JP2006511579A5 - - Google Patents

Download PDF

Info

Publication number
JP2006511579A5
JP2006511579A5 JP2004563642A JP2004563642A JP2006511579A5 JP 2006511579 A5 JP2006511579 A5 JP 2006511579A5 JP 2004563642 A JP2004563642 A JP 2004563642A JP 2004563642 A JP2004563642 A JP 2004563642A JP 2006511579 A5 JP2006511579 A5 JP 2006511579A5
Authority
JP
Japan
Prior art keywords
alkyl
group
halo
alkoxy
phenyl
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
JP2004563642A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006511579A (ja
JP4516430B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2003/040129 external-priority patent/WO2004058149A2/en
Publication of JP2006511579A publication Critical patent/JP2006511579A/ja
Publication of JP2006511579A5 publication Critical patent/JP2006511579A5/ja
Application granted granted Critical
Publication of JP4516430B2 publication Critical patent/JP4516430B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2004563642A 2002-12-20 2003-12-16 1−(アミノ)インダン並びに(1,2−ジヒドロ−3−アミノ)−ベンゾフラン、ベンゾチオフェン及びインドール Expired - Fee Related JP4516430B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US43538102P 2002-12-20 2002-12-20
PCT/US2003/040129 WO2004058149A2 (en) 2002-12-20 2003-12-16 1-(amino)indanes and (1,2-dihydro-3-amino)-benzofurans, benzothiophenes and indoles

Publications (3)

Publication Number Publication Date
JP2006511579A JP2006511579A (ja) 2006-04-06
JP2006511579A5 true JP2006511579A5 (https=) 2006-10-12
JP4516430B2 JP4516430B2 (ja) 2010-08-04

Family

ID=32682229

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004563642A Expired - Fee Related JP4516430B2 (ja) 2002-12-20 2003-12-16 1−(アミノ)インダン並びに(1,2−ジヒドロ−3−アミノ)−ベンゾフラン、ベンゾチオフェン及びインドール

Country Status (8)

Country Link
US (1) US7220734B2 (https=)
EP (1) EP1581509B1 (https=)
JP (1) JP4516430B2 (https=)
AT (1) ATE496024T1 (https=)
AU (1) AU2003297232B2 (https=)
CA (1) CA2509218C (https=)
DE (1) DE60335827D1 (https=)
WO (1) WO2004058149A2 (https=)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1661881B1 (en) 2003-08-29 2014-12-17 Ono Pharmaceutical Co., Ltd. Compound capable of binding s1p receptor and pharmaceutical use thereof
US7605171B2 (en) 2003-12-17 2009-10-20 Merck & Co., Inc. (3,4-disubstituted)propanoic carboxylates as S1P (Edg) receptor agonists
CN101014329B (zh) 2004-07-16 2010-09-08 杏林制药株式会社 用于对器官或组织的移植的排异反应或骨髓移植的移植物抗宿主反应预防或治疗的药物组合物
MX2007001661A (es) 2004-08-13 2007-04-23 Praecis Pharm Inc Metodos y composiciones para modular la actividad del receptor de esfingosina -1 fosfato (sip).
EP1806338B1 (en) 2004-10-12 2016-01-20 Kyorin Pharmaceutical Co., Ltd. Process for producing 2-amino-2-[2-[4-(3-benzyloxy-phenylthio)-2-chlorophenyl[ethyl]-1,3-propanediol hydrochloride and hydrates thereof. and intermediates the production thereof
ATE397582T1 (de) * 2004-10-22 2008-06-15 Bioprojet Soc Civ Neue dicarbonsäurederivate
EP2592066B1 (en) 2004-12-13 2014-12-03 Ono Pharmaceutical Co., Ltd. Aminocarboxylic acid derivative and medical use thereof
WO2006090849A1 (ja) * 2005-02-25 2006-08-31 Redox Bioscience Inc. 炎症性眼表面疾患の予防ないし治療剤
CN101203512A (zh) * 2005-04-22 2008-06-18 第一三共株式会社 杂环化合物
SI1932522T1 (sl) * 2005-10-07 2012-08-31 Kyorin Seiyaku Kk Terapevtsko sredstvo za jetrno bolezen, ki vsebuje 2-amino-1,3- propandiolni derivat kot aktivno sestavino
EP1988083B1 (en) 2006-02-03 2014-04-02 Taisho Pharmaceutical Co., Ltd. Triazole derivative
JP5218737B2 (ja) 2006-02-06 2013-06-26 大正製薬株式会社 スフィンゴシン−1−リン酸結合阻害物質
TWI389683B (zh) * 2006-02-06 2013-03-21 Kyorin Seiyaku Kk A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient
WO2007099423A1 (en) * 2006-03-02 2007-09-07 Pfizer Products Inc. 1-pyrrolidine indane derivatives as histamine-3 receptor antagonists
MX2008012738A (es) * 2006-04-03 2009-02-06 Astellas Pharma Inc Heterocompuesto.
JPWO2007129745A1 (ja) 2006-05-09 2009-09-17 第一三共株式会社 ヘテロアリールアミド低級カルボン酸誘導体
MX2009001457A (es) 2006-08-08 2009-02-19 Kyorin Seiyaku Kk Derivados de aminoalcohol e inmunosupresores que contienen lo mismo como ingrediente activo.
JP5188972B2 (ja) * 2006-08-08 2013-04-24 杏林製薬株式会社 アミノリン酸エステル誘導体及びそれらを有効成分とするs1p受容体調節剤
JP2009269819A (ja) * 2006-08-25 2009-11-19 Asahi Kasei Pharma Kk アミン化合物
EP2014653A1 (en) * 2007-06-15 2009-01-14 Bioprojet Novel dicarboxylic acid derivatives as S1P1 receptor agonists
DK2177512T3 (da) 2007-08-01 2012-06-18 Taisho Pharmaceutical Co Ltd S1P1-bindingshæmmer
TWI580356B (zh) 2007-08-13 2017-05-01 孟山都科技有限責任公司 控制植物寄生性線蟲的化合物及方法以及被覆有該化合物之種子
WO2009099174A1 (ja) 2008-02-07 2009-08-13 Kyorin Pharmaceutical Co., Ltd. アミノアルコール誘導体を有効成分とする炎症性腸疾患の治療剤又は予防剤
US20090298894A1 (en) * 2008-04-21 2009-12-03 Asahi Kasei Pharma Corporation Amino acid compounds
BRPI0912545B1 (pt) * 2008-05-14 2022-02-01 The Scripps Research Institute Compostos moduladores de receptores de esfingosina fosfato, uso dos mesmos e composição e combinação farmacêutica compreendendo os ditos compostos
SI2291080T1 (sl) 2008-05-14 2015-11-30 The Scripps Research Institute Novi modulatorji sfingosinskih fosfatnih receptorjev
EA019252B1 (ru) 2008-07-23 2014-02-28 Арена Фармасьютикалз, Инк. ЗАМЕЩЕННЫЕ ПРОИЗВОДНЫЕ (1,2,3,4-ТЕТРАГИДРОЦИКЛОПЕНТА[b]ИНДОЛ-3-ИЛ)УКСУСНОЙ КИСЛОТЫ, ПРИМЕНИМЫЕ В ЛЕЧЕНИИ АУТОИММУННЫХ И ВОСПАЛИТЕЛЬНЫХ РАССТРОЙСТВ
SI2342205T1 (sl) 2008-08-27 2016-09-30 Arena Pharmaceuticals, Inc. Substituirani triciklični kislinski derivati kot agonisti S1P1 receptorja, uporabni v zdravljenju avtoimunskih in vnetnih obolenj
ES2405054T3 (es) 2009-01-23 2013-05-30 Bristol-Myers Squibb Company Derivados de pirazol-1,2,4-oxadiazol como agonistas de esfingosina-1-fosfato
JP2012515787A (ja) 2009-01-23 2012-07-12 ブリストル−マイヤーズ スクイブ カンパニー 自己免疫疾患および炎症性疾患の処置におけるs1pアゴニストとしての置換オキサジアゾール誘導体
EP2389377B1 (en) 2009-01-23 2014-07-16 Bristol-Myers Squibb Company Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases
US8399451B2 (en) 2009-08-07 2013-03-19 Bristol-Myers Squibb Company Heterocyclic compounds
NZ599914A (en) * 2009-11-13 2014-08-29 Receptos Inc Selective heterocyclic sphingosine 1 phosphate receptor modulators
EA024801B1 (ru) * 2009-11-13 2016-10-31 Рецептос Ллк Селективные модуляторы рецептора сфингозин-1-фосфата
NZ599913A (en) * 2009-11-13 2014-08-29 Receptos Inc Sphingosine 1 phosphate receptor modulators and methods of chiral synthesis
US9062015B2 (en) 2009-12-14 2015-06-23 Merck Patent Gmbh Inhibitors of sphingosine kinase
SG10201906876PA (en) 2010-01-27 2019-09-27 Arena Pharm Inc Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof
SG183416A1 (en) 2010-03-03 2012-09-27 Arena Pharm Inc Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof
WO2011133734A1 (en) 2010-04-23 2011-10-27 Bristol-Myers Squibb Company 4 - (5 - isoxazolyl or 5 - pyrrazolyl -1,2,4- oxadiazol - 3 - yl) -mandelic acid amides as sphingosin- 1 - phosphate 1 rreceptor agonists
EP2619190B1 (en) 2010-09-24 2015-08-12 Bristol-Myers Squibb Company Substituted oxadiazole compounds and their use as s1p1 agonists
EP2706999B1 (en) 2011-05-13 2019-08-28 Celgene International II Sàrl Selective heterocyclic sphingosine 1 phosphate receptor modulators
MX386419B (es) 2015-01-06 2025-03-18 Arena Pharm Inc Metodos de condiciones de tratamiento relacionadas con el receptor s1p1.
EP3939965A1 (en) 2015-06-22 2022-01-19 Arena Pharmaceuticals, Inc. Crystalline l-arginine salt of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta[b]indol-3-yl)acetic acid for use in sipi receptor-associated disorders
MA47504A (fr) 2017-02-16 2019-12-25 Arena Pharm Inc Composés et méthodes de traitement de l'angiocholite biliaire primitive
WO2018151834A1 (en) 2017-02-16 2018-08-23 Arena Pharmaceuticals, Inc. Compounds and methods for treatment of inflammatory bowel disease with extra-intestinal manifestations
ES2987794T3 (es) 2018-06-06 2024-11-18 Arena Pharm Inc Procedimientos de tratamiento de afecciones relacionadas con el receptor S1P1
CN112955431A (zh) 2018-09-06 2021-06-11 艾尼纳制药公司 可用于治疗自身免疫性病症和炎性病症的化合物
EP4267117B1 (en) * 2020-12-23 2026-04-08 Celgene Corporation Carboxylic acid containing indanyl compounds for the treatment of neurodegenerative diseases
US11919879B2 (en) 2021-06-16 2024-03-05 Celgene Corporation Carboxylic acid containing azetidinyl compounds for the treatment of neurodegenerative diseases

