JP2005522432A5 - - Google Patents

Download PDF

Info

Publication number
JP2005522432A5
JP2005522432A5 JP2003565480A JP2003565480A JP2005522432A5 JP 2005522432 A5 JP2005522432 A5 JP 2005522432A5 JP 2003565480 A JP2003565480 A JP 2003565480A JP 2003565480 A JP2003565480 A JP 2003565480A JP 2005522432 A5 JP2005522432 A5 JP 2005522432A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
pharmaceutically acceptable
acceptable salt
composition according
methoxy
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.)
Withdrawn
Application number
JP2003565480A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005522432A (ja
Filing date
Publication date
Priority claimed from GB0202680A external-priority patent/GB0202680D0/en
Priority claimed from GB0222616A external-priority patent/GB0222616D0/en
Application filed filed Critical
Priority claimed from PCT/GB2003/000462 external-priority patent/WO2003066056A1/en
Publication of JP2005522432A publication Critical patent/JP2005522432A/ja
Publication of JP2005522432A5 publication Critical patent/JP2005522432A5/ja
Withdrawn legal-status Critical Current

Links

JP2003565480A 2002-02-05 2003-02-04 ニューロン成長の促進方法 Withdrawn JP2005522432A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0202680A GB0202680D0 (en) 2002-02-05 2002-02-05 Novel method
GB0222616A GB0222616D0 (en) 2002-09-30 2002-09-30 Novel method
PCT/GB2003/000462 WO2003066056A1 (en) 2002-02-05 2003-02-04 Method of promoting neuronal growth

Publications (2)

Publication Number Publication Date
JP2005522432A JP2005522432A (ja) 2005-07-28
JP2005522432A5 true JP2005522432A5 (enExample) 2006-03-16

Family

ID=27736189

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003565480A Withdrawn JP2005522432A (ja) 2002-02-05 2003-02-04 ニューロン成長の促進方法

Country Status (5)

Country Link
US (1) US20070270432A1 (enExample)
EP (1) EP1471912A1 (enExample)
JP (1) JP2005522432A (enExample)
AU (1) AU2003244452A1 (enExample)
WO (1) WO2003066056A1 (enExample)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7452888B2 (en) 2002-03-27 2008-11-18 Glaxo Group Limited Quinoline derivatives and their use as 5-ht6 ligands
EA009367B1 (ru) 2002-12-18 2007-12-28 Сувен Лайф Сайенсиз Лимитед ПРОИЗВОДНЫЕ 5-ТИА-5-ДИОКСО-4b-АЗАИНДЕНО[2,1-a]ИНДЕНА, ОБЛАДАЮЩИЕ АФФИННОСТЬЮ К РЕЦЕПТОРУ СЕРОТОНИНА
BRPI0412263B1 (pt) 2003-07-22 2019-10-15 Arena Pharmaceuticals, Inc. Derivados de diaril e aril heteroaril uréia, uso e composição farmacêutica contendo os mesmos, bem como processo para preparação da dita composição
MXPA06007415A (es) 2004-01-02 2007-01-26 Suven Life Sciences Ltd Inden [2, 1a] indenos e isoindol [2,1-a] indoles novedosos.
US7713954B2 (en) 2004-09-30 2010-05-11 Roche Palo Alto Llc Compositions and methods for treating cognitive disorders
KR101016972B1 (ko) 2005-08-12 2011-02-25 수벤 라이프 사이언시스 리미티드 기능성 5-ht6 리간드인 아미노아릴 설폰아미드 유도체
WO2007020654A1 (en) 2005-08-16 2007-02-22 Suven Life Sciences An improved process for the preparation of losartan
CA2670717C (en) 2007-01-08 2012-01-10 Suven Life Sciences Limited 5-(heterocyclyl)alkyl-n-(arylsulfonyl)indole compounds and their use as 5-ht6 ligands
US20080176861A1 (en) 2007-01-23 2008-07-24 Kalypsys, Inc. Sulfonyl-substituted bicyclic compounds as ppar modulators for the treatment of non-alcoholic steatohepatitis
SI2155674T1 (sl) 2007-05-03 2011-10-28 Suven Life Sciences Ltd Aminoalkoksi aril sulfonamid spojine in njih uporaba kot 5-ht6 ligandi
MX2010003765A (es) 2007-10-26 2010-04-30 Suven Life Sciences Ltd Compuestos de aminoarilsulfonamida y su uso como ligandos de la 5-hidroxitriptamina6.
EP2254564A1 (en) 2007-12-12 2010-12-01 Glaxo Group Limited Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-quinoline
US20110021538A1 (en) 2008-04-02 2011-01-27 Arena Pharmaceuticals, Inc. Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor
WO2010032257A1 (en) 2008-09-17 2010-03-25 Suven Life Sciences Limited Aryl indolyl sulfonamide compounds and their use as 5-ht6 ligands
MX2011002884A (es) 2008-09-17 2011-04-21 Suven Life Sciences Ltd Compuestos de aril-sulfonamida-amina y su uso como ligandos de 5-ht6.
US9126946B2 (en) 2008-10-28 2015-09-08 Arena Pharmaceuticals, Inc. Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto
WO2011083487A1 (en) 2010-01-05 2011-07-14 Suven Life Sciences Limited Sulfone compounds as 5-ht6 receptor ligands
KR101608499B1 (ko) 2013-10-08 2016-04-01 이화여자대학교 산학협력단 4-니트로인돌 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 포함하는 5-ht6 수용체 관련 질환의 예방 또는 치료용 약학적 조성물
WO2016201373A1 (en) 2015-06-12 2016-12-15 Axovant Sciences Ltd. Diaryl and arylheteroaryl urea derivatives useful for the prophylaxis and treatment of rem sleep behavior disorder
CA2992518A1 (en) 2015-07-15 2017-01-19 Axovant Sciences Gmbh Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis and treatment of hallucinations associated with a neurodegenerative disease

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DZ2376A1 (fr) * 1996-12-19 2002-12-28 Smithkline Beecham Plc Dérivés de sulfonamides nouveaux procédé pour leurpréparation et compositions pharmaceutiques les c ontenant.

Similar Documents

Publication Publication Date Title
JP2005522432A5 (enExample)
HRP20161657T1 (hr) Kinazolinoni kao inhibitori humane fosfatidilinozitol 3- kinaze delta
MY148487A (en) Biphenyl derivatives
CA2364718A1 (en) Monoamine reuptake inhibitors for treatment of cns disorders
JP2006526031A5 (enExample)
MY130803A (en) New quinuclidine amide derivatives
WO2006098918A3 (en) Substituted gamma lactams as therapeutic agents
GEP20094723B (en) Tetraazabenzo [e] azulene derivatives and analogs thereof
JP2007521280A5 (enExample)
NO20050883D0 (no) Ny fremgangsmate for syntesen (IS)-4,5-dimetoksy-1-(metylaminometyl)-benzocyklobutan og addisjonssalter derav, og anvendelse i syntesen av ivabradin og addisjonssalter derav med en farmasoytisk akseptabel syre
ATE442135T1 (de) 5ht2c-rezeptor-modulator-zusammensetzungen und anwendungsverfahren
EP2397476A3 (en) Indole derivative having PGD2 receptor antagonist activity
EP1741712A3 (en) Nebivolol and its pharmaceutically acceptable salts, process for preparation and pharmaceutical compositions of Nebivolol
JP2005504782A5 (enExample)
FR2882556B1 (fr) Forme cristalline gamma d du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent
CA2522813A1 (en) 2-alkynyl-and 2-alkenyl-pyrazolo-¬4,3-e|-1,2,4-triazolo-¬1,5-c|-pyrimidine adenosine a2a receptor antagonists
JP2008513510A5 (enExample)
WO2006066173A3 (en) Novel mch receptor antagonists
JP2004532828A5 (enExample)
WO2007039462A3 (en) Indane derivatives as mch receptor antagonists
RU2000100362A (ru) Применение специфического антагониста 5нт2 рецепторов для приготовления лекарств, пригодных для лечения синдрома апноэ во сне
NO20050888D0 (no) Ny fremgangsmate for syntesen av 1,3,4,5-tetrahydro-2H-3-benzazepin-2-onforbindelser, og anvendelse i syntesen av ivabradin og addisjonssalter derav med en farmasoytisk akseptabel syre
SE0401655D0 (sv) New compounds
NO20063602L (no) Benzyl(iden)-laktam-derivater
DE60311942D1 (de) Verfahren für die Synthese von Perindopril und seiner pharmazeutischen annehmbaren Salzen