DK0975602T3 - Imidazol- og imidazolinderivater samt anvendelse heraf - Google Patents
Imidazol- og imidazolinderivater samt anvendelse herafInfo
- Publication number
- DK0975602T3 DK0975602T3 DK98915550T DK98915550T DK0975602T3 DK 0975602 T3 DK0975602 T3 DK 0975602T3 DK 98915550 T DK98915550 T DK 98915550T DK 98915550 T DK98915550 T DK 98915550T DK 0975602 T3 DK0975602 T3 DK 0975602T3
- Authority
- DK
- Denmark
- Prior art keywords
- imidazoline derivatives
- imidazole
- compounds
- receptors
- alpha2
- Prior art date
Links
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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/50—Nitrogen atoms not forming part of a nitro radical with carbocyclic radicals directly attached to said nitrogen atoms
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/834,658 US5866579A (en) | 1997-04-11 | 1997-04-11 | Imidazole and imidazoline derivatives and uses thereof |
PCT/US1998/007453 WO1998046572A1 (en) | 1997-04-11 | 1998-04-10 | Imidazole and imidazoline derivatives and uses thereof |
EP98915550A EP0975602B1 (en) | 1997-04-11 | 1998-04-10 | Imidazole and imidazoline derivatives and uses thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
DK0975602T3 true DK0975602T3 (da) | 2005-10-17 |
Family
ID=25267478
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK98915550T DK0975602T3 (da) | 1997-04-11 | 1998-04-10 | Imidazol- og imidazolinderivater samt anvendelse heraf |
Country Status (11)
Country | Link |
---|---|
US (4) | US5866579A (da) |
EP (1) | EP0975602B1 (da) |
AT (1) | ATE297899T1 (da) |
AU (1) | AU6970598A (da) |
DE (1) | DE69830576T2 (da) |
DK (1) | DK0975602T3 (da) |
ES (1) | ES2245029T3 (da) |
HK (1) | HK1026892A1 (da) |
PT (1) | PT975602E (da) |
SI (1) | SI0975602T1 (da) |
WO (1) | WO1998046572A1 (da) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19514579A1 (de) * | 1995-04-20 | 1996-10-24 | Boehringer Ingelheim Kg | Verwendung von alpha¶1¶¶L¶-Agonisten zur Behandlung der Harninkontinenz |
US6503935B1 (en) | 1998-08-07 | 2003-01-07 | Abbott Laboratories | Imidazoles and related compounds as α1A agonists |
US6410562B1 (en) | 1998-12-18 | 2002-06-25 | Eli Lilly And Company | Hypoglycemic imidazoline compounds |
EP1385823B1 (en) * | 2001-04-09 | 2006-12-13 | Chiron Corporation | Guanidino compounds as melanocortin-4 receptor (mc4-r) agonists |
FR2846328B1 (fr) * | 2002-10-23 | 2004-12-10 | Servier Lab | Nouveaux derives de l'imidazoline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
EP1562786A2 (en) * | 2002-11-20 | 2005-08-17 | Johnson Controls Technology Company | Covered illuminated vanity mirror assembly |
US20060293359A1 (en) * | 2003-06-25 | 2006-12-28 | Allergan, Inc. | Methods and compositions for the treatment of diabetes |
US20050059664A1 (en) * | 2003-09-12 | 2005-03-17 | Allergan, Inc. | Novel methods for identifying improved, non-sedating alpha-2 agonists |
FR2858619B1 (fr) * | 2003-08-08 | 2006-12-22 | Aventis Pharma Sa | Derives de quinoleines-4-substituees, leurs procede et intermediaires de preparation et les compositions pharmaceutiques qui les contiennent |
US7348434B2 (en) | 2003-08-08 | 2008-03-25 | Antony Bigot | 4-substituted quinoline derivatives, method and intermediates for their preparation and pharmaceutical compositions containing them |
US20050058696A1 (en) * | 2003-09-12 | 2005-03-17 | Allergan, Inc. | Methods and compositions for the treatment of pain and other alpha 2 adrenergic-mediated conditions |
CA2593788A1 (en) * | 2005-01-28 | 2006-08-10 | Merck And Co., Inc. | Antidiabetic bicyclic compounds |
BRPI0615307A2 (pt) * | 2005-08-25 | 2009-08-04 | Schering Corp | agonistas de adrenorreceptor alfa2c |
JP2009524619A (ja) * | 2006-01-27 | 2009-07-02 | エフ.ホフマン−ラ ロシュ アーゲー | Cns障害の処置のための2−イミダゾールの使用 |
EP2076496B1 (en) * | 2006-10-19 | 2010-03-31 | F. Hoffmann-Roche AG | Aminomethyl-2-imidazoles with affinity with the trace amine associated receptors |
CA2666762C (en) * | 2006-10-19 | 2014-12-30 | F. Hoffmann-La Roche Ag | Aminomethyl-4-imidazoles |
JP5064511B2 (ja) | 2006-11-02 | 2012-10-31 | エフ.ホフマン−ラ ロシュ アーゲー | 痕跡アミン関連受容体調節剤としての置換2−イミダゾール |
RU2456281C2 (ru) * | 2006-11-16 | 2012-07-20 | Ф. Хоффманн-Ля Рош Аг | Замещенные 4-имидазолы, способ их получения и их применение |
AU2007332641A1 (en) * | 2006-12-13 | 2008-06-19 | F. Hoffmann-La Roche Ag | Novel 2 -imidazoles as ligands for trace amine associated receptors (TAAR) |
US20080146523A1 (en) * | 2006-12-18 | 2008-06-19 | Guido Galley | Imidazole derivatives |
US8119807B2 (en) | 2007-01-12 | 2012-02-21 | Allergan, Inc. | Quinolynylmethylimidizoles as therapeutic agents |
US8013169B2 (en) | 2007-01-12 | 2011-09-06 | Allergan, Inc | Naphthylmethylimidizoles as therapeutic agents |
WO2008088936A1 (en) | 2007-01-12 | 2008-07-24 | Allergan, Inc. | Quinolynylmethylimidizoles as therapeutic agents |
RU2473545C2 (ru) * | 2007-02-02 | 2013-01-27 | Ф.Хоффманн-Ля Рош Аг | Новые 2-аминооксазолины в качестве лигандов taar1 для заболеваний цнс |
KR101335845B1 (ko) * | 2007-02-15 | 2013-12-02 | 에프. 호프만-라 로슈 아게 | Taar1 리간드로서의 2-아미노옥사졸린 |
BRPI0812840A2 (pt) | 2007-07-02 | 2014-12-09 | Hoffmann La Roche | 2-imidazolinas |
JP2010531836A (ja) * | 2007-07-03 | 2010-09-30 | エフ.ホフマン−ラ ロシュ アーゲー | 4−イミダゾリン及びそれらの抗うつ剤としての使用 |
KR101133862B1 (ko) * | 2007-07-27 | 2012-04-06 | 에프. 호프만-라 로슈 아게 | Taar 리간드로서의 2-아제티딘메테인아민 및 2-피롤리딘메테인아민 |
CA2695071A1 (en) * | 2007-08-02 | 2009-02-05 | F. Hoffmann-La Roche Ag | The use of benzamide derivatives for the treatment of cns disorders |
WO2009019149A1 (en) * | 2007-08-03 | 2009-02-12 | F. Hoffmann-La Roche Ag | Pyridinecarboxamide and benzamide derivatives as taar1 ligands |
RU2491284C2 (ru) * | 2007-08-15 | 2013-08-27 | Аллерган, Инк. | Адренергические соединения |
US20090286829A1 (en) * | 2008-05-13 | 2009-11-19 | Allergan, Inc. | Quinolynylmethylimidizoles as therapeutic agents |
US8242153B2 (en) * | 2008-07-24 | 2012-08-14 | Hoffmann-La Roche Inc. | 4,5-dihydro-oxazol-2YL derivatives |
PE20110215A1 (es) * | 2008-07-24 | 2011-03-31 | Hoffmann La Roche | Derivados de 4,5-dihidro-oxazol-2-ilo |
AU2010210513A1 (en) * | 2009-02-06 | 2011-09-01 | Allergan, Inc. | Pyridine compounds as subtype selective modulators of alpha2B and/or alpha 2C adrenergic receptors |
US20100311798A1 (en) * | 2009-06-05 | 2010-12-09 | Decoret Guillaume | 2-aminooxazolines as taar1 ligands |
US8354441B2 (en) * | 2009-11-11 | 2013-01-15 | Hoffmann-La Roche Inc. | Oxazoline derivatives |
US9452980B2 (en) | 2009-12-22 | 2016-09-27 | Hoffmann-La Roche Inc. | Substituted benzamides |
JP6052685B2 (ja) | 2011-07-25 | 2016-12-27 | アラーガン、インコーポレイテッドAllergan,Incorporated | α2アドレナリン受容体の調節因子としてのN−(イミダゾリジン−2−イリデン)−ヘテロシクロペンタ[b]ピリジン誘導体 |
CN104507913B (zh) | 2012-07-13 | 2017-07-28 | 霍夫曼-拉罗奇有限公司 | 抗增殖的苯并[b]氮杂*‑2‑酮 |
MY195528A (en) | 2016-03-17 | 2023-01-30 | Hoffmann La Roche | 5-Ethyl-4-Methyl-Pyrazole-3-Carboxamide Derivative Having Activity as Agonist of Taar |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3288805A (en) * | 1966-11-29 | Amino-eviid azoline | ||
US3636219A (en) * | 1964-03-02 | 1972-01-18 | Du Pont | Anticholinergic compositions containing certain thiazolines or imidazolines |
CH632268A5 (de) * | 1977-01-14 | 1982-09-30 | Sandoz Ag | Verfahren zur herstellung von neuen heterocyclylaminoderivaten. |
NL7711390A (nl) * | 1977-10-18 | 1979-04-20 | Philips Nv | Nieuwe 2-arylimino-hexahydopyrimidinen en - imi- dazolidinen, zouten en complexen daarvan, werk- wijze ter bereiding van de nieuwe verbindingen, alsmede fungicide preparaten op basis van de nieuwe verbindingen. |
GB2206880B (en) * | 1987-07-16 | 1991-04-24 | Farmos Oy | Optical isomers of an imidazole derivative |
GB8827822D0 (en) * | 1988-11-29 | 1988-12-29 | Janssen Pharmaceutica Nv | (1h-azol-1-ylmethyl)substituted quinoline derivatives |
JPH06507392A (ja) * | 1991-02-26 | 1994-08-25 | エイアールシー 1,インコーポレイテッド | 交感神経性の持続性疼痛の治療のための組成物および方法 |
US5663189A (en) * | 1993-07-01 | 1997-09-02 | The Procter & Gamble Company | 2-imidazolinylamino heterocyclic compounds useful as alpha-2 adrenoceptor agonists |
US5389638A (en) * | 1993-09-10 | 1995-02-14 | Abbott Laboratories | Tetrahydroisoquinolines as alpha-2 antagonists and biogenic amine uptake inhibitors |
CA2181909C (en) * | 1994-01-24 | 2008-10-07 | Stephen A. Munk | Aromatic 2-amino-imidazole derivatives as alpha-2a adrenoceptor agonists |
US5684031A (en) * | 1996-02-01 | 1997-11-04 | The Procter & Gamble Company | Dihydrobenzofuran and related compounds useful as anti-inflammatory agents |
JP2001506981A (ja) * | 1996-11-25 | 2001-05-29 | ザ プロクター アンド ギャンブル カンパニー | α―2アドレナリン受容体作動薬として有用な2―イミダゾリニルアミノインドール化合物 |
-
1997
- 1997-04-11 US US08/834,658 patent/US5866579A/en not_active Expired - Fee Related
-
1998
- 1998-04-10 AU AU69705/98A patent/AU6970598A/en not_active Abandoned
- 1998-04-10 WO PCT/US1998/007453 patent/WO1998046572A1/en active IP Right Grant
- 1998-04-10 DE DE69830576T patent/DE69830576T2/de not_active Expired - Fee Related
- 1998-04-10 SI SI9830790T patent/SI0975602T1/sl unknown
- 1998-04-10 EP EP98915550A patent/EP0975602B1/en not_active Expired - Lifetime
- 1998-04-10 PT PT98915550T patent/PT975602E/pt unknown
- 1998-04-10 DK DK98915550T patent/DK0975602T3/da active
- 1998-04-10 ES ES98915550T patent/ES2245029T3/es not_active Expired - Lifetime
- 1998-04-10 AT AT98915550T patent/ATE297899T1/de not_active IP Right Cessation
- 1998-10-20 US US09/175,253 patent/US6093727A/en not_active Expired - Fee Related
-
1999
- 1999-09-20 US US09/398,861 patent/US6294566B1/en not_active Expired - Fee Related
-
2000
- 2000-08-02 HK HK00104824A patent/HK1026892A1/xx not_active IP Right Cessation
-
2001
- 2001-08-20 US US09/933,106 patent/US6777426B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US20020019390A1 (en) | 2002-02-14 |
US6777426B2 (en) | 2004-08-17 |
ES2245029T3 (es) | 2005-12-16 |
US6093727A (en) | 2000-07-25 |
WO1998046572A1 (en) | 1998-10-22 |
US5866579A (en) | 1999-02-02 |
EP0975602A1 (en) | 2000-02-02 |
DE69830576D1 (de) | 2005-07-21 |
AU6970598A (en) | 1998-11-11 |
EP0975602B1 (en) | 2005-06-15 |
EP0975602A4 (en) | 2003-01-22 |
DE69830576T2 (de) | 2006-05-04 |
HK1026892A1 (en) | 2000-12-29 |
SI0975602T1 (sl) | 2005-12-31 |
ATE297899T1 (de) | 2005-07-15 |
US6294566B1 (en) | 2001-09-25 |
PT975602E (pt) | 2005-10-31 |
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