NO20003945L - N-acyl cyclic amine derivatives - Google Patents
N-acyl cyclic amine derivativesInfo
- Publication number
- NO20003945L NO20003945L NO20003945A NO20003945A NO20003945L NO 20003945 L NO20003945 L NO 20003945L NO 20003945 A NO20003945 A NO 20003945A NO 20003945 A NO20003945 A NO 20003945A NO 20003945 L NO20003945 L NO 20003945L
- Authority
- NO
- Norway
- Prior art keywords
- group
- atom
- hydrogen atoms
- cyclic amine
- amine derivatives
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Oppfinnelsen omhandler forbindelser representert ved den generelle formelen [X] [I] [hvor Ar betyr en arylgruppe eller en heteroarylgruppe som kan ha en substituentgruppe valgt fra en gruppe bestående av et halogenatom, en lavere alkylgruppe og en lavere alkoksygruppe; R1 betyr en C3-C, sykloalkylgruppe som er substituerbar med et fluoratom; RJ og R4 betyr hydrogen- atomer, grupper representert ved -(A^.-NH-B eller lignende; R3 og R5 betyr hydrogenatomer, Cj-C, alifatiske hydrokarbon- grupper eller lignende som er substituerbare med en lavere alkylgruppe(r); n betyr O eller 1; og X betyr et oksygen- atom eller et svovelatom]. Forbindelser i henhold til oppfinnelsen, siden de ikke bare har svært selektiv antagonistisk aktivitet mot muskarine M3 reseptorer men også viser utmerket oral aktivitet, virk- ningsvarighet og farmakokinetikk, er svært anvendbare som sikre og effektive legemidler mot luftveis-, urinveis- og fordøyelsessykdommer med få ugunstige bivirkninger.The invention relates to compounds represented by the general formula [X] [I] [wherein Ar represents an aryl group or a heteroaryl group which may have a substituent group selected from a group consisting of a halogen atom, a lower alkyl group and a lower alkoxy group; R1 represents a C3-C, cycloalkyl group which is substitutable with a fluorine atom; R 1 and R 4 are hydrogen atoms, groups represented by - (A 1 -NH-B or the like; R 3 and R 5 are hydrogen atoms, C n represents O or 1; and X represents an oxygen atom or a sulfur atom.] Compounds of the invention, since they not only exhibit highly selective antagonistic activity against muscarinic M3 receptors but also exhibit excellent oral activity, duration of action and pharmacokinetics. are very useful as safe and effective medicines for respiratory, urinary and digestive diseases with few adverse side effects.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10038036A JPH11224848A (en) | 1998-02-04 | 1998-02-04 | Exposure apparatus and device manufacturing method |
| JP22872698 | 1998-07-29 | ||
| PCT/JP1999/000462 WO1999040070A1 (en) | 1998-02-04 | 1999-02-03 | N-acyl cyclic amine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO20003945D0 NO20003945D0 (en) | 2000-08-04 |
| NO20003945L true NO20003945L (en) | 2000-10-03 |
Family
ID=26377219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20003945A NO20003945L (en) | 1998-02-04 | 2000-08-04 | N-acyl cyclic amine derivatives |
Country Status (1)
| Country | Link |
|---|---|
| NO (1) | NO20003945L (en) |
-
2000
- 2000-08-04 NO NO20003945A patent/NO20003945L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20003945D0 (en) | 2000-08-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE164575T1 (en) | SUBSTITUTED AROMATIC COMPOUNDS AS CAMP PHOSPHODIESTERASE AND TNF INHIBITORS | |
| MY142807A (en) | Benzimidazole derivative and use thereof. | |
| HUP0402310A2 (en) | 1,6-naphthyridine derivatives as antidiabetics and pharmaceutical compositions containing them | |
| NO20065830L (en) | Substituted 2-quinolyloxazoles useful as PDE4 inhibitors. | |
| DE60017115D1 (en) | AMID DERIVATIVES AND THEIR MEDICAL USE | |
| DK1260512T3 (en) | Hitherto unknown cyclic amide derivatives | |
| TW200605883A (en) | Condensed heterocycle derivative having HCV inhibitory activity | |
| TW200519088A (en) | Aryl or heteroaryl amide compounds | |
| MY153045A (en) | Oxopyrazine derivative and herbicide | |
| CA2324418A1 (en) | Novel opiate compounds, methods of making and methods of use | |
| MXPA02011417A (en) | Substituted 1 aminoalkyl lactams and their use as muscarinic receptor antagonists. | |
| WO2005092858A3 (en) | Alpha aryl or heteroaryl methyl beta piperidino propanamide compounds as orl1-receptor antagonist | |
| HUP0002353A2 (en) | 1-cycloalkyl-1,8-naphthyridin-4-one derivatives with phoshodiesterase iv inhibitory activity and pharmaceutical compositions containing them | |
| MXPA04002886A (en) | Nicotinic acid-heterocyclyl-amides and analogous pyrimidine derivatives serving as pesticides. | |
| DE602004031722D1 (en) | CONDENSED BICYCLIC SUBSTITUTED AMINE AS HISTAMIN 3 RECEPTOR LIGANDS | |
| NO20004485L (en) | Cycloalken derivatives, their preparation and use | |
| ATE83773T1 (en) | 3(2H)PYRIDAZINONE, PROCESS FOR ITS PREPARATION AND ANTI-SRS-A AGENT CONTAINING IT. | |
| MXPA02011418A (en) | Substituted 1 aminoalkyl lactams and their use as muscarinic receptor antagonists. | |
| TR200103349T2 (en) | Purin derivatives, preparation method and pharmaceutical compositions containing them. | |
| EP1775289A4 (en) | NEW IMIDAZOLIDINE DERIVATIVES | |
| DE69022744D1 (en) | PIPERIDINE AND PYRROLIDINE DERIVATIVES. | |
| BR0308759A (en) | Siliconated phenyl amide derivatives usable as a microbiocide | |
| NO20032291L (en) | pyrimidine | |
| MEP12108A (en) | Novel branched substituted amino derivatives of 3-amino-1-phenyl-1h[1,2,4]triazol, methods for producing them and pharmaceutical compositions containing them | |
| NO20023251D0 (en) | New tetrahydropyridines, processes for their preparation and pharmaceutical compositions containing the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |