ES2138594T3 - Agentes derivados de piridina e imidazol para enfermedades cardiovasculares. - Google Patents
Agentes derivados de piridina e imidazol para enfermedades cardiovasculares.Info
- Publication number
- ES2138594T3 ES2138594T3 ES92906439T ES92906439T ES2138594T3 ES 2138594 T3 ES2138594 T3 ES 2138594T3 ES 92906439 T ES92906439 T ES 92906439T ES 92906439 T ES92906439 T ES 92906439T ES 2138594 T3 ES2138594 T3 ES 2138594T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- pct
- thromboxane
- optionally
- chch3
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/55—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Treating Waste Gases (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Abstract
SE DESCRIBEN LOS COMPUESTOS DE FORMULA (I) O UN ESTER BIOCALIFICABLE DE LOS MISMOS, UNA SAL FARMACEUTICAMENTE ACEPTABLE O AMBOS, EN DONDE R1,R2,R3 Y R4 SON CADA UNO SELECCIONADOS INDEPENDIENTEMENTE DE H O ALQUILO C1-C4; R5 ES (CH2)MSO2R6, (CH2)MNHSO2R6 O (CH2)NHCOR7; R6 Y R7 SON ALQUILO C1-C6, PERFLUOROALQUILO(CH2)N C1-C3, CICLOALQIL(CH2)N C3-C6, ARIL(CH2)N O HETEROARIL(CH2)N; O R6 E NR8R9; R8 ES H O ALQUILO C1-C4; R9 ES ALQUILO C1-C6, CICLOALQUIL(CH2)N C3-C6, ARIL(CH2)N O HETEROARIL(CH2); O R8 Y R9 JUNTOS CON EL ATOMO DE NITROGENO AL CUAL ESTAN ADJUNTOS FORMAN UN ANILLO HETEROCICLICO DE 5 A 7 MIEMBROS QUE PUEDE OPCIONALMENTE INCORPORAR UN DOBLE ENLACE CARBON-CARBON O UNA UNION ATOMICA SELECCIONADA DE O, S, NH, N(ALQUIL C1-C4) Y N(ALCANOIL C1C5), Y QUE PUEDE SER OPCIONALMENTE SUSTITUIDO CON UNO DE TRES SUSTITUYENTES INDEPENDIENTEMENTE SELECCIONADOS DE ALQUILO C2-C4 Y ALCOXI C1-C4, QUE PUEDEN OPCIONALMENTE SER BENZO-FISIONADOS; X E CH2, CHCH3, C(OH)CH3, C=CH2 U O; M ES 0 O 1; N ES 0, 1, 2 O3; Y HET ES PIRIMIDIL 3CON LA PREVISION DE CUANDO HET ES IMIDAZILIL-1 ENTONCES X ES CH2 O CHCH3.LOS COMPUESTOS SON INHIBIDORES DE SINTETASA A2 TROMOXANA COMBINADA Y ANTAGONISTAS DE ENDOPEROXIDO/A2 TROMBOXANA DE UTILIDAD EN EL TRATAMIENTO DE ENFERMEDADES EN LAS CUALES LA TOMBOXANA A2 ES UN AGENTE CAUSATIVO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB919107043A GB9107043D0 (en) | 1991-04-04 | 1991-04-04 | Therapeutic agents |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2138594T3 true ES2138594T3 (es) | 2000-01-16 |
Family
ID=10692617
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES92906439T Expired - Lifetime ES2138594T3 (es) | 1991-04-04 | 1992-03-17 | Agentes derivados de piridina e imidazol para enfermedades cardiovasculares. |
Country Status (14)
Country | Link |
---|---|
US (2) | US5457118A (es) |
EP (1) | EP0579618B1 (es) |
JP (1) | JP3088015B2 (es) |
AT (1) | ATE185560T1 (es) |
CA (1) | CA2104456C (es) |
DE (1) | DE69230141T2 (es) |
DK (1) | DK0579618T3 (es) |
ES (1) | ES2138594T3 (es) |
FI (2) | FI104070B (es) |
GB (1) | GB9107043D0 (es) |
GR (1) | GR3032308T3 (es) |
IE (1) | IE921060A1 (es) |
PT (1) | PT100332B (es) |
WO (1) | WO1992017451A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9220137D0 (en) * | 1992-09-23 | 1992-11-04 | Pfizer Ltd | Therapeutic agents |
AU2044297A (en) * | 1996-03-29 | 1997-10-22 | Meiji Seika Kaisha Ltd. | Novel heterocyclic compounds having platelet aggregation inhibitory effects |
KR20010042125A (ko) * | 1998-03-23 | 2001-05-25 | 오흘러 로스 제이. | 피페리디디닐 및 n-아미디노피페리디닐 유도체 |
