DE602005027307D1 - Arylanilinderivate als agonisten des beta2-adrenergen rezeptors - Google Patents
Arylanilinderivate als agonisten des beta2-adrenergen rezeptorsInfo
- Publication number
- DE602005027307D1 DE602005027307D1 DE602005027307T DE602005027307T DE602005027307D1 DE 602005027307 D1 DE602005027307 D1 DE 602005027307D1 DE 602005027307 T DE602005027307 T DE 602005027307T DE 602005027307 T DE602005027307 T DE 602005027307T DE 602005027307 D1 DE602005027307 D1 DE 602005027307D1
- Authority
- DE
- Germany
- Prior art keywords
- adreneer
- arylaniline
- beta2
- agonists
- receptor
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/56—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups
- C07C215/58—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
- C07C215/60—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain the chain having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53578404P | 2004-01-12 | 2004-01-12 | |
PCT/US2005/000810 WO2005070872A1 (en) | 2004-01-12 | 2005-01-11 | Aryl aniline derivatives as beta2 adrenergic receptor agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
DE602005027307D1 true DE602005027307D1 (de) | 2011-05-19 |
Family
ID=34806964
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE602005027307T Active DE602005027307D1 (de) | 2004-01-12 | 2005-01-11 | Arylanilinderivate als agonisten des beta2-adrenergen rezeptors |
Country Status (19)
Country | Link |
---|---|
US (3) | US7622467B2 (de) |
EP (1) | EP1706371B1 (de) |
JP (1) | JP5041814B2 (de) |
CN (1) | CN1910137B (de) |
AR (1) | AR047098A1 (de) |
AT (1) | ATE504559T1 (de) |
AU (1) | AU2005206510A1 (de) |
BR (1) | BRPI0506823A (de) |
CA (1) | CA2551821A1 (de) |
DE (1) | DE602005027307D1 (de) |
ES (1) | ES2364450T3 (de) |
IL (1) | IL176549A0 (de) |
MA (1) | MA28304A1 (de) |
NO (1) | NO20063620L (de) |
NZ (1) | NZ548196A (de) |
RU (1) | RU2370490C2 (de) |
TW (1) | TW200531692A (de) |
WO (1) | WO2005070872A1 (de) |
ZA (1) | ZA200605720B (de) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6200134B1 (en) | 1998-01-20 | 2001-03-13 | Kerr Corporation | Apparatus and method for curing materials with radiation |
TWI249515B (en) * | 2001-11-13 | 2006-02-21 | Theravance Inc | Aryl aniline beta2 adrenergic receptor agonists |
US7182597B2 (en) | 2002-08-08 | 2007-02-27 | Kerr Corporation | Curing light instrument |
TW200526547A (en) * | 2003-09-22 | 2005-08-16 | Theravance Inc | Amino-substituted ethylamino β2 adrenergic receptor agonists |
CN1984876A (zh) * | 2004-06-03 | 2007-06-20 | 施万制药 | 二胺类β2肾上腺素能受体激动剂 |
EP1778638A1 (de) * | 2004-07-21 | 2007-05-02 | Theravance, Inc. | Adrenergische diaryl ether beta2-rezeptoragonisten |
JP2008512470A (ja) * | 2004-09-10 | 2008-04-24 | セラヴァンス, インコーポレーテッド | アミジン置換アリールアニリン化合物 |
GB0424284D0 (en) | 2004-11-02 | 2004-12-01 | Novartis Ag | Organic compounds |
BRPI0606712A2 (pt) * | 2005-01-11 | 2010-03-16 | Glaxo Group Ltd | sal do composto, formulação farmacêutica, combinação, uso de um composto, e, método para preparar um composto cristalino |
ES2265276B1 (es) * | 2005-05-20 | 2008-02-01 | Laboratorios Almirall S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico. |
US8113830B2 (en) | 2005-05-27 | 2012-02-14 | Kerr Corporation | Curing light instrument |
EP2281813A1 (de) | 2005-08-08 | 2011-02-09 | Pulmagen Therapeutics (Synergy) Limited | Bicyclo[2.2.1]Hept-7-Ylamin Derivate und deren Verwendung |
