JP2006528147A5 - - Google Patents

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Publication number
JP2006528147A5
JP2006528147A5 JP2006520762A JP2006520762A JP2006528147A5 JP 2006528147 A5 JP2006528147 A5 JP 2006528147A5 JP 2006520762 A JP2006520762 A JP 2006520762A JP 2006520762 A JP2006520762 A JP 2006520762A JP 2006528147 A5 JP2006528147 A5 JP 2006528147A5
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JP
Japan
Prior art keywords
alkyl
formula
group
compound
optionally substituted
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
JP2006520762A
Other languages
English (en)
Japanese (ja)
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JP2006528147A (ja
Filing date
Publication date
Priority claimed from GB0316893A external-priority patent/GB0316893D0/en
Priority claimed from GB0411167A external-priority patent/GB0411167D0/en
Application filed filed Critical
Priority claimed from PCT/EP2004/008061 external-priority patent/WO2005014571A1/en
Publication of JP2006528147A publication Critical patent/JP2006528147A/ja
Publication of JP2006528147A5 publication Critical patent/JP2006528147A5/ja
Pending legal-status Critical Current

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JP2006520762A 2003-07-18 2004-07-16 ヒスタミンh3受容体リガンドとしての置換ピペリジン Pending JP2006528147A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0316893A GB0316893D0 (en) 2003-07-18 2003-07-18 Novel compounds
GB0411167A GB0411167D0 (en) 2004-05-19 2004-05-19 Novel compounds
PCT/EP2004/008061 WO2005014571A1 (en) 2003-07-18 2004-07-16 Substituted piperidines as histamine h3 receptor ligands

Publications (2)

Publication Number Publication Date
JP2006528147A JP2006528147A (ja) 2006-12-14
JP2006528147A5 true JP2006528147A5 (enExample) 2007-07-19

Family

ID=34137741

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006520762A Pending JP2006528147A (ja) 2003-07-18 2004-07-16 ヒスタミンh3受容体リガンドとしての置換ピペリジン

Country Status (9)

Country Link
US (1) US20060247227A1 (enExample)
EP (1) EP1646620B1 (enExample)
JP (1) JP2006528147A (enExample)
AR (1) AR045999A1 (enExample)
AT (1) ATE370135T1 (enExample)
DE (1) DE602004008291T2 (enExample)
ES (1) ES2291913T3 (enExample)
TW (1) TW200514781A (enExample)
WO (1) WO2005014571A1 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007010350A1 (en) * 2005-07-19 2007-01-25 Pfizer Products Inc. Synthesis of therapeutic diphenyl ethers
JP2009506987A (ja) 2005-08-02 2009-02-19 ニューロゲン コーポレイション ジピペラジニルケトンおよび関連する類似体
CA2687931C (en) 2007-05-31 2016-05-24 Boehringer Ingelheim International Gmbh Ccr2 receptor antagonists and uses thereof
EP2205588A2 (en) * 2007-09-28 2010-07-14 Schering Corporation Oxypiperidine derivatives as histamine receptor antagonists
CN103724328B (zh) 2008-12-19 2015-10-14 贝林格尔.英格海姆国际有限公司 作为ccr2受体拮抗剂用于治疗炎症、哮喘和copd的环状嘧啶-4-甲酰胺
PL2513093T3 (pl) 2009-12-17 2015-03-31 Centrexion Therapeutics Corp Nowi antagoniści receptora CCR2 i ich zastosowanie
EP2569295B1 (en) 2010-05-12 2014-11-19 Boehringer Ingelheim International GmbH New ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments
JP2013526507A (ja) 2010-05-12 2013-06-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用
US8841313B2 (en) 2010-05-17 2014-09-23 Boehringer Ingelheim International Gmbh CCR2 antagonists and uses thereof
CN102260277B (zh) 2010-05-24 2013-07-24 中国科学院上海药物研究所 新型苯并噁嗪噁唑烷酮类化合物及其制备方法和用途
JP5636094B2 (ja) 2010-05-25 2014-12-03 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Ccr2受容体アンタゴニスト
EP2576538B1 (en) 2010-06-01 2015-10-28 Boehringer Ingelheim International GmbH New CCR2 antagonists
CA2806341C (en) * 2010-07-29 2020-03-24 Rigel Pharmaceuticals, Inc. Ampk-activating heterocyclic compounds and methods for using the same
WO2013010839A1 (en) 2011-07-15 2013-01-24 Boehringer Ingelheim International Gmbh Novel and selective ccr2 antagonists
CA2863022A1 (en) * 2012-01-16 2013-07-25 Glaxosmithkline Intellectual Property Development Limited Therapeutic uses
CN104114538B (zh) * 2012-01-16 2016-04-13 葛兰素史克知识产权发展有限公司 治疗用途
WO2013151982A1 (en) 2012-04-03 2013-10-10 Arena Pharmaceuticals, Inc. Methods and compounds useful in treating pruritus, and methods for identifying such compounds
EP2647377A1 (en) 2012-04-06 2013-10-09 Sanofi Use of an h3 receptor antagonist for the treatment of alzheimer's disease
AU2016287584B2 (en) 2015-07-02 2020-03-26 Centrexion Therapeutics Corporation (4-((3R,4R)-3-methoxytetrahydro-pyran-4-ylamino)piperidin-1-yl)(5-methyl-6-(((2R,6S)-6-(p-tolyl)tetrahydro-2H-pyran-2-yl)methylamino)pyrimidin-4yl)methanone citrate
WO2017095758A1 (en) * 2015-12-01 2017-06-08 Merck Sharp & Dohme Corp. Homobispiperidinyl derivatives as liver x receptor beta agonists, compositions, and their use
AU2023247609A1 (en) * 2022-03-31 2024-10-17 Bebetter Med Inc. 1,4-diheterocyclic substituted aromatic ring or aromatic heterocyclic compound and use thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20020507A1 (es) * 2000-10-17 2002-06-25 Schering Corp Compuestos no-imidazoles como antagonistas del receptor histamina h3
CA2436083A1 (en) * 2001-02-08 2002-09-19 Schering Corporation Use of dual h3/m2 antagonists in the treatment of cognition deficit disorders
EP1444219A1 (en) * 2001-10-12 2004-08-11 Novo Nordisk A/S Substituted piperidines and their use for the treatment of diseases related to the histamine h3 receptor
AU2003242252A1 (en) * 2002-06-07 2003-12-22 Kyowa Hakko Kogyo Co., Ltd. Bicyclic pyrimidine derivatives

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