ES2152558T3 - Derivados de l-n6-(1-iminoetil)lisina utiles como inhibidores de oxido nitrico sintasa. - Google Patents
Derivados de l-n6-(1-iminoetil)lisina utiles como inhibidores de oxido nitrico sintasa.Info
- Publication number
- ES2152558T3 ES2152558T3 ES96929765T ES96929765T ES2152558T3 ES 2152558 T3 ES2152558 T3 ES 2152558T3 ES 96929765 T ES96929765 T ES 96929765T ES 96929765 T ES96929765 T ES 96929765T ES 2152558 T3 ES2152558 T3 ES 2152558T3
- Authority
- ES
- Spain
- Prior art keywords
- inhibitors
- derivatives
- nitrico
- iminoetil
- sintasa
- 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
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- -1 amino alcohol amine derivatives of L-N6-(1-iminoethyl)lysine Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000236 nitric oxide synthase inhibitor Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- CSYSULGPHGCBQD-UHFFFAOYSA-N s-ethylisothiouronium diethylphosphate Chemical compound CCSC(N)=N.CCOP(O)(=O)OCC CSYSULGPHGCBQD-UHFFFAOYSA-N 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/05—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/14—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
- C07C279/12—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical 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)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
SE PRESENTAN DERIVADOS DE L - N 6 - (1 - IMINOETIL)LISINA DE FORMULA GENERAL (I), COMPOSICIONES FARMACEUTICAS QUE CONTIENE ESTOS COMPUESTOS Y SU USO TERAPEUTICO, EN PARTICULAR SU USO COMO INHIBIDORES DE LA OXIDO NITRICO SINTASA. Y ES UN ATOMO DE HIDROGENO, UN RADICAL ALQUILO MENOR, UN RADICAL ALQUENILO MENOR, UN RADICAL ALQUINILO MENOR, UN RADICAL HIDROCARBURO AROMATICO, UN RADICAL HIDROCARBURO ALICICLICO, UN RADICAL AMINO, UN RADICAL HETEROCICLILO EN EL QUE SE SELECCIONAN INDEPENDIENTEMENTE DE 1 A 4 HETEROATOMOS ENTRE OXIGENO, NITROGENO Y AZUFRE, DONDE TODOS ESTOS RADICALES PUEDEN SER SUSTITUIDOS OPCIONALMENTE CON HIDROGENO, UN RADICAL CIANO, ALQUILO MENOR, NITRO, AMINO O HIDROCARBURO ALICICLICO, O HIDROCARBUROS ALICICLICOS AROMATICOS QUE PUEDEN SUSTITUIRSE OPCIONALMENTE CON UN RADICAL ALQUILO MENOR; X ES UN RADICAL ALQUILO MENOR, UN RADICAL ALQUENILO MENOR, UN RADICAL ALQUINILO MENOR, UN RADICAL HIDROCARBURO AROMATICO, UN RADICAL (CH 2 ) M Q(CH 2 ) N , DONDE M=1-3, N=1-3, Y Q ES AZUFRE, UN GRUPO SULFINILO, SULFONILO U OXIGENO, C=O, UN RADICAL ALQUINILO MENOR, UN RADICAL HIDROCARBURO AROMATICO, UN RADICAL HIDROCARBURO ALICICLICO O RADICALES HETEROCICLILOS EN LOS QUE SE SELECCIONAN INDEPENDIENTEMENTE DE 1 A 4 HETEROATOMOS ENTRE OXIGENO, NITROGENO Y AZUFRE, DONDE TODOS ESTOS RADICALES PUEDEN SER SUSTITUIDOS OPCIONALMENTE CON HIDROGENO, UN HALOGENO O UN RADICAL ALQUILO MENOR; R 1, R 2 , R 3 Y R 4 SE SELECCIONAN INDEPENDIENTEM ENTE DEL GRUPO FORMADO POR HIDROGENO Y UN RADICAL ALQUILO MENOR; A ES UN RADICAL ALQUILO MENOR QUE PUEDE SUSTITUIRSE OPCIONALMENTE CON HIDROGENO, UN RADICAL ALQUILO MENOR, HIDROXILO, ALQUIOXILO MENOR, ALQUIOXICARBONILO, ALQUILARILOXILO, TIOL, TIOALQUIOXILO MENOR, TIOALQUILARILOXILO, TIOARILOXILO, SULFINILALQUILO, SULFINILALQUILARILO, SULFINILARILO, SULFONILALQUILO, SULFONILALQUILARILO, SULFONILARILO, HALOGENO, HIDROCARBUROS AROMATICOS O HIDROCARBUROS ALICICLICOS; O A PUEDE SER UN ENLACE DIRECTO CON EL RESTO DE LA MOLECULA; B ES CH 2 R 5 DONDE R 5 ES UNA AMIDINA, GUANIDINA, SULFONAMIDA, UN GRUPO AMINO QUE PUEDE SUSTITUIRSE OPCIONALMENTE CON RADICALES ALQUILO, ALQUILARILO O ARILO.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/526,147 US5830917A (en) | 1995-09-11 | 1995-09-11 | L-N6 -(1-iminoethyl) lysine derivatives useful as nitric oxide synthase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2152558T3 true ES2152558T3 (es) | 2001-02-01 |
Family
ID=24096116
