PE20080311A1 - Derivados de oxadiazol como agentes afines a receptores nicotinicos - Google Patents
Derivados de oxadiazol como agentes afines a receptores nicotinicosInfo
- Publication number
- PE20080311A1 PE20080311A1 PE2007000661A PE2007000661A PE20080311A1 PE 20080311 A1 PE20080311 A1 PE 20080311A1 PE 2007000661 A PE2007000661 A PE 2007000661A PE 2007000661 A PE2007000661 A PE 2007000661A PE 20080311 A1 PE20080311 A1 PE 20080311A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- oxadiazol
- propyl
- phenyl
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- 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
- C07D471/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Child & Adolescent Psychology (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
REFERIDA A UN DERIVADO DE OXADIAZOL DE FORMULA 8I), DONDE Q ES -(CH2)n-; n ES 3 O 4; Ra ES HIDROGENO O METILO; R1 ES -NR6COR7; R2 ES H, HALOGENO, ALQUILO C1-C6; R3 ES H, ALQUILO C1-C6, ALCOXI C1-C6, ENTRE OTROS; R4 Y R5 SON H, ALQUILO C1-C6, CICLOALQUILO C3-C6, ENTRE OTROS; R6 ES HIDROGENO; R7 ES ALQUILO C1-C5, CICLOALQUILO C3-C8, PIRIDILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 3-FLUORO-N-[4-(5-{[3-(4-MORFOLINIL)PROPIL]AMINO}-1,3,4-OXADIAZOL-2-IL)FENIL]BENZAMIDA, N-[3-(METILOXI)-4-(5-{[3-(4-MORFOLINIL)PROPIL]AMINO}-1,3,4-OXADIAZOL-2-IL)FENIL]CICLOPENTANO-CARBOXAMIDA, N-[4-(5-{[3-(DIETILAMINO)PROPIL]AMINO}-1,3,4-OXADIAZOL-2-IL)-3-(METILOXI)FENIL]-2,6-DIFLUOROBENZAMIDA, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS TIENEN AFINIDAD POR LOS RECEPTORES NICOTINICOS, PARTICULARMENTE POR EL RECEPTOR NICOTINICO ALFA 7 Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES NEUROLOGICAS, TRASTORNOS PSIQUIATRICOS, TRASTORNOS RELACIONADOS CON EL DOLOR, ENTRE OTROS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0610657.9A GB0610657D0 (en) | 2006-05-30 | 2006-05-30 | Compounds |
| GB0619710A GB0619710D0 (en) | 2006-10-05 | 2006-10-05 | Compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20080311A1 true PE20080311A1 (es) | 2008-05-23 |
Family
ID=38294122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007000661A PE20080311A1 (es) | 2006-05-30 | 2007-05-28 | Derivados de oxadiazol como agentes afines a receptores nicotinicos |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090105217A1 (es) |
| EP (1) | EP2021331A1 (es) |
| JP (1) | JP2009538865A (es) |
| KR (1) | KR20090014223A (es) |
| AR (1) | AR061196A1 (es) |
| AU (1) | AU2007267170A1 (es) |
| BR (1) | BRPI0711779A2 (es) |
| CA (1) | CA2653771A1 (es) |
| EA (1) | EA200870591A1 (es) |
| PE (1) | PE20080311A1 (es) |
| TW (1) | TW200811155A (es) |
| WO (1) | WO2007138033A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0723719D0 (en) * | 2007-12-04 | 2008-01-16 | Glaxo Group Ltd | Compounds |
| GB0723815D0 (en) * | 2007-12-05 | 2008-01-16 | Glaxo Group Ltd | Compounds |
| TWI490214B (zh) * | 2008-05-30 | 2015-07-01 | 艾德克 上野股份有限公司 | 苯或噻吩衍生物及該等作為vap-1抑制劑之用途 |
| EP2323971B1 (en) * | 2008-08-12 | 2012-05-09 | F. Hoffmann-La Roche AG | Salicylamide derivatives as nicotinic alpha 7 modulators |
| AU2009289329A1 (en) * | 2008-09-02 | 2010-03-11 | Neurosearch A/S | Triazole derivatives and their use as nicotinic acetylcholine receptor modulators |
| WO2011079439A1 (en) * | 2009-12-30 | 2011-07-07 | Zannan Scitech Co., Ltd. | Highly active metathesis catalysts selective for romp and rcm reactions |
| CN110709394B (zh) * | 2017-03-31 | 2025-02-21 | 中美博瑞纳制药有限公司 | 可用作alcat1抑制剂的化合物 |
| CN111960983A (zh) * | 2020-08-31 | 2020-11-20 | 南通大学 | 一种n-甲基-3-(1-甲基吡咯烷-3-基)丙-1-胺及其合成方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60326894D1 (de) * | 2002-09-30 | 2009-05-07 | Neurosearch As | 1,4-Diazabicycloalkanderivate, deren Herstellung und Verwendung |
-
