JP2006506414A5 - - Google Patents
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- Publication number
- JP2006506414A5 JP2006506414A5 JP2004549780A JP2004549780A JP2006506414A5 JP 2006506414 A5 JP2006506414 A5 JP 2006506414A5 JP 2004549780 A JP2004549780 A JP 2004549780A JP 2004549780 A JP2004549780 A JP 2004549780A JP 2006506414 A5 JP2006506414 A5 JP 2006506414A5
- Authority
- JP
- Japan
- Prior art keywords
- inflammatory
- combination
- inhibitor
- inflammation
- compounds
- 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.)
- Withdrawn
Links
- 150000001875 compounds Chemical class 0.000 description 7
- 206010061218 Inflammation Diseases 0.000 description 4
- 230000004054 inflammatory process Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 208000027866 inflammatory disease Diseases 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 2
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 2
- 229940111134 coxibs Drugs 0.000 description 2
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- KAVIOGXCVVZYEM-SMDDNHRTSA-N (4s)-4-[(2r)-2-[2-chloro-5-(trifluoromethyl)phenyl]sulfanyl-2-(1,3-thiazol-5-yl)ethyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylic acid Chemical compound OC(=O)N1C(C)(C)OC[C@@H]1C[C@H](C=1SC=NC=1)SC1=CC(C(F)(F)F)=CC=C1Cl KAVIOGXCVVZYEM-SMDDNHRTSA-N 0.000 description 1
- -1 4-chloro-3-fluorobenzoyl triflate Chemical compound 0.000 description 1
- 229940122204 Cyclooxygenase inhibitor Drugs 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102000008299 Nitric Oxide Synthase Human genes 0.000 description 1
- 108010021487 Nitric Oxide Synthase Proteins 0.000 description 1
- 102000001708 Protein Isoforms Human genes 0.000 description 1
- 108010029485 Protein Isoforms Proteins 0.000 description 1
- 229940124639 Selective inhibitor Drugs 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000004968 inflammatory condition Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002599 prostaglandin synthase inhibitor Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0203304A SE0203304D0 (sv) | 2002-11-07 | 2002-11-07 | Novel Coumpounds |
| PCT/SE2003/001712 WO2004041794A1 (en) | 2002-11-07 | 2003-11-06 | Antiinflammatory 3-arylthio-3-thiazolyl-alkylamines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006506414A JP2006506414A (ja) | 2006-02-23 |
| JP2006506414A5 true JP2006506414A5 (enExample) | 2006-12-21 |
Family
ID=20289508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004549780A Withdrawn JP2006506414A (ja) | 2002-11-07 | 2003-11-06 | 抗炎症性３−アリールチオ−３−チアゾリル−アルキルアミン |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20060040992A1 (enExample) |
| EP (1) | EP1562920B1 (enExample) |
| JP (1) | JP2006506414A (enExample) |
| AT (1) | ATE331711T1 (enExample) |
| AU (1) | AU2003278667A1 (enExample) |
| DE (1) | DE60306546T2 (enExample) |
| ES (1) | ES2268441T3 (enExample) |
| SE (1) | SE0203304D0 (enExample) |
| WO (1) | WO2004041794A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR035700A1 (es) * | 2001-05-08 | 2004-06-23 | Astrazeneca Ab | Derivados de arilheteroalquilamina, composicion farmaceutica, usos de estos derivados para la fabricacion de medicamentos, metodos de tratamiento, y proceso para la preparacion de estos derivados |
| CN104069112A (zh) | 2007-10-19 | 2014-10-01 | 贝林格尔.英格海姆国际有限公司 | 取代的哌啶子基-二氢噻吩并嘧啶 |
| DK2379525T3 (en) | 2008-12-19 | 2015-10-19 | Boehringer Ingelheim Int | Cyclic pyrimidin-4-carboxamides, as CCR2 receptor antagonists for the treatment of inflammation, asthma and COPD |
| WO2011073154A1 (en) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | New ccr2 receptor antagonists and uses thereof |
| WO2011073155A1 (en) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Novel antagonists for ccr2 and uses thereof |
| CN102822172A (zh) | 2010-01-29 | 2012-12-12 | 贝林格尔.英格海姆国际有限公司 | 取代的二氮杂萘及其作为syk 激酶抑制剂的用途 |
| EP2569295B1 (en) | 2010-05-12 | 2014-11-19 | Boehringer Ingelheim International GmbH | New ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| US8877745B2 (en) | 2010-05-12 | 2014-11-04 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| US8841313B2 (en) | 2010-05-17 | 2014-09-23 | Boehringer Ingelheim International Gmbh | CCR2 antagonists and uses thereof |
| US9018212B2 (en) | 2010-05-25 | 2015-04-28 | Boehringer Ingelheim International Gmbh | Pyridazine carboxamides as CCR2 receptor antagonists |
| EP2576538B1 (en) | 2010-06-01 | 2015-10-28 | Boehringer Ingelheim International GmbH | New CCR2 antagonists |
| JP5959537B2 (ja) | 2011-01-28 | 2016-08-02 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 置換ピリジニル−ピリミジン及び医薬としてのその使用 |
| WO2012171863A1 (en) | 2011-06-16 | 2012-12-20 | Boehringer Ingelheim International Gmbh | New selective ccr2 antagonists |
| JP5786258B2 (ja) | 2011-07-15 | 2015-09-30 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規かつ選択的なｃｃｒ２拮抗薬 |
| CA2843022C (en) | 2011-07-26 | 2019-09-24 | Boehringer Ingelheim International Gmbh | Substituted quinolines and their use as medicaments |
| US20130059866A1 (en) | 2011-08-24 | 2013-03-07 | Boehringer Ingelheim International Gmbh | Novel piperidino-dihydrothienopyrimidine sulfoxides and their use for treating copd and asthma |
| US9096579B2 (en) | 2012-04-20 | 2015-08-04 | Boehringer Ingelheim International Gmbh | Amino-indolyl-substituted imidazolyl-pyrimidines and their use as medicaments |
| CA2942997C (en) | 2014-03-19 | 2022-09-13 | Boehringer Ingelheim International Gmbh | Heteroaryl syk inhibitors |
| GB201512635D0 (en) | 2015-07-17 | 2015-08-26 | Ucl Business Plc | Uses of therapeutic compounds |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2688638A (en) * | 1951-07-17 | 1954-09-07 | Givaudan Corp | Nu-(beta-phenoxyethyl) haloethylamines |
| US4314081A (en) * | 1974-01-10 | 1982-02-02 | Eli Lilly And Company | Arloxyphenylpropylamines |
| FR2432500A1 (fr) * | 1978-02-24 | 1980-02-29 | Roussel Uclaf | Nouveaux derives de la benzene propanamine et leurs sels, procede de preparation et application a titre de medicaments |
| US4325953A (en) * | 1979-09-14 | 1982-04-20 | John Wyeth And Brother Limited | 4-Aryl-4-aryloxypiperidines |
| DE3138550A1 (de) * | 1981-09-28 | 1983-04-07 | Boehringer Ingelheim KG, 6507 Ingelheim | Substituierte 2-phenyl-2-(pyridyloxy)-ethylamine und isostere verbindungen, verfahren zu ihrer herstellung und verwendung |
| DE3328348A1 (de) * | 1983-08-05 | 1985-02-14 | Degussa Ag, 6000 Frankfurt | Verfahren zur duennschichtchromatographischen trennung von enantiomeren |
| US4902710A (en) * | 1988-12-14 | 1990-02-20 | Eli Lilly And Company | Serotonin and norepinephrine uptake inhibitors |
| GB0004151D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
| GB0004149D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel compounds |
| GB0004152D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel compounds |
| GB0004153D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
| AR035700A1 (es) * | 2001-05-08 | 2004-06-23 | Astrazeneca Ab | Derivados de arilheteroalquilamina, composicion farmaceutica, usos de estos derivados para la fabricacion de medicamentos, metodos de tratamiento, y proceso para la preparacion de estos derivados |
| SE0102640D0 (sv) * | 2001-07-31 | 2001-07-31 | Astrazeneca Ab | Novel compounds |
| SE0102641D0 (sv) * | 2001-07-31 | 2001-07-31 | Astrazeneca Ab | Novel compounds |
| US7084122B2 (en) * | 2001-11-21 | 2006-08-01 | Erik Larsen | Use of glycosides of mono- and diacyglycerol as anti-inflammatory agents |
-
2002
- 2002-11-07 SE SE0203304A patent/SE0203304D0/xx unknown
-
2003
- 2003-11-06 AT AT03770201T patent/ATE331711T1/de not_active IP Right Cessation
- 2003-11-06 EP EP03770201A patent/EP1562920B1/en not_active Expired - Lifetime
- 2003-11-06 AU AU2003278667A patent/AU2003278667A1/en not_active Abandoned
- 2003-11-06 WO PCT/SE2003/001712 patent/WO2004041794A1/en not_active Ceased
- 2003-11-06 ES ES03770201T patent/ES2268441T3/es not_active Expired - Lifetime
- 2003-11-06 DE DE60306546T patent/DE60306546T2/de not_active Expired - Fee Related
- 2003-11-06 US US10/534,191 patent/US20060040992A1/en not_active Abandoned
- 2003-11-06 JP JP2004549780A patent/JP2006506414A/ja not_active Withdrawn
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