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES96929765T Expired - Lifetime ES2152558T3 (es) | 1995-09-11 | 1996-09-09 | Derivados de l-n6-(1-iminoetil)lisina utiles como inhibidores de oxido nitrico sintasa. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5830917A (es) |
| EP (1) | EP0861231B1 (es) |
| JP (1) | JPH11512428A (es) |
| AT (1) | ATE197449T1 (es) |
| AU (1) | AU720070B2 (es) |
| BR (1) | BR9610912A (es) |
| CA (1) | CA2231768A1 (es) |
| DE (1) | DE69610932T2 (es) |
| DK (1) | DK0861231T3 (es) |
| ES (1) | ES2152558T3 (es) |
| GR (1) | GR3034944T3 (es) |
| NZ (1) | NZ316735A (es) |
| PT (1) | PT861231E (es) |
| WO (1) | WO1997010204A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK1265859T3 (da) * | 2000-03-24 | 2006-05-01 | Pharmacia Corp | Amidinoforbindelser der er nyttige som nitrogenoxidsyntaseinhibitorer |
| AR034120A1 (es) | 2000-04-13 | 2004-02-04 | Pharmacia Corp | Compuesto derivado halogenado del acido 2-amino-4,5 heptenoico, composicion farmaceutica que lo comprende y el uso de dicho compuesto y dicha composicion en la fabricacion de un medicamento para inhibir o modular la sintesis de acido nitrico |
| AR030416A1 (es) | 2000-04-13 | 2003-08-20 | Pharmacia Corp | COMPUESTO DERIVADO HALOGENADO DEL ACIDO 2-AMINO-3,4 HEPTENOICO, COMPOSICION FARMACEUTICA QUE LO COMPRENDE Y SU USO EN LA FABRICACION DE UN MEDICAMENTO uTIL COMO INHIBIDOR DE LA OXIDO NITRICO SINTETASA |
| US6956131B2 (en) | 2000-04-13 | 2005-10-18 | Pharmacia Corporation | 2-amino-3, 4 heptenoic compounds useful as nitric oxide synthase inhibitors |
| US6787668B2 (en) | 2000-04-13 | 2004-09-07 | Pharmacia Corporation | 2-amino-4,5 heptenoic acid derivatives useful as nitric oxide synthase inhibitors |
| US6545170B2 (en) | 2000-04-13 | 2003-04-08 | Pharmacia Corporation | 2-amino-5, 6 heptenoic acid derivatives useful as nitric oxide synthase inhibitors |
| AR032318A1 (es) | 2000-04-13 | 2003-11-05 | Pharmacia Corp | Compuesto derivado halogenado del acido 2-amino-5,6 heptenoico; composicion farmaceutica que lo comprende y su uso en la fabricacion de un medicamento util como inhibidor de la oxido nitrico sintetasa |
| US7012098B2 (en) * | 2001-03-23 | 2006-03-14 | Pharmacia Corporation | Inhibitors of inducible nitric oxide synthase for chemoprevention and treatment of cancers |
| US7470815B1 (en) * | 2001-06-22 | 2008-12-30 | Northwestern University | Selective neuronal nitric oxide synthase inhibitors |
| US20030109522A1 (en) * | 2001-09-24 | 2003-06-12 | Manning Pamela T. | Ophthalmologic treatment methods using selective iNOS inhibitors |
| CA2494284A1 (en) * | 2002-08-02 | 2004-02-12 | Pharmacia Corporation | Methods for treatment and prevention of gastrointestinal conditions |
| DE102008061247A1 (de) * | 2008-12-10 | 2010-06-24 | Christian-Albrechts-Universität Zu Kiel | Inhibitoren der Dimethylarginin Dimethylaminohydrolase |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1114155A (en) * | 1964-08-24 | 1968-05-15 | Evans Medical Ltd | Guanidino derivatives |
| DE3505555A1 (de) * | 1985-02-18 | 1986-09-11 | Behringwerke Ag, 3550 Marburg | Neue oligopeptidylargininolderivate und deren homologe, verfahren zu deren herstellung, deren verwendung und diese enthaltende mittel |
| ZA852512B (en) * | 1985-04-03 | 1985-11-27 | Toray Industries | Guanidine derivatives |
| US5196450A (en) * | 1985-12-19 | 1993-03-23 | Merrell Dow Pharmaceuticals Inc. | Method of inhibiting protozoal growth |
| US5242947A (en) * | 1988-02-10 | 1993-09-07 | New York University | Use of polyamines as ionic-channel regulating agents |
| AU619613B2 (en) * | 1988-11-10 | 1992-01-30 | Merrell Dow Pharmaceuticals Inc. | Lactamimides in the treatment of drug-resistant protozoal infections |
| US5380945A (en) * | 1989-06-21 | 1995-01-10 | Abbott Laboratories | Guanidino compounds as regulators of nitric oxide synthase |
