DE69922528T2 - N-imidazolyl-alkyl substituierte cyklische amine als histamin-h3 agonisten oder antagonisten - Google Patents
N-imidazolyl-alkyl substituierte cyklische amine als histamin-h3 agonisten oder antagonisten Download PDFInfo
- Publication number
- DE69922528T2 DE69922528T2 DE69922528T DE69922528T DE69922528T2 DE 69922528 T2 DE69922528 T2 DE 69922528T2 DE 69922528 T DE69922528 T DE 69922528T DE 69922528 T DE69922528 T DE 69922528T DE 69922528 T2 DE69922528 T2 DE 69922528T2
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- DE
- Germany
- Prior art keywords
- compound according
- compound
- ring
- substituted
- nhr
- 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.)
- Expired - Fee Related
Links
- 0 O=C*c(nc1)c[n]1[Po] Chemical compound O=C*c(nc1)c[n]1[Po] 0.000 description 9
- HZKQAAPUFWRVQF-UHFFFAOYSA-N CCCC(C)CC1CCN(CCCCc2c[nH]cn2)CC1 Chemical compound CCCC(C)CC1CCN(CCCCc2c[nH]cn2)CC1 HZKQAAPUFWRVQF-UHFFFAOYSA-N 0.000 description 1
- ZWAFECIRGVWPCG-UHFFFAOYSA-N CCCN(CC1CCN(CCCCc(nc2)c[n]2[Tl])CC1)Cc(cc1)ccc1Cl Chemical compound CCCN(CC1CCN(CCCCc(nc2)c[n]2[Tl])CC1)Cc(cc1)ccc1Cl ZWAFECIRGVWPCG-UHFFFAOYSA-N 0.000 description 1
- XBBVHXSPWYPPEC-UHFFFAOYSA-M O=C(C1CCN(CCCCC(N=[I]2)=CN2[Tl])CC1)Nc1cc(C(F)(F)F)ccc1 Chemical compound O=C(C1CCN(CCCCC(N=[I]2)=CN2[Tl])CC1)Nc1cc(C(F)(F)F)ccc1 XBBVHXSPWYPPEC-UHFFFAOYSA-M 0.000 description 1
- NOVPIORYEAPJLY-UHFFFAOYSA-M O=C(C1CCN(CCCCc(nc2)c[n]2[Tl])CC1)Nc(cc1)ccc1Cl Chemical compound O=C(C1CCN(CCCCc(nc2)c[n]2[Tl])CC1)Nc(cc1)ccc1Cl NOVPIORYEAPJLY-UHFFFAOYSA-M 0.000 description 1
- DMANRJXAVWTKSS-UHFFFAOYSA-N O=CCCCC(NC1)=CN1[Tl] Chemical compound O=CCCCC(NC1)=CN1[Tl] DMANRJXAVWTKSS-UHFFFAOYSA-N 0.000 description 1
- ZQEXIXXJFSQPNA-UHFFFAOYSA-N O=Cc1c[nH]cn1 Chemical compound O=Cc1c[nH]cn1 ZQEXIXXJFSQPNA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D401/02—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
- 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
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- 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
- C07D401/14—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 three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/173,642 US6133291A (en) | 1998-10-16 | 1998-10-16 | N-(imidazolylalkyl)substituted cyclic amines as histamine-H3 agonists or antagonists |
| US173642 | 1998-10-16 | ||
| PCT/US1999/021461 WO2000023438A1 (en) | 1998-10-16 | 1999-10-15 | N-(imidazolylalkyl)substituted cyclic amines as histamine-h3 agonists or antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69922528D1 DE69922528D1 (de) | 2005-01-13 |
| DE69922528T2 true DE69922528T2 (de) | 2005-12-15 |
Family
ID=22632924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69922528T Expired - Fee Related DE69922528T2 (de) | 1998-10-16 | 1999-10-15 | N-imidazolyl-alkyl substituierte cyklische amine als histamin-h3 agonisten oder antagonisten |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6133291A (https=) |
| EP (1) | EP1121354B1 (https=) |
| JP (1) | JP2002527513A (https=) |
| CN (1) | CN1198817C (https=) |
| AT (1) | ATE284398T1 (https=) |
| AU (1) | AU1092800A (https=) |
| CA (1) | CA2346436A1 (https=) |
| DE (1) | DE69922528T2 (https=) |
| ES (1) | ES2229782T3 (https=) |
| WO (1) | WO2000023438A1 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7361666B2 (en) | 1999-05-25 | 2008-04-22 | Sepracor, Inc. | Heterocyclic analgesic compounds and methods of use thereof |
| US6635661B2 (en) | 2000-05-25 | 2003-10-21 | Sepracor Inc. | Heterocyclic analgesic compounds and methods of use thereof |
| US6677332B1 (en) | 1999-05-25 | 2004-01-13 | Sepracor, Inc. | Heterocyclic analgesic compounds and methods of use thereof |
| US6645980B1 (en) | 2000-05-25 | 2003-11-11 | Sepracor Inc. | Heterocyclic analgesic compounds and methods of use thereof |
| US6476050B2 (en) | 2000-03-14 | 2002-11-05 | Sepracor, Inc. | 3-substituted piperidines comprising urea functionality, and methods of use thereof |
| ATE283853T1 (de) * | 2000-09-20 | 2004-12-15 | Schering Corp | Substituierte imidazole als duale histamine h1 und h3 agonisten oder antagonisten |
| FR2827863A1 (fr) * | 2001-07-27 | 2003-01-31 | Sanofi Synthelabo | Derives d'aminoalkylimidazole, leur preparation et leur utilisation en therapeutique |
| KR100432577B1 (ko) | 2002-02-08 | 2004-05-24 | 주식회사유한양행 | 이미다졸 유도체의 제조방법 |
| PT1499316E (pt) * | 2002-04-18 | 2008-06-30 | Schering Corp | Derivados de (1-4-piperidinil)benzimidazole úteis como antagonistas de histamina h3 |
| WO2004000831A1 (en) * | 2002-06-24 | 2003-12-31 | Schering Corporation | Indole derivatives useful as histamine h3 antagonists |
| US7880017B2 (en) | 2003-11-11 | 2011-02-01 | Allergan, Inc. | Process for the synthesis of imidazoles |
| US7183305B2 (en) | 2003-11-11 | 2007-02-27 | Allergan, Inc. | Process for the synthesis of imidazoles |
| EP1896453B1 (en) * | 2005-06-20 | 2009-12-02 | Schering Corporation | Carbon-linked substituted piperidines and derivatives thereof useful as histamine h3 antagonists |
| CL2007002958A1 (es) * | 2006-10-12 | 2008-05-09 | Epix Delaware Inc | Compuestos derivados de heteroaril-carboxamida, antagonistas del receptor de quimioquina; composicion farmaceutica; y uso para el tratamiento o prevencion de enfermedades tales como rechazo de transplante de organos, artritis reumatoidea, lupus, entr |
| WO2009076512A1 (en) | 2007-12-11 | 2009-06-18 | Epix Delaware, Inc. | Carboxamidξ compounds and their use as chemokine receptor agonists |
| WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
| WO2016100940A1 (en) | 2014-12-19 | 2016-06-23 | The Broad Institute, Inc. | Dopamine d2 receptor ligands |
| US10752588B2 (en) * | 2014-12-19 | 2020-08-25 | The Broad Institute, Inc. | Dopamine D2 receptor ligands |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4006137A (en) * | 1975-08-21 | 1977-02-01 | E. R. Squibb & Sons, Inc. | 2-Ethenyl imidazolium derivatives |
| ZA792608B (en) * | 1978-05-30 | 1980-06-25 | Smith Kline French Lab | Nitro compounds |
