CO5721001A2 - Derivados sustituidos de morfolina y tiomorfolina - Google Patents

Derivados sustituidos de morfolina y tiomorfolina

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Publication number
CO5721001A2
CO5721001A2 CO06091597A CO06091597A CO5721001A2 CO 5721001 A2 CO5721001 A2 CO 5721001A2 CO 06091597 A CO06091597 A CO 06091597A CO 06091597 A CO06091597 A CO 06091597A CO 5721001 A2 CO5721001 A2 CO 5721001A2
Authority
CO
Colombia
Prior art keywords
cycloalkyl
ilo
alky
halo
alkyl
Prior art date
Application number
CO06091597A
Other languages
English (en)
Inventor
Tornoe Christian Wenzel
Mario Rottlander
Nikolay Khanzhin
Andrea Ritzen
William Patrick Watson
Original Assignee
Lundbeck & Co As H
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37730781&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CO5721001(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lundbeck & Co As H filed Critical Lundbeck & Co As H
Publication of CO5721001A2 publication Critical patent/CO5721001A2/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/041,3-Oxazines; Hydrogenated 1,3-oxazines
    • C07D265/061,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D279/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D279/101,4-Thiazines; Hydrogenated 1,4-thiazines
    • C07D279/121,4-Thiazines; Hydrogenated 1,4-thiazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/135Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
    • C07D307/84Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D307/85Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

1.- Un derivado sustituido de morfolina o tiomorfolina de formula general Ien el cualq es 0 o 1;W es O o S;X es CO;Z es O;R1 se selecciona del grupo formado por halogeno, ciano, alqu(en/in)iIo C1-6, cicloalqu(en)ilo C3-8, cicloalqu(en)iIo C3-8-alqu(en/in)iIo C1-6, halo-alqu(en/in)iIo C1-6, halo-cicloalqu(en)iIo C3-8, halo-cicloalqu(en)ilo C3-8-alqu(en/in)ilo C1-6, alqu(en/in)iIoxi C1-6, cicloalqu(en)iloxi C3-8 y cicloalqu(en)ilo C3-8-alqu(en/in)iIoxi C1-6;R2 se selecciona del grupo formado por halogeno, ciano, alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8, cicloalqu(en)ilo C3-8-alqu(en/in)ilo C1-6, halo-alqu(en/in)ilo C1-6, halo-cicloalqu(en)ilo C3-8, halo-cicloalqu(en)ilo C3-8-alqu(en/in)ilo C1-6, alqu(en/in)iloxi C1-6, cicloalqu(en)iloxi C3-8, cicloalqu(en)ilo C3-8-alqu(en/in)iIoxi C1-6, el fenilo sustituido en forma opcional y el piridilo sustituido en forma opcional; en los que el fenilo y el piridilo estan sustituidos en forma opcional con uno o mas sustituyentes que son, en forma independiente, halogeno, alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8 o cicloalqu(en)iIo C3-8-alqu(en/in)ilo C1-6;R3 se selecciona del grupo formado por alqu(en/in)ilo C1-10, cicloalqu(en)ilo C3-8, cicloalqu(en)ilo C3-8-alqu(en/in)ilo C1-6, Ar-alqu(en/in)ilo C1-6, Ar-cicloalqu(en)ilo C3-8, Ar-cicloalqu(en)ilo C3-8-alqu(en/in)iIo C1-6 y Ar; ycada uno de R4, R5, R6 y R7 se selecciona en forma independiente del grupo formado por hidrogeno y Ar;como base libre o sus sales.
CO06091597A 2004-03-12 2006-09-12 Derivados sustituidos de morfolina y tiomorfolina CO5721001A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DKPA200400412 2004-03-12

Publications (1)

Publication Number Publication Date
CO5721001A2 true CO5721001A2 (es) 2007-01-31

Family

ID=37730781

Family Applications (1)

Application Number Title Priority Date Filing Date
CO06091597A CO5721001A2 (es) 2004-03-12 2006-09-12 Derivados sustituidos de morfolina y tiomorfolina

Country Status (32)

