンパク質b阻害剤としての複素環式アミド化合物 |
| AR037746A1 (es) | 2001-12-06 | 2004-12-01 | Novartis Ag | Compuestos derivados de amidoacetonitrilo, un procedimiento para su preparacion, un procedimiento para la preparacion de compuestos intermediarios, una composicion para combatir parasitos, un procedimiento para combatir dichos parasitos, y el empleo de dichos derivados para la preparacion de una com |
| SE0104248D0 (sv) | 2001-12-14 | 2001-12-14 | Astrazeneca Ab | Method of treatment |
| CN100383124C (zh) | 2002-02-04 | 2008-04-23 | 霍夫曼-拉罗奇有限公司 | 作为npy拮抗剂的喹啉衍生物 |
| IL164212A0 (en) | 2002-03-28 | 2005-12-18 | Applied Research Systems | Thiazolidine carboxamide derivatives, their preparation and pharmaceutical compositions containing them |
| US7282591B2 (en) | 2002-04-11 | 2007-10-16 | Merck & Co., Inc. | 1h-benzo{f}indazol-5-yl derivatives as selective glucocorticoid receptor modulators |
| FR2838739B1 (fr) | 2002-04-19 | 2004-05-28 | Sanofi Synthelabo | Derives de n-[phenyl(piperidin-2-yl)methyl)benzamide, leur preparation et leur application en therapeutique |
| WO2003091217A1 (fr) | 2002-04-26 | 2003-11-06 | Ishihara Sangyo Kaisha, Ltd. | Composes pyridine ou sels de ces derniers et herbicides les contenant |
| US7375093B2 (en) | 2002-07-05 | 2008-05-20 | Intrexon Corporation | Ketone ligands for modulating the expression of exogenous genes via an ecdysone receptor complex |
| FR2842805A1 (fr) | 2002-07-29 | 2004-01-30 | Sanofi Synthelabo | Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide,leur preparation et leur application et therapeutique |
| GB0221697D0 (en) | 2002-09-18 | 2002-10-30 | Unilever Plc | Novel compouds and their uses |
| WO2004029204A2 (fr) | 2002-09-27 | 2004-04-08 | Merck & Co., Inc. | Pyrimidines substituees |
| WO2004039795A2 (fr) | 2002-10-29 | 2004-05-13 | Fujisawa Pharmaceutical Co., Ltd. | Composes amide |
| EP1560488B1 (fr) | 2002-11-05 | 2010-09-01 | Glaxo Group Limited | Agents antibacteriens |
| AU2003290333A1 (en) | 2002-12-24 | 2004-07-22 | Biofocus Plc | Compound libraries of imidazo(1,5-a)pyridin-3-yl derivatives and related heterobicycles for targetting compounds capable of binding to g-protein coupled receptors |
| US7601868B2 (en) | 2003-02-12 | 2009-10-13 | Takeda Pharmaceutical Company Limited | Amine derivative |
| EP1625115A1 (fr) | 2003-05-09 | 2006-02-15 | Pharmacia & Upjohn Company LLC | Derives pyrimidiques substitues |
| EP1660454A1 (fr) * | 2003-07-07 | 2006-05-31 | Vernalis (R&D) Limited | Composes azacycliques convenant comme inhibiteurs des canaux specifiques des neurones sensoriels |
| EP1776362A1 (fr) | 2003-07-18 | 2007-04-25 | Virochem Pharma Inc. | Composes spiro et procedes pour moduler une activite de recepteur de chimiokime |
| US7094791B2 (en) | 2003-07-31 | 2006-08-22 | Avalon Pharmaceuticals, Inc. | Derivatives of 3-hydroxy-pyrrole-2,4-dicarboxylic acid and uses thereof |
| WO2005021545A1 (fr) | 2003-09-03 | 2005-03-10 | Galapagos Nv | Derives d'imidazo[1,5-a]pyridine ou d'imidazo[1,5-a]piperidine et leur utilisation dans la preparation d'un medicament dirige contre les troubles lies au recepteur 5-ht2a |
| GB0320983D0 (en) | 2003-09-08 | 2003-10-08 | Biofocus Plc | Compound libraries |
| EP1786816A4 (fr) | 2003-09-10 | 2009-11-04 | Virochem Pharma Inc | Composes de spirohydantoine et procedes de modulation de l'activite des recepteurs de chimiokine |
| WO2005046683A1 (fr) * | 2003-10-07 | 2005-05-26 | Renovis, Inc. | Derives d'amide utilises comme ligands du canal ionique et compositions pharmaceutiques et methodes d'utilisation de ces derives |
| WO2005042524A1 (fr) | 2003-10-30 | 2005-05-12 | Virochem Pharma Inc. | Carboxamide de pyridine et methodes permettant d'inhiber l'integrase du vih |
| CA2555133A1 (fr) | 2004-02-04 | 2005-09-01 | Pfizer Products Inc. | Composes de quinoline substitues |
| GB0403578D0 (en) | 2004-02-18 | 2004-03-24 | Biofocus Discovery Ltd | Compounds which interact with the G-protein coupled receptor family |
| JP2007526324A (ja) | 2004-03-02 | 2007-09-13 | スミスクライン・ビーチャム・コーポレイション | Akt活性のある阻害剤 |
| CA2561791A1 (fr) | 2004-03-31 | 2005-10-20 | Janssen Pharmaceutica, N.V. | Composes heterocycliques non-imidazole |
| DE102004022897A1 (de) | 2004-05-10 | 2005-12-08 | Bayer Cropscience Ag | Azinyl-imidazoazine |
| US7550499B2 (en) | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| WO2005115374A1 (fr) | 2004-05-29 | 2005-12-08 | 7Tm Pharma A/S | Ligands du recepteur crth2 utilises a des fins therapeutiques |
| DE102004039876A1 (de) | 2004-06-23 | 2006-01-26 | Lanxess Deutschland Gmbh | Herstellung von fluorierten 1,3-Benzodioxanen |
| DE102004031323A1 (de) | 2004-06-29 | 2006-01-19 | Bayer Cropscience Ag | Substituierte Pyridazincarboxamide und Derivate hiervon |
| JP2008511552A (ja) * | 2004-08-30 | 2008-04-17 | ニューロメッド ファーマシューティカルズ リミテッド | カルシウムチャネルブロッカーとしての尿素誘導体 |
| AR050926A1 (es) | 2004-09-03 | 2006-12-06 | Astrazeneca Ab | Derivados de benzamida como inhibidores de la histonadesacetilasa(hdac) |
| KR100677149B1 (ko) | 2004-11-12 | 2007-02-02 | 삼성전자주식회사 | 잉크 조성물 |
| EP1829863A4 (fr) | 2004-11-26 | 2009-04-22 | Takeda Pharmaceutical | Derive d'acide arylalcanoique |
| EP1831194A4 (fr) | 2004-12-21 | 2009-12-02 | Astrazeneca Ab | ANTAGONISTES HETEROCYCLIQUES DE MCHr1 ET LEURS APPLICATIONS THERAPEUTIQUES |
| US20080207677A1 (en) | 2004-12-31 | 2008-08-28 | Gpc Biotech Ag | Napthyridine Compounds As Rock Inhibitors |
| US20060173183A1 (en) | 2004-12-31 | 2006-08-03 | Alantos Pharmaceuticals, Inc., | Multicyclic bis-amide MMP inhibitors |
| EP1844003A4 (fr) | 2005-01-27 | 2010-09-22 | Astrazeneca Ab | Nouveaux composes biaromatiques, inhibiteurs du recepteur p2x7 |
| WO2006094246A2 (fr) | 2005-03-03 | 2006-09-08 | Sirtris Pharmaceuticals, Inc. | Modulateurs de sirtuine a base de n-arylmethyl benzamide |
| US20070155738A1 (en) | 2005-05-20 | 2007-07-05 | Alantos Pharmaceuticals, Inc. | Heterobicyclic metalloprotease inhibitors |
| JP2008545744A (ja) | 2005-06-02 | 2008-12-18 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | フェニルアルキル置換ヘテロアリール誘導体 |
| ES2536351T3 (es) | 2005-06-13 | 2015-05-22 | Merck Sharp & Dohme Limited | Agentes terapéuticos |
| ES2525217T3 (es) | 2005-06-27 | 2014-12-19 | Exelixis Patent Company Llc | Moduladores de LXR basados en imidazol |
| CA2609319C (fr) | 2005-07-15 | 2014-02-04 | Nissan Chemical Industries, Ltd. | Composes thiophenes et activateurs du recepteur thrombopoietine |
| CN100494167C (zh) | 2005-08-02 | 2009-06-03 | 天津大学 | 抗乙肝病毒的叔胺氧化物及制备方法和制备药物的应用 |
| WO2007017093A1 (fr) | 2005-08-04 | 2007-02-15 | Bayer Healthcare Ag | Derives amides d'acide 2-benzyloxy-benzoique substitue |
| EP1764098A1 (fr) | 2005-09-17 | 2007-03-21 | Speedel Experimenta AG | Dérivés de diaminoalcols et leur utilization pour le traitement de la malaria, de la maladie d'Alzheimer et du SIDA |
| CA2628875A1 (fr) | 2005-11-10 | 2007-05-18 | Bayer Healthcare Ag | Diaryle-urees servant a traiter une neuropathie diabetique |
| US20090176791A1 (en) | 2005-11-10 | 2009-07-09 | Bayer Healthcare Ag | Diaryl Ureas for Treating Pulmonary Hypertension |
| US7888376B2 (en) | 2005-11-23 | 2011-02-15 | Bristol-Myers Squibb Company | Heterocyclic CETP inhibitors |
| DE102005059479A1 (de) | 2005-12-13 | 2007-06-14 | Merck Patent Gmbh | Hydroxychinolinderivate |
| EP1962829A1 (fr) | 2005-12-15 | 2008-09-03 | Bayer HealthCare AG | Urees de diaryle pour le traitement des infections virales |
| CA2633411A1 (fr) | 2005-12-15 | 2007-06-21 | Bayer Healthcare Ag | Diaryle-urees pour le traitement de maladies inflammatoires de la peau, l'oeil et/ou l'oreille |
| TWI412322B (zh) | 2005-12-30 | 2013-10-21 | Du Pont | 控制無脊椎害蟲之異唑啉 |
| JP2009524656A (ja) | 2006-01-27 | 2009-07-02 | アストラゼネカ・アクチエボラーグ | アミド置換キノリン |
| JP2009527459A (ja) | 2006-02-23 | 2009-07-30 | 武田薬品工業株式会社 | 縮合窒素含有複素環化合物 |
| DE102006012251A1 (de) | 2006-03-15 | 2007-11-08 | Grünenthal GmbH | Substituierte 4-Amino-chinazolin-Derivate und ihre Verwendung zur Herstellung von Arzneimitteln |
| EP2010493B1 (fr) | 2006-04-12 | 2016-01-27 | Merck Sharp & Dohme Corp. | Composés de pyridylamide antagonistes des canaux calciques de type t |
| JP2009538317A (ja) | 2006-05-26 | 2009-11-05 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 癌治療のための置換ジアリールウレアを用いた薬物の組み合わせ |
| GB0611152D0 (en) | 2006-06-06 | 2006-07-19 | Ucb Sa | Therapeutic agents |
| WO2008003746A1 (fr) | 2006-07-06 | 2008-01-10 | Bayer Cropscience Sa | Nouveaux dérivés de n-(4-pyridin-2-ylbutyle) carboxamide, procédé de préparation et utilisation comme fongicides |
| CN101611009A (zh) | 2006-07-25 | 2009-12-23 | 伊维沃制药股份有限公司 | 喹啉衍生物 |
| CA2661459A1 (fr) * | 2006-08-21 | 2008-02-28 | F. Hoffmann-La Roche Ag | Amides di-aromatiques substitues en tant qu'inhibiteurs de la glyt1 |
| US7834023B2 (en) | 2006-09-20 | 2010-11-16 | Portola Pharmaceuticals, Inc. | Substituted dihydroquinazolines as platelet ADP receptor inhibitors |
| WO2008056687A1 (fr) | 2006-11-09 | 2008-05-15 | Daiichi Sankyo Company, Limited | Nouveau dérivé de spiropipéridine |
| AU2007321920A1 (en) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Heterotricyclic metalloprotease inhibitors |
| WO2008063670A1 (fr) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Inhibiteurs de métalloprotéases hétérobicycliques |
| EP2121621B1 (fr) | 2006-12-08 | 2014-05-07 | Exelixis Patent Company LLC | Modulateurs lxr et fxr |
| US7872018B2 (en) | 2006-12-21 | 2011-01-18 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US20080293711A1 (en) | 2007-03-08 | 2008-11-27 | Clark Michael P | Chemokine receptor modulators |
| EP2146715A4 (fr) | 2007-04-11 | 2011-08-31 | Merck Sharp & Dohme | Antagonistes du récepteur cgrp comprenant des groupes terminaux amide tertiaire, sulfamide, carbamate et urée |
| ES2504565T3 (es) | 2007-06-05 | 2014-10-08 | Merck Sharp & Dohme Corp. | Antagonistas del receptor CGRP de carboxamida heterocíclica |
| US20100261723A1 (en) | 2007-07-09 | 2010-10-14 | Astrazeneca Ab | Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases |
| WO2009023179A2 (fr) | 2007-08-10 | 2009-02-19 | Genelabs Technologies, Inc. | Entités chimiques bicycliques azotées pour traiter les infections virales |
| EP2188295A4 (fr) | 2007-08-10 | 2011-11-16 | Crystalgenomics Inc | Dérivés de pyridine et leurs procédés d'utilisation |
| WO2009038812A1 (fr) | 2007-09-20 | 2009-03-26 | Amgen Inc. | Dérivés de pipéridine condensée, utiles en tant que ligands des récepteurs vanilloïdes |
| US8476297B2 (en) | 2007-12-04 | 2013-07-02 | Amgen Inc. | TRP-M8 receptor ligands and their use in treatments |
| WO2009072621A1 (fr) | 2007-12-07 | 2009-06-11 | Nissan Chemical Industries, Ltd. | Composé dihydroazole substitué et agent antiparasitaire |
| WO2009117269A1 (fr) | 2008-03-18 | 2009-09-24 | Merck & Co., Inc. | 4-hydroxypyrimidine-5-carboxamides substitués |
| US20110015198A1 (en) | 2008-03-28 | 2011-01-20 | Banyu Pharmaceutical Co., Inc. | Diarylmethylamide derivative having melanin-concentrating hormone receptor antagonism |
| AR071310A1 (es) | 2008-04-11 | 2010-06-09 | Merck Serono Sa | Sulfonamidas |
| DE102008019838A1 (de) | 2008-04-19 | 2009-12-10 | Boehringer Ingelheim International Gmbh | Neue Arylsulfonylglycin-Derivate, deren Herstellung und deren Verwendung als Arzneimittel |
| CA2727243A1 (fr) | 2008-06-12 | 2009-12-17 | Merck Sharp & Dohme Corp. | Quinoleines 3- et 6-substituees ramifiees en tant qu'antagonistes de recepteur cgrp |
| RU2011102471A (ru) | 2008-06-25 | 2012-07-27 | Байер Шеринг Фарма Акциенгезелльшафт (De) | Диарилмочевины для лечения сердечной недостаточности |
| ES2610882T3 (es) * | 2008-08-19 | 2017-05-03 | Janssen Pharmaceutica, N.V. | Antagonistas del receptor al mentol frío |
| CN101343313B (zh) | 2008-09-03 | 2011-11-16 | 南京农业大学 | 一种葡萄糖二肽类化合物及其制备方法和用途 |
| TWI389913B (zh) | 2008-09-08 | 2013-03-21 | Lg Life Sciences Ltd | 并合雜環化合物 |
| CN102209541B (zh) | 2008-09-08 | 2016-05-18 | 小利兰·斯坦福大学托管委员会 | 醛脱氢酶活性调节剂和其使用方法 |
| WO2010046780A2 (fr) | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Composés antiviraux |
| TW201030001A (en) | 2008-11-14 | 2010-08-16 | Amgen Inc | Pyridine and pyrimidine derivatives as phosphodiesterase 10 inhibitors |
| UY32525A (es) | 2009-04-03 | 2010-10-29 | Astrazeneca Ab | Compuestos que tienen actividad agonista del receptor de glucocorticosteroides |
| MX2011011428A (es) * | 2009-05-01 | 2011-11-29 | Raqualia Pharma Inc | Derivados de acido sulfamoilbenzoico como antagonistas de trpm8. |
| CA2761639C (fr) | 2009-05-29 | 2016-06-07 | Raqualia Pharma Inc. | Derives de carboxamide substitues par aryle comme inhibiteurs des canaux calciques ou sodiques |
| WO2010141330A1 (fr) | 2009-06-02 | 2010-12-09 | Boehringer Ingelheim International Gmbh | Dérivés d'amides d'acide 6,7-dihydro-5h-imidazo [1,2-a] imidazole-3-carboxylique |
| TW201103941A (en) * | 2009-06-10 | 2011-02-01 | Janssen Pharmaceutica Nv | Benzimidazole derivatives useful as TRPM8 channel modulators |
| CA2769512C (fr) | 2009-07-29 | 2019-07-09 | Duke University | Compositions renfermant des antagonistes du recepteur fp et leur utilisation pour inhiber la croissance des poils |
| DE102009028929A1 (de) | 2009-08-27 | 2011-07-07 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Heterocyclisch-substituierte 2-Acetamido-5-Aryl-1,2,4-triazolone und deren Verwendung |
| UY32940A (es) | 2009-10-27 | 2011-05-31 | Bayer Cropscience Ag | Amidas sustituidas con halogenoalquilo como insecticidas y acaricidas |
| CA2786277A1 (fr) | 2010-01-06 | 2011-07-14 | Joseph P. Errico | Methodes et compositions pour le developpement de medicaments cibles |
| WO2011094890A1 (fr) | 2010-02-02 | 2011-08-11 | Argusina Inc. | Dérivés phénylalanines et leur utilisation comme modulateurs non peptidiques du récepteur de glp-1 |
| US20110212969A1 (en) | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| TW201211053A (en) | 2010-05-10 | 2012-03-16 | Nissan Chemical Ind Ltd | Spiro compound and drug for activating adiponectin receptor |
| WO2011146300A1 (fr) | 2010-05-17 | 2011-11-24 | Merck Sharp & Dohme Corp. | Nouveaux inhibiteurs de prolylcarboxypeptidase |
| ES2660611T3 (es) | 2010-05-27 | 2018-03-23 | Bayer Cropscience Ag | Derivados de ácido piridinilcarboxílico como fungicidas |
| JP2013540145A (ja) | 2010-10-21 | 2013-10-31 | ウニベルシテート デス ザールランデス | コルチゾール依存性疾患の治療用の選択的cyp11b1阻害剤 |
| CN103201279A (zh) | 2010-11-05 | 2013-07-10 | 赛诺米克斯公司 | 作为trpm8的调节剂有用的化合物 |
| RS63320B1 (sr) | 2010-12-08 | 2022-07-29 | The U S A As Represented By The Secretary Department Of Health And Human Services | Supstituisani pirazolopirimidini kao aktivatori glukocerebrozidaze |
| US20140088187A1 (en) | 2010-12-14 | 2014-03-27 | Beth Israel Deaconess Medical Center | Androgen receptor inhibitors and methods of use thereof |
| PT2652025T (pt) | 2010-12-15 | 2018-11-02 | Ppg Europe B V | Composição secante e a sua utilização |
| US20130324522A1 (en) | 2010-12-17 | 2013-12-05 | The Rockefeller University | Insect odorant receptor antagonists |
| WO2012118850A1 (fr) | 2011-02-28 | 2012-09-07 | Array Biopharma Inc. | Inhibiteurs de sérine/thréonine kinase |
| WO2012120398A1 (fr) | 2011-03-04 | 2012-09-13 | Pfizer Limited | Dérivés de carboxamide substitués par aryle en tant que modulateurs de trpm8 |
| WO2012177896A1 (fr) | 2011-06-24 | 2012-12-27 | Amgen Inc. | Antagonistes de trpm8 et leur utilisation dans le cadre thérapeutique |
-
2012
- 2012-06-21 BR BR112013033316A patent/BR112013033316A2/pt not_active IP Right Cessation
- 2012-06-21 JP JP2014517168A patent/JP2014527511A/ja active Pending
- 2012-06-21 AP AP2013007331A patent/AP2013007331A0/xx unknown
- 2012-06-21 MX MX2013015274A patent/MX2013015274A/es not_active Application Discontinuation
- 2012-06-21 US US13/529,860 patent/US8710043B2/en active Active
- 2012-06-21 CA CA2839699A patent/CA2839699A1/fr not_active Abandoned
- 2012-06-21 EP EP12730134.9A patent/EP2723717A2/fr not_active Withdrawn
- 2012-06-21 WO PCT/US2012/043566 patent/WO2012177893A2/fr not_active Ceased
- 2012-06-21 PH PH1/2013/502611A patent/PH12013502611A1/en unknown
- 2012-06-21 CN CN201280041145.5A patent/CN103906733A/zh active Pending
- 2012-06-21 KR KR1020147001927A patent/KR20140045507A/ko not_active Withdrawn
- 2012-06-21 MY MYPI2013004627A patent/MY157429A/en unknown
- 2012-06-21 EA EA201490152A patent/EA201490152A1/ru unknown
- 2012-06-21 PE PE2013002869A patent/PE20140868A1/es not_active Application Discontinuation
- 2012-06-21 AU AU2012272895A patent/AU2012272895B2/en not_active Ceased
- 2012-06-22 TW TW103114426A patent/TW201429948A/zh unknown
- 2012-06-22 TW TW101122538A patent/TWI448454B/zh not_active IP Right Cessation
- 2012-06-25 UY UY0001034160A patent/UY34160A/es not_active Application Discontinuation
- 2012-06-25 AR ARP120102273A patent/AR086750A1/es not_active Application Discontinuation
-
2013
- 2013-12-23 TN TNP2013000529A patent/TN2013000529A1/fr unknown
- 2013-12-24 CL CL2013003715A patent/CL2013003715A1/es unknown
-
2014
- 2014-01-10 CO CO14004185A patent/CO6852073A2/es active IP Right Grant
- 2014-01-20 MA MA36692A patent/MA35271B1/fr unknown
- 2014-01-24 CR CR20140037A patent/CR20140037A/es unknown
- 2014-02-24 US US14/187,677 patent/US9096527B2/en active Active
- 2014-02-24 US US14/187,732 patent/US20140171406A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| KR20140045507A (ko) | 2014-04-16 |
| AU2012272895B2 (en) | 2015-01-22 |
| MX2013015274A (es) | 2014-03-31 |
| EP2723717A2 (fr) | 2014-04-30 |
| US9096527B2 (en) | 2015-08-04 |
| CO6852073A2 (es) | 2014-01-30 |
| EA201490152A1 (ru) | 2014-05-30 |
| UY34160A (es) | 2012-08-31 |
| TW201311643A (zh) | 2013-03-16 |
| PE20140868A1 (es) | 2014-07-18 |
| MY157429A (en) | 2016-06-15 |
| CN103906733A (zh) | 2014-07-02 |
| BR112013033316A2 (pt) | 2017-01-31 |
| CR20140037A (es) | 2014-03-13 |