2007
- 2007-05-28 PE PE2007000661A patent/PE20080311A1/es not_active Application Discontinuation
- 2007-05-28 TW TW096118892A patent/TW200811155A/zh unknown
- 2007-05-28 AR ARP070102281A patent/AR061196A1/es unknown
- 2007-05-29 KR KR1020087031726A patent/KR20090014223A/ko not_active Withdrawn
- 2007-05-29 EP EP07729582A patent/EP2021331A1/en not_active Withdrawn
- 2007-05-29 EA EA200870591A patent/EA200870591A1/ru unknown
- 2007-05-29 WO PCT/EP2007/055159 patent/WO2007138033A1/en not_active Ceased
- 2007-05-29 US US12/302,054 patent/US20090105217A1/en not_active Abandoned
- 2007-05-29 AU AU2007267170A patent/AU2007267170A1/en not_active Abandoned
- 2007-05-29 JP JP2009512565A patent/JP2009538865A/ja active Pending
- 2007-05-29 BR BRPI0711779-5A patent/BRPI0711779A2/pt not_active IP Right Cessation
- 2007-05-29 CA CA002653771A patent/CA2653771A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AR061196A1 (es) | 2008-08-13 |
| EP2021331A1 (en) | 2009-02-11 |
| BRPI0711779A2 (pt) | 2011-11-29 |
| AU2007267170A1 (en) | 2007-12-06 |
| WO2007138033A1 (en) | 2007-12-06 |
| CA2653771A1 (en) | 2007-12-06 |
| EA200870591A1 (ru) | 2009-06-30 |
| JP2009538865A (ja) | 2009-11-12 |
| TW200811155A (en) | 2008-03-01 |
| KR20090014223A (ko) | 2009-02-06 |
| US20090105217A1 (en) | 2009-04-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20080311A1 (es) | Derivados de oxadiazol como agentes afines a receptores nicotinicos | |
| PE20141375A1 (es) | Activadores de glucoquinasa | |
| PE20090884A1 (es) | Compuestos de indol como activadores de glucoquinasa | |
| PE20090297A1 (es) | Derivados de pirazol sustituidos con heteroarilo utiles para tratar trastornos hiperproliferativos y enfermedades asociadas con angiogenesis | |
| RU2008135690A (ru) | Соединения и композиции в качестве ингибиторов протеинкиназы | |
| PE20090617A1 (es) | Compuestos amino-5-[-4-(difluorometoxi)fenil]-5-fenilimidazolona para la inhibicion de -secretasa | |
| PE20070189A1 (es) | COMPUESTO DE AMINO-5-HETEROARILO (5 MIEMBROS) IMIDAZOLONA Y SU USO PARA MODULACION DE LA ß-SECRETASA | |
| PE20142099A1 (es) | Derivados de sulfonamida | |
| PE20080925A1 (es) | DERIVADOS DE PIRROLO[2,3-b]PIRIDINA COMO INHIBIDORES DE QUINASA, EN PARTICULAR INHIBIDORES IKK2 (O IKK BETA) | |
| PE20040833A1 (es) | Derivado de 1-aminociclohexano sustituidos en la posicion 4 | |
| PE20090160A1 (es) | COMPUESTOS AMINO-5-[4-(DIFLUOROMETOXI)FENIL SUSTITUIDO]-5-FENILIMIDAZOLONA COMO INHIBIDORES DE ß-SECRETASA | |
| PE20110028A1 (es) | Derivados de isoxazol y su uso como potenciadores de los receptores metabotropicos de glutamato | |
| PE20091201A1 (es) | AMIDAS SUSTITUIDAS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON (Btk) | |
| PE20061150A1 (es) | Derivados de n-(n-sulfonilaminoarilmetil)ciclopropanocarboxamida sustituidos como antagonistas del receptor vainilloide tipo 1 (vdr1) | |
| PE20090641A1 (es) | Amidas heterociclicas | |
| PE20081229A1 (es) | Antagonistas de receptor de orexina de diazepam sustituido | |
| PE20020544A1 (es) | Derivados de indolilmaleimida | |
| PE20081378A1 (es) | Derivados de 1,2,4-triazol como moduladores de mglur5 | |
| PE20110308A1 (es) | 1,2,5-oxadiazoles como inhibidores de indolamina 2,3-dioxigenasa | |
| PE20090477A1 (es) | Derivados de oxazol como inhibidores de los canales de sodio | |
| PE20200293A1 (es) | Inhibidores pirazolicos de magl | |
| PE20090435A1 (es) | Inhibidores de tetrahidropiranocromeno de gamma secretasa | |
| PE20081665A1 (es) | Antagonistas del receptor de dopamina 2 de rapida disociacion | |
| PE20090592A1 (es) | Nuevos derivados de piperazina-amida | |
| RU2008120850A (ru) | Соединения и композиции в качестве ингибиторов протеинкиназ |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |