JP2017532294A5 - - Google Patents

Download PDF

Info

Publication number
JP2017532294A5
JP2017532294A5 JP2017510289A JP2017510289A JP2017532294A5 JP 2017532294 A5 JP2017532294 A5 JP 2017532294A5 JP 2017510289 A JP2017510289 A JP 2017510289A JP 2017510289 A JP2017510289 A JP 2017510289A JP 2017532294 A5 JP2017532294 A5 JP 2017532294A5
Authority
JP
Japan
Prior art keywords
och
phenyl
compound
chch
sch
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
JP2017510289A
Other languages
English (en)
Japanese (ja)
Other versions
JP2017532294A (ja
JP6607924B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/046005 external-priority patent/WO2016028959A1/en
Publication of JP2017532294A publication Critical patent/JP2017532294A/ja
Publication of JP2017532294A5 publication Critical patent/JP2017532294A5/ja
Application granted granted Critical
Publication of JP6607924B2 publication Critical patent/JP6607924B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017510289A 2014-08-20 2015-08-20 置換二環式化合物 Active JP6607924B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462039622P 2014-08-20 2014-08-20
US62/039,622 2014-08-20
PCT/US2015/046005 WO2016028959A1 (en) 2014-08-20 2015-08-20 Substituted bicyclic compounds

Publications (3)

Publication Number Publication Date
JP2017532294A JP2017532294A (ja) 2017-11-02
JP2017532294A5 true JP2017532294A5 (enExample) 2018-09-27
JP6607924B2 JP6607924B2 (ja) 2019-11-20

Family

ID=54012322

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017510289A Active JP6607924B2 (ja) 2014-08-20 2015-08-20 置換二環式化合物

Country Status (34)

Country Link
US (6) US9522888B2 (enExample)
EP (1) EP3183242B1 (enExample)
JP (1) JP6607924B2 (enExample)
KR (1) KR102559465B1 (enExample)
CN (1) CN107148409B (enExample)
AR (1) AR101591A1 (enExample)
AU (1) AU2015305501B2 (enExample)
CA (1) CA2958560C (enExample)
CL (1) CL2017000382A1 (enExample)
CO (1) CO2017002312A2 (enExample)
CY (1) CY1124355T1 (enExample)
DK (1) DK3183242T3 (enExample)
EA (1) EA032415B1 (enExample)
ES (1) ES2877627T3 (enExample)
HR (1) HRP20211121T1 (enExample)
HU (1) HUE055567T2 (enExample)
IL (1) IL250613B (enExample)
LT (1) LT3183242T (enExample)
MA (1) MA40082B1 (enExample)
MX (1) MX381458B (enExample)
MY (1) MY179783A (enExample)
PE (1) PE20170445A1 (enExample)
PH (1) PH12017500261A1 (enExample)
PL (1) PL3183242T3 (enExample)
PT (1) PT3183242T (enExample)
RS (1) RS62118B1 (enExample)
SG (1) SG11201701221SA (enExample)
SI (1) SI3183242T1 (enExample)
SM (1) SMT202100391T1 (enExample)
TN (1) TN2017000026A1 (enExample)
TW (1) TWI689487B (enExample)
UY (1) UY36274A (enExample)
WO (1) WO2016028959A1 (enExample)
ZA (1) ZA201701210B (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR101591A1 (es) * 2014-08-20 2016-12-28 Bristol Myers Squibb Co Compuestos bicíclicos sustituidos
ES2859478T3 (es) * 2016-09-02 2021-10-04 Bristol Myers Squibb Co Compuestos heterocíclicos tricíclicos sustituidos
CA3066423A1 (en) * 2017-06-14 2018-12-20 Trevena, Inc. Compounds for modulating s1p1 activity and methods of using the same
US11059784B2 (en) * 2017-08-09 2021-07-13 Bristol-Myers Squibb Company Oxime ether compounds
WO2019032632A1 (en) 2017-08-09 2019-02-14 Bristol-Myers Squibb Company ALKYLPHENYL COMPOUNDS
MX2022005766A (es) 2019-11-19 2022-08-08 Trevena Inc Compuestos y métodos para la preparación de compuestos moduladores de esfingosina 1-fosfato tipo 1 (s1p1).
JP7653447B2 (ja) * 2020-03-27 2025-03-28 レセプトス・リミテッド・ライアビリティ・カンパニー スフィンゴシン1ホスフェート受容体モジュレーター
CN116903578B (zh) * 2023-09-04 2023-11-24 江西省药品检验检测研究院 连钱草中的酚酸类化合物及其提取分离方法与应用

