CL2011001436A1 - Compuestos derivados de 4-[(2r)-4-terc-butilpiperazina-2-carbonil]-n-(4-cloro-3-fluorofenil)piperazina-1-carboxamida; antagonista del receptor crr2b; composicion farmaceutica; util en tratamiento de enfermedades inflamatorias y/o dolor neuropatico. - Google Patents
Compuestos derivados de 4-[(2r)-4-terc-butilpiperazina-2-carbonil]-n-(4-cloro-3-fluorofenil)piperazina-1-carboxamida; antagonista del receptor crr2b; composicion farmaceutica; util en tratamiento de enfermedades inflamatorias y/o dolor neuropatico.Info
- Publication number
- CL2011001436A1 CL2011001436A1 CL2011001436A CL2011001436A CL2011001436A1 CL 2011001436 A1 CL2011001436 A1 CL 2011001436A1 CL 2011001436 A CL2011001436 A CL 2011001436A CL 2011001436 A CL2011001436 A CL 2011001436A CL 2011001436 A1 CL2011001436 A1 CL 2011001436A1
- Authority
- CL
- Chile
- Prior art keywords
- butylpiperazine
- fluorophenyl
- piperazine
- carbonyl
- chloro
- Prior art date
Links
Classifications
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/195—Radicals derived from nitrogen analogues of carboxylic acids
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
- 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
- C07D417/14—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 three or more hetero rings
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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compuestos derivados de 4-[(2r)-4-terc-butilpiperazina-2-carbonil]-n-(4-cloro-3-fluorofenil)piperazina-1-carboamida; composición farmacéutica que los comprende; y su uso en el tratamiento del dolor.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12244508P | 2008-12-15 | 2008-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2011001436A1 true CL2011001436A1 (es) | 2011-08-26 |
Family
ID=42241254
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2011001436A CL2011001436A1 (es) | 2008-12-15 | 2011-06-13 | Compuestos derivados de 4-[(2r)-4-terc-butilpiperazina-2-carbonil]-n-(4-cloro-3-fluorofenil)piperazina-1-carboxamida; antagonista del receptor crr2b; composicion farmaceutica; util en tratamiento de enfermedades inflamatorias y/o dolor neuropatico. |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US20100152197A1 (es) |
| EP (2) | EP2727913A1 (es) |
| JP (1) | JP2012512153A (es) |
| KR (1) | KR20110099012A (es) |
| CN (1) | CN102317273A (es) |
| AR (1) | AR074737A1 (es) |
| AU (1) | AU2009327575B2 (es) |
| BR (1) | BRPI0922439A2 (es) |
| CA (1) | CA2746990A1 (es) |
| CL (1) | CL2011001436A1 (es) |
| CO (1) | CO6440554A2 (es) |
| CR (1) | CR20110332A (es) |
| CU (1) | CU20110133A7 (es) |
| DO (1) | DOP2011000191A (es) |
| EA (1) | EA201190019A1 (es) |
| EC (1) | ECSP11011131A (es) |
| IL (1) | IL213163A0 (es) |
| MX (1) | MX2011006087A (es) |
| NI (1) | NI201100125A (es) |
| PE (1) | PE20120082A1 (es) |
| TW (1) | TW201028400A (es) |
| UY (1) | UY32321A (es) |
| WO (1) | WO2010071567A1 (es) |
| ZA (1) | ZA201105219B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0519288A2 (pt) * | 2004-12-24 | 2009-01-06 | Astrazeneca Ab | compostos heterocÍclicos como antagonistas de ccr2b |
| GB0525957D0 (en) * | 2005-12-21 | 2006-02-01 | Astrazeneca Ab | Methods |
| WO2018134731A1 (en) | 2017-01-17 | 2018-07-26 | Glaxosmithkline Intellectual Property Development Limited | Non peptidic heterobivalent molecules for treating inflammatory diseases |
| US12319958B2 (en) | 2020-07-21 | 2025-06-03 | Rutgers, The State University Of New Jersey | Method and kit for CCR2 expression profiling and disease stratification |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133061A (en) * | 1962-11-13 | 1964-05-12 | Sterling Drug Inc | Piperidine carboxamides and derivatives thereof |
| US3541085A (en) * | 1969-05-09 | 1970-11-17 | American Cyanamid Co | Method of preparing thiotricyclic compounds |
| DE4234295A1 (de) * | 1992-10-12 | 1994-04-14 | Thomae Gmbh Dr K | Carbonsäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| WO1997030035A1 (en) | 1996-02-13 | 1997-08-21 | Zeneca Limited | Quinazoline derivatives as vegf inhibitors |
| ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| DE19743435A1 (de) * | 1997-10-01 | 1999-04-08 | Merck Patent Gmbh | Benzamidinderivate |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| IL152682A0 (en) | 2000-05-31 | 2003-06-24 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| HUP0301742A3 (en) | 2000-07-07 | 2005-08-29 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors, process for producing them, pharmaceutical compositions containing them and their use |
| BR0112224A (pt) | 2000-07-07 | 2003-06-10 | Angiogene Pharm Ltd | Composto, composição farmacêutica, uso de um composto ou de um sal, solvato ou pró-droga farmaceuticamente aceitável do mesmo, e, processo para preparar um composto |
| US20060205761A1 (en) | 2003-06-06 | 2006-09-14 | Catherine Abbadie | Ccr-2 antagonists for treatment of neuropathic pain |
| GB0428327D0 (en) * | 2004-12-24 | 2005-02-02 | Astrazeneca Ab | Method |
| BRPI0519288A2 (pt) * | 2004-12-24 | 2009-01-06 | Astrazeneca Ab | compostos heterocÍclicos como antagonistas de ccr2b |
| GB0525957D0 (en) * | 2005-12-21 | 2006-02-01 | Astrazeneca Ab | Methods |
-
2009
- 2009-12-10 US US12/634,739 patent/US20100152197A1/en not_active Abandoned
- 2009-12-14 PE PE2011001229A patent/PE20120082A1/es not_active Application Discontinuation
- 2009-12-14 MX MX2011006087A patent/MX2011006087A/es active IP Right Grant
- 2009-12-14 BR BRPI0922439A patent/BRPI0922439A2/pt not_active IP Right Cessation
- 2009-12-14 UY UY0001032321A patent/UY32321A/es not_active Application Discontinuation
- 2009-12-14 CA CA2746990A patent/CA2746990A1/en not_active Abandoned
- 2009-12-14 EP EP14153398.4A patent/EP2727913A1/en not_active Withdrawn
- 2009-12-14 KR KR1020117013597A patent/KR20110099012A/ko not_active Withdrawn
- 2009-12-14 AR ARP090104853A patent/AR074737A1/es not_active Application Discontinuation
- 2009-12-14 TW TW098142762A patent/TW201028400A/zh unknown
- 2009-12-14 AU AU2009327575A patent/AU2009327575B2/en not_active Ceased
- 2009-12-14 JP JP2011540662A patent/JP2012512153A/ja active Pending
- 2009-12-14 EP EP09833731A patent/EP2379519A4/en not_active Ceased
- 2009-12-14 WO PCT/SE2009/051416 patent/WO2010071567A1/en not_active Ceased
- 2009-12-14 EA EA201190019A patent/EA201190019A1/ru unknown
- 2009-12-14 CN CN2009801567238A patent/CN102317273A/zh active Pending
-
2011
- 2011-05-26 CO CO11065428A patent/CO6440554A2/es not_active Application Discontinuation
- 2011-05-26 IL IL213163A patent/IL213163A0/en unknown
- 2011-06-13 CL CL2011001436A patent/CL2011001436A1/es unknown
- 2011-06-15 DO DO2011000191A patent/DOP2011000191A/es unknown
- 2011-06-15 CU CU20110133A patent/CU20110133A7/es unknown
- 2011-06-15 NI NI201100125A patent/NI201100125A/es unknown
- 2011-06-15 CR CR20110332A patent/CR20110332A/es not_active Application Discontinuation
- 2011-06-15 EC EC2011011131A patent/ECSP11011131A/es unknown
- 2011-07-14 ZA ZA2011/05219A patent/ZA201105219B/en unknown
-
2012
- 2012-07-25 US US13/557,559 patent/US20120289513A1/en not_active Abandoned
-
2013
- 2013-06-27 US US13/928,803 patent/US20130289043A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201105219B (en) | 2012-03-28 |
| CU20110133A7 (es) | 2012-01-31 |
| EP2379519A1 (en) | 2011-10-26 |
| EA201190019A1 (ru) | 2012-02-28 |
| EP2727913A1 (en) | 2014-05-07 |
| ECSP11011131A (es) | 2011-07-29 |
| IL213163A0 (en) | 2011-07-31 |
| CO6440554A2 (es) | 2012-05-15 |
| MX2011006087A (es) | 2011-06-21 |
| DOP2011000191A (es) | 2011-07-15 |
| US20120289513A1 (en) | 2012-11-15 |
| CR20110332A (es) | 2011-08-05 |
| AU2009327575A1 (en) | 2011-06-23 |
| WO2010071567A1 (en) | 2010-06-24 |
| BRPI0922439A2 (pt) | 2017-06-06 |
| AU2009327575B2 (en) | 2013-07-04 |
| US20130289043A1 (en) | 2013-10-31 |
| PE20120082A1 (es) | 2012-03-04 |
| KR20110099012A (ko) | 2011-09-05 |
| JP2012512153A (ja) | 2012-05-31 |
| EP2379519A4 (en) | 2012-06-20 |
| NI201100125A (es) | 2012-03-19 |
| UY32321A (es) | 2010-07-30 |
| TW201028400A (en) | 2010-08-01 |
| CN102317273A (zh) | 2012-01-11 |
| AR074737A1 (es) | 2011-02-09 |
| US20100152197A1 (en) | 2010-06-17 |
| CA2746990A1 (en) | 2010-06-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CL2011003147A1 (es) | Compuestos derivados de n-(1-4-(1h-pirazol-5-il)ftalazina-1-il) piperidina-4-il) benzamida; composicion farmaceutica que los contiene, utiles como antagonista de la trayectoria de hedgehog, en el tratamiento del cancer. | |
| CL2013000304A1 (es) | Compuestos derivados de 2-arilamino-bencimidazoles inhibidores de prostaglandina e2 (mpges-1); composicion farmaceutica que los comprende; compuestos intermediarios; uso en el tratamiento de enfermedades inflamatorias y/o afecciones asociadas, en particular el dolor. | |
| CL2009000394A1 (es) | Compuestos derivados de n-(1h-indazol-5-il)pirrolidin-3-carboxamida sustituida, inhibidores de erk; composicion farmaceutica; y su uso en el tratamiento del cancer. | |
| CL2008003591A1 (es) | Compuestos derivados de isoxazolo-piridina sustituida; procedimiento de preparacion; composicion farmaceutica; y su uso en el tratamiento de trastornos cognitivos y alzheimer, mediado por la union al sitio de fijacion del receptor gaba a alfa 5. | |
| CL2015000942A1 (es) | Compuestos de benceno sustituido. | |
| UY32036A (es) | Derivados de ciclohexil-amida, composiciones farmacéuticas que los contienen, su preparación y aplicaciones | |
| UY28766A1 (es) | Compuestos heteropolicíclicos adicionales y su uso como antagonistas del receptor de glutamato metabotrópico | |
| CL2011000846A1 (es) | Compuestos heterociclicos sustituidos; composicion farmaceutica; y su uso para el tratamiento de la hepatitis c. | |
| CL2011002942A1 (es) | Compuestos derivados de 2,4-diamino-pirimidina, agonistas de receptor tipo toll-7 (tlr7); composicion farmaceutica; y su uso para el tratamiento del cancer. | |
| EA201170151A1 (ru) | Пиперидиниловые агонисты gpcr | |
| CL2009000368A1 (es) | 3-(amido o sulfamido)-4-(4-azinil sustituido) benzamidas o benzosulfonamidas; la composicion farmaceutica que los contiene; el uso de los compuestos; y un kit que contiene dichos compeustos; utiles como inhibidores del receptor de quimioquinas cxcr3. | |
| CL2009000119A1 (es) | Compuestos derivados de amino-bencimidazoles sustituidos; composicion farmaceutica; y su uso en el tratamiento del alzheimer. | |
| ATE544759T1 (de) | 5-pyridinon-substituierte indazole und pharmazeutische zusammensetzungen davon | |
| CL2011002300A1 (es) | Compuestos derivados de 2,4-diamiropirimidinas 5-sustitudas inhibidoras de quinasa ptk2; preparaciones farmaceuticas; y su uso para el tratamiento y/o la prevencion de cancer, infecciones, enfermedades inflamatorias y autoinmunes. | |
| CL2008000202A1 (es) | Compuestos derivados de n-aril-acetamida, antagonista trpv1;composicion farmaceutica que los comprende, utiles en el tratamiento del dolor. | |
| PA8845601A1 (es) | Antagonistas del receptor transitorio potencial de vanilloides 1(trpv1) | |
| CL2011000979A1 (es) | Compuestos derivados ftalazina 1,4-disustituida; composicion farmaceutica; y su uso en el tratamiento del cancer. | |
| CL2007001663A1 (es) | Uso de un antagonista de cgrp de formula definida (a), sus enantiomeros, sus diastereomeros, sus mezclas y sus sales para preparar un medicamento util para prevenir o tratar el dolor visceral. | |
| CR9722A (es) | Derivados de benzilpiperazina y su uso medico | |
| AR074222A1 (es) | Derivados lantibioticos carboxiamida con actividad antibacterial mejorada, procedimiento de obtencion sus composiciones farmaceuticas derivados carboxamida y empleo de los mismos | |
| SV2011003916A (es) | Nuevas lactamas como inhibidores de beta secretasa | |
| UY32520A (es) | Compuestos que tienen actividad agonista del receptor de glucocorticoesteroides | |
| CL2008003602A1 (es) | Compuestos derivados de triazolotriazinas y triazolopirazinas sustituidas; composicion farmaceutica; y su uso en el tratamiento y/o profilaxis de trastornos hematologicos. | |
| CL2008003182A1 (es) | Compuestos derivados de 1,2,4-triazol-3-amino; composicion farmaceutica; y su uso en el tratamiento del dolor, reflujo gastroesofagico, ansiedad, sindrome del intestino irritable. | |
| BRPI0818450A2 (pt) | Antagonistas do receptor de 5-ht7 |