Country Link
US (6) US7501414B2 (es)
EP (3) EP1727809B8 (es)
JP (1) JP5006184B2 (es)
KR (2) KR20120136422A (es)
CN (2) CN1930138A (es)
AR (1) AR049784A1 (es)
AT (2) ATE398112T1 (es)
AU (1) AU2005221762B2 (es)
BR (1) BRPI0508570B8 (es)
CA (1) CA2559397C (es)
CO (1) CO5721001A2 (es)
CY (2) CY1110392T1 (es)
DE (2) DE602005016849D1 (es)
DK (2) DK1727809T3 (es)
EA (1) EA015120B1 (es)
EG (1) EG25344A (es)
ES (2) ES2306087T3 (es)
HK (1) HK1172618A1 (es)
HR (1) HRP20090685T1 (es)
IL (1) IL177859A (es)
MY (2) MY147786A (es)
NO (1) NO337161B1 (es)
NZ (1) NZ549133A (es)
PL (2) PL1947093T3 (es)
PT (2) PT1947093E (es)
RS (2) RS50606B (es)
SG (1) SG151254A1 (es)
SI (2) SI1947093T1 (es)
TW (2) TWI349666B (es)
UA (2) UA102517C2 (es)
WO (1) WO2005087754A1 (es)
ZA (2) ZA200607286B (es)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7799832B2 (en) 2003-10-23 2010-09-21 Valeant Pharmaceuticals North America Combinations of retigabine and sodium channel inhibitors or sodium channel-influencing active compounds for treating pains
TWI349666B (en) * 2004-03-12 2011-10-01 Lundbeck & Co As H Substituted morpholine and thiomorpholine derivatives
UA89503C2 (uk) * 2004-09-13 2010-02-10 Х. Луннбек А/С Заміщені похідні аніліну
JP5237643B2 (ja) * 2005-03-03 2013-07-17 ハー・ルンドベック・アクチエゼルスカベット 置換されたピリジン誘導体
UA92340C2 (en) * 2005-03-03 2010-10-25 Х. Луннбек А/С Substituted pyridine derivatives
BRPI0707495A2 (pt) * 2006-02-07 2011-05-03 H Lundbeck & Co As método para tratar ou reduzir os sintomas de esquizofrenia, uso de um abridor seletivo de canal de potássio kcnq, método de triagem de um composto, e, uso de um composto
US7960436B2 (en) 2006-06-05 2011-06-14 Valeant Pharmaceuticals International Substituted arylamino-1,2,3,4-tetrahydro naphthalenes and-2,3-dihydro-1H-indenes as potassium channel modulators
PL2061465T3 (pl) 2006-08-23 2014-03-31 Valeant Pharmaceuticals Int Pochodne 4-(N-azacykloalkilo) anilidów jako modulatory kanałów potasowych
US8993593B2 (en) 2006-08-23 2015-03-31 Valeant Pharmaceuticals International N-(4-(6-fluoro-3,4-dihydroisoquinolin-2(1H)-yl)-2,6-dimethylphenyl)-3,3-dimethylbutanamide as potassium channel modulators
NZ577740A (en) 2006-11-28 2012-06-29 Valeant Pharmaceuticals Int 1,4 diamino bicyclic retigabine analogues as potassium channel modulators
WO2008130616A2 (en) * 2007-04-19 2008-10-30 Schering Corporation Diaryl morpholines as cb1 modulators
US8367684B2 (en) 2007-06-13 2013-02-05 Valeant Pharmaceuticals International Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators
WO2009015667A1 (en) * 2007-08-01 2009-02-05 H. Lundbeck A/S Use of kncq potassium channel openers for reducing symptoms of or treating disorders or conditions wherein the dopaminergic system is disrupted
US7786146B2 (en) * 2007-08-13 2010-08-31 Valeant Pharmaceuticals International Derivatives of 5-amino-4,6-disubstituted indole and 5-amino-4,6-disubstituted indoline as potassium channel modulators
SG176464A1 (en) * 2008-05-09 2011-12-29 Agency Science Tech & Res Diagnosis and treatment of kawasaki disease
WO2010094644A1 (en) * 2009-02-17 2010-08-26 Neurosearch A/S Substituted pyridine derivatives and their medical use
WO2010094645A1 (en) * 2009-02-17 2010-08-26 Neurosearch A/S Substituted pyridine derivatives and their medical use
TW201041857A (en) * 2009-05-11 2010-12-01 Lundbeck & Co As H Stable forms of N-(2,6-dimethyl-4-morpholin-4-yl-phenyl)-3,3-dimethyl-butyramide
US20100286138A1 (en) * 2009-05-11 2010-11-11 H. Lundbeck A/S Stable forms of N-(2,6-Dimethyl-4-morpholin-4-yl-phenyl)-3,3-dimethyl-butyramide
US20120232058A1 (en) * 2009-09-07 2012-09-13 Neurosearch A/S Substituted pyridine derivatives and their medical use
KR101449348B1 (ko) 2010-07-08 2014-10-08 화이자 인코포레이티드 Kv7 칼륨 채널 개방제로서의 피페리디닐 피리미딘 아미드
CN103073455B (zh) 2011-10-25 2015-08-19 中国科学院上海药物研究所 一类新型的kcnq钾通道激动剂、其制备方法和用途
US9321750B2 (en) * 2012-04-20 2016-04-26 Innov17 Llc ROR modulators and their uses
CN103044431A (zh) * 2012-10-22 2013-04-17 中国药科大学 制备五氟磺草胺的新方法
US8652527B1 (en) 2013-03-13 2014-02-18 Upsher-Smith Laboratories, Inc Extended-release topiramate capsules
US9101545B2 (en) 2013-03-15 2015-08-11 Upsher-Smith Laboratories, Inc. Extended-release topiramate capsules
US20170360726A1 (en) * 2014-12-05 2017-12-21 Aquinnah Pharmaceuticals, Inc. Compounds, compositions and methods of use
EP3366683A1 (en) * 2017-02-28 2018-08-29 Acousia Therapeutics GmbH Cyclic amides, acteamides and ureas useful as potassium channel openers
WO2020157126A1 (en) 2019-01-29 2020-08-06 Università degli Studi di Salerno Modulators of potassium ion channels and uses thereof
IL282188A (en) * 2021-04-08 2022-11-01 Yeda Res & Dev Combined use of ketamine and bretigabine for the treatment of psychiatric disorders

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03175086A (ja) * 1989-09-14 1991-07-30 Fuji Photo Film Co Ltd ジアゾ感熱記録材料
DE4200259A1 (de) 1992-01-08 1993-07-15 Asta Medica Ag Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung
US5688792A (en) * 1994-08-16 1997-11-18 Pharmacia & Upjohn Company Substituted oxazine and thiazine oxazolidinone antimicrobials
DE19539861A1 (de) 1995-10-26 1997-04-30 Asta Medica Ag Verwendung von 4-Amino-4-(4-fluorbenzylamino)-1-ethoxy-carbonylaminobenzen zur Prophylaxe und Behandlung der Folgen der akuten und chronischen zerebralen Minderdurchblutung sowie neurodegenerativer Erkrankungen
NZ329200A (en) * 1996-12-16 1999-05-28 Hoechst Ag Sulphonamide substituted quinazoline, isoquinoline, quinoline or benzo[1,3-]oxazine derivatives and medicaments
US6187797B1 (en) * 1996-12-23 2001-02-13 Dupont Pharmaceuticals Company Phenyl-isoxazoles as factor XA Inhibitors
US6020357A (en) * 1996-12-23 2000-02-01 Dupont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
PL334250A1 (en) 1996-12-23 2000-02-14 Du Pont Pharm Co Nitrogen containing hetero-aromatic compounds and inhibitors of xa factor
JP2001506271A (ja) * 1996-12-23 2001-05-15 デュポン ファーマシューティカルズ カンパニー Xa因子阻害剤としての酸素またはイオウを含む複素環式芳香族化合物
CA2314401A1 (en) 1997-12-22 1999-07-01 Du Pont Pharmaceuticals Company Nitrogen containing heteroaromatics with ortho-substituted p1's as factor xa inhibitors
WO1999050255A2 (en) 1998-03-27 1999-10-07 Du Pont Pharmaceuticals Company Disubstituted pyrazolines and triazolines as factor xa inhibitors
NZ516743A (en) * 1999-08-04 2004-02-27 Icagen Inc Methods for treating or preventing pain and anxiety
US6495550B2 (en) * 1999-08-04 2002-12-17 Icagen, Inc. Pyridine-substituted benzanilides as potassium ion channel openers
US6117900A (en) 1999-09-27 2000-09-12 Asta Medica Aktiengesellschaft Use of retigabine for the treatment of neuropathic pain
AU2001263486A1 (en) 2000-05-26 2001-12-11 Bristol-Myers Squibb Company Human KCNQ5 potassium channel, methods and compositions thereof
WO2001096540A2 (en) 2000-06-11 2001-12-20 Dupont Pharmaceuticals Company Hepatitis c protease exosite for inhibitor design
PE20020044A1 (es) * 2000-06-16 2002-01-30 Upjohn Co Tiazina oxazolidinona
US6589986B2 (en) * 2000-12-20 2003-07-08 Wyeth Methods of treating anxiety disorders
IL156601A0 (en) * 2001-01-16 2004-01-04 Astrazeneca Ab Therapeutic chroman compounds
JP2004517129A (ja) * 2001-01-16 2004-06-10 アストラゼネカ・アクチエボラーグ 治療用クロモン化合物
CN1250519C (zh) * 2001-01-19 2006-04-12 中国人民解放军军事医学科学院毒物药物研究所 具有调节钾通道功能的胺衍生物及其制备方法和应用
MXPA03007395A (es) * 2001-02-20 2003-12-04 Bristol Myers Squibb Co Derivados de pirimidin-5-carboxamida 2,4-disustituida como moduladores del canal de potasio kcnq.
SE0103649D0 (sv) * 2001-11-01 2001-11-01 Astrazeneca Ab Therapeutic quinoline compounds
SE0103648D0 (sv) * 2001-11-01 2001-11-01 Astrazeneca Ab Therapeutic quinolone compounds
TWI349666B (en) * 2004-03-12 2011-10-01 Lundbeck & Co As H Substituted morpholine and thiomorpholine derivatives

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DE602005007474D1 (en) 2008-07-24
IL177859A (en) 2013-02-28
CA2559397A1 (en) 2005-09-22
KR20120136422A (ko) 2012-12-18
AR049784A1 (es) 2006-09-06
ES2334076T3 (es) 2010-03-04
US7501414B2 (en) 2009-03-10
CN1930138A (zh) 2007-03-14
KR101411204B1 (ko) 2014-06-23
UA90670C2 (en) 2010-05-25
EP1947093B1 (en) 2009-09-23
US20090137571A1 (en) 2009-05-28
IL177859A0 (en) 2006-12-31
JP2007528880A (ja) 2007-10-18
EP2138487A1 (en) 2009-12-30
DE602005016849D1 (de) 2009-11-05
US7632835B2 (en) 2009-12-15
BRPI0508570B1 (pt) 2018-11-21
KR20060128004A (ko) 2006-12-13
DK1727809T3 (da) 2008-09-29
TW200811121A (en) 2008-03-01
ATE398112T1 (de) 2008-07-15
DK1947093T3 (da) 2010-02-01
CY1110392T1 (el) 2015-04-29
US8012962B2 (en) 2011-09-06
HK1172618A1 (zh) 2013-04-26
BRPI0508570B8 (pt) 2021-05-25
ZA200709718B (en) 2008-09-25
HRP20090685T1 (hr) 2010-02-28
TW200533359A (en) 2005-10-16
PL1947093T3 (pl) 2010-02-26
EP1727809A1 (en) 2006-12-06
EG25344A (en) 2011-12-14
US20100063036A1 (en) 2010-03-11
TWI357901B (en) 2012-02-11
ZA200607286B (en) 2008-04-30
NO20064599L (no) 2006-12-08
SI1947093T1 (sl) 2010-01-29
US20100063033A1 (en) 2010-03-11
EA015120B1 (ru) 2011-06-30
MY147786A (en) 2013-01-31
CN102516204B (zh) 2016-01-20
CN102516204A (zh) 2012-06-27
CA2559397C (en) 2010-08-10
UA102517C2 (ru) 2013-07-25
MY143698A (en) 2011-06-30
NZ549133A (en) 2010-09-30
BRPI0508570A (pt) 2007-08-14
EP1727809B8 (en) 2008-10-29
CY1109656T1 (el) 2014-08-13
US20110294787A1 (en) 2011-12-01
PL1727809T3 (pl) 2008-11-28
NO337161B1 (no) 2016-02-01
RS50606B (sr) 2010-05-07
PT1727809E (pt) 2008-08-13
JP5006184B2 (ja) 2012-08-22
AU2005221762B2 (en) 2011-06-09
ES2306087T3 (es) 2008-11-01
RS51066B (sr) 2010-10-31
ATE443702T1 (de) 2009-10-15
AU2005221762A1 (en) 2005-09-22
US7812023B2 (en) 2010-10-12
US8299075B2 (en) 2012-10-30
US20060167248A1 (en) 2006-07-27
EP1947093A1 (en) 2008-07-23
EP1947093B9 (en) 2010-03-03
SG151254A1 (en) 2009-04-30
EP1727809B1 (en) 2008-06-11
WO2005087754A1 (en) 2005-09-22
EA200601686A1 (ru) 2007-02-27
TWI349666B (en) 2011-10-01
US20090143369A1 (en) 2009-06-04
SI1727809T1 (sl) 2008-10-31
PT1947093E (pt) 2009-12-22

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