WO2005000845A3 - Derives bicycliques utilises en tant qu'antagonistes des recepteurs nk-1 et nk-2 - Google Patents
Derives bicycliques utilises en tant qu'antagonistes des recepteurs nk-1 et nk-2 Download PDFInfo
- Publication number
- WO2005000845A3 WO2005000845A3 PCT/EP2004/051210 EP2004051210W WO2005000845A3 WO 2005000845 A3 WO2005000845 A3 WO 2005000845A3 EP 2004051210 W EP2004051210 W EP 2004051210W WO 2005000845 A3 WO2005000845 A3 WO 2005000845A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antagonists
- bicyclic derivatives
- neurokinin
- receptors
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
-
- 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
- C07D295/04—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/155—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne des nouveaux dérivés de formule (1) qui présentent une activité antagoniste envers les récepteurs neurokinine 1 (NK-1) et neurokinine 2 (NK-2), ainsi que le procédé de préparation de ceux-ci. Ces composés sont utiles dans la prévention et/ou le traitement des maladies associées à la stimulation des récepteurs NK-1 et NK-2.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI2003A001292 | 2003-06-25 | ||
| IT001292A ITMI20031292A1 (it) | 2003-06-25 | 2003-06-25 | Derivati biciclici nk-2 antagonisti selettivi. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2005000845A2 WO2005000845A2 (fr) | 2005-01-06 |
| WO2005000845A3 true WO2005000845A3 (fr) | 2005-04-07 |
Family
ID=30131291
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2004/051210 Ceased WO2005000845A2 (fr) | 2003-06-25 | 2004-06-23 | Derives bicycliques utilises en tant qu'antagonistes des recepteurs nk-1 et nk-2 |
Country Status (2)
| Country | Link |
|---|---|
| IT (1) | ITMI20031292A1 (fr) |
| WO (1) | WO2005000845A2 (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8835426B2 (en) | 2007-02-26 | 2014-09-16 | Vitae Pharmaceuticals, Inc. | Cyclic urea and carbamate inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| US8883778B2 (en) | 2009-07-01 | 2014-11-11 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11 beta-hydroxysteroid dehydrogenase 1 |
| US9079861B2 (en) | 2007-11-07 | 2015-07-14 | Vitae Pharmaceuticals, Inc. | Cyclic urea inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009075835A1 (fr) | 2007-12-11 | 2009-06-18 | Vitae Pharmaceutical, Inc | Inhibiteurs cycliques d'urée de la 11-hydroxystéroïde déhydrogénase 1 |
| ES2421537T3 (es) | 2008-05-01 | 2013-09-03 | Vitae Pharmaceuticals Inc | Inhibidores cíclicos de la 11beta-hidroxiesteroide deshidrogenasa 1 |
| CA2729998A1 (fr) | 2008-07-25 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Inhibiteurs de la 11 beta-hydroxysteroide deshydrogenase 1 |
| CA2730499A1 (fr) | 2008-07-25 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Inhibiteurs cycliques de la 11 beta-hydroxysteroide deshydrogenase 1 |
| WO2010089303A1 (fr) | 2009-02-04 | 2010-08-12 | Boehringer Ingelheim International Gmbh | Inhibiteurs cycliques de la 11β-hydroxystéroïde déshydrogénase de type 1 |
| MA33216B1 (fr) | 2009-04-30 | 2012-04-02 | Boehringer Ingelheim Int | Inhibiteurs cycliques de la 11béta-hydroxysteroïde déshydrogénase 1 |
| EP2440537A1 (fr) | 2009-06-11 | 2012-04-18 | Vitae Pharmaceuticals, Inc. | Inhibiteurs cycliques de la 11-bêta-hydroxystéroïde déshydrogénase 1 basée sur la structure 1,3-oxazinan-2-one |
| WO2011159760A1 (fr) | 2010-06-16 | 2011-12-22 | Vitae Pharmaceuticals, Inc. | Hétérocycles à 5, 6 et 7 chaînons substitués, médicaments contenant ces composés et leur utilisation |
| EP2585444B1 (fr) | 2010-06-25 | 2014-10-22 | Boehringer Ingelheim International GmbH | Azaspirohexanones comme inhibiteurs de 11-beta -hsd1 pour le traitement de troubles métaboliques |
| MX2013004699A (es) | 2010-11-02 | 2013-05-22 | Boehringer Ingelheim Int | Combinaciones farmaceuticas para el tratamiento de trastornos metabolicos. |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044154A1 (fr) * | 2000-11-28 | 2002-06-06 | Glaxosmithkline Spa | Nouveaux composés |
| WO2002083663A1 (fr) * | 2001-04-11 | 2002-10-24 | Glaxosmithkline S.P.A. | Derives de quinoline-4-carboxamide comme antagonistes de recepteurs de nk-3 et nk-4 |
-
2003
- 2003-06-25 IT IT001292A patent/ITMI20031292A1/it unknown
-
2004
- 2004-06-23 WO PCT/EP2004/051210 patent/WO2005000845A2/fr not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044154A1 (fr) * | 2000-11-28 | 2002-06-06 | Glaxosmithkline Spa | Nouveaux composés |
| WO2002083663A1 (fr) * | 2001-04-11 | 2002-10-24 | Glaxosmithkline S.P.A. | Derives de quinoline-4-carboxamide comme antagonistes de recepteurs de nk-3 et nk-4 |
Non-Patent Citations (2)
| Title |
|---|
| BLANEY, F.E. ET AL.: "Stepwise Modulation of Neurokinin-3 and Neurokin-2 Receptor Affinity and Selectivity", JOURNAL OF MEDICINAL CHEMISTRY, vol. 44, 2001, pages 1675 - 1689, XP002301972 * |
| WERMUTH ET AL: "The Practise of Medicinal Chemistry", PRACTICE OF MEDICINAL CHEMISTRY, XX, XX, 1996, pages 203 - 237, XP002190259 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8835426B2 (en) | 2007-02-26 | 2014-09-16 | Vitae Pharmaceuticals, Inc. | Cyclic urea and carbamate inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| US9079861B2 (en) | 2007-11-07 | 2015-07-14 | Vitae Pharmaceuticals, Inc. | Cyclic urea inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| US8883778B2 (en) | 2009-07-01 | 2014-11-11 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11 beta-hydroxysteroid dehydrogenase 1 |
Also Published As
| Publication number | Publication date |
|---|---|
| ITMI20031292A1 (it) | 2004-12-26 |
| WO2005000845A2 (fr) | 2005-01-06 |
| ITMI20031292A0 (it) | 2003-06-25 |
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