| US5059712A (en) * | 1989-09-13 | 1991-10-22 | Cornell Research Foundation, Inc. | Isolating aminoarginine and use to block nitric oxide formation in body |
| US5028627A (en) * | 1989-09-13 | 1991-07-02 | Cornell Research Foundation, Inc. | Method of using arginine derivatives to inhibit systemic hypotension associated with nitric oxide production or endothelial derived relaxing factor |
| GB8929076D0 (en) * | 1989-12-22 | 1990-02-28 | Scras | Treatment of shock by blocking agents of edrf effect or formation |
| CA2036770C (en) * | 1990-02-26 | 2003-09-09 | Jeffrey P. Whitten | Inhibitors of nitric oxide biosynthesis |
| US5132453A (en) * | 1991-03-22 | 1992-07-21 | Cornell Research Foundation, Inc. | N6 -(hydrazinoiminomethyl)lysine and method of inhibiting nitric oxide formation in body |
| US5273875A (en) * | 1991-03-22 | 1993-12-28 | Cornell Research Foundation, Inc. | N6 -(hydrazinoiminomethyl)lysine and method of inhibiting nitric oxide formation in body |
| GB9127376D0 (en) * | 1991-12-24 | 1992-02-19 | Wellcome Found | Amidino derivatives |
| US5296466A (en) * | 1992-02-19 | 1994-03-22 | Board Of Regents, The University Of Texas System | Inhibition of nitric oxide-mediated hypotension and septic shock with iron-containing hemoprotein |
| US5281627A (en) * | 1992-05-28 | 1994-01-25 | Cornell Research Foundation, Inc. | Substituted arginines and substituted homoarginines and use thereof |
| WO1994014780A1 (en) * | 1992-12-18 | 1994-07-07 | The Wellcome Foundation Limited | Pyrimidine, pyridine, pteridinone and indazole derivatives as enzyme inhibitors |
| GB9312761D0 (en) * | 1993-06-21 | 1993-08-04 | Wellcome Found | Amino acid derivatives |
| WO1995011014A1 (en) * | 1993-10-21 | 1995-04-27 | G.D. Searle & Co. | Amidino derivatives useful as nitric oxide synthase inhibitors |
| US5362744A (en) * | 1993-11-22 | 1994-11-08 | Warner-Lambert Company | Tetrazole-substituted urea acat inhibitors |
| DE19536219C1 (de) * | 1995-09-28 | 1996-11-07 | Siemens Ag | Hydraulikleitung mit integriertem, drucklosem Rücklauf |
-
1995
- 1995-09-11 US US08/526,147 patent/US5830917A/en not_active Expired - Fee Related
-
1996
- 1996-09-09 NZ NZ316735A patent/NZ316735A/xx unknown
- 1996-09-09 JP JP9511983A patent/JPH11512428A/ja not_active Abandoned
- 1996-09-09 ES ES96929765T patent/ES2152558T3/es not_active Expired - Lifetime
- 1996-09-09 DE DE69610932T patent/DE69610932T2/de not_active Expired - Fee Related
- 1996-09-09 PT PT96929765T patent/PT861231E/pt unknown
- 1996-09-09 WO PCT/US1996/013819 patent/WO1997010204A1/en not_active Ceased
- 1996-09-09 CA CA002231768A patent/CA2231768A1/en not_active Abandoned
- 1996-09-09 EP EP96929765A patent/EP0861231B1/en not_active Expired - Lifetime
- 1996-09-09 DK DK96929765T patent/DK0861231T3/da active
- 1996-09-09 BR BR9610912A patent/BR9610912A/pt not_active Application Discontinuation
- 1996-09-09 AU AU69037/96A patent/AU720070B2/en not_active Ceased
- 1996-09-09 AT AT96929765T patent/ATE197449T1/de not_active IP Right Cessation
-
2000
- 2000-11-30 GR GR20000402646T patent/GR3034944T3/el not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69610932D1 (de) | 2000-12-14 |
| BR9610912A (pt) | 1999-03-30 |
| MX9801897A (es) | 1998-05-31 |
| DE69610932T2 (de) | 2001-04-26 |
| JPH11512428A (ja) | 1999-10-26 |
| AU6903796A (en) | 1997-04-01 |
| DK0861231T3 (da) | 2001-01-08 |
| US5830917A (en) | 1998-11-03 |
| AU720070B2 (en) | 2000-05-25 |
| CA2231768A1 (en) | 1997-03-20 |
| EP0861231A1 (en) | 1998-09-02 |
| PT861231E (pt) | 2001-02-28 |
| WO1997010204A1 (en) | 1997-03-20 |
| GR3034944T3 (en) | 2001-02-28 |
| ATE197449T1 (de) | 2000-11-11 |
| NZ316735A (en) | 1999-01-28 |
| EP0861231B1 (en) | 2000-11-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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