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4200750A (en) 1977-01-07 1980-04-29 Westwood Pharmaceuticals Inc. 4-Substituted imidazo [1,2-a]quinoxalines
US6069143A (en) 1994-12-20 2000-05-30 Smithkline Beecham Corporation Fibrinogen receptor antagonists
ATE441654T1 (de) 2002-01-18 2009-09-15 Merck & Co Inc Edg-rezeptoragonisten
US20050070506A1 (en) 2002-01-18 2005-03-31 Doherty George A. Selective s1p1/edg1 receptor agonists
AU2003202994B2 (en) 2002-01-18 2007-11-22 Merck Sharp & Dohme Corp. N-(benzyl)aminoalkylcarboxylates, phosphinates, phosphonates and tetrazoles as Edg receptor agonists
JP2005531506A (ja) 2002-03-01 2005-10-20 メルク エンド カムパニー インコーポレーテッド Edg受容体作動薬としてのアミノアルキルホスホネートおよび関連化合物
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
AU2004251146A1 (en) 2003-05-19 2005-01-06 Irm, Llc Immunosuppressant compounds and compositions
AU2004299456B2 (en) 2003-12-17 2010-10-07 Merck Sharp & Dohme Corp. (3,4-disubstituted)propanoic carboxylates as S1P (Edg) receptor agonists
TW200538433A (en) 2004-02-24 2005-12-01 Irm Llc Immunosuppressant compounds and compositiions
JP2008517915A (ja) 2004-10-22 2008-05-29 メルク エンド カムパニー インコーポレーテッド S1p受容体アゴニストとしての2−(アリール)アザシクリルメチルカルボキシレート、スルホネート、ホスホネート、ホスフィネート及びヘテロ環
MX2007009848A (es) * 2005-02-14 2008-03-10 Univ Virginia Agonistas de esfingosina 1-fosfato comprendiendo cicloalcanos y heterociclos de 5 miembros substituidos por grupos amino y fenilo.
JP2008530197A (ja) 2005-02-18 2008-08-07 イノディア インク. 4−ヒドロキシイソロイシンの類似体及びその使用
EP1858889A1 (en) 2005-03-08 2007-11-28 Biota Scientific Management Pty. Ltd. Bicyclic nucleosides and nucleotides as therapeutic agents
BRPI0609668A2 (pt) 2005-03-23 2011-10-18 Actelion Pharmaceuticals Ltd composto, composição farmacêutica, e, uso de um composto
CN101203512A (zh) 2005-04-22 2008-06-18 第一三共株式会社 杂环化合物
JP2008545767A (ja) 2005-06-08 2008-12-18 ノバルティス アクチエンゲゼルシャフト 多環式オキサジアゾールまたはイソキサゾールおよびsip受容体リガンドとしてのそれらの使用
JP2009506046A (ja) 2005-08-23 2009-02-12 アイアールエム・リミテッド・ライアビリティ・カンパニー 免疫抑制剤化合物および組成物
EP1976513B1 (en) 2006-01-06 2016-08-24 Sunovion Pharmaceuticals Inc. Cycloalkylamines as monoamine reuptake inhibitors
MX2008009579A (es) 2006-01-27 2008-09-25 Univ Virginia Metodo para el tratamiento de dolor neuropatico.
WO2007088450A2 (en) 2006-02-01 2007-08-09 Pfizer Products Inc. Chromane antagonist of the h-3 receptor
US7790707B2 (en) 2006-03-21 2010-09-07 Epix Pharmaceuticals Inc. S1P receptor modulating compounds and use thereof
EP2001472A2 (en) 2006-03-23 2008-12-17 Merck and Co., Inc. Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use
MX2008012738A (es) 2006-04-03 2009-02-06 Astellas Pharma Inc Heterocompuesto.
JP2009269819A (ja) 2006-08-25 2009-11-19 Asahi Kasei Pharma Kk アミン化合物
SI2069335T1 (sl) 2006-09-08 2013-04-30 Actelion Pharmaceuticals Ltd. Derivati piridin-3-ila kot imunomodulacijska sredstva
CN101610674A (zh) * 2006-12-21 2009-12-23 艾博特公司 鞘氨醇-1-磷酸酯受体激动剂和拮抗剂化合物
CA2672727A1 (en) * 2006-12-21 2008-07-03 Abbott Laboratories Sphingosine-1-phosphate receptor agonist and antagonist compounds
US8217027B2 (en) 2006-12-21 2012-07-10 Abbott Laboratories Sphingosine-1-phosphate receptor agonist and antagonist compounds
GB0625648D0 (en) 2006-12-21 2007-01-31 Glaxo Group Ltd Compounds
JP2010521450A (ja) 2007-03-16 2010-06-24 アクテリオン ファーマシューティカルズ リミテッド S1p1/edg1受容体アゴニストとしてのアミノ−ピリジン誘導体
EA201070422A1 (ru) 2007-10-04 2010-12-30 Мерк Сероно С.А. Производные оксадиазола
CN101970430B (zh) 2007-11-01 2013-05-08 埃科特莱茵药品有限公司 嘧啶衍生物
GB0725105D0 (en) 2007-12-21 2008-01-30 Glaxo Group Ltd Compounds
