CL2003002770A1 - Compuestos derivados de pirrol e imiddazol; composiciones farmaceuticas que los contienen; procedimiento de preparacion; y su uso en el tratamiento y/o prevencion de enfermedades que estan asociadas con la modulacion de los receptores a canabinoides - Google Patents
Compuestos derivados de pirrol e imiddazol; composiciones farmaceuticas que los contienen; procedimiento de preparacion; y su uso en el tratamiento y/o prevencion de enfermedades que estan asociadas con la modulacion de los receptores a canabinoidesInfo
- Publication number
- CL2003002770A1 CL2003002770A1 CL200302770A CL2003002770A CL2003002770A1 CL 2003002770 A1 CL2003002770 A1 CL 2003002770A1 CL 200302770 A CL200302770 A CL 200302770A CL 2003002770 A CL2003002770 A CL 2003002770A CL 2003002770 A1 CL2003002770 A1 CL 2003002770A1
- Authority
- CL
- Chile
- Prior art keywords
- diseases
- modulation
- prevention
- treatment
- pharmaceutical compositions
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 230000002265 prevention Effects 0.000 title abstract 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 title 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
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- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C—CHEMISTRY; METALLURGY
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- 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
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- 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
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Reproductive Health (AREA)
- Cardiology (AREA)
- Psychology (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Pregnancy & Childbirth (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Virology (AREA)
- Otolaryngology (AREA)
- Gynecology & Obstetrics (AREA)
- Rheumatology (AREA)
Abstract
COMPUESTOS DE LA FORMULA (I) EN DONDE R1,R2,R3,R4,R5,R6 M y X SON TAL COMO SE DEFINEN EN LA DESCRIPCION Y REIVINDICACIONES, Y SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS, COMPOSICIONES FARMACEUTICAS QUE LOS COMPRENDEN Y PROCEDIMIENTO DE PREPARACION; UTILES PARA EL TRATAMIENTO Y/O PREVENCION DE ENFERMEDADES QUE ESTAN ASOCIADAS CON LA MODULACION DE LOS RECEPTORES CB1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03000003 | 2003-01-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2003002770A1 true CL2003002770A1 (es) | 2005-01-07 |
Family
ID=32695582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL200302770A CL2003002770A1 (es) | 2003-01-02 | 2003-12-29 | Compuestos derivados de pirrol e imiddazol; composiciones farmaceuticas que los contienen; procedimiento de preparacion; y su uso en el tratamiento y/o prevencion de enfermedades que estan asociadas con la modulacion de los receptores a canabinoides |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US7294644B2 (es) |
| EP (1) | EP1583742B1 (es) |
| JP (1) | JP4444120B2 (es) |
| KR (1) | KR100704097B1 (es) |
| CN (2) | CN100395234C (es) |
| AR (1) | AR042691A1 (es) |
| AT (1) | ATE450505T1 (es) |
| AU (1) | AU2003298227A1 (es) |
| BR (1) | BR0317926A (es) |
| CA (1) | CA2511859A1 (es) |
| CL (1) | CL2003002770A1 (es) |
| DE (1) | DE60330392D1 (es) |
| ES (1) | ES2334565T3 (es) |
| MX (1) | MXPA05007114A (es) |
| PL (1) | PL378206A1 (es) |
| RU (1) | RU2339618C2 (es) |
| TW (1) | TW200413328A (es) |
| WO (1) | WO2004060870A1 (es) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003007887A2 (en) | 2001-07-20 | 2003-01-30 | Merck & Co., Inc. | Substituted imidazoles as cannabinoid receptor modulators |
| EP1496838B1 (en) | 2002-03-12 | 2010-11-03 | Merck Sharp & Dohme Corp. | Substituted amides |
| FR2845382A1 (fr) * | 2002-10-02 | 2004-04-09 | Sanofi Synthelabo | Derives d'indazolecarboxamides, leur preparation et leur utilisation en therapeutique |
| RU2330035C2 (ru) * | 2003-01-02 | 2008-07-27 | Ф.Хоффманн-Ля Рош Аг | Пирролилтиазолы и фармацевтическая композиция, обладающая свойством модулятора рецептора св1 |
| WO2005040128A1 (en) * | 2003-10-24 | 2005-05-06 | Glaxo Group Limited | Heterocyclyl compounds |
| GB0403780D0 (en) * | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Therapeutic agents |
| EP1568698A1 (en) * | 2004-02-27 | 2005-08-31 | Aventis Pharma Deutschland GmbH | Pyrrole-derivatives as factor Xa inhibitors |
| JP4177435B2 (ja) | 2004-04-03 | 2008-11-05 | アストラゼネカ アクチボラグ | 治療薬 |
| JP4703649B2 (ja) | 2004-07-30 | 2011-06-15 | エグゼリクシス, インコーポレイテッド | 薬学的因子としてのピロール誘導体 |
| FR2874012B1 (fr) * | 2004-08-09 | 2008-08-22 | Sanofi Synthelabo | Derives de pyrrole, leur preparation et leur utlisation en therapeutique |
| SG163577A1 (en) * | 2004-12-03 | 2010-08-30 | Schering Corp | Substituted piperazines as cb1 antagonists |
| CA2594488C (en) * | 2005-01-10 | 2015-04-28 | University Of Connecticut | Novel heteropyrrole analogs acting on cannabinoid receptors |
| BRPI0613505A2 (pt) | 2005-06-30 | 2011-01-11 | Prosidion Ltd | agonistas de gpcr |
| GB0518819D0 (en) * | 2005-09-15 | 2005-10-26 | Astrazeneca Ab | Therapeutic agents |
| US7897601B2 (en) * | 2006-01-18 | 2011-03-01 | Intervet, Inc. | Cannabinoid receptor modulators |
| US8222274B2 (en) | 2006-02-20 | 2012-07-17 | Astellas Pharma Inc. | Pyrrole derivative or salt thereof |
| CL2008000017A1 (es) | 2007-01-04 | 2008-08-01 | Prosidion Ltd | Compuestos derivados de heterociclos de nitrogeno y oxigeno, agonistas de gpcr; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de la obesidad, diabetes, sindrome metabolico, hiperlipidemia, toleranci |
| US20100048632A1 (en) | 2007-01-04 | 2010-02-25 | Matthew Colin Thor Fyfe | Piperidine GPCR Agonists |
| AR064735A1 (es) | 2007-01-04 | 2009-04-22 | Prosidion Ltd | Agonistas de gpcr y composicion farmaceutica en base al compuesto |
| GB0700122D0 (en) | 2007-01-04 | 2007-02-14 | Prosidion Ltd | GPCR agonists |
| WO2008081208A1 (en) | 2007-01-04 | 2008-07-10 | Prosidion Limited | Piperidine gpcr agonists |
| US20100197564A1 (en) * | 2007-04-19 | 2010-08-05 | Schering Corporation | Diaryl morpholines as cb1 modulators |
| JP2010531874A (ja) * | 2007-06-28 | 2010-09-30 | インターベット インターナショナル ベー. フェー. | Cb1アンタゴニストとしての置換ピペラジン |
| WO2009005646A2 (en) * | 2007-06-28 | 2009-01-08 | Schering Corporation | Substituted piperazines as cb1 antagonists |
| HUE026446T2 (en) | 2007-07-19 | 2016-05-30 | Lundbeck H As | 5-membered heterocyclic amides and related compounds |
| GB0720390D0 (en) | 2007-10-18 | 2007-11-28 | Prosidion Ltd | G-Protein coupled receptor agonists |
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| CN103842140B (zh) | 2011-10-05 | 2016-09-07 | 埃克森美孚化学专利公司 | 轮胎硫化气囊 |
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| JO3215B1 (ar) * | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
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| US3940418A (en) | 1972-04-07 | 1976-02-24 | G. D. Searle & Co. | Esters and amides of 4,5-dihydrobenz[g]indazole-3-carboxylic acids and related compounds |
| FR2713225B1 (fr) | 1993-12-02 | 1996-03-01 | Sanofi Sa | N-pipéridino-3-pyrazolecarboxamide substitué. |
| FR2692575B1 (fr) | 1992-06-23 | 1995-06-30 | Sanofi Elf | Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| FR2714057B1 (fr) | 1993-12-17 | 1996-03-08 | Sanofi Elf | Nouveaux dérivés du 3-pyrazolecarboxamide, procédé pour leur préparation et compositions pharmaceutiques les contenant. |
| US5596106A (en) | 1994-07-15 | 1997-01-21 | Eli Lilly And Company | Cannabinoid receptor antagonists |
| US6613789B2 (en) * | 1994-07-28 | 2003-09-02 | G. D. Searle & Co. | Heterocyclo-substituted imidazoles for the treatment of inflammation |
| FR2741621B1 (fr) * | 1995-11-23 | 1998-02-13 | Sanofi Sa | Nouveaux derives de pyrazole, procede pour leur preparation et compositions pharmaceutiques en contenant |
| FR2742148B1 (fr) * | 1995-12-08 | 1999-10-22 | Sanofi Sa | Nouveaux derives du pyrazole-3-carboxamide, procede pour leur preparation et compositions pharmaceutiques les contenant |
| FR2783246B1 (fr) | 1998-09-11 | 2000-11-17 | Aventis Pharma Sa | Derives d'azetidine, leur preparation et les medicaments les contenant |
| FR2789079B3 (fr) | 1999-02-01 | 2001-03-02 | Sanofi Synthelabo | Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant |
| WO2001015609A1 (en) | 1999-08-31 | 2001-03-08 | Fox Hollow Technologies | Atherectomy catheter with a rotating and telescoping cutter |
| FR2800375B1 (fr) | 1999-11-03 | 2004-07-23 | Sanofi Synthelabo | Derives tricycliques d'acide pyrazolecarboxylique, leur preparation, les compositions pharmaceutiques en contenant |
| FR2805817B1 (fr) | 2000-03-03 | 2002-04-26 | Aventis Pharma Sa | Compositions pharmaceutiques contenant des derives d'azetidine, les nouveaux derives d'azetidine et leur preparation |
| FR2805818B1 (fr) | 2000-03-03 | 2002-04-26 | Aventis Pharma Sa | Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant |
| FR2805810B1 (fr) | 2000-03-03 | 2002-04-26 | Aventis Pharma Sa | Compositions pharmaceutiques contenant des derives de 3- amino-azetidine, les nouveaux derives et leur preparation |
| CN1205188C (zh) | 2000-03-23 | 2005-06-08 | 索尔瓦药物有限公司 | 具有cb1-拮抗活性的4,5-二氢-1h-吡唑衍生物 |
| FR2809621B1 (fr) * | 2000-05-12 | 2002-09-06 | Sanofi Synthelabo | Utilisation d'un antagoniste des recepteurs aux cannabinoides centraux pour la preparation de medicaments utiles comme antidiarrheiques |
| FR2814678B1 (fr) | 2000-10-04 | 2002-12-20 | Aventis Pharma Sa | Association d'un antagoniste du recepteur cb1 et de sibutramine, les compositions pharmaceutiques les contenant et leur utilisation pour la traitement de l'obesite |
| WO2003007887A2 (en) * | 2001-07-20 | 2003-01-30 | Merck & Co., Inc. | Substituted imidazoles as cannabinoid receptor modulators |
| TWI231757B (en) | 2001-09-21 | 2005-05-01 | Solvay Pharm Bv | 1H-Imidazole derivatives having CB1 agonistic, CB1 partial agonistic or CB1-antagonistic activity |
| WO2003027114A1 (en) | 2001-09-24 | 2003-04-03 | Bayer Pharmaceuticals Corporation | Preparation and use of 1,5,6,7-tetrahydropyrrolo[3,2-c]pyridine derivatives for treatment of obesity |
| JP2005532982A (ja) | 2001-09-24 | 2005-11-04 | バイエル・フアーマシユーチカルズ・コーポレーシヨン | 肥満の処置のためのピロール誘導体の製造及び使用 |
| HN2002000266A (es) | 2001-09-24 | 2003-11-16 | Bayer Corp | Preparacion y uso de derivados de imidazol para el tratamiento de la obesidad. |
| RU2330035C2 (ru) | 2003-01-02 | 2008-07-27 | Ф.Хоффманн-Ля Рош Аг | Пирролилтиазолы и фармацевтическая композиция, обладающая свойством модулятора рецептора св1 |
-
2003
- 2003-12-22 TW TW092136400A patent/TW200413328A/zh unknown
- 2003-12-22 US US10/743,642 patent/US7294644B2/en not_active Expired - Fee Related
- 2003-12-22 EP EP03795949A patent/EP1583742B1/en not_active Expired - Lifetime
- 2003-12-22 KR KR1020057012530A patent/KR100704097B1/ko not_active Expired - Fee Related
- 2003-12-22 DE DE60330392T patent/DE60330392D1/de not_active Expired - Lifetime
- 2003-12-22 CN CNB2003801082687A patent/CN100395234C/zh not_active Expired - Fee Related
- 2003-12-22 WO PCT/EP2003/014720 patent/WO2004060870A1/en not_active Ceased
- 2003-12-22 ES ES03795949T patent/ES2334565T3/es not_active Expired - Lifetime
- 2003-12-22 AT AT03795949T patent/ATE450505T1/de not_active IP Right Cessation
- 2003-12-22 MX MXPA05007114A patent/MXPA05007114A/es active IP Right Grant
- 2003-12-22 BR BR0317926-5A patent/BR0317926A/pt not_active IP Right Cessation
- 2003-12-22 CN CNA200710085476XA patent/CN101012193A/zh active Pending
- 2003-12-22 RU RU2005124360/04A patent/RU2339618C2/ru not_active IP Right Cessation
- 2003-12-22 JP JP2004564210A patent/JP4444120B2/ja not_active Expired - Fee Related
- 2003-12-22 AU AU2003298227A patent/AU2003298227A1/en not_active Abandoned
- 2003-12-22 PL PL378206A patent/PL378206A1/pl not_active Application Discontinuation
- 2003-12-22 CA CA002511859A patent/CA2511859A1/en not_active Abandoned
- 2003-12-29 CL CL200302770A patent/CL2003002770A1/es unknown
- 2003-12-30 AR ARP030104878A patent/AR042691A1/es unknown
-
2007
- 2007-05-10 US US11/801,727 patent/US7579369B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA05007114A (es) | 2005-08-26 |
| US7579369B2 (en) | 2009-08-25 |
| ATE450505T1 (de) | 2009-12-15 |
| ES2334565T3 (es) | 2010-03-12 |
| US7294644B2 (en) | 2007-11-13 |
| EP1583742B1 (en) | 2009-12-02 |
| KR100704097B1 (ko) | 2007-04-06 |
| CN101012193A (zh) | 2007-08-08 |
| US20070238754A1 (en) | 2007-10-11 |
| AU2003298227A1 (en) | 2004-07-29 |
| PL378206A1 (pl) | 2006-03-20 |
| CN1735593A (zh) | 2006-02-15 |
| AR042691A1 (es) | 2005-06-29 |
| US20040167129A1 (en) | 2004-08-26 |
| EP1583742A1 (en) | 2005-10-12 |
| KR20050091055A (ko) | 2005-09-14 |
| WO2004060870A1 (en) | 2004-07-22 |
| RU2339618C2 (ru) | 2008-11-27 |
| RU2005124360A (ru) | 2006-06-10 |
| TW200413328A (en) | 2004-08-01 |
| JP2006521281A (ja) | 2006-09-21 |
| CA2511859A1 (en) | 2004-07-22 |
| BR0317926A (pt) | 2005-11-29 |
| JP4444120B2 (ja) | 2010-03-31 |
| DE60330392D1 (de) | 2010-01-14 |
| CN100395234C (zh) | 2008-06-18 |
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