AU2002322720B2 (en) | 2001-07-25 | 2008-11-13 | Raptor Pharmaceutical Inc. | Compositions and methods for modulating blood-brain barrier transport |
US6722688B2 (en) | 2001-11-21 | 2004-04-20 | The Burton Corporation | Snowboard binding system |
WO2004050040A2 (en) * | 2002-12-03 | 2004-06-17 | Vela Pharmaceuticals, Inc. | Pharmaceutical composition of 1-(3,4-dimethoxyphenyl)-4-methyl-5-ethyl-7-methoxy-8-hydroxy-5h-2,3-benzodiazepine and uses thereof |
WO2004069155A2 (en) * | 2002-12-03 | 2004-08-19 | Vela Pharmaceuticals, Inc. | Pharmaceutical composition of 1-(3-hydroxy-4-methoxyphenyl)-4-methyl-5-ethyl-7,8-dimethoxy-5h-2,3-benzodiazepine and uses therof |
US20070032479A1 (en) * | 2003-12-03 | 2007-02-08 | Leventer Steven M | Treatment of inflammatory disorders of the epithelium with low dose 2,3-benzodiazepines |
CN103259027A (zh) | 2005-04-28 | 2013-08-21 | 普罗透斯数字保健公司 | 药物信息系统 |
EP2061761A1 (en) * | 2006-09-07 | 2009-05-27 | Millennium Pharmaceuticals, Inc. | Phenethylamide derivatives with kinase inhibitory activity |
EP2063905B1 (en) | 2006-09-18 | 2014-07-30 | Raptor Pharmaceutical Inc | Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates |
CN102316902B (zh) | 2009-02-20 | 2014-09-24 | to-BBB控股股份有限公司 | 基于谷胱甘肽的药物递送系统 |
CN110075069A (zh) | 2009-05-06 | 2019-08-02 | 实验室护肤股份有限公司 | 包含活性剂-磷酸钙颗粒复合物的皮肤递送组合物及其应用 |
US20120077778A1 (en) | 2010-09-29 | 2012-03-29 | Andrea Bourdelais | Ladder-Frame Polyether Conjugates |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60172964A (ja) * | 1984-02-15 | 1985-09-06 | Tanabe Seiyaku Co Ltd | 桂皮酸誘導体及びその製法 |
US4837333A (en) * | 1987-05-14 | 1989-06-06 | G. D. Searle & Co. | Substituted alkylidene imidazoles |
DE3932403A1 (de) * | 1989-05-12 | 1991-04-11 | Thomae Gmbh Dr K | Neue arylsulfonamide, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
IL94805A (en) * | 1989-06-28 | 1994-04-12 | Ciba Geigy Ag | Certain translocated carboxylic acids (a) Arylsulfonamide - and pyridyl - or imidazolil (), process for their preparation and pharmaceutical preparations containing them |
-
1991
- 1991-04-04 GB GB919107043A patent/GB9107043D0/en active Pending
-
1992
- 1992-03-17 ES ES92906439T patent/ES2138594T3/es not_active Expired - Lifetime
- 1992-03-17 EP EP92906439A patent/EP0579618B1/en not_active Expired - Lifetime
- 1992-03-17 CA CA002104456A patent/CA2104456C/en not_active Expired - Fee Related
- 1992-03-17 DK DK92906439T patent/DK0579618T3/da active
- 1992-03-17 DE DE69230141T patent/DE69230141T2/de not_active Expired - Fee Related
- 1992-03-17 US US08/133,155 patent/US5457118A/en not_active Expired - Fee Related
- 1992-03-17 WO PCT/EP1992/000591 patent/WO1992017451A1/en active IP Right Grant
- 1992-03-17 AT AT92906439T patent/ATE185560T1/de not_active IP Right Cessation
- 1992-03-17 JP JP04505819A patent/JP3088015B2/ja not_active Expired - Fee Related
- 1992-04-02 PT PT100332A patent/PT100332B/pt not_active IP Right Cessation
- 1992-04-03 IE IE106092A patent/IE921060A1/en not_active IP Right Cessation
-
1993
- 1993-09-15 FI FI934045A patent/FI104070B/fi not_active IP Right Cessation
-
1995
- 1995-07-14 US US08/502,748 patent/US5705523A/en not_active Expired - Fee Related
-
1999
- 1999-02-01 FI FI990179A patent/FI990179A0/fi unknown
-
2000