PE20091339A1 (es) 2007-12-21 2009-09-26 Glaxo Group Ltd Derivados de oxadiazol con actividad sobre receptores s1p1
EP2280933B1 (en) 2008-04-01 2013-07-24 Theravance, Inc. 2 -aminotetralin derivatives as mu opioid receptor antagonists
AU2009304596A1 (en) 2008-10-17 2010-04-22 Akaal Pharma Pty Ltd S1P receptors modulators
WO2010065760A1 (en) 2008-12-04 2010-06-10 Exelixis, Inc. Imidazo [1,2a] pyridine derivatives, their use as s1p1 agonists and methods for their production
CA2743397C (en) 2008-12-18 2017-02-28 Mathilde Muzerelle Oxadiazole fused heterocyclic derivatives useful for the treatment of multiple sclerosis
EP2202232A1 (en) 2008-12-26 2010-06-30 Laboratorios Almirall, S.A. 1,2,4-oxadiazole derivatives and their therapeutic use
EP2210890A1 (en) 2009-01-19 2010-07-28 Almirall, S.A. Oxadiazole derivatives as S1P1 receptor agonists
WO2010085582A1 (en) 2009-01-23 2010-07-29 Bristol-Myers Squibb Company Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases
WO2010085581A1 (en) 2009-01-23 2010-07-29 Bristol-Myers Squibb Company Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases
WO2010085584A1 (en) 2009-01-23 2010-07-29 Bristol-Myers Squibb Company Pyrazole-i, 2, 4 -oxad iazole derivatives as s.phing0sine-1-ph0sphate agonists
EP2395986A1 (en) 2009-02-10 2011-12-21 Abbott Laboratories Methods for preparing s1p receptor agonists and antagonists
US8399451B2 (en) 2009-08-07 2013-03-19 Bristol-Myers Squibb Company Heterocyclic compounds
CN102686571B (zh) * 2009-10-29 2015-11-25 百时美施贵宝公司 三环杂环化合物
TW201130488A (en) * 2010-02-03 2011-09-16 Daiichi Sankyo Co Ltd Pyrrole compound
ES2548683T3 (es) 2010-04-23 2015-10-20 Bristol-Myers Squibb Company Amidas del ácido 4-(5-isoxazolil o 5-pirrazolil-1,2,4-oxadiazol-3-il)-mandélico como agonistas de receptor de esfingosina-1-fosfato 1
CN102260617B (zh) 2010-05-25 2013-11-13 张孝忠 一种王浆特制酒及其制作工艺
CN102260177A (zh) 2010-05-25 2011-11-30 中国医学科学院药物研究所 丙二醇类衍生物、其制备方法和其药物组合物与用途
CN103124727B (zh) 2010-07-20 2015-03-25 百时美施贵宝公司 取代的3-苯基-1,2,4-噁二唑化合物
WO2012040532A1 (en) 2010-09-24 2012-03-29 Bristol-Myers Squibb Company Substituted oxadiazole compounds and their use as s1p1 agonists
WO2012061459A1 (en) 2010-11-03 2012-05-10 Bristol-Myers Squibb Company Heterocyclic compounds as s1p1 agonists for the treatment of autoimmune and vascular diseases
CN102250035A (zh) 2011-06-10 2011-11-23 北京富卡生物技术有限公司 二芳基取代-1,3,4-噁二唑化合物的合成方法和其药物用途
JP5984051B2 (ja) 2012-07-12 2016-09-06 株式会社Gsユアサ 電極体
TWI631097B (zh) 2012-07-27 2018-08-01 百健Ma公司 作爲s1p調節劑及/或atx調節劑之化合物
US9115054B2 (en) 2013-02-21 2015-08-25 Bristol-Myers Squibb Company Tetrahydronaphthalenyl compounds useful as sipi agonists
AR101591A1 (es) * 2014-08-20 2016-12-28 Bristol Myers Squibb Co Compuestos bicíclicos sustituidos

Similar Documents

Publication Publication Date Title
JP6952695B2 (ja) インフルエンザウイルス複製の阻害剤、その適用方法および使用
JP2015514808A5 (enExample)
JP2016506369A5 (enExample)
JP2018516963A5 (enExample)
JP2018535963A5 (enExample)
JP2015504067A5 (enExample)
JP2016514719A5 (enExample)
JP2019509276A5 (enExample)
JP2018517746A5 (enExample)
JP2015501833A5 (enExample)
JP2016525130A5 (enExample)
JP2016517417A5 (enExample)
JP2017504650A5 (enExample)
JP2012533630A5 (enExample)
JP2013533883A5 (enExample)
JP2012519691A5 (enExample)
JP2016530259A5 (enExample)
JP2016503797A5 (enExample)
RU2015127827A (ru) Производные бензилиденгуанидина и их терапевтическое применение для лечения заболеваний, связанных с неправильным сворачиванием белков
JP2013529210A5 (enExample)
JP2009526761A5 (enExample)
JP2017533968A5 (enExample)
JP2005526857A5 (enExample)
JP2016504400A5 (enExample)
JP2013510825A5 (enExample)