| AU2012272895A1 (en) | 2013-04-11 |
| US20140171639A1 (en) | 2014-06-19 |
| CL2013003715A1 (es) | 2014-06-27 |
| CA2839699A1 (fr) | 2012-12-27 |
| US20130157996A1 (en) | 2013-06-20 |
| US8710043B2 (en) | 2014-04-29 |
| TN2013000529A1 (en) | 2015-03-30 |
| WO2012177893A2 (fr) | 2012-12-27 |
| AP2013007331A0 (en) | 2013-12-31 |
| JP2014527511A (ja) | 2014-10-16 |
| AR086750A1 (es) | 2014-01-22 |
| PH12013502611A1 (en) | 2014-04-28 |
| TWI448454B (zh) | 2014-08-11 |
| US20140171406A1 (en) | 2014-06-19 |
| WO2012177893A3 (fr) | 2013-06-13 |
| TW201429948A (zh) | 2014-08-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA35271B1 (fr) | Antagonistes de trpm8 et leur utilisation dans des traitements | |
| MA37762B1 (fr) | Composés n-aryltriazole utilisés comme antagonistes de lpar | |
| MA37764A1 (fr) | Composés n-alkyltriazole utilisés comme antagonistes de lpar | |
| MA41562B1 (fr) | Agonistes d'apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires | |
| MA33467B1 (fr) | Promédicaments comprenant un conjugué insuline-lieur | |
| MA40111B1 (fr) | Dérivés du tétrahydronaphtalène inhibant la protéine mcl-1 | |
| EA201290519A1 (ru) | Положительные аллостерические модуляторы рецептора хинолин амида m1 | |
| MA42397B1 (fr) | 4-azaindoles substituées et leur utilisation comme modulatoeurs de la récepteur glun2b | |
| MA34517B1 (fr) | Promédicaments comprenant un conjugué exendine-lieur | |
| MA34898B1 (fr) | Nouveaux dérivés hétérocycliques et leur utilisation dans le traitement de troubles neurologiques | |
| EP2582676A4 (fr) | Modulateurs allostériques positifs du récepteur m1 de l'amide tétrahydroquinoline | |
| EA201170624A1 (ru) | Изоникотинамидные антагонисты рецепторов орексинов | |
| EP2614860A4 (fr) | Composition pharmaceutique pour le traitement de l'oeil sec | |
| EP2827856A4 (fr) | Composés et compositions pour le traitement d'affections musculaires | |
| MA38391A1 (fr) | Dérivés de pyridinyl et triazolone pyridinyl de fusion | |
| EA200901373A1 (ru) | Аминогетероциклические соединения | |
| MA35348B1 (fr) | 4-imidazopyridazin-1-yl-benzamides et 4-imidazotriazin-1-yl-benzamides en tant qu'inhibiteurs de btk | |
| EA201491592A1 (ru) | Соединения индолов и индазолов, активирующие ampk | |
| MA37765A1 (fr) | Composés de pyrazole substitués utilisés comme antagonistes de lpar | |
| TN2011000209A1 (en) | Aryl methyl benzoquinazolinone m1 receptor positive allosteric modulators | |
| MA35444B1 (fr) | Ligands du récepteur ep1 | |
| MA29377B1 (fr) | Derives de la pyrimidine pour traitement de troubles a caractere hyperproliferatif | |
| EA201491606A1 (ru) | Ингибиторы кинуренин-3-монооксигеназы, фармацевтические композиции и способы их применения | |
| EA200970065A1 (ru) | Производные пиперазинила, предназначенные для лечения заболеваний, опосредованных рецептором gpr38 | |
| MY183111A (en) | 3-(heteroaryl-amino)-1,2,3,4-tetrahydro-9h-carbazole derivatives and their use as prostaglandin d2 receptor modulators |