GB0516313D0 (en) | 2005-08-08 | 2005-09-14 | Argenta Discovery Ltd | Azole derivatives and their uses |
TW200738658A (en) | 2005-08-09 | 2007-10-16 | Astrazeneca Ab | Novel compounds |
GB0601951D0 (en) | 2006-01-31 | 2006-03-15 | Novartis Ag | Organic compounds |
TW200745067A (en) * | 2006-03-14 | 2007-12-16 | Astrazeneca Ab | Novel compounds |
EP2322525B1 (de) | 2006-04-21 | 2013-09-18 | Novartis AG | Purinderivate als Adenosin A2A Rezeptoragonisten |
TW200833670A (en) | 2006-12-20 | 2008-08-16 | Astrazeneca Ab | Novel compounds 569 |
GB0702458D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | Salts 668 |
ES2306595B1 (es) * | 2007-02-09 | 2009-09-11 | Laboratorios Almirall S.A. | Sal de napadisilato de 5-(2-((6-(2,2-difluoro-2-feniletoxi)hexil)amino)-1-hidroxietil)-8-hidroxiquinolin-2(1h)-ona como agonista del receptor adrenergico beta2. |
ES2320961B1 (es) * | 2007-11-28 | 2010-03-17 | Laboratorios Almirall, S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor adrenergico beta2. |
EP2096105A1 (de) * | 2008-02-28 | 2009-09-02 | Laboratorios Almirall, S.A. | 4-(2-Amino-1-hydroxyethyl)Phenol-Derivate als Agonisten des b2-adrenergen Rezeptors |
TW201002696A (en) | 2008-06-18 | 2010-01-16 | Astrazeneca Ab | Novel compounds 409 |
US8236786B2 (en) * | 2008-08-07 | 2012-08-07 | Pulmagen Therapeutics (Inflammation) Limited | Respiratory disease treatment |
UY32297A (es) | 2008-12-22 | 2010-05-31 | Almirall Sa | Sal mesilato de 5-(2-{[6-(2,2-difluoro-2-fenilitoxi) hexil]amino}-1-hidroxietil)-8-hidroxiquinolin-2( 1h)-ona como agonista del receptor b(beta)2 acrenérgico |
CA2748331C (en) | 2008-12-30 | 2016-08-02 | Pulmagen Therapeutics (Inflammation) Limited | Sulfonamide compounds for the treatment of respiratory disorders |
EP2228368A1 (de) | 2009-03-12 | 2010-09-15 | Almirall, S.A. | Verfahren zur Herstellung von 5-(2-{[6-(2,2-Difluor-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxychinolin-2(1H)-on |
WO2010150014A1 (en) | 2009-06-24 | 2010-12-29 | Pulmagen Therapeutics (Inflammation) Limited | 5r- 5 -deuterated glitazones for respiratory disease treatment |
GB0913342D0 (en) | 2009-07-31 | 2009-09-16 | Astrazeneca Ab | Compounds - 801 |
WO2011048409A1 (en) | 2009-10-20 | 2011-04-28 | Astrazeneca Ab | Cyclic amine derivatives having beta2 adrenergic receptor agonist and muscarinic receptor antagonist activity |
GB0918922D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminopyridine derivatives |
GB0918923D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Aminothiazole derivatives |
GB0918924D0 (en) | 2009-10-28 | 2009-12-16 | Vantia Ltd | Azaindole derivatives |
GB201002243D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
GB201002224D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
GB201009801D0 (en) | 2010-06-11 | 2010-07-21 | Astrazeneca Ab | Compounds 950 |
GEP20156285B (en) | 2011-02-25 | 2015-05-11 | Aierem Elelsi | Compounds and compositions as trk inhibitors |
EP2578570A1 (de) | 2011-10-07 | 2013-04-10 | Almirall, S.A. | Neues Verfahren zur Herstellung von 5-(2-{[6-(2,2-Difluor-2-phenylethoxy)hexyl]amino}-1(R)-hydroxyethyl)-8-hydroxychinolin-2(1H)-on mittels neuen Synthesezwischenstoffen |
EP2641900A1 (de) | 2012-03-20 | 2013-09-25 | Almirall, S.A. | Neuartige polymorphe Kristallformen von 5-(2-{[6-(2,2-difluor-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxychinolin-2(1H)-on, Heminapadisylat als Agonist des beta2-adrenergen Rezeptors |
Family Cites Families (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE630296A (de) | 1962-03-31 | |||
AT310146B (de) | 1971-04-26 | 1973-09-25 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung von neuen N,N'-Bis-(β-hydroxyaryläthyl)-diaminoalkanen und deren Säureadditionssalzen |
CH545764A (de) | 1971-07-27 | 1974-02-15 | ||
BE794414A (fr) | 1972-01-25 | 1973-07-23 | Sandoz Sa | Nouveaux amino-alcools, leur preparation et leur application comme medicament |
FR2266497B1 (de) | 1974-04-03 | 1977-11-04 | Roussel Uclaf | |
JPS5913510B2 (ja) | 1975-12-26 | 1984-03-30 | オオツカセイヤク カブシキガイシヤ | カルボスチリルユウドウタイノセイゾウホウ |
JPS5283619A (en) | 1976-01-01 | 1977-07-12 | Yamanouchi Pharmaceut Co Ltd | Alpha-substituted aminomethyl benzyl alcohol derivative |
JPS609713B2 (ja) | 1976-10-08 | 1985-03-12 | 大塚製薬株式会社 | カルボスチリル誘導体 |
ZW6584A1 (en) | 1983-04-18 | 1985-04-17 | Glaxo Group Ltd | Phenethanolamine derivatives |
GB8334494D0 (en) | 1983-12-24 | 1984-02-01 | Tanabe Seiyaku Co | Carbostyril derivatives |
GB8507942D0 (en) | 1985-03-27 | 1985-05-01 | Beecham Group Plc | Compounds |
DK9987A (da) | 1986-01-11 | 1987-07-12 | Beecham Group Plc | Ethanolaminderivater |
US5223614A (en) | 1987-12-19 | 1993-06-29 | Boehringer Ingelheim Gmbh | New quaternary ammonium compounds, their preparation and use |
US4894219A (en) | 1988-03-29 | 1990-01-16 | University Of Florida | Beta-agonist carbostyril derivatives, assay method and pharmacological composition |
US5434304A (en) | 1990-09-26 | 1995-07-18 | Aktiebolaget Astra | Process for preparing formoterol and related compounds |
GB9405019D0 (en) | 1994-03-15 | 1994-04-27 | Smithkline Beecham Plc | Novel compounds |
US6075040A (en) | 1996-09-05 | 2000-06-13 | Eli Lilly And Company | Selective β3 adrenergic agonists |
US6040344A (en) | 1996-11-11 | 2000-03-21 | Sepracor Inc. | Formoterol process |
GB9713819D0 (en) | 1997-06-30 | 1997-09-03 | Glaxo Group Ltd | Method of reducing the systemic effects of compounds |
US6362371B1 (en) | 1998-06-08 | 2002-03-26 | Advanced Medicine, Inc. | β2- adrenergic receptor agonists |
US6713651B1 (en) | 1999-06-07 | 2004-03-30 | Theravance, Inc. | β2-adrenergic receptor agonists |
US20020143034A1 (en) | 1998-12-30 | 2002-10-03 | Fujisawa Pharmaceutical Co. Ltd. | Aminoalcohol derivatives and their use as beta 3 adrenergic agonists |
GB9913083D0 (en) | 1999-06-04 | 1999-08-04 | Novartis Ag | Organic compounds |
WO2001007026A2 (en) | 1999-07-22 | 2001-02-01 | Eli Lilly And Company | Improved method of treating type ii diabetes and obesity |
UA73965C2 (en) | 1999-12-08 | 2005-10-17 | Theravance Inc | b2 ADRENERGIC RECEPTOR ANTAGONISTS |
OA11558A (en) | 1999-12-08 | 2004-06-03 | Advanced Medicine Inc | Beta 2-adrenergic receptor agonists. |
CA2405745A1 (en) | 2000-04-27 | 2001-11-08 | Boehringer Ingelheim Pharma Kg | New betamimetics having a long-lasting activity, processes for preparingthem and their use as medicaments |
AUPQ841300A0 (en) | 2000-06-27 | 2000-07-20 | Fujisawa Pharmaceutical Co., Ltd. | New aminoalcohol derivatives |
US6759398B2 (en) | 2000-08-05 | 2004-07-06 | Smithkline Beecham Corporation | Anti-inflammatory androstane derivative |
EP1341759B1 (de) | 2000-11-10 | 2006-06-14 | Eli Lilly And Company | 3-substituierte oxindolderivate als beta-3-agonisten |
GB0103630D0 (en) | 2001-02-14 | 2001-03-28 | Glaxo Group Ltd | Chemical compounds |
US7144908B2 (en) | 2001-03-08 | 2006-12-05 | Glaxo Group Limited | Agonists of beta-adrenoceptors |
ATE381537T1 (de) | 2001-03-22 | 2008-01-15 | Glaxo Group Ltd | Formanilid-derivative als beta2-adrenorezeptor- agonisten |
PT1425001E (pt) | 2001-09-14 | 2009-02-18 | Glaxo Group Ltd | Derivados de fenetanolamina para o tratamento de doenças respiratórias |
US6653323B2 (en) * | 2001-11-13 | 2003-11-25 | Theravance, Inc. | Aryl aniline β2 adrenergic receptor agonists |
US20030229058A1 (en) | 2001-11-13 | 2003-12-11 | Moran Edmund J. | Aryl aniline beta2 adrenergic receptor agonists |
TWI249515B (en) | 2001-11-13 | 2006-02-21 | Theravance Inc | Aryl aniline beta2 adrenergic receptor agonists |
GB0204719D0 (en) | 2002-02-28 | 2002-04-17 | Glaxo Group Ltd | Medicinal compounds |
JP2005523920A (ja) | 2002-04-25 | 2005-08-11 | グラクソ グループ リミテッド | フェネタノールアミン誘導体 |
JP2005527618A (ja) | 2002-05-28 | 2005-09-15 | セラヴァンス インコーポレーテッド | アルコキシアリールβ2アドレナリン作動性レセプターアゴニスト |
PL375195A1 (en) | 2002-06-27 | 2005-11-28 | Astellas Pharma Inc. | Aminoalcohol derivatives |
GB0217225D0 (en) | 2002-07-25 | 2002-09-04 | Glaxo Group Ltd | Medicinal compounds |
TW200409746A (en) | 2002-07-26 | 2004-06-16 | Theravance Inc | Crystalline β2 adrenergic receptor agonist |
PE20040950A1 (es) | 2003-02-14 | 2005-01-01 | Theravance Inc | DERIVADOS DE BIFENILO COMO AGONISTAS DE LOS RECEPTORES ADRENERGICOS ß2 Y COMO ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS |
US7317102B2 (en) | 2003-04-01 | 2008-01-08 | Theravance, Inc. | Diarylmethyl and related compounds |
EP1622875B1 (de) | 2003-05-08 | 2009-12-02 | Theravance, Inc. | Kristalline formen eines arylanilin-beta-2-adrenergenrezeptor-agonists |
US7556785B2 (en) * | 2003-05-12 | 2009-07-07 | United Phosphorus, Ltd. | Apparatus and method for rapid and continuous generation of phosphine gas |
TW200510277A (en) | 2003-05-27 | 2005-03-16 | Theravance Inc | Crystalline form of β2-adrenergic receptor agonist |
TW200526547A (en) | 2003-09-22 | 2005-08-16 | Theravance Inc | Amino-substituted ethylamino β2 adrenergic receptor agonists |
CN1984876A (zh) | 2004-06-03 | 2007-06-20 | 施万制药 | 二胺类β2肾上腺素能受体激动剂 |
EP1778638A1 (de) | 2004-07-21 | 2007-05-02 | Theravance, Inc. | Adrenergische diaryl ether beta2-rezeptoragonisten |
JP2008512470A (ja) | 2004-09-10 | 2008-04-24 | セラヴァンス, インコーポレーテッド | アミジン置換アリールアニリン化合物 |
-
2004
- 2004-12-30 TW TW093141433A patent/TW200531692A/zh unknown
-
2005
- 2005-01-11 NZ NZ548196A patent/NZ548196A/xx unknown
- 2005-01-11 AU AU2005206510A patent/AU2005206510A1/en not_active Abandoned
- 2005-01-11 DE DE602005027307T patent/DE602005027307D1/de active Active
- 2005-01-11 US US11/033,198 patent/US7622467B2/en active Active
- 2005-01-11 CA CA002551821A patent/CA2551821A1/en not_active Abandoned
- 2005-01-11 EP EP05711348A patent/EP1706371B1/de active Active
- 2005-01-11 WO PCT/US2005/000810 patent/WO2005070872A1/en active Application Filing
- 2005-01-11 CN CN2005800022796A patent/CN1910137B/zh not_active Expired - Fee Related
- 2005-01-11 JP JP2006549523A patent/JP5041814B2/ja not_active Expired - Fee Related
- 2005-01-11 AR ARP050100092A patent/AR047098A1/es unknown
- 2005-01-11 BR BRPI0506823-1A patent/BRPI0506823A/pt not_active IP Right Cessation
- 2005-01-11 AT AT05711348T patent/ATE504559T1/de not_active IP Right Cessation
- 2005-01-11 ES ES05711348T patent/ES2364450T3/es active Active
- 2005-01-11 RU RU2006129312/04A patent/RU2370490C2/ru not_active IP Right Cessation
-
2006
- 2006-06-26 IL IL176549A patent/IL176549A0/en unknown
- 2006-07-11 ZA ZA200605720A patent/ZA200605720B/xx unknown
- 2006-07-24 MA MA29204A patent/MA28304A1/fr unknown
- 2006-08-09 NO NO20063620A patent/NO20063620L/no not_active Application Discontinuation
-
2009
- 2009-10-06 US US12/574,066 patent/US7994165B2/en not_active Expired - Fee Related
-
2011
- 2011-06-28 US US13/170,386 patent/US20120071654A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20100087410A1 (en) | 2010-04-08 |
BRPI0506823A (pt) | 2007-05-29 |
TW200531692A (en) | 2005-10-01 |
CN1910137A (zh) | 2007-02-07 |
KR20070000466A (ko) | 2007-01-02 |
US7622467B2 (en) | 2009-11-24 |
JP5041814B2 (ja) | 2012-10-03 |
IL176549A0 (en) | 2006-10-31 |
NO20063620L (no) | 2006-10-06 |
ZA200605720B (en) | 2008-09-25 |
US20120071654A1 (en) | 2012-03-22 |
ATE504559T1 (de) | 2011-04-15 |
JP2007518738A (ja) | 2007-07-12 |
AR047098A1 (es) | 2006-01-04 |
NZ548196A (en) | 2009-08-28 |
RU2006129312A (ru) | 2008-02-20 |
US7994165B2 (en) | 2011-08-09 |
RU2370490C2 (ru) | 2009-10-20 |
EP1706371B1 (de) | 2011-04-06 |
WO2005070872A1 (en) | 2005-08-04 |
US20050159448A1 (en) | 2005-07-21 |
AU2005206510A1 (en) | 2005-08-04 |
CA2551821A1 (en) | 2005-08-04 |
MA28304A1 (fr) | 2006-11-01 |
CN1910137B (zh) | 2010-05-26 |
EP1706371A1 (de) | 2006-10-04 |
ES2364450T3 (es) | 2011-09-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE602005027307D1 (de) | Arylanilinderivate als agonisten des beta2-adrenergen rezeptors | |
ATE451364T1 (de) | Als modulatoren des dopamin-d3-rezeptors geeignete azabicycloä3.1.0ühexanderivate | |
ATE421511T1 (de) | Indol-3-carbonyl-spiro-piperidinderivate als antagonisten des v1a-rezeptors | |
DE602006015607D1 (de) | Thiazol-4-carboxamid-derivate als mglur5-antagonisten | |
DK1735304T3 (da) | Quinolinoncarboxamidforbindelser som 5-HT4-receptoragonister | |
ATE517883T1 (de) | Imidazolderivate als funktionelle selektive agonisten des alpha2c-adrenorezeptors | |
DE602006019624D1 (de) | Piperidin-4-yl-pyridazin-3-yl-aminderivate als schnell dissoziierende antagonisten des dopamin-2-rezeptors | |
ATE400271T1 (de) | Aryl-pyridinderivate als 11-beta-hsd1-hemmer | |
DE602007014374D1 (de) | Ä4,5'ü-bipyrimidinyl-6,4'-diaminderivate als proteinkinase-hemmer | |
ATE420076T1 (de) | Indozolonderivate als 11b-hsd1-inhibitoren | |
DE602006003628D1 (de) | Purinderivate als a2a-rezeptoragonisten | |
ATE497953T1 (de) | Thiazolderivate als modulatoren des cannabinoidrezeptors | |
ATE518834T1 (de) | 2,3,4,9-tetrahydro-1h-carbazol-derivative als crth2-rezeptorantagonisten | |
NL2000241A1 (nl) | Carboxamidederivaten als muscarine-receptorantagonisten. | |
ATE549350T1 (de) | Neuropeptid-2-rezeptor-agonisten | |
ATE481405T1 (de) | Thiazolpyrazolopyrimidine als antagonisten des crf1-rezeptors | |
DE602005015204D1 (de) | Oxadiazolonderivate als ppar-delta-agonisten | |
ATE429428T1 (de) | Indanderivate als antagonisten des mch-rezeptors | |
DK1899324T3 (da) | Benzimidazolcarboxamid-forbindelser som 5-HT4-receptoragonister | |
DE602004014772D1 (de) | Pyrrol-2,5-dithionderivate als modulatoren des liver-x-rezeptors | |
ATE459618T1 (de) | 3-piperidinylisochroman-5-ole als dopaminagonisten | |
DE112005002826A5 (de) | Ausgleichseinheit | |
ATE512137T1 (de) | Benzoylpiperidinderivate als doppelmodulatoren des 5-ht2a- und des d3-rezeptors | |
DE602006005242D1 (de) | Pyrazolopyridinderivate als inhibitoren der kinase 1 des beta-adrenergen rezeptors | |
DE602006008002D1 (de) | Benzofuranylderivate als 5-ht6-rezeptorinhibitoren |