ES2117551B1 - NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME. - Google Patents
NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME.Info
- Publication number
- ES2117551B1 ES2117551B1 ES9502547A ES9502547A ES2117551B1 ES 2117551 B1 ES2117551 B1 ES 2117551B1 ES 9502547 A ES9502547 A ES 9502547A ES 9502547 A ES9502547 A ES 9502547A ES 2117551 B1 ES2117551 B1 ES 2117551B1
- Authority
- ES
- Spain
- Prior art keywords
- hydrogen
- leukotrenees
- quinolins
- alkyl
- naphthalenic
- 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 - Fee Related
Links
- 239000005557 antagonist Substances 0.000 title abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- -1 CARBONYLAMYL Chemical class 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D215/12—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
- C07C17/14—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the side-chain of aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/54—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to acyclic carbon atoms and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
QUINOLINAS NAFTALENICAS CON ACCION ANTAGONISTA DE LOS LEUCOTRIENOS, PROCEDIMIENTO PARA SU PREPARACION Y UTILIZACION DE LAS MISMAS. NUEVAS QUINOLINAS I EL SUSTITUYENTE QUE CONTIENE A ESTA UNIDO A LA POSICION 6 O 7 DEL SISTEMA 2-NAFTOLICO; R1, R2, R6 SON HIDROGENO, FLUOR, CLORO, BROMO, -OCH3 O (C1-C4)-ALQUILO; R3 ES HIDROGENO O METILO; R4, R5 SON HIDROGENO, -OH, -NH2 (C1-C4)-ALQUILCARBONILAMINO (C1-C4)-ALCOXICARBONILALQUILO, CARBAMOILO, CARBAMOILALQUILO, N,N-DIALQUILCARBAMOILALQUILO; -A- ES UN BIRRADICAL -O-, -S-, SO2-, -SO-, -SO2NR7- O -NR7SO2-, R7 ES HIDROGENO O UN (C1-C4)-ALQUILO; B ES OXIGENO O AZUFRE O -SO2- O UN ENLACE SENCILLO; D ES UN GRUPO 5-TETRAZOLILO O -COOR8-, DONDE R8 ES HIDROGENO, UN (C1-C4)-ALQUILO O UN GRUPO FENILALQUILO DE MENOS DE 10 ATOMOS DE CARBONO; M ES UN ENTERO 0-4; N Y P SON 0-6, SIENDO N+P MENOR O IGUAL A 6. PRESENTAN ACCION ANTAGONISTA DE LOS LEUCOTRIENOS.NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME. NEW QUINOLINS AND THE SUBSTITUTE CONTAINING THIS UNIT AT POSITION 6 OR 7 OF THE 2-NAFTOLIC SYSTEM; R1, R2, R6 ARE HYDROGEN, FLUORINE, CHLORINE, BROMINE, -OCH3 O (C1-C4) -ALKYL; R3 IS HYDROGEN OR METHYL; R4, R5 ARE HYDROGEN, -OH, -NH2 (C1-C4) -ALKYL CARBONYLAMYL (C1-C4) -ALCOXYCARBONYLALKYL, N, N-DIALKYL CARBAMOYLALKYL; -A- IS A BIRRADICAL -O-, -S-, SO2-, -SO-, -SO2NR7- OR -NR7SO2-, R7 IS HYDROGEN OR A (C1-C4) -ALKYL; B IS OXYGEN OR SULFUR OR -SO2- OR A SIMPLE LINK; D IS A GROUP 5-TETRAZOLYL OR -COOR8-, WHERE R8 IS HYDROGEN, A (C1-C4) -ALKYL OR A PHENYLALKYL GROUP OF LESS THAN 10 CARBON ATOMS; M IS AN INTEGER 0-4; N AND P ARE 0-6, BEING N + P LESS THAN OR EQUAL TO 6. THEY PRESENT ANTAGONISTIC ACTION OF THE LEUKOTRENEES.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9502547A ES2117551B1 (en) | 1995-12-29 | 1995-12-29 | NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME. |
| AU13783/97A AU1378397A (en) | 1995-12-29 | 1996-12-23 | Naphthalene quinolines having leukotriene-antagonistic action |
| PCT/EP1996/005811 WO1997024331A1 (en) | 1995-12-29 | 1996-12-23 | Naphthalene quinolines having leukotriene-antagonistic action |
| EP96944059A EP0874826A1 (en) | 1995-12-29 | 1996-12-23 | Naphthalene quinolines having leukotriene-antagonistic action |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9502547A ES2117551B1 (en) | 1995-12-29 | 1995-12-29 | NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2117551A1 ES2117551A1 (en) | 1998-08-01 |
| ES2117551B1 true ES2117551B1 (en) | 1999-04-01 |
Family
ID=8292586
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES9502547A Expired - Fee Related ES2117551B1 (en) | 1995-12-29 | 1995-12-29 | NAPHTHALENIC QUINOLINS WITH ANTAGONIST ACTION OF THE LEUKOTRENEES, PROCEDURE FOR THE PREPARATION AND USE OF THE SAME. |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP0874826A1 (en) |
| AU (1) | AU1378397A (en) |
| ES (1) | ES2117551B1 (en) |
| WO (1) | WO1997024331A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1177176E (en) * | 1999-04-28 | 2006-08-31 | Aventis Pharma Gmbh | DERIVATIVES OF TRIARILIC ACIDS AS LIGANDS OF PPAR RECEPTORS. |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5084575A (en) * | 1987-07-31 | 1992-01-28 | American Home Products Corporation | Quinoline substituted naphthalenepropionic acid derivatives as anti-inflammatory/antiallergic agents |
| US4920132A (en) * | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| US4920130A (en) * | 1987-11-02 | 1990-04-24 | Rorer Pharamceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| US4920131A (en) * | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| GB8728051D0 (en) * | 1987-12-01 | 1988-01-06 | Leo Pharm Prod Ltd | Chemical compounds |
| ES2103181B1 (en) * | 1994-08-01 | 1998-04-01 | Menarini Lab | NAFTALENIC AMIDES WITH ANTAGONIST ACTION OF THE LEUKOTRENEES. |
| ES2103180B1 (en) * | 1994-08-01 | 1998-04-01 | Menarini Lab | PHENYLACETAMIDES WITH ANTAGONIST ACTION OF THE LEUCOTRENEES. |
-
1995
- 1995-12-29 ES ES9502547A patent/ES2117551B1/en not_active Expired - Fee Related
-
1996
- 1996-12-23 EP EP96944059A patent/EP0874826A1/en not_active Withdrawn
- 1996-12-23 WO PCT/EP1996/005811 patent/WO1997024331A1/en not_active Ceased
- 1996-12-23 AU AU13783/97A patent/AU1378397A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ES2117551A1 (en) | 1998-08-01 |
| EP0874826A1 (en) | 1998-11-04 |
| WO1997024331A1 (en) | 1997-07-10 |
| AU1378397A (en) | 1997-07-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EC2A | Search report published |
Date of ref document: 19980801 Kind code of ref document: A1 Effective date: 19980801 |
|
| FD1A | Patent lapsed |
Effective date: 20051230 |