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU7686891A (en) 1990-04-05 1991-10-30 American National Red Cross, The A protein family related to immediate-early protein expressed by human endothelial cells during differentiation
US5585476A (en) 1994-02-15 1996-12-17 Maclennan; Alexander J. Molecular cloning and expression of G-protein coupled receptors
US6495579B1 (en) * 1996-12-02 2002-12-17 Angiotech Pharmaceuticals, Inc. Method for treating multiple sclerosis
US5912144A (en) 1997-04-24 1999-06-15 Incyte Pharmaceuticals, Inc. Edg-1-receptor homolog
US6060272A (en) 1997-05-07 2000-05-09 Human Genome Sciences, Inc. Human G-protein coupled receptors
AU1865499A (en) 1997-12-30 1999-07-26 Allelix Biopharmaceuticals Inc. Identification of lysolipid receptors involved in inflammatory response
ATE273390T1 (de) 1997-12-30 2004-08-15 Nps Allelix Corp Säugertier edg-7 rezeptor homologen
WO1999046277A1 (en) 1998-03-09 1999-09-16 Smithkline Beecham Corporation HUMAN EDG-1c POLYNUCLEOTIDES AND POLYPEPTIDES AND METHODS OF USE
EP1071708A4 (en) 1998-04-23 2005-01-19 Smithkline Beecham Corp GENE OF THE EDG FAMILY, HUMAN H218
US6130067A (en) 1998-05-20 2000-10-10 Smithkline Beecham Corporation Human EDG3sb gene
AU5575299A (en) 1998-08-19 2000-03-14 Millennium Pharmaceuticals, Inc. 14274 receptor, a g-protein coupled receptor related to the edg receptor family
WO2000014233A1 (en) 1998-09-03 2000-03-16 Millennium Pharmaceuticals, Inc. 14275 receptor, a novel g-protein coupled receptor related to the edg receptor family
EP1112365A2 (de) 1998-09-11 2001-07-04 Max-Delbrück-Centrum Für Molekulare Medizin Humaner un muriner g-protein gekoppelter rezeptor edg6 (endothelial differentiation gen) und seine verwendung
KR20080104062A (ko) 1998-11-20 2008-11-28 아레나 파마슈티칼스, 인크. 사람의 오르판 g 단백질 커플링 수용체
US6812335B1 (en) 1999-03-23 2004-11-02 The Regents Of The University Of California Human polypeptide receptors for lysophospholipids and sphingolipids and nucleic acids encoding the same
US6323333B1 (en) 1999-04-05 2001-11-27 Smithkline Beecham Corporation Mouse EDG1
WO2000060056A1 (en) 1999-04-05 2000-10-12 Smithkline Beecham Corporation Mouse edg5 gene
CN1347411A (zh) * 1999-04-19 2002-05-01 盐野义制药株式会社 含有噁二唑环的磺酰胺衍生物
WO2001004139A2 (en) 1999-07-13 2001-01-18 Smithkline Beecham Corporation Human axor29 receptor
SE9902763D0 (sv) 1999-07-21 1999-07-21 Astra Pharma Inc Novel receptor
WO2001011022A1 (en) 1999-08-05 2001-02-15 Smithkline Beecham Corporation Mouse g-protein coupled receptor edg3
GB9923890D0 (en) 1999-10-08 1999-12-08 Pfizer Ltd Novel polypeptide
WO2001027137A2 (en) 1999-10-12 2001-04-19 Smithkline Beecham Corporation Rattus norvegicus (edg3)
WO2002059081A2 (en) * 2001-01-26 2002-08-01 Kirin Beer Kabushiki Kaisha Urea derivatives as inhibitors of ccr-3 receptor
ATE448193T1 (de) * 2002-01-18 2009-11-15 Merck & Co Inc ßN-(BENZYL)AMINOALKYL CARBOXYLATE, PHOSPHINATE, PHOSPHONATE UND TETRAZOLE ALS EDG REZEPTORAGONISTENß
US7479504B2 (en) * 2002-01-18 2009-01-20 Merck & Co., Inc. Edg receptor agonists
US20050070506A1 (en) 2002-01-18 2005-03-31 Doherty George A. Selective s1p1/edg1 receptor agonists
AU2003218056A1 (en) 2002-03-01 2003-09-16 Merck & Co., Inc. Aminoalkylphosphonates and related compounds as edg receptor agonists
US7309721B2 (en) 2002-03-01 2007-12-18 Merck + Co., Inc. Aminoalkylphosphonates and related compounds as Edg receptor agonists
JP2005533058A (ja) 2002-06-17 2005-11-04 メルク エンド カムパニー インコーポレーテッド Edg受容体アゴニストとしての1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)アゼチジン−3−カルボキシラートおよび1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)ピロリジン−3−カルボキシラート

Similar Documents

Publication Publication Date Title
JP2006511579A5 (https=)
JP2006528980A5 (https=)
CA2509218A1 (en) 1-(amino)indanes and (1,2-dihydro-3-amino)-benzofurans, benzothiophenes and indoles as edg receptor agonists
JP2008517915A5 (https=)
CA2952541C (en) Pyridazones and triazinones for the treatment and prophylaxis of hepatitis b virus infection
JP2007515432A5 (https=)
JP2010540593A5 (https=)
JP6813665B2 (ja) 4−ピリドン化合物またはその塩、それを含む医薬組成物および剤
ES2405054T3 (es) Derivados de pirazol-1,2,4-oxadiazol como agonistas de esfingosina-1-fosfato
CA2498051C (en) Pyrimidinone derivatives as therapeutic agents against acute and chronic inflammatory, ischaemic and remodelling processes
AU2012312305B2 (en) Acyclic cyanoethylpyrazoles as janus kinase inhibitors
WO2018011100A1 (en) Novel tetrahydropyrazolopyridine compounds for the treatment of infectious diseases
ES2649475T3 (es) Derivados de piridin-4-ilo
JP2010509342A5 (https=)
JP2009532417A5 (https=)
JP2013542994A5 (https=)
TW201010997A (en) Nicotinamide derivatives
ES2533095T3 (es) Agonistas de receptores de esfingosina-1-fosfato
JPH06506450A (ja) 喘息および呼吸器官の炎症の治療に有用なヘテロサイクリックアミン類
JP2011525192A5 (https=)
JP2002528490A5 (https=)
JP2002528493A5 (https=)
JP2009507909A5 (https=)
HRP20211121T1 (hr) Supstituirani biciklični spojevi
CA2475712A1 (en) Nicotinamide derivatives useful as pde4 inhibitors