PE20071171A1 - Derivados de acido nicotinico como moduladores de receptores de glutamato metabotropicos - Google Patents
Derivados de acido nicotinico como moduladores de receptores de glutamato metabotropicosInfo
- Publication number
- PE20071171A1 PE20071171A1 PE2006001666A PE2006001666A PE20071171A1 PE 20071171 A1 PE20071171 A1 PE 20071171A1 PE 2006001666 A PE2006001666 A PE 2006001666A PE 2006001666 A PE2006001666 A PE 2006001666A PE 20071171 A1 PE20071171 A1 PE 20071171A1
- Authority
- PE
- Peru
- Prior art keywords
- amine
- alkyl
- hydroxyl
- halogen
- phenyl
- Prior art date
Links
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 title abstract 3
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 title abstract 3
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical class OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 title 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical group [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- -1 4-CHLORO-PHENYL-AMINO Chemical class 0.000 abstract 1
- QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 abstract 1
- 150000003973 alkyl amines Chemical group 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 230000002496 gastric effect Effects 0.000 abstract 1
- 210000001035 gastrointestinal tract Anatomy 0.000 abstract 1
- 210000000653 nervous system Anatomy 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 210000001635 urinary tract Anatomy 0.000 abstract 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- C07D401/06—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 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Chemical & Material Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Addiction (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Nutrition Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE R1 ES ALQUILO, BENCILO OPCIONALMENTE SUSTITUIDOS, R2 ES H, ALQUILO O BENCILO OPCIONALMENTE SUSTITUIDOS; O JUNTOS R1 Y R2 JUNTO AL ATOMO DE NITROGENO, HETEROCICLO OPCIONALMENTE SUSTITUIDOS; R3 ES HALOGENO, HIDROXILO, ALQUILO, ALCOXILO, AMINO, ENTRE OTROS; R4 ES HIDROXILO, HALOGENO, AMINO, ALQUIL-AMINO, ENTRE OTROS; Q ES CH, CR4, N; V ES CH, CR4, N; X ES CH, N; Y ES CH, CR3, N; Z ES CR6aR6b, NR5, O; R5 ES H, HIDROXILO; R6a Y R6b SON CADA UNO H, HALOGENO, HIDROXILO, AMINO, ALQUILO, ALCOXILO, HALOALQUILO. SON COMPUESTOS PREFERIDOS: CLORHIDRATO DE 6-(4-CLORO-FENIL-AMINO)-N,N-DIETIL-NICOTIN-AMIDA; CLORHIDRATO DE N,N-DIETIL-6-(4-METOXI-FENIL-AMINO)-NICOTIDIN-AMIDA; AZEPAN-1-IL-[6-(4-CLORO-FENIL-AMINO)-PIRIDIN-3-IL]-METANONA; ENTRE OTROS. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DE LOS RECEPTORES DE GLUTAMATO METABOTROPICOS HUMANOS (mGLURs) UTILES EN DISTINTOS TRASTORNOS RELACIONADOS CON EL TRACTO GASTROINTESTINAL Y URINARIO ASI COMO TRASTORNOS DEL SISTEMA NERVIOSO
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05027934 | 2005-12-20 | ||
| EP06120424 | 2006-09-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20071171A1 true PE20071171A1 (es) | 2008-01-22 |
Family
ID=37744569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006001666A PE20071171A1 (es) | 2005-12-20 | 2006-12-20 | Derivados de acido nicotinico como moduladores de receptores de glutamato metabotropicos |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090005363A1 (es) |
| EP (1) | EP1966144A1 (es) |
| JP (1) | JP2009519986A (es) |
| KR (1) | KR20080076962A (es) |
| AR (1) | AR058554A1 (es) |
| AU (1) | AU2006329007A1 (es) |
| BR (1) | BRPI0620066A2 (es) |
| CA (1) | CA2627630A1 (es) |
| PE (1) | PE20071171A1 (es) |
| RU (1) | RU2008129622A (es) |
| TW (1) | TW200732323A (es) |
| WO (1) | WO2007071358A1 (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2009002684A (es) * | 2006-09-11 | 2009-06-05 | Novartis Ag | Derivados de acido nicotinico como moduladores de receptores de glutamato metabotropico. |
