JP2012500205A5 - - Google Patents

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Publication number
JP2012500205A5
JP2012500205A5 JP2011523131A JP2011523131A JP2012500205A5 JP 2012500205 A5 JP2012500205 A5 JP 2012500205A5 JP 2011523131 A JP2011523131 A JP 2011523131A JP 2011523131 A JP2011523131 A JP 2011523131A JP 2012500205 A5 JP2012500205 A5 JP 2012500205A5
Authority
JP
Japan
Prior art keywords
alkoxy
alkylamino
heteroaryl
cycloalkyl
aryl
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.)
Granted
Application number
JP2011523131A
Other languages
English (en)
Japanese (ja)
Other versions
JP5546540B2 (ja
JP2012500205A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/053524 external-priority patent/WO2010019646A1/en
Publication of JP2012500205A publication Critical patent/JP2012500205A/ja
Publication of JP2012500205A5 publication Critical patent/JP2012500205A5/ja
Application granted granted Critical
Publication of JP5546540B2 publication Critical patent/JP5546540B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2011523131A 2008-08-12 2009-08-12 スフィンゴシン‐1‐リン酸(s1p)レセプター拮抗薬およびその使用方法 Expired - Fee Related JP5546540B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US8821708P 2008-08-12 2008-08-12
US61/088,217 2008-08-12
PCT/US2009/053524 WO2010019646A1 (en) 2008-08-12 2009-08-12 Sphingosine-1-phosphate (s1p) receptor antagonists and methods for use thereof

Publications (3)

Publication Number Publication Date
JP2012500205A JP2012500205A (ja) 2012-01-05
JP2012500205A5 true JP2012500205A5 (enExample) 2012-09-27
JP5546540B2 JP5546540B2 (ja) 2014-07-09

Family

ID=41165710

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011523131A Expired - Fee Related JP5546540B2 (ja) 2008-08-12 2009-08-12 スフィンゴシン‐1‐リン酸(s1p)レセプター拮抗薬およびその使用方法

Country Status (10)

Country Link
US (1) US8049037B2 (enExample)
EP (1) EP2328863A1 (enExample)
JP (1) JP5546540B2 (enExample)
KR (1) KR20110044893A (enExample)
CN (1) CN102119140B (enExample)
AU (1) AU2009282017B2 (enExample)
BR (1) BRPI0918399A2 (enExample)
CA (1) CA2733970A1 (enExample)
RU (1) RU2505527C2 (enExample)
WO (1) WO2010019646A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8802692B2 (en) 2008-10-17 2014-08-12 Exelixis, Inc. Synergistic effects between sphingosine-1-phosphate receptor antagonists and antimicrotubule agents
US8168795B2 (en) * 2009-08-11 2012-05-01 Allergan, Inc. Selective sphingosine-1-phosphate receptor antagonists
WO2011028927A1 (en) * 2009-09-04 2011-03-10 Allergan, Inc. Selective sphingosine-1-phosphate receptor antagonists
JP2013533286A (ja) * 2010-07-30 2013-08-22 セントルイス ユニバーシティ 疼痛を治療する方法
KR101625872B1 (ko) 2015-01-27 2016-06-01 국민대학교산학협력단 스마트단말기의 이벤트 기반의 차량조명 제어시스템 및 그 제어방법, 그리고 이를 위한 컴퓨터로 판독가능한 기록매체

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE756062A (fr) * 1969-09-11 1971-03-11 Boehringer Sohn Ingelheim Derives de 1,1,1-trichlorethane leurs procedes de fabrication et leur utilisation en tant que substances biocides
JPS55111451A (en) 1979-02-19 1980-08-28 Nippon Kayaku Co Ltd Novel 2-hydroxybenzamide derivative and agricultural and horticultural soil bactericide
EP0146810A3 (de) 1983-12-05 1987-05-13 Solco Basel AG Verfahren zur Herstellung von Sphingosinderivaten
JPS61172860A (ja) * 1985-01-28 1986-08-04 Nippon Kayaku Co Ltd 新規ピリジン誘導体及びそれを有効成分とする農園芸用細菌病防除剤
US4659722A (en) * 1984-08-20 1987-04-21 Nippon Kayaku Kabushiki Kaisha Bactericidal N-(2,2,2 trichloroethyl)pyridinecarboxamides
US5110987A (en) 1988-06-17 1992-05-05 Emory University Method of preparing sphingosine derivatives
ZA902794B (en) 1989-04-18 1991-04-24 Duphar Int Res New 3-n substituted carbamoyl-indole derivatives
US5294722A (en) 1992-04-16 1994-03-15 E. R. Squibb & Sons, Inc. Process for the preparation of imidazoles useful in angiotensin II antagonism
US5403851A (en) 1994-04-05 1995-04-04 Interneuron Pharmaceuticals, Inc. Substituted tryptamines, phenalkylamines and related compounds
ATE314342T1 (de) 1997-03-12 2006-01-15 Takara Bio Inc Spingosinanaloga
ATE332888T1 (de) 1997-09-11 2006-08-15 Takara Bio Inc Sphingosinderivate und medizinische zubereitung
AU5322399A (en) * 1998-07-27 2000-02-21 President And Fellows Of Harvard College Method of high-throughput screening of molecules and compounds for their effectson biological and chemical processes
CA2422044A1 (en) * 2000-09-14 2002-03-21 Gliatech, Inc. Nitrogen-containing compounds and their use as glycine transport inhibitors
JP2004529100A (ja) * 2001-01-30 2004-09-24 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 スフィンゴシン−1−ホスフェートレセプターのアゴニストおよびアンタゴニスト
AU2002310099A1 (en) * 2001-05-22 2002-12-03 President And Fellows Of Harvard College Identification of anti-protozoal agents
US7074817B2 (en) 2001-06-20 2006-07-11 Wyeth Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)
GB0324210D0 (en) * 2003-10-15 2003-11-19 Novartis Ag Organic compounds
GB0405289D0 (en) * 2004-03-09 2004-04-21 Novartis Ag Organic compounds

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