| JPS6287573A (ja) * | 1985-10-11 | 1987-04-22 | Banyu Pharmaceut Co Ltd | 四級アンモニウム塩の製造法 |
| GB8916947D0 (en) * | 1989-07-25 | 1989-09-13 | Smith Kline French Lab | Medicaments |
| GB9115740D0 (en) * | 1991-07-20 | 1991-09-04 | Smithkline Beecham Plc | Medicaments |
| DE69212164T2 (de) * | 1991-12-18 | 1996-12-05 | Schering Corp., Kenilworth, N.J. | Imidolylalkyl-derivate substituiert mit einem stickstoffenthaltende-6 gliedrigen ring |
| MX9207393A (es) * | 1991-12-18 | 1994-06-30 | Schering Corp | Imidazoil o alquilo de imidazoil susbtituido con una cadena heterociclica de cuatro o cinco miembros que contienen nitrogeno. |
| WO1993012093A1 (en) * | 1991-12-18 | 1993-06-24 | Schering Corporation | Imidazolyl-alkyl-piperazine and -diazepine derivatives as histamine h3 agonists/antagonists |
| US5807872A (en) * | 1992-12-16 | 1998-09-15 | Schering Corporation | Imidazoylalkyl substituted with a six membered nitrogen containing heterocyclic ring |
| FI92843C (fi) * | 1993-02-25 | 1995-01-10 | Eija Anitta Maeensivu | Uusi menetelmä optisesti aktiivisten glyserolijohdannaisten valmistamiseksi |
| ATE234290T1 (de) * | 1993-11-15 | 2003-03-15 | Schering Corp | Phenylalkyl-imidazole als h3-rezeptor- antagonisten |
| FR2732017B1 (fr) * | 1995-03-21 | 2000-09-22 | Inst Nat Sante Rech Med | Nouveaux derives de l'imidazole antagonistes et/ou agonistes du recepteur h3 de l'histamine, leur preparation et leurs applications therapeutiques |
| DK0841923T3 (da) * | 1995-06-07 | 2003-01-27 | Gliatech Inc | 1H-4(5)-substituerede imidazolderivater |
-
1998
- 1998-10-16 US US09/173,642 patent/US6133291A/en not_active Expired - Fee Related
-
1999
- 1999-10-15 EP EP99954622A patent/EP1121354B1/en not_active Expired - Lifetime
- 1999-10-15 WO PCT/US1999/021461 patent/WO2000023438A1/en not_active Ceased
- 1999-10-15 CN CNB99812236XA patent/CN1198817C/zh not_active Expired - Fee Related
- 1999-10-15 AU AU10928/00A patent/AU1092800A/en not_active Abandoned
- 1999-10-15 DE DE69922528T patent/DE69922528T2/de not_active Expired - Fee Related
- 1999-10-15 AT AT99954622T patent/ATE284398T1/de not_active IP Right Cessation
- 1999-10-15 JP JP2000577165A patent/JP2002527513A/ja active Pending
- 1999-10-15 ES ES99954622T patent/ES2229782T3/es not_active Expired - Lifetime
- 1999-10-15 CA CA002346436A patent/CA2346436A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ES2229782T3 (es) | 2005-04-16 |
| WO2000023438A1 (en) | 2000-04-27 |
| US6133291A (en) | 2000-10-17 |
| JP2002527513A (ja) | 2002-08-27 |
| EP1121354A1 (en) | 2001-08-08 |
| EP1121354B1 (en) | 2004-12-08 |
| AU1092800A (en) | 2000-05-08 |
| CN1323302A (zh) | 2001-11-21 |
| CN1198817C (zh) | 2005-04-27 |
| CA2346436A1 (en) | 2000-04-27 |
| ATE284398T1 (de) | 2004-12-15 |
| DE69922528D1 (de) | 2005-01-13 |
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| AU1296799A (en) | Imidazoylalkyl substituted with a five, six or seven membered heterocyclic ring containing one nitrogen atom |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |