ES2196806T3 - Derivados de fenilurea y de feniltiourea. - Google Patents
Derivados de fenilurea y de feniltiourea.Info
- Publication number
- ES2196806T3 ES2196806T3 ES99923540T ES99923540T ES2196806T3 ES 2196806 T3 ES2196806 T3 ES 2196806T3 ES 99923540 T ES99923540 T ES 99923540T ES 99923540 T ES99923540 T ES 99923540T ES 2196806 T3 ES2196806 T3 ES 2196806T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- alkoxy
- sulfur
- phenyl
- nitrogen
- 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
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth 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)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
1. Un compuesto de fórmula (I): en la cual: uno de X e Y es N, y el otro es CH; Z representa oxígeno o azufre; R1 representa alquilo(C1-6), alquenilo(C2-6) o alcoxi(C1-6); halógeno, R7CO- ó NR8R9CO-; R2, R3, R4, R5 y R6 representan independientemente alquilo(C1-6), alquenilo(C2-6), alcoxi(C1-6) o tioalquilo(C1-6); hidrógeno, halógeno, nitro, ciano, fenoxi, naftiloxi, fenilalcoxi(C1-6), naftilalcoxi(C1-6), fenilalquilo(C1-6), naftilalquilo(C1-6), R7CO-, R7SO2NH-, R7CON(R10)-, NR8R9-, NR8R9CO-, -COOR8, un anillo monocíclico o bicíclico de 5 a 10 miembros, que puede estar insaturado o saturado, que contiene 1 a 3 heteroátomos seleccionados entre oxígeno, nitrógeno o azufre, o un alquilo(C1-6) sustituido con un anillo monocíclico o bicíclico de 5 a 10 miembros, que puede estar insaturado o saturado, que contiene 1 a 3 heteroátomos seleccionados entre oxígeno, nitrógeno o azufre; o un par adyacente de R2, R3, R4, R5 y R6 junto con los átomos de carbono a los cuales están unidos, forman un anillocarbocíclico o heterocíclico aromático o no aromático de 5 a 7 miembros, en el que el anillo heterocíclico contiene 1, 2 ó o 3 heteroátomos seleccionados entre oxígeno, nitrógeno y azufre, y en el que el anillo carbocíclico o heterocíclico puede estar insustituido o sustituido en el carbono o nitrógeno con uno o más sustituyentes seleccionados entre =O, alquilo(C1-4), fenilalquilo(C1-4), naftilalquilo(C1-4), fenilo, naftilo, alcoxi(C1-4), alcoxi(C1-4)alquil(C1-4)hidroxi, hidroxialquilo(C1-4), RaCO2-, RaCO2alquilo(C1-4), ciano, cianoalquilo(C1-4), RaRbN y RaRbNalquilo(C1-4); en el cual, Ra y Rb son independientemente seleccionados entre hidrógeno y alquilo(C1-4); R7 es alquilo(C1-6), fenilo o naftilo; R8 y R9 representan independientemente hidrógeno, alquilo (C1-6), fenilo, naftilo, fenilalquilo(C1-6) o naftilalquilo(C1-6); R10 es hidrógeno o alquilo(C1-6); y n es 0, 1, 2 ó 3; en donde alquilo puede ser una cadena lineal, ramificada o cíclica; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9809988.0A GB9809988D0 (en) | 1998-05-08 | 1998-05-08 | Compounds |
GBGB9809972.4A GB9809972D0 (en) | 1998-05-08 | 1998-05-08 | Compounds |
GBGB9903268.2A GB9903268D0 (en) | 1999-02-12 | 1999-02-12 | Compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2196806T3 true ES2196806T3 (es) | 2003-12-16 |
Family
ID=27269308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES99923540T Expired - Lifetime ES2196806T3 (es) | 1998-05-08 | 1999-05-04 | Derivados de fenilurea y de feniltiourea. |
Country Status (8)
Country | Link |
---|---|
US (1) | US6372757B1 (es) |
EP (1) | EP1075478B1 (es) |
JP (1) | JP4633925B2 (es) |
AU (1) | AU4037799A (es) |
CA (1) | CA2331735A1 (es) |
DE (1) | DE69906960T2 (es) |
ES (1) | ES2196806T3 (es) |
WO (1) | WO1999058533A1 (es) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6093820A (en) | 1997-10-02 | 2000-07-25 | Taro Pharmaceutical Industries Ltd. | Method and reagents for N-alkylating ureides |
ATE241345T1 (de) * | 1999-02-12 | 2003-06-15 | Smithkline Beecham Plc | Neue verwendung von orexinrezeptorantagonisten |
WO2000047576A1 (en) * | 1999-02-12 | 2000-08-17 | Smithkline Beecham Plc | Cinnamide derivatives as orexin-1 receptors antagonists |
DE60015927T2 (de) * | 1999-02-12 | 2005-04-07 | Smithkline Beecham P.L.C., Brentford | Phenylharnstoff und phenylthioharnstoffderivate |
BRPI0109200B8 (pt) | 2000-03-14 | 2021-05-25 | Actelion Pharmaceuticals Ltd | compostos e composições farmacêuticas |
EP1288202A4 (en) * | 2000-05-11 | 2003-07-02 | Banyu Pharma Co Ltd | N-ACYLTETRAHYDROISOQUINOLINE DERIVATIVES |
PT1289955E (pt) | 2000-06-16 | 2005-08-31 | Smithkline Beecham Plc | Piperidinas para utilizacao como antagonistas dos receptores da orexina |
US7683071B2 (en) * | 2000-07-26 | 2010-03-23 | Taro Pharmaceuticals Industries Ltd. | Composition and method for improved bioavailability and enhanced brain delivery of 5,5-diphenyl barbituric acid |
US6939873B2 (en) * | 2000-07-26 | 2005-09-06 | Taro Pharmaceuticals Industries Limited | Non-sedating barbituric acid derivatives |
US6756379B2 (en) | 2001-07-26 | 2004-06-29 | Taro Pharmaceutical Industries Ltd. | Non-sedating barbiturate compounds as neuroprotective agents |
IL158463A0 (en) | 2001-05-05 | 2004-05-12 | Smithkline Beecham Plc | N-aroyl cyclic amines |
GB0115862D0 (en) * | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
GB0130335D0 (en) * | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
AU2003246657A1 (en) | 2002-07-09 | 2004-01-23 | Actelion Pharmaceuticals Ltd. | 7,8,9,10-tetrahydro-6H-azepino, 6,7,8,9-tetrahydro-pyrido and 2,3-dihydro-2H-pyrrolo[2,1-b]-quinazolinone derivatives |
JP4528125B2 (ja) | 2002-10-11 | 2010-08-18 | アクテリオン ファーマシューティカルズ リミテッド | スルホニルアミノ−酢酸誘導体 |
AR042444A1 (es) * | 2002-12-11 | 2005-06-22 | Taro Pharmaceuticals Ireland L | Metodo para el tratamiento de desordenes del movimiento mediante la utilizacion de acido barbiturico |
CA2520839A1 (en) | 2003-04-28 | 2004-11-11 | Actelion Pharmaceuticals Ltd | Quinoxalinone-3- one derivatives as orexin receptor antagonists |
US20050032794A1 (en) * | 2003-08-05 | 2005-02-10 | Padia Janak K. | Diamine derivatives of quinone and uses thereof |
HUP0304101A3 (en) * | 2003-12-22 | 2008-10-28 | Sanofi Aventis | Pyrazole derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates |
BRPI0508263B8 (pt) | 2004-03-01 | 2021-05-25 | Idorsia Pharmaceuticals Ltd | derivados de 1, 2, 3, 4-tetra-hidro-isoquinolina, composição farmacêutica, e, uso de derivado de 1, 2, 3, 4-tetra-hidro-isoquinolina |
WO2005097127A2 (en) | 2004-04-02 | 2005-10-20 | Merck & Co., Inc. | Method of treating men with metabolic and anthropometric disorders |
CA2572797A1 (en) * | 2004-07-02 | 2006-01-12 | Daniella Gutman | A process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid |
US20060178307A1 (en) * | 2005-01-26 | 2006-08-10 | The Regents Of The University Of California | Modulation of NMDA receptor currents via orexin receptor and/or CRF receptor |
US7501395B2 (en) | 2005-04-25 | 2009-03-10 | Eisai R & D Management Co., Ltd. | Method of screening for antianxiety drugs |
US7547782B2 (en) | 2005-09-30 | 2009-06-16 | Bristol-Myers Squibb Company | Met kinase inhibitors |
EP2049110B1 (en) | 2006-07-14 | 2014-08-20 | Merck Sharp & Dohme Corp. | Bridged diazepan orexin receptor antagonists |
US20080132529A1 (en) * | 2006-11-14 | 2008-06-05 | Avraham Yacobi | Method of improving bioavailability for non-sedating barbiturates |
PE20081229A1 (es) | 2006-12-01 | 2008-08-28 | Merck & Co Inc | Antagonistas de receptor de orexina de diazepam sustituido |
CL2008001003A1 (es) | 2007-04-11 | 2008-10-17 | Actelion Pharmaceuticals Ltd | Compuestos derivados de oxazolidinona; composicion farmaceutica que comprende a dichos compuestos; y su uso para preparar un medicamento para tratar una infeccion bacteriana. |
US8263586B2 (en) | 2007-05-18 | 2012-09-11 | Merck Sharp & Dohme Corp. | OXO bridged diazepan orexin receptor antagonists |
US8242121B2 (en) | 2007-05-23 | 2012-08-14 | Merck Sharp & Dohme Corp. | Pyridyl piperidine orexin receptor antagonists |
WO2008150364A1 (en) | 2007-05-23 | 2008-12-11 | Merck & Co., Inc. | Cyclopropyl pyrrolidine orexin receptor antagonists |
WO2009133522A1 (en) * | 2008-04-30 | 2009-11-05 | Actelion Pharmaceuticals Ltd | Piperidine and pyrrolidine compounds |
CA2745420A1 (en) | 2008-12-02 | 2010-06-10 | Glaxo Group Limited | N-{[(ir,4s,6r-3-(2-pyridinylcarbonyl)-3-azabicyclo [4.1.0] hept-4-yl] methyl}-2-heteroarylamine derivatives and uses thereof |
GB0823467D0 (en) | 2008-12-23 | 2009-01-28 | Glaxo Group Ltd | Novel Compounds |
EA201171293A1 (ru) | 2009-04-24 | 2012-05-30 | Глэксо Груп Лимитед | 3-азабицикло[4.1.0]гептаны, применяемые в качестве антагонистов орексина |
EP2470525A1 (en) | 2009-08-24 | 2012-07-04 | Glaxo Group Limited | Piperidine derivatives used as orexin antagonists |
JP2013502447A (ja) | 2009-08-24 | 2013-01-24 | グラクソ グループ リミテッド | 睡眠障害の治療のためのオレキシン受容体アンタゴニストとしての5−メチル−ピペリジン誘導体 |
WO2011031745A1 (en) | 2009-09-09 | 2011-03-17 | Achaogen, Inc. | Antibacterial fluoroquinolone analogs |
EP2332939A1 (en) | 2009-11-26 | 2011-06-15 | Æterna Zentaris GmbH | Novel Naphthyridine derivatives and the use thereof as kinase inhibitors |
WO2012089607A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Novel compounds with a 3a-azabicyclo [4.1.0] heptane core acting on orexin receptors |
WO2012089606A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Azabicyclo [4.1.0] hept - 4 - yl derivatives as human orexin receptor antagonists |
AR088352A1 (es) | 2011-10-19 | 2014-05-28 | Merck Sharp & Dohme | Antagonistas del receptor de 2-piridiloxi-4-nitrilo orexina |
US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
WO2013119639A1 (en) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Substituted prolines / piperidines as orexin receptor antagonists |
JP6663909B2 (ja) | 2014-08-13 | 2020-03-13 | エオラス セラピューティクス, インコーポレイテッド | オレキシンレセプターモジュレーターとしてのジフルオロピロリジン |
EP3414241B1 (en) | 2016-02-12 | 2022-05-04 | Astrazeneca AB | Halo-substituted piperidines as orexin receptor modulators |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0222839A4 (en) | 1985-05-17 | 1988-11-09 | Univ Australian | ANTI-MALARIA COMPOUNDS. |
JPH05213884A (ja) | 1991-06-14 | 1993-08-24 | Upjohn Co:The | 新規な4−アミノキノリン類およびこれを有効成分とする高血圧・鬱血性心不全の予防・治療剤 |
EP0842933B1 (en) | 1995-05-31 | 2004-08-04 | Sumitomo Pharmaceuticals Company, Limited | Novel naphthyridine derivatives |
US5972936A (en) | 1996-05-20 | 1999-10-26 | Darwin Discover Limited | Benzofuran carboxamides and their therapeutic use |
AR016817A1 (es) * | 1997-08-14 | 2001-08-01 | Smithkline Beecham Plc | Derivados de fenilurea o feniltiourea, procedimiento para su preparacion, coleccion de compuestos, compuestos intermediarios, composicion farmaceutica,metodo de tratamiento y uso de dichos compuestos para la manufactura de un medicamento |
-
1999
- 1999-05-04 CA CA002331735A patent/CA2331735A1/en not_active Abandoned
- 1999-05-04 EP EP99923540A patent/EP1075478B1/en not_active Expired - Lifetime
- 1999-05-04 DE DE69906960T patent/DE69906960T2/de not_active Expired - Lifetime
- 1999-05-04 ES ES99923540T patent/ES2196806T3/es not_active Expired - Lifetime
- 1999-05-04 JP JP2000548337A patent/JP4633925B2/ja not_active Expired - Fee Related
- 1999-05-04 US US09/700,002 patent/US6372757B1/en not_active Expired - Fee Related
- 1999-05-04 WO PCT/EP1999/003100 patent/WO1999058533A1/en active IP Right Grant
- 1999-05-04 AU AU40377/99A patent/AU4037799A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
DE69906960T2 (de) | 2004-01-29 |
AU4037799A (en) | 1999-11-29 |
US6372757B1 (en) | 2002-04-16 |
CA2331735A1 (en) | 1999-11-18 |
DE69906960D1 (en) | 2003-05-22 |
JP2003522101A (ja) | 2003-07-22 |
EP1075478A1 (en) | 2001-02-14 |
EP1075478B1 (en) | 2003-04-16 |
WO1999058533A1 (en) | 1999-11-18 |
JP4633925B2 (ja) | 2011-02-16 |
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