JP2009508949A5 - - Google Patents

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Publication number
JP2009508949A5
JP2009508949A5 JP2008532213A JP2008532213A JP2009508949A5 JP 2009508949 A5 JP2009508949 A5 JP 2009508949A5 JP 2008532213 A JP2008532213 A JP 2008532213A JP 2008532213 A JP2008532213 A JP 2008532213A JP 2009508949 A5 JP2009508949 A5 JP 2009508949A5
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Japan
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groups
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JP2008532213A
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English (en)
Japanese (ja)
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JP5133889B2 (ja
JP2009508949A (ja
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Priority claimed from PCT/US2006/024393 external-priority patent/WO2007040682A1/en
Publication of JP2009508949A publication Critical patent/JP2009508949A/ja
Publication of JP2009508949A5 publication Critical patent/JP2009508949A5/ja
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Expired - Fee Related legal-status Critical Current
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JP2008532213A 2005-09-21 2006-06-23 炎症治療のためのビアリール基置換複素環ｌｔａ４ｈ阻害剤 Expired - Fee Related JP5133889B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US71901605P 2005-09-21 2005-09-21
US60/719,016 2005-09-21
PCT/US2006/024393 WO2007040682A1 (en) 2005-09-21 2006-06-23 Biaryl substituted heterocycle inhibitors of lta4h for treating inflammation

Publications (3)

Publication Number Publication Date
JP2009508949A JP2009508949A (ja) 2009-03-05
JP2009508949A5 true JP2009508949A5 (enExample) 2009-08-13
JP5133889B2 JP5133889B2 (ja) 2013-01-30

Family

ID=37205825

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008532213A Expired - Fee Related JP5133889B2 (ja) 2005-09-21 2006-06-23 炎症治療のためのビアリール基置換複素環ｌｔａ４ｈ阻害剤

Country Status (15)

Country Link
US (3) US20070078263A1 (enExample)
EP (1) EP1926708B1 (enExample)
JP (1) JP5133889B2 (enExample)
KR (1) KR101328306B1 (enExample)
CN (1) CN101312948B (enExample)
AU (1) AU2006297798B2 (enExample)
BR (1) BRPI0616187A2 (enExample)
CA (1) CA2623348A1 (enExample)
EA (1) EA017618B1 (enExample)
IL (1) IL190372A0 (enExample)
NO (1) NO20081829L (enExample)
NZ (1) NZ566788A (enExample)
SG (1) SG166769A1 (enExample)
UA (1) UA101943C2 (enExample)
WO (2) WO2007040682A1 (enExample)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7576102B2 (en) * 2005-12-21 2009-08-18 Decode Genetics Ehf Biaryl substituted nitrogen containing heterocycle inhibitors of LTA4H for treating inflammation
EP3205644A1 (en) 2005-12-29 2017-08-16 Celtaxsys Inc. Diamine derivatives as inhibitors of leukotriene a4 hydrolase
CN101443330B (zh) * 2006-06-13 2012-12-19 上海海和药物研究开发有限公司 杂环非核苷类化合物及其制备方法、药物组合物和作为抗病毒抑制剂的用途
US8115005B2 (en) 2006-08-04 2012-02-14 Decode Genetics Ehf. Pyrazolylphenyl and pyrrolylphenyl inhibitors of LTA4H for treating inflammation
KR101133862B1 (ko) * 2007-07-27 2012-04-06 에프. 호프만-라 로슈 아게 Ｔａａｒ 리간드로서의 2-아제티딘메테인아민 및 2-피롤리딘메테인아민
PE20091017A1 (es) 2007-10-31 2009-07-16 Janssen Pharmaceutica Nv Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno a4 hidrolasa
US20090312558A1 (en) * 2008-06-13 2009-12-17 Reliance Life Sciences Pvt. Ltd. Process for the preparation of arylcyclopropoane carboxylic carbonitriles, and compounds derived therefrom
WO2010045633A2 (en) * 2008-10-17 2010-04-22 National Jewish Health Measurement and analysis of leukotrienes
NZ596137A (en) * 2009-05-14 2013-08-30 Janssen Pharmaceutica Nv Compounds with two fused bicyclic heteroaryl moieties as modulators of leukotriene a4 hydrolase
WO2011011598A1 (en) 2009-07-24 2011-01-27 Decode Genetics Ehf Process for preparing 4- { (s) -2- (4-(4-chlorophenoxy) phenoxymethyl) pyrrolidin-1-yl) } butyric acid and salts thereof
WO2011078303A1 (ja) 2009-12-25 2011-06-30 宇部興産株式会社 アミノピリジン化合物
JP2013532734A (ja) 2010-08-04 2013-08-19 ユニバーシティ オブ バージニア パテント ファウンデーション 炎症性疾患を治療するための組成物及び方法
TR201802550T4 (tr) 2011-03-14 2018-03-21 Boehringer Ingelheim Int Lökotrien üretiminin benzodioksan inhibitörleri.
US9139567B2 (en) 2011-07-19 2015-09-22 Boehringer Ingelheim International Gmbh Arylpyrazole ethers as inhibitors of leukotriene A4 hydrolase
KR20140138851A (ko) 2012-03-06 2014-12-04 베링거 인겔하임 인터내셔날 게엠베하 류코트리엔 생성 억제를 위해 기타 활성제와 병용된 벤조디옥산
WO2013134226A1 (en) 2012-03-06 2013-09-12 Boehringer Ingelheim International Gmbh Benzodioxanes for inhibiting leukotriene production
TWI593678B (zh) * 2012-04-27 2017-08-01 葛蘭素集團有限公司 作為類視色素相關孤兒受體γ(RORγ)調節劑之化合物、其醫藥組合物及用途
WO2014014874A1 (en) * 2012-07-17 2014-01-23 Boehringer Ingelheim International Gmbh Pyrazole derivatives which inhibit leukotriene production
WO2014164658A1 (en) 2013-03-12 2014-10-09 Celtaxsys, Inc. Methods of inhibiting leukotriene a4 hydrolase
CA2906086A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
CA2906084A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
EP2968264A4 (en) 2013-03-14 2016-11-02 Celtaxsys Inc INHIBITORS OF LEUCOTRIENE A4 HYDROLASE
US9573957B2 (en) 2013-07-15 2017-02-21 Boehringer Ingelheim International Gmbh Inhibitors of leukotriene production
WO2015009609A1 (en) 2013-07-15 2015-01-22 Boehringer Ingelheim International Gmbh Inhibitors of leukotriene production
DK3102209T3 (da) 2014-02-04 2021-07-12 Bioscience Pharma Partners Llc Anvendelse af flap-hæmmere til at reducere neuroinflammationsmedieret læsion i centralnervesystemet
WO2020039094A1 (en) * 2018-08-24 2020-02-27 Xeniopro GmbH Phenoxy(hetero)aryl ethers of antiproliferative activity
CN108640864A (zh) * 2018-03-27 2018-10-12 深圳大学 一种查尔酮基荧光探针及其制备方法与应用
ES3014615T3 (en) 2018-05-31 2025-04-23 Celltaxis Llc Method of reducing pulmonary exacerbations in respiratory disease patients
CA3105542A1 (en) * 2018-07-31 2020-02-06 Novartis Ag Crystalline forms of a lta4h inhibitor
CN111100063B (zh) * 2018-10-25 2022-05-17 南京药石科技股份有限公司 一种合成2-氟甲基取代的吡咯烷、哌啶以及哌嗪衍生物的制备方法
CN111620942B (zh) * 2020-06-12 2021-10-15 中国科学院昆明动物研究所 布氏鼠耳蝠白三烯A4水解酶抑制剂Motistin的成熟肽及其应用
AU2022376563A1 (en) 2021-11-01 2023-12-07 Alkahest, Inc. Benzodioxane modulators of leukotriene a4 hydrolase (lta4h) for prevention and treatment of aging-associated diseases

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE103599T1 (de) * 1988-09-21 1994-04-15 Searle & Co 3-oxiranbenzoesaeuren und derivate.
IE70521B1 (en) * 1989-02-28 1996-12-11 Zeneca Pharma Sa Heterocycles with inhibitory activity of 5-lipoxygenase
US5149704A (en) * 1991-05-03 1992-09-22 Abbott Laboratories Platelet activating antagonists
GB9226111D0 (en) * 1992-12-15 1993-02-10 Smithkline Beecham Plc Madicaments
GB9411045D0 (en) 1994-06-02 1994-07-20 Smithkline Beecham Plc Compounds and use
US5925654A (en) 1997-03-12 1999-07-20 G.D. Searle & Co. LTA4 , hydrolase inhibitors
US6110944A (en) * 1997-03-12 2000-08-29 G. D. Searle & Co. LTA4, hydrolase inhibitors
DE69830218T2 (de) * 1997-08-07 2006-02-02 Eli Lilly And Co., Indianapolis 1-[4-Substituierte Alkoxy)benzylnaphthalinderivate als Östrogeninhibitoren
WO2003075921A2 (en) * 2002-03-05 2003-09-18 Transtech Pharma, Inc. Mono- and bicyclic azole derivatives that inhibit the interaction of ligands with rage
US6982259B2 (en) * 2002-04-30 2006-01-03 Schering Aktiengesellschaft N-heterocyclic derivatives as NOS inhibitors
SE0202463D0 (sv) * 2002-08-14 2002-08-14 Astrazeneca Ab Novel compounds
KR20060054408A (ko) 2003-07-28 2006-05-22 얀센 파마슈티카 엔.브이. 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및ｌｔａ4 ｈ 조정자로서의 그의 용도
WO2006038594A1 (ja) * 2004-10-04 2006-04-13 Ono Pharmaceutical Co., Ltd. Ｎ型カルシウムチャネル阻害薬

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