PE20090839A1 - Derivados de isoxazol-imidazol - Google Patents
Derivados de isoxazol-imidazolInfo
- Publication number
- PE20090839A1 PE20090839A1 PE2008001060A PE2008001060A PE20090839A1 PE 20090839 A1 PE20090839 A1 PE 20090839A1 PE 2008001060 A PE2008001060 A PE 2008001060A PE 2008001060 A PE2008001060 A PE 2008001060A PE 20090839 A1 PE20090839 A1 PE 20090839A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- isoxazole
- trifluoromethyl
- isoxazol
- imidazol
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- -1 4-FLUORO-PHENYL Chemical class 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 208000010877 cognitive disease Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
Classifications
-
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P25/28—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
- 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
- C07D413/14—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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
REFERIDO A DERIVADOS DE ISOXAZOL-IMIDAZOL DE FORMULA (I), DONDE R1 Y R2 SON CADA UNO H, HALOGENO, HALOALCOXI C1-C7; R3 ES FENILO, HETEROARILO DE 6 MIEMBROS, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 3-FENIL-4-(1-FENIL-1H-IMIDAZOL-4-IL)-5-TRIFLUOROMETIL-ISOXAZOL; 4-[1-(4-FLUORO-FENIL)-1H-MIDAZOL-4-IL]-3-FENIL-5-TRIFLUOROMETIL-ISOXAZOL; 1-{4-[4-(3-FENIL-5-TRIFLUOROMETIL-ISOXAZOL-4-IL)-IMIDAZOL-1-IL]-FENIL}-ETANONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA Y A UN PROCESO DE PREPARACION. DICHO COMPUESTO TIENE ACTIVIDAD Y SELECTIVIDAD PARA EL SITIO DE UNION DEL RECEPTOR GABA A ALFA5 SIENDO UTIL EN EL TRATAMIENTO DE TRANSTORNOS COGNITIVOS TAL COMO LA ENFERMEDAD DE ALZHEIMER
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07110846 | 2007-06-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090839A1 true PE20090839A1 (es) | 2009-07-02 |
Family
ID=39735035
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008001060A PE20090839A1 (es) | 2007-06-22 | 2008-06-20 | Derivados de isoxazol-imidazol |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7851469B2 (es) |
| EP (1) | EP2170873B1 (es) |
| JP (1) | JP5416103B2 (es) |
| KR (1) | KR101228194B1 (es) |
| CN (1) | CN101965344B (es) |
| AR (1) | AR067075A1 (es) |
| AT (1) | ATE519760T1 (es) |
| AU (1) | AU2008267894B2 (es) |
| BR (1) | BRPI0814718A2 (es) |
| CA (1) | CA2690975A1 (es) |
| CL (1) | CL2008001820A1 (es) |
| ES (1) | ES2369805T3 (es) |
| IL (1) | IL202667A0 (es) |
| MX (1) | MX2009014001A (es) |
| PE (1) | PE20090839A1 (es) |
| TW (1) | TW200911795A (es) |
| WO (1) | WO2009000662A1 (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112013001265A2 (pt) | 2010-07-19 | 2016-05-17 | Syngenta Participations Ag | microbicidas |
| EP2595985A1 (en) | 2010-07-19 | 2013-05-29 | Syngenta Participations AG | Isoxazole, isothiazole, furane and thiophene compounds as microbicides |
| US8466181B2 (en) * | 2010-12-10 | 2013-06-18 | Hoffmann-La Roche Inc. | 1,2,3-triazole-imidazole compounds |
| US20150374705A1 (en) | 2012-02-14 | 2015-12-31 | Shanghai Institues for Biological Sciences | Substances for treatment or relief of pain |
| WO2014001279A1 (en) | 2012-06-26 | 2014-01-03 | Aniona Aps | A phenyl triazole derivative and its use for modulating the gabaa receptor complex |
| WO2014001280A1 (en) | 2012-06-26 | 2014-01-03 | Aniona Aps | A phenyl triazole derivative and its use for modulating the gabaa receptor complex |
| CA2876778A1 (en) | 2012-06-26 | 2014-01-03 | Saniona Aps | A phenyl triazole derivative and its use for modulating the gabaa receptor complex |
| AU2013283488A1 (en) | 2012-06-26 | 2015-01-15 | Saniona Aps | A phenyl triazole derivative and its use for modulating the GABAA receptor complex |
| WO2014001278A1 (en) | 2012-06-26 | 2014-01-03 | Aniona Aps | A phenyl triazole derivative and its use for modulating the gabaa receptor complex |
| EP3619207B1 (en) | 2017-05-04 | 2021-06-23 | Basf Se | Substituted 5-(haloalkyl)-5-hydroxy-isoxazolines for combating phytopathogenic fungi |