- 2000-01-04 GR GR20000400008T patent/GR3032308T3/el not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH06506200A (ja) | 1994-07-14 |
FI934045A (fi) | 1993-09-15 |
CA2104456C (en) | 1996-12-10 |
FI990179A (fi) | 1999-02-01 |
DE69230141T2 (de) | 2000-02-03 |
FI104070B1 (fi) | 1999-11-15 |
FI934045A0 (fi) | 1993-09-15 |
WO1992017451A1 (en) | 1992-10-15 |
IE921060A1 (en) | 1992-10-07 |
GB9107043D0 (en) | 1991-05-22 |
JP3088015B2 (ja) | 2000-09-18 |
EP0579618B1 (en) | 1999-10-13 |
DE69230141D1 (de) | 1999-11-18 |
PT100332B (pt) | 1999-06-30 |
US5457118A (en) | 1995-10-10 |
CA2104456A1 (en) | 1992-10-05 |
ATE185560T1 (de) | 1999-10-15 |
FI104070B (fi) | 1999-11-15 |
PT100332A (pt) | 1993-07-30 |
GR3032308T3 (en) | 2000-04-27 |
EP0579618A1 (en) | 1994-01-26 |
US5705523A (en) | 1998-01-06 |
DK0579618T3 (da) | 2000-01-03 |
FI990179A0 (fi) | 1999-02-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2138594T3 (es) | Agentes derivados de piridina e imidazol para enfermedades cardiovasculares. | |
GB9317764D0 (en) | Therapeutic compound | |
ES2163295T3 (es) | Derivados de imidazol y su uso como inhibidores de la farnesil-protein-transferasa. | |
DE69309670D1 (de) | Heterocyclische carbonsäure-derivate, die an rar rezeptoren binden können | |
TW200738706A (en) | Pyrido-, pyrazo-and pyrimido-pyrimidine derivatives and their use as mTOR inhibitors | |
BG94282A (bg) | 2,9-дизаместени-4н-пиридо/1,2,-а/пиримидин-4-они | |
DK0607193T3 (da) | Antifugale triazolderivater | |
AP9901578A0 (en) | Sulfonylbenzene compounds as anti-inflammatory/analgesic agents. | |
NZ513594A (en) | Heterocyclic compounds, intermediates thereof and elastase inhibitors | |
AR045006A1 (es) | Derivados de quinazolinona 5-sustituidos | |
BG104717A (en) | Water soluble azoles as broad-spectrum antifungals | |
MXPA02011464A (es) | Derivados 1,4-diazepan-2,5-diona y su uso como antagonistas del receptor de la nk-1. | |
IL182547A0 (en) | 4-[(2,4-dichloro-5-methoxyphenyl)amino]-6-alkoxy-7-ethynyl-3-quinolinecarbonitriles for the treatment of ischemic injury | |
SE9904177D0 (sv) | Novel compounds | |
DE60144246D1 (de) | Imidazolderivate, verfahren zu deren herstellung und deren verwendung | |
AR027035A1 (es) | Pirroles sustituidos | |
HRP20090617T1 (hr) | Protutumorska kombinacija koja sadrži substituirane akriloil distamicinske derivate i protutijela koja inhibiraju čimbenike rasta ili njihove receptore | |
CO4940439A1 (es) | COMPUESTOS 4-AMINO-6,7-DISUSTITUIDOS-PIRIDO-[2,3-d] PIRIMI- DINA | |
PE20010167A1 (es) | Amidas de acidos fenilciclohexanocarboxilicos sustituidos con actividad inhibidora de la incorporacion de adenosina | |
BRPI0417626A (pt) | derivado de 1-[(indol-3-il) carbonil] piperazina tricìclica, composição farmacêutica, uso de um derivado de 1-[(indol-3-il) carbonil] piperazina tricìclica | |
EP0375451A3 (en) | Compounds having a renin-inhibiting activity | |
ECSP993005A (es) | Compuestos de sulfonilbenceno como agentes anti-inflamatorios / analgesicos | |
RU2000130705A (ru) | Производные индола, лекарственное средство их содержащее, способ их получения (варианты) и применение в качестве ингибитора тирозинкиназы (варианты), применение для лечения опухолевых и других заболеваний (варианты) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
Ref document number: 579618 Country of ref document: ES |