ZA914491B - Inhibition of 5-lipoxygenase and cyclooxygenase products - Google Patents
Inhibition of 5-lipoxygenase and cyclooxygenase productsInfo
- Publication number
- ZA914491B ZA914491B ZA914491A ZA914491A ZA914491B ZA 914491 B ZA914491 B ZA 914491B ZA 914491 A ZA914491 A ZA 914491A ZA 914491 A ZA914491 A ZA 914491A ZA 914491 B ZA914491 B ZA 914491B
- Authority
- ZA
- South Africa
- Prior art keywords
- lipoxygenase
- inhibition
- cyclooxygenase products
- cyclooxygenase
- products
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53719590A | 1990-06-12 | 1990-06-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA914491B true ZA914491B (en) | 1992-12-30 |
Family
ID=24141624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA914491A ZA914491B (en) | 1990-06-12 | 1991-06-10 | Inhibition of 5-lipoxygenase and cyclooxygenase products |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0533837A4 (en) |
JP (1) | JPH05508153A (en) |
KR (1) | KR930700104A (en) |
AU (1) | AU8205991A (en) |
CA (1) | CA2084290A1 (en) |
IE (1) | IE911977A1 (en) |
NZ (1) | NZ238485A (en) |
PT (1) | PT97960A (en) |
WO (1) | WO1991019497A1 (en) |
ZA (1) | ZA914491B (en) |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0679396A1 (en) * | 1994-03-02 | 1995-11-02 | Pfizer Inc. | Use of 3-substituted-2-oxidole-1-carboxamides for the manufacture of a medicament in the treatment and prevention of ischemia induced myocardial injury and cytokine mediated myocardial injury |
US5552422A (en) * | 1995-01-11 | 1996-09-03 | Merck Frosst Canada, Inc. | Aryl substituted 5,5 fused aromatic nitrogen compounds as anti-inflammatory agents |
US6136839A (en) * | 1995-06-12 | 2000-10-24 | G. D. Searle & Co. | Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitor and a 5-lipoxygenase inhibitor |
US7301021B2 (en) | 1997-07-02 | 2007-11-27 | Smithkline Beecham Corporation | Substituted imidazole compounds |
WO1999012930A1 (en) | 1997-09-05 | 1999-03-18 | Glaxo Group Limited | 2,3-diaryl-pyrazolo[1,5-b]pyridazines derivatives, their prepa ration and their use as cyclooxygenase 2 (cox-2) inhibitors |
JP2001526230A (en) | 1997-12-19 | 2001-12-18 | スミスクライン・ビーチャム・コーポレイション | Heteroaryl-substituted imidazole compounds, pharmaceutical compositions and uses thereof |
US6858617B2 (en) | 1998-05-26 | 2005-02-22 | Smithkline Beecham Corporation | Substituted imidazole compounds |
ATE266399T1 (en) | 1998-08-20 | 2004-05-15 | Smithkline Beecham Corp | NEW SUBSTITUTED TRIAZOLE COMPOUNDS |
WO2000026216A1 (en) | 1998-11-03 | 2000-05-11 | Glaxo Group Limited | Pyrazolopyridine derivatives as selective cox-2 inhibitors |
AU1909200A (en) | 1998-11-04 | 2000-05-22 | Smithkline Beecham Corporation | Pyridin-4-yl or pyrimidin-4-yl substituted pyrazines |
JP2002538157A (en) | 1999-02-27 | 2002-11-12 | グラクソ グループ リミテッド | Pyrazolopyridine |
CN1255406C (en) * | 1999-11-10 | 2006-05-10 | 奥索-麦克尼尔药品公司 | Substituted 2-acyl-3-(heteroaryl)-imidazo [1,2-a] pyrimidines, and related pharmaceutical compoistions and methods |
JP2003528043A (en) | 1999-11-23 | 2003-09-24 | スミスクライン・ビーチャム・コーポレイション | 3,4-Dihydro- (1H) quinazolin-2-one compounds as CSBP / p38 kinase inhibitors |
US6759410B1 (en) | 1999-11-23 | 2004-07-06 | Smithline Beecham Corporation | 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors |
US7053099B1 (en) | 1999-11-23 | 2006-05-30 | Smithkline Beecham Corporation | 3,4-dihydro-(1H)quinazolin-2-one compounds as CSBP/p38 kinase inhibitors |
EP1233951B1 (en) | 1999-11-23 | 2005-06-01 | SmithKline Beecham Corporation | 3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors |
GB9930358D0 (en) | 1999-12-22 | 2000-02-09 | Glaxo Group Ltd | Process for the preparation of chemical compounds |
US7235551B2 (en) | 2000-03-02 | 2007-06-26 | Smithkline Beecham Corporation | 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases |
PE20020506A1 (en) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | PIRAZOLE DERIVATIVES FUSED AS PROTEIN KINASE INHIBITORS |
ATE300541T1 (en) | 2000-12-15 | 2005-08-15 | Glaxo Group Ltd | PYRAZOLOPYRIDINE DERIVATIVES |
EP1341788B1 (en) | 2000-12-15 | 2005-08-10 | Glaxo Group Limited | Pyrazolopyridines |
WO2002072581A2 (en) | 2001-03-08 | 2002-09-19 | Smithkline Beecham Corporation | Pyrazolopyriadine derivatives |
US6596731B2 (en) | 2001-03-27 | 2003-07-22 | Hoffmann-La Roche Inc. | Substituted imidazo[1,2-A] pyridine derivatives |
JP4237497B2 (en) | 2001-03-30 | 2009-03-11 | スミスクライン ビーチャム コーポレーション | Pyrazolopyridines, their preparation and their use as therapeutic compounds |
DE60212949T2 (en) | 2001-04-10 | 2007-01-04 | Smithkline Beecham Corp. | ANTIVIRAL PYRAZOLOPYRIDINE COMPOUNDS |
US6756498B2 (en) | 2001-04-27 | 2004-06-29 | Smithkline Beecham Corporation | Process for the preparation of chemical compounds |
WO2002088124A2 (en) | 2001-04-27 | 2002-11-07 | Smithkline Beecham Corporation | Pyrazolo'1,5-a!pyridine derivatives |
EP1401836B1 (en) * | 2001-06-21 | 2006-08-23 | SmithKline Beecham Corporation | Imidazo¬1,2-a|pyridine derivatives for the prophylaxis and treatment of herpes viral infections |
ES2262893T3 (en) | 2001-10-05 | 2006-12-01 | Smithkline Beecham Corporation | IMIDAZO-PIRIDINE DERIVATIVES FOR USE IN THE TREATMENT OF VIRIC INFECTION BY HERPES. |
US7199120B2 (en) | 2001-12-11 | 2007-04-03 | Smithkline Beecham Corporation | Pyrazolo-pyridine derivatives as antiherpes agents |
US7153863B2 (en) | 2002-10-03 | 2006-12-26 | Smithkline Beecham Corporation | Therapeutic compounds based on pyrazolopyridline derivatives |
JP2009507032A (en) | 2005-09-02 | 2009-02-19 | アボット・ラボラトリーズ | New imidazo heterocycle |
US8188083B2 (en) | 2007-06-28 | 2012-05-29 | Abbott Laboratories | Triazolopyridazines |
CA2778949C (en) | 2009-10-30 | 2018-02-27 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as pde10 inhibitors |
WO2011074658A1 (en) | 2009-12-18 | 2011-06-23 | 田辺三菱製薬株式会社 | Novel anti-platelet agent |
AR080754A1 (en) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | IMIDAZO DERIVATIVES (1,2-A) PIRAZINA AND ITS USE AS PDE10 INHIBITORS |
CA2822357A1 (en) | 2010-12-22 | 2012-06-28 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
BR112013033375B1 (en) | 2011-06-27 | 2022-05-10 | Janssen Pharmaceutica N.V | Derivatives of 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline, their use, pharmaceutical composition that comprises them, process of preparation thereof, sterile solution and intermediate compound |
WO2014001314A1 (en) | 2012-06-26 | 2014-01-03 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
JP6174695B2 (en) | 2012-07-09 | 2017-08-02 | ヤンセン ファーマシューティカ エヌ.ベー. | Inhibitor of phosphodiesterase 10 enzyme |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5002941A (en) * | 1985-12-12 | 1991-03-26 | Smithkline Beecham Corporation | Pyrrolo(1,2-a)imidazole and imidazo(1,2-a)pyridine derivatives and their use as 5-lipoxygenase pathway inhibitors |
ZW24186A1 (en) * | 1985-12-12 | 1987-07-08 | Smithkline Beckman Corp | Inhibition of the 5-lipoxygenase pathway |
JPH05503919A (en) * | 1989-06-13 | 1993-06-24 | スミスクライン・ビーチャム・コーポレイション | Suppression of interleukin-1 or tumor necrosis factor production by monocytes and/or macrophages |
-
1991
- 1991-06-07 EP EP19910912750 patent/EP0533837A4/en not_active Withdrawn
- 1991-06-07 CA CA002084290A patent/CA2084290A1/en not_active Abandoned
- 1991-06-07 WO PCT/US1991/004022 patent/WO1991019497A1/en not_active Application Discontinuation
- 1991-06-07 JP JP91512077A patent/JPH05508153A/en active Pending
- 1991-06-07 KR KR1019920703188A patent/KR930700104A/en not_active Application Discontinuation
- 1991-06-07 AU AU82059/91A patent/AU8205991A/en not_active Abandoned
- 1991-06-10 ZA ZA914491A patent/ZA914491B/en unknown
- 1991-06-11 IE IE197791A patent/IE911977A1/en unknown
- 1991-06-11 NZ NZ238485A patent/NZ238485A/en unknown
- 1991-06-12 PT PT97960A patent/PT97960A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CA2084290A1 (en) | 1991-12-13 |
AU8205991A (en) | 1992-01-07 |
EP0533837A4 (en) | 1994-11-17 |
EP0533837A1 (en) | 1993-03-31 |
NZ238485A (en) | 1994-03-25 |
WO1991019497A1 (en) | 1991-12-26 |
JPH05508153A (en) | 1993-11-18 |
PT97960A (en) | 1992-03-31 |
KR930700104A (en) | 1993-03-13 |
IE911977A1 (en) | 1991-12-18 |
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