| BR102019014802A2 (pt) | 2018-07-20 | 2020-02-04 | Boehringer Ingelheim Int | difluorometil-fenil triazóis |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3525205A1 (de) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
| GB9808663D0 (en) | 1998-04-23 | 1998-06-24 | Merck Sharp & Dohme | Therapeutic agents |
| US6660753B2 (en) | 1999-08-19 | 2003-12-09 | Nps Pharmaceuticals, Inc. | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
| IT1314191B1 (it) | 1999-10-18 | 2002-12-06 | Recordati Chem Pharm | Derivati isossazolcarbossamidici |
| US6511987B1 (en) | 1999-11-12 | 2003-01-28 | Neurogen Corporation | Bicyclic and tricyclic heteroaromatic compounds |
| PA8535601A1 (es) | 2000-12-21 | 2002-11-28 | Pfizer | Derivados benzimidazol y piridilimidazol como ligandos para gabaa |
| GB0108475D0 (en) | 2001-04-04 | 2001-05-23 | Merck Sharp & Dohme | New compounds |
| EP1411942A4 (en) | 2001-07-05 | 2005-01-26 | Synaptic Pharma Corp | SUBSTITUTED ANILINPIPERIDINES AS MCH-SELECTIVE ANTAGONISTS |
| ES2299618T3 (es) | 2001-11-20 | 2008-06-01 | Eli Lilly And Company | Agonistas beta-3-adrenergicos. |
| GB0128160D0 (en) | 2001-11-23 | 2002-01-16 | Merck Sharp & Dohme | Novel compounds |
| WO2004022555A1 (en) | 2002-09-06 | 2004-03-18 | Vertex Pharmaceuticals Incorporated | Isoxazoles and their use in the treatment of ischemic diseases |
| ES2770035T3 (es) * | 2003-04-11 | 2020-06-30 | Ptc Therapeutics Inc | Compuesto de ácido 1,2,4-oxadiazol benzoico y su uso para la supresión sin sentido y el tratamiento de enfermedades |
| WO2005118568A1 (en) | 2004-06-01 | 2005-12-15 | F. Hoffmann-La Roche Ag | Pyridin-4-yl-ethynyl-imidazoles and pyrazoles as mglu5 receptor antagonists |
| GB0318447D0 (en) | 2003-08-05 | 2003-09-10 | Merck Sharp & Dohme | Therapeutic agents |
| EP1773807A2 (en) | 2004-06-14 | 2007-04-18 | Takeda San Diego, Inc. | Kinase inhibitors |
| EP1812427A4 (en) | 2004-10-15 | 2009-10-14 | Scripps Research Inst | FATTY ACID AMIDE HYDROLASE OXADIAZOLE KETONE INHIBITORS |
| US20070060589A1 (en) | 2004-12-21 | 2007-03-15 | Purandare Ashok V | Inhibitors of protein arginine methyl transferases |
| KR101181692B1 (ko) * | 2004-12-28 | 2012-09-19 | 아스카 세이야쿠 가부시키가이샤 | 피리미디닐이속사졸 유도체 |
| KR101121372B1 (ko) * | 2005-12-27 | 2012-04-12 | 에프. 호프만-라 로슈 아게 | 아릴-이속사졸-4-일-이미다졸 유도체 |
| BRPI0620760A2 (pt) * | 2005-12-27 | 2011-11-22 | Hoffmann La Roche | derivados de aril-isoxazol-4-il-imidazo[1,5]piridina |
| BRPI0706560A2 (pt) * | 2006-01-17 | 2011-03-29 | Hoffmann La Roche | derivados de aril-isoxazol-4-il-imidazo [1,2-a] piridina úteis para o tratamento de doença de alzheimer por intermédio de receptores gaba |
-
2008
- 2008-06-12 AT AT08760925T patent/ATE519760T1/de active
- 2008-06-12 BR BRPI0814718-3A2A patent/BRPI0814718A2/pt not_active IP Right Cessation
- 2008-06-12 JP JP2010512649A patent/JP5416103B2/ja not_active Expired - Fee Related
- 2008-06-12 ES ES08760925T patent/ES2369805T3/es active Active
- 2008-06-12 MX MX2009014001A patent/MX2009014001A/es active IP Right Grant
- 2008-06-12 EP EP08760925A patent/EP2170873B1/en not_active Not-in-force
- 2008-06-12 CN CN2008800239424A patent/CN101965344B/zh not_active Expired - Fee Related
- 2008-06-12 CA CA2690975A patent/CA2690975A1/en not_active Abandoned
- 2008-06-12 KR KR1020107001422A patent/KR101228194B1/ko not_active Expired - Fee Related
- 2008-06-12 AU AU2008267894A patent/AU2008267894B2/en not_active Ceased
- 2008-06-12 WO PCT/EP2008/057384 patent/WO2009000662A1/en not_active Ceased
- 2008-06-16 US US12/139,535 patent/US7851469B2/en not_active Expired - Fee Related
- 2008-06-19 CL CL2008001820A patent/CL2008001820A1/es unknown
- 2008-06-19 TW TW097122892A patent/TW200911795A/zh unknown
- 2008-06-20 PE PE2008001060A patent/PE20090839A1/es not_active Application Discontinuation
- 2008-06-20 AR ARP080102628A patent/AR067075A1/es unknown
-
2009
- 2009-12-10 IL IL202667A patent/IL202667A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN101965344B (zh) | 2013-03-06 |
| MX2009014001A (es) | 2010-01-28 |