| BRPI0814758A2 (pt) * | 2007-08-03 | 2015-03-03 | Hoffmann La Roche | Piridinacarboxamida e derivados de benzamida como ligantes taar1 |
| EP2211859B1 (en) * | 2007-10-12 | 2016-01-06 | Novartis AG | Metabotropic glutamate receptor modulators for the treatment of parkinson's disease |
| WO2009047303A2 (en) * | 2007-10-12 | 2009-04-16 | Novartis Ag | Metabotropic glutamate receptor modulators for the treatment of pervasive developmental disorder |
| KR20110027817A (ko) * | 2008-06-30 | 2011-03-16 | 노파르티스 아게 | Mglur 조절제를 포함하는 파킨슨병 치료용 조합물 |
| KR101754698B1 (ko) * | 2008-12-19 | 2017-07-26 | 센트렉시온 테라퓨틱스 코포레이션 | 염증, 천식 및 copd 치료용 ccr2 수용체 길항제로서의 사이클릭 피리미딘-4-카복스아미드 |
| US8748623B2 (en) | 2009-02-17 | 2014-06-10 | Syntrix Biosystems, Inc. | Pyridinecarboxamides as CXCR2 modulators |
| WO2011009890A2 (en) | 2009-07-23 | 2011-01-27 | Novartis Ag | Use of azabicycloalkyl derivatives or pyrrolidine-2-one derivatives |
| HRP20140621T1 (hr) * | 2009-08-24 | 2014-11-21 | Neuralstem, Inc. | Sinteza neurostimulativnog piperazina |
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| DE817911C (de) * | 1947-12-16 | 1951-10-22 | Chem Fab Tempelhof Preuss & Te | Verfahren zur Darstellung von in 6-Stellung basisch substituierten Pyridin-3-carbonsaeureamiden |
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| CN1361768A (zh) * | 1999-06-02 | 2002-07-31 | Nps药物有限公司 | 代谢移变的谷氨酸盐受体拮抗剂和它们治疗中枢神经系统疾病的用途 |
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| EP1381603A2 (en) * | 2000-08-18 | 2004-01-21 | PHARMACIA & UPJOHN COMPANY | Quinuclidine-substituedaryl moieties for treatment of disease ( nicotinic acetylcholine receptor ligands ) |
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| DE102004020908A1 (de) * | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituierte 5,6,7,8,-Tetrahydro-pyrido[4,3-d]pyrimidin-2-yl- und 5,6,7,8,-Tetrahydro-chinazolin-2-yl-Verbindungen |
| SE0401969D0 (sv) * | 2004-08-02 | 2004-08-02 | Astrazeneca Ab | Piperidine derivatives |
| ATE538124T1 (de) * | 2004-11-12 | 2012-01-15 | Bristol Myers Squibb Co | Imidazokondensierte tricyclische verbindungen auf thiazoloä4,5-büpyridin-basis und pharmazeutische zusammensetzungen damit |
| WO2006064286A1 (en) * | 2004-12-13 | 2006-06-22 | Medivir Uk Ltd | Cathepsin s inhibitors |
| CN101133027B (zh) * | 2005-03-04 | 2011-03-30 | 弗·哈夫曼-拉罗切有限公司 | 作为mglur5拮抗剂的吡啶-2-甲酰胺衍生物 |
-
2006
- 2006-12-18 US US12/158,387 patent/US20090005363A1/en not_active Abandoned
- 2006-12-18 AU AU2006329007A patent/AU2006329007A1/en not_active Abandoned
- 2006-12-18 BR BRPI0620066-4A patent/BRPI0620066A2/pt not_active IP Right Cessation
- 2006-12-18 CA CA002627630A patent/CA2627630A1/en not_active Abandoned
- 2006-12-18 EP EP06829702A patent/EP1966144A1/en not_active Withdrawn
- 2006-12-18 AR ARP060105586A patent/AR058554A1/es not_active Application Discontinuation
- 2006-12-18 RU RU2008129622/04A patent/RU2008129622A/ru not_active Application Discontinuation
- 2006-12-18 WO PCT/EP2006/012181 patent/WO2007071358A1/en not_active Ceased
- 2006-12-18 KR KR1020087014836A patent/KR20080076962A/ko not_active Withdrawn
- 2006-12-18 JP JP2008546217A patent/JP2009519986A/ja active Pending
- 2006-12-19 TW TW095147659A patent/TW200732323A/zh unknown
- 2006-12-20 PE PE2006001666A patent/PE20071171A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1966144A1 (en) | 2008-09-10 |
| AR058554A1 (es) | 2008-02-13 |
| RU2008129622A (ru) | 2010-01-27 |
| WO2007071358A1 (en) | 2007-06-28 |
| TW200732323A (en) | 2007-09-01 |
| BRPI0620066A2 (pt) | 2011-11-01 |
| JP2009519986A (ja) | 2009-05-21 |
| US20090005363A1 (en) | 2009-01-01 |
| KR20080076962A (ko) | 2008-08-20 |
| AU2006329007A1 (en) | 2007-06-28 |
| CA2627630A1 (en) | 2007-06-28 |
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