JP2006522771A5 - - Google Patents

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Publication number
JP2006522771A5
JP2006522771A5 JP2006505136A JP2006505136A JP2006522771A5 JP 2006522771 A5 JP2006522771 A5 JP 2006522771A5 JP 2006505136 A JP2006505136 A JP 2006505136A JP 2006505136 A JP2006505136 A JP 2006505136A JP 2006522771 A5 JP2006522771 A5 JP 2006522771A5
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JP
Japan
Prior art keywords
piperidinyl
phenyl
oxy
carbonyl
alkyl
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.)
Pending
Application number
JP2006505136A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006522771A (ja
Filing date
Publication date
Priority claimed from GBGB0308333.4A external-priority patent/GB0308333D0/en
Application filed filed Critical
Publication of JP2006522771A publication Critical patent/JP2006522771A/ja
Publication of JP2006522771A5 publication Critical patent/JP2006522771A5/ja
Pending legal-status Critical Current

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JP2006505136A 2003-04-10 2004-04-08 アルツハイマーなどの神経疾患の治療用のヒスタミンh3アンタゴニストとしての4−(4−{ヘテロサイクリルアルコキシ}フェニル)−1−(ヘテロサイクリル−カルボニル)ピペリジン誘導体およびその関連化合物 Pending JP2006522771A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0308333.4A GB0308333D0 (en) 2003-04-10 2003-04-10 Novel compounds
PCT/EP2004/003985 WO2004089373A1 (en) 2003-04-10 2004-04-08 4- (4-(heterocyclylalkoxy}phenyl)-1-(heterocyclyl-carbonyl)piperidine derivatives and related compounds as histamine h3 antagonists for the treatment of neurological diseases such as alzheimer’s

Publications (2)

Publication Number Publication Date
JP2006522771A JP2006522771A (ja) 2006-10-05
JP2006522771A5 true JP2006522771A5 (cg-RX-API-DMAC7.html) 2007-05-31

Family

ID=9956580

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006505136A Pending JP2006522771A (ja) 2003-04-10 2004-04-08 アルツハイマーなどの神経疾患の治療用のヒスタミンh3アンタゴニストとしての4−(4−{ヘテロサイクリルアルコキシ}フェニル)−1−(ヘテロサイクリル−カルボニル)ピペリジン誘導体およびその関連化合物

Country Status (22)

Country Link
US (1) US20060205774A1 (cg-RX-API-DMAC7.html)
EP (1) EP1610786B9 (cg-RX-API-DMAC7.html)
JP (1) JP2006522771A (cg-RX-API-DMAC7.html)
KR (1) KR20050111638A (cg-RX-API-DMAC7.html)
CN (1) CN1805747A (cg-RX-API-DMAC7.html)
AR (1) AR044006A1 (cg-RX-API-DMAC7.html)
AT (1) ATE365039T1 (cg-RX-API-DMAC7.html)
AU (1) AU2004228949B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0409110A (cg-RX-API-DMAC7.html)
CA (1) CA2521899A1 (cg-RX-API-DMAC7.html)
CO (1) CO5640135A2 (cg-RX-API-DMAC7.html)
DE (1) DE602004007119T2 (cg-RX-API-DMAC7.html)
ES (1) ES2288681T3 (cg-RX-API-DMAC7.html)
GB (1) GB0308333D0 (cg-RX-API-DMAC7.html)
IS (1) IS8118A (cg-RX-API-DMAC7.html)
MA (1) MA27726A1 (cg-RX-API-DMAC7.html)
MX (1) MXPA05010816A (cg-RX-API-DMAC7.html)
NO (1) NO20055256L (cg-RX-API-DMAC7.html)
RU (1) RU2005134006A (cg-RX-API-DMAC7.html)
TW (1) TW200503710A (cg-RX-API-DMAC7.html)
WO (1) WO2004089373A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA200507795B (cg-RX-API-DMAC7.html)

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US20050256118A1 (en) * 2004-05-12 2005-11-17 Altenbach Robert J Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
EP1717235A3 (en) * 2005-04-29 2007-02-28 Bioprojet Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands
KR101397913B1 (ko) 2005-05-30 2014-05-26 엠에스디 가부시키가이샤 신규 피페리딘 유도체
US7553964B2 (en) * 2005-06-03 2009-06-30 Abbott Laboratories Cyclobutyl amine derivatives
ATE450526T1 (de) 2005-06-20 2009-12-15 Schering Corp Als antagonisten von histamin h3 geeignete piperidinderivate
US7408066B2 (en) 2005-06-20 2008-08-05 Schering Corproation Carbon-linked substituted piperidines and derivatives thereof useful as histamine H3 antagonists
GB0514812D0 (en) * 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
CA2623025A1 (en) 2005-09-20 2007-03-29 Schering Corporation 1- [ [1- [ (2-amin0-6-methyl-4-pyridinyl) methyl] -4-flu0r0-4-piperidinyl,] carbonyl] -4- [2- (2-pyridinyl) -3h-imidaz0 [4 , 5-b] pyridin-3-yl] piperidine useful as histamine h3 antagonist
US7943605B2 (en) 2005-10-27 2011-05-17 Ucb Pharma S.A. Compounds comprising a lactam or a lactam derivative moiety, processes for making them, and their uses
TW200730498A (en) 2005-12-20 2007-08-16 Glaxo Group Ltd Compounds
CA2634847A1 (en) 2005-12-21 2007-07-05 Schering Corporation Substituted aniline derivatives useful as histamine h3 antagonists
CA2634250A1 (en) 2005-12-21 2007-07-05 Schering Corporation Phenoxypiperidines and analogs thereof useful as histamine h3 antagonists
BRPI0713836A2 (pt) 2006-07-25 2013-05-28 Cephalon Inc composto, composiÇço farmacÊutica e mÉtodo para tratar distérbio
TW200823204A (en) * 2006-10-17 2008-06-01 Arena Pharm Inc Biphenyl sulfonyl and phenyl-heteroaryl sulfonyl modulators of the histamine H3-receptor useful for the treatment of disorders related thereto
US7638541B2 (en) 2006-12-28 2009-12-29 Metabolex Inc. 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
AU2008208653B2 (en) * 2007-01-22 2012-11-22 Pfizer Products Inc. Tosylate salt of a therapeutic compound and pharmaceutical compositions thereof
CA2693169C (en) 2007-07-19 2016-01-12 Metabolex, Inc. N-linked heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders
BRPI0914891A2 (pt) * 2008-06-20 2015-11-24 Metabolex Inc agonistas de aril gpr119 e usos dos mesmos
JP5909185B2 (ja) 2009-10-01 2016-04-26 シマベイ セラピューティクス, インコーポレーテッド 置換テトラゾール−1−イルフェノキシメチルチアゾール−2−イルピペリジニルピリミジン塩
WO2011163090A1 (en) 2010-06-23 2011-12-29 Metabolex, Inc. Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
BR112014013461A2 (pt) 2011-12-08 2017-06-13 Taisho Pharmaceutical Co Ltd derivado de fenilpirrol
WO2013151982A1 (en) 2012-04-03 2013-10-10 Arena Pharmaceuticals, Inc. Methods and compounds useful in treating pruritus, and methods for identifying such compounds
HUP1300139A2 (en) * 2013-03-06 2014-09-29 Richter Gedeon Nyrt Phenoxypiperidine h3 antagonists
EP2970196B1 (en) 2013-03-15 2020-11-25 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
EA201992707A1 (ru) 2013-11-18 2020-06-30 Глобал Блад Терапьютикс, Инк. Соединения и их применения для модуляции гемоглобина
WO2016169421A1 (zh) 2015-04-21 2016-10-27 江苏恒瑞医药股份有限公司 咪唑并异吲哚类衍生物、其制备方法及其在医药上的应用
US10292983B2 (en) 2016-08-03 2019-05-21 Cymabay Therapeutics, Inc. Oxymethylene aryl compounds for treating inflammatory gastrointestinal diseases or gastrointestinal conditions
TWI821537B (zh) * 2019-03-05 2023-11-11 日商衛材R&D企管股份有限公司 五環式雜環化合物

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US4166853A (en) * 1978-05-05 1979-09-04 The Upjohn Company Antihypertensive 7-trifluoromethyl-4-aminoquinolones
US5364791A (en) * 1992-05-14 1994-11-15 Elisabetta Vegeto Progesterone receptor having C. terminal hormone binding domain truncations
DE69334150T2 (de) * 1992-05-14 2008-03-13 Baylor College Of Medicine, Houston Mutierte steroidhormonrezeptoren, methoden für ihre benutzung und molekularer schalter für gentherapie
DE4407139A1 (de) * 1994-03-04 1995-09-07 Thomae Gmbh Dr K Aryl-1-azacycloalkane und deren Salze, diese Verbindungen enthaltende Arzneimittel und deren Verwendung sowie Verfahren zu ihrer Herstellung
CA2214288C (en) * 1996-09-18 2006-07-18 Lonza Ag Process for the preparation of 1-acyl-4-arylpiperidines
EP0837065A1 (de) * 1996-10-16 1998-04-22 Ciba SC Holding AG Phenylglycidylether-HALS
BR0108088A (pt) * 2000-07-13 2004-04-06 Abbott Lab Pirrolidinas 1,3-dissubstituìdas e 1,3,3-trissubstituìdas como ligandos receptores de histamina-3 e suas aplicações terapêuticas
US6515013B2 (en) * 2000-07-13 2003-02-04 Abbott Laboratories 1,3-disubstituted and 1,3,3-trisubstituted pyrrolidines as histamine-3 receptor ligands and their therapeutic applications
BRPI0113162B8 (pt) * 2000-08-08 2021-05-25 Johnson & Johnson compostos ariloxialquilaminas nao-imidazólicos e composição farmacêutica compreendendo os referidos compostos
PL210793B1 (pl) * 2001-02-28 2012-03-30 Merck & Co Inc Acylowane pochodne piperydyny
AU2002306848A1 (en) * 2001-03-23 2002-10-08 Elan Pharmaceuticals, Inc. Methods of treating alzheimer's disease with piperidin derivates
US7459461B2 (en) * 2001-10-19 2008-12-02 Ortho-Mcneil Pharmaceutical, Inc. Phosphonic acid compounds as inhibitors of serine proteases

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