| IL202667A0 (en) | 2010-06-30 |
| KR20100023042A (ko) | 2010-03-03 |
| AU2008267894B2 (en) | 2012-08-23 |
| CL2008001820A1 (es) | 2009-05-29 |
| EP2170873A1 (en) | 2010-04-07 |
| JP5416103B2 (ja) | 2014-02-12 |
| CA2690975A1 (en) | 2008-12-31 |
| AR067075A1 (es) | 2009-09-30 |
| JP2010530862A (ja) | 2010-09-16 |
| KR101228194B1 (ko) | 2013-01-30 |
| ES2369805T3 (es) | 2011-12-07 |
| WO2009000662A1 (en) | 2008-12-31 |
| US20090005370A1 (en) | 2009-01-01 |
| EP2170873B1 (en) | 2011-08-10 |
| ATE519760T1 (de) | 2011-08-15 |
| TW200911795A (en) | 2009-03-16 |
| BRPI0814718A2 (pt) | 2015-02-24 |
| US7851469B2 (en) | 2010-12-14 |
| AU2008267894A1 (en) | 2008-12-31 |
| CN101965344A (zh) | 2011-02-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20090839A1 (es) | Derivados de isoxazol-imidazol | |
| PE20121050A1 (es) | Compuestos de n-(1-(4-(1h-pirazol-5-il)ftalazin-1-il)piperidin-4-il)-benzamida sustituidos como antagonistas de la trayectoria hedgehog | |
| PE20142301A1 (es) | Uracilos sustituidos biciclicamente y uso de los mismos | |
| NO20083909L (no) | Bisykliske benzimidazolforbindelser, og deres anvendelse som metabotropiske glutamatreseptorforsterkere | |
| PE20100087A1 (es) | Compuestos y composiciones como inhibidores de cinasa | |
| PE20141203A1 (es) | Benzilindazoles sustituidos para uso como inhibidores de la quinasa bub1 en el tratamiento de enfermedades hiperproliferativas | |
| EA201001585A1 (ru) | Производные тиенопиридона в качестве активаторов амр-активированной протеинкиназы (амрк) | |
| PE20091173A1 (es) | Derivados de heteroarilo como antagonistas de receptor de orexina | |
| NO20063470L (no) | Tetrazolforbindelser og deres anvendelse av metabotrofe glutamatreseptorantagonister | |
| PE20121640A1 (es) | Derivados de pirazina como inhibidores de bace | |
| NO20063599L (no) | Ytterligere heterosykliske forbindelser og deres anvendelse som metabotrofiske glutamatreseptorantagonister | |
| PE20080362A1 (es) | Derivados de ciclohexilpirazol-lactama como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1 | |
| EA200601266A1 (ru) | Соединения триазола и их применение в качестве антагонистов метаботропного рецептора глутамата | |
| CL2007003826A1 (es) | Compuestos derivados de n-(amino-(hetero)aril)-1h-pirrolopiridin-2-carboxamidas, antagonistas de receptores tipo trpv1; procedimiento de preparacion; composicion farmaceutica; y uso para el tratamiento de enfermedades tales como trastornos gastrointestinales, trastornos respiratorios, psoriasis y depresion. | |
| PE20110433A1 (es) | Antagonistas de la via hedgehog de ftalazina disustituida | |
| PE20130215A1 (es) | Nuevos derivados de ciclohexilamina que tienen actividad como agonistas adrenergicos beta2 y como antagonistas muscarinicos m3 | |
| UY29421A1 (es) | Nuevos compuestos de n-(n-sulfonilaminoarilmetil) ciclopropanocarboxanida sustituidos, comoposiciones farmacéuticas que los contienen a aplicaciones. | |
| PE20090898A1 (es) | Pirrolidina-aril-eteres como antagonistas de receptor de nk3 | |
| UY29389A1 (es) | Derivados sustituidos del ácido1-((4-((((3,3-dimetil-2-oxo-2,3-dihidro-1h-indol-1-il)carbonil)amino)metil)piperidin-1-il)metil)ciclobutanocarboxílico, sales farmaceuticamente aceptables, composiciones que los contienen y aplicaciones. | |
| PE20090621A1 (es) | Pirrolidina-aril-eteres como antagonistas de receptores de nk3 | |
| PE20161363A1 (es) | Moduladores del receptor acoplado a la proteina g40 (gpr40) de pirrolidina para el tratamiento de enfermedades como la diabetes | |
| BRPI0816219B8 (pt) | compostos contendo guanidina úteis como antagonistas de receptor muscarínico, composição farmacêutica e uso | |
| PE20081665A1 (es) | Antagonistas del receptor de dopamina 2 de rapida disociacion | |
| PE20120026A1 (es) | 2-metil-1-(fenilsulfonil)-4-piperazin-1-il-1h-benzimidazol como ligando de 5-hidroxitriptamina-6 (5-ht6) | |
| PE20160846A1 (es) | Piperidiniltetrahidroquinolinas sustituidas y su uso como antagonistas de los adenoreceptores alpha-2c |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |