DE3853704D1 - Pyrrolo[1,2-a]imidazol- und Imidazo[1,2-a]pyridinderivate und ihre Anwendung als 5-Lipoxygenase Inhibitoren. - Google Patents
Pyrrolo[1,2-a]imidazol- und Imidazo[1,2-a]pyridinderivate und ihre Anwendung als 5-Lipoxygenase Inhibitoren.Info
- Publication number
- DE3853704D1 DE3853704D1 DE3853704T DE3853704T DE3853704D1 DE 3853704 D1 DE3853704 D1 DE 3853704D1 DE 3853704 T DE3853704 T DE 3853704T DE 3853704 T DE3853704 T DE 3853704T DE 3853704 D1 DE3853704 D1 DE 3853704D1
- Authority
- DE
- Germany
- Prior art keywords
- pyrrolo
- imidazo
- imidazole
- pyridine derivatives
- lipoxygenase inhibitors
- 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.)
- Expired - Lifetime
Links
- IIOKDOJKJGCOEP-UHFFFAOYSA-N 3h-pyrrolo[1,2-a]imidazole Chemical compound C1=CN2CC=NC2=C1 IIOKDOJKJGCOEP-UHFFFAOYSA-N 0.000 title abstract 2
- 150000005234 imidazo[1,2-a]pyridines Chemical class 0.000 title abstract 2
- 239000000867 Lipoxygenase Inhibitor Substances 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 102000001381 Arachidonate 5-Lipoxygenase Human genes 0.000 abstract 1
- 108010093579 Arachidonate 5-lipoxygenase Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000037361 pathway Effects 0.000 abstract 1
Classifications
-
- 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
-
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9225887A | 1987-09-02 | 1987-09-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3853704D1 true DE3853704D1 (de) | 1995-06-08 |
Family
ID=22232414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE3853704T Expired - Lifetime DE3853704D1 (de) | 1987-09-02 | 1988-09-01 | Pyrrolo[1,2-a]imidazol- und Imidazo[1,2-a]pyridinderivate und ihre Anwendung als 5-Lipoxygenase Inhibitoren. |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP0306300B1 (de) |
| JP (1) | JPS6471876A (de) |
| KR (1) | KR900003167A (de) |
| CN (1) | CN1032011A (de) |
| AT (1) | ATE122044T1 (de) |
| AU (1) | AU1815092A (de) |
| DE (1) | DE3853704D1 (de) |
| DK (1) | DK483288A (de) |
| FI (1) | FI884017A (de) |
| HU (1) | HUT50475A (de) |
| IL (1) | IL87604A0 (de) |
| MY (1) | MY103766A (de) |
| NO (1) | NO883882L (de) |
| NZ (1) | NZ225967A (de) |
| PT (1) | PT88390B (de) |
Families Citing this family (6)
| 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 |
| AU6355190A (en) * | 1989-06-13 | 1991-01-17 | Smithkline Beecham Corporation | Inhibition of interleukin-1 and tumor necrosis factor production by monocytes and/or macrophages |
| PA8595001A1 (es) * | 2003-03-04 | 2004-09-28 | Pfizer Prod Inc | Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf) |
| CN102093366B (zh) * | 2011-03-04 | 2012-11-28 | 中国医学科学院医药生物技术研究所 | 双环氨基吡唑类化合物及其在抗柯萨奇病毒中的应用 |
| US10526345B2 (en) | 2016-04-08 | 2020-01-07 | Mankind Pharma Ltd. | Compounds as GPR119 agonists |
| US10954229B2 (en) | 2016-04-08 | 2021-03-23 | Mankind Pharma Ltd. | GPR119 agonist compounds |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4175127A (en) * | 1978-09-27 | 1979-11-20 | Smithkline Corporation | Pyridyl substituted 2,3-dihydroimidazo[2,1-b]thiazoles |
| US4186205A (en) * | 1979-01-08 | 1980-01-29 | Smithkline Corporation | 2,3-Di(4-substituted phenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazoles |
| ZW24186A1 (en) * | 1985-12-12 | 1987-07-08 | Smithkline Beckman Corp | Inhibition of the 5-lipoxygenase pathway |
-
1988
- 1988-08-29 MY MYPI88000971A patent/MY103766A/en unknown
- 1988-08-29 NZ NZ225967A patent/NZ225967A/en unknown
- 1988-08-30 JP JP63218235A patent/JPS6471876A/ja active Pending
- 1988-08-30 IL IL87604A patent/IL87604A0/xx unknown
- 1988-08-30 DK DK483288A patent/DK483288A/da not_active Application Discontinuation
- 1988-08-31 PT PT88390A patent/PT88390B/pt not_active IP Right Cessation
- 1988-08-31 HU HU884506A patent/HUT50475A/hu unknown
- 1988-08-31 NO NO88883882A patent/NO883882L/no unknown
- 1988-08-31 FI FI884017A patent/FI884017A/fi not_active Application Discontinuation
- 1988-08-31 CN CN88106330A patent/CN1032011A/zh active Pending
- 1988-08-31 KR KR1019880011126A patent/KR900003167A/ko not_active Application Discontinuation
- 1988-09-01 AT AT88308077T patent/ATE122044T1/de not_active IP Right Cessation
- 1988-09-01 EP EP88308077A patent/EP0306300B1/de not_active Expired - Lifetime
- 1988-09-01 DE DE3853704T patent/DE3853704D1/de not_active Expired - Lifetime
-
1992
- 1992-06-11 AU AU18150/92A patent/AU1815092A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| FI884017A (fi) | 1989-03-03 |
| HUT50475A (en) | 1990-02-28 |
| NZ225967A (en) | 1992-03-26 |
| EP0306300A2 (de) | 1989-03-08 |
| DK483288D0 (da) | 1988-08-30 |
| NO883882L (no) | 1989-03-03 |
| EP0306300B1 (de) | 1995-05-03 |
| ATE122044T1 (de) | 1995-05-15 |
| AU621308B2 (en) | 1992-03-12 |
| AU2174488A (en) | 1989-05-25 |
| PT88390A (pt) | 1989-07-31 |
| FI884017A0 (fi) | 1988-08-31 |
| NO883882D0 (no) | 1988-08-31 |
| JPS6471876A (en) | 1989-03-16 |
| IL87604A0 (en) | 1989-01-31 |
| EP0306300A3 (en) | 1990-08-16 |
| MY103766A (en) | 1993-09-30 |
| DK483288A (da) | 1989-03-03 |
| AU1815092A (en) | 1992-08-27 |
| PT88390B (pt) | 1992-10-30 |
| CN1032011A (zh) | 1989-03-29 |
| KR900003167A (ko) | 1990-03-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69108138D1 (de) | Imidazopyridinderivate und ihre Verwendung. | |
| FI843001A (fi) | Pyrrolo(1,2-a)imidazol- och imidatzo (1,2-a)pyridinimmunomodulatorer. | |
| ATE174596T1 (de) | Imidazo (1,2-a)pyridine als bradykinin- antagonisten | |
| PT582810E (pt) | Novas 7-(substituidas)-8-(substituidas)-9-(substituidas)-6-desmetil-6-desoxitetraciclinas como agentes antibioticos | |
| DE3777735D1 (de) | Imid-derivate, ihre herstellung und ihre verwendung. | |
| DE3855549D1 (de) | Benzimidazol-Derivate und therapeutische, diese enthaltende Mittel gegen Ulcer | |
| EP0404797A4 (en) | 1h/3h- 4-(n,n-dicycloalkyl/branched-alkylcarboxamido)-benzyl)imidazo 4,5-c)pyridines as paf antagonists | |
| HUT61552A (en) | N-pyrazolyl-1,2,4-triazolo/1,5-c/pyrimidine-2-sulfonamide derivatives, process for producing and applying same, as well as herbicidal compositions comprising such compounds as active ingredient | |
| DE3484549D1 (de) | (3-amino-1h-pyrazol-4-yl)(aryl)ketone. | |
| AU6418086A (en) | Imidazo``1,5-a``quinazoline derivatives, their preparation and use. | |
| DE3853704D1 (de) | Pyrrolo[1,2-a]imidazol- und Imidazo[1,2-a]pyridinderivate und ihre Anwendung als 5-Lipoxygenase Inhibitoren. | |
| NO159854C (no) | Analogifremgangsm te til fremstilling av terapeutisk aktive beta-karbolin-3-karboksylsyrederivater. | |
| AU3397789A (en) | Imidazo(1,2-a)furo-and thieno pyridine derivatives | |
| ATE71378T1 (de) | Purin-histamin-h1-antagonisten, ihre herstellung und sie enthaltende pharmazeutische praeparate. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8332 | No legal effect for de |