JP2015500795A5 - - Google Patents

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Publication number
JP2015500795A5
JP2015500795A5 JP2014535990A JP2014535990A JP2015500795A5 JP 2015500795 A5 JP2015500795 A5 JP 2015500795A5 JP 2014535990 A JP2014535990 A JP 2014535990A JP 2014535990 A JP2014535990 A JP 2014535990A JP 2015500795 A5 JP2015500795 A5 JP 2015500795A5
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Japan
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optionally substituted
compound according
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alkyl
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JP2014535990A
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Japanese (ja)
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JP6254088B2 (ja
JP2015500795A (ja
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Priority claimed from PCT/US2012/060464 external-priority patent/WO2013059215A1/en
Publication of JP2015500795A publication Critical patent/JP2015500795A/ja
Publication of JP2015500795A5 publication Critical patent/JP2015500795A5/ja
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Publication of JP6254088B2 publication Critical patent/JP6254088B2/ja
Expired - Fee Related legal-status Critical Current
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JP2014535990A 2011-10-17 2012-10-16 置換ビアリールアルキルアミド Expired - Fee Related JP6254088B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161548076P 2011-10-17 2011-10-17
US61/548,076 2011-10-17
PCT/US2012/060464 WO2013059215A1 (en) 2011-10-17 2012-10-16 Substituted biaryl alkyl amides

Publications (3)

Publication Number Publication Date
JP2015500795A JP2015500795A (ja) 2015-01-08
JP2015500795A5 true JP2015500795A5 (OSRAM) 2015-12-03
JP6254088B2 JP6254088B2 (ja) 2017-12-27

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ID=47148954

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014535990A Expired - Fee Related JP6254088B2 (ja) 2011-10-17 2012-10-16 置換ビアリールアルキルアミド

Country Status (8)

Country Link
US (3) US8822527B2 (OSRAM)
EP (1) EP2768799B1 (OSRAM)
JP (1) JP6254088B2 (OSRAM)
CN (1) CN104011013B (OSRAM)
AU (1) AU2012326361B2 (OSRAM)
CA (1) CA2850987C (OSRAM)
MX (2) MX360188B (OSRAM)
WO (1) WO2013059215A1 (OSRAM)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2850987C (en) 2011-10-17 2019-10-15 Biotheryx, Inc. Substituted biaryl alkyl amides
WO2016199688A1 (ja) * 2015-06-10 2016-12-15 住友化学株式会社 カーバメート化合物の製造方法
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
EP3454862B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
WO2017197055A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN110769822A (zh) 2017-06-20 2020-02-07 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
US20200157144A1 (en) * 2017-08-01 2020-05-21 Agency For Science, Technology And Research Antimicrobial peptidomimetics
EP3679026A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Glutarimide
EP3679028A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Dihydroquinolinones
CN111315735B (zh) 2017-09-04 2024-03-08 C4医药公司 二氢苯并咪唑酮
CN107540574B (zh) * 2017-09-19 2021-06-11 成都西岭源药业有限公司 R-联苯丙氨醇的制备方法
EP3710002A4 (en) 2017-11-16 2021-07-07 C4 Therapeutics, Inc. DEGRADATION AND DEGRADATION AGENTS FOR TARGETED PROTEIN DEGRADATION
WO2019191112A1 (en) 2018-03-26 2019-10-03 C4 Therapeutics, Inc. Cereblon binders for the degradation of ikaros
WO2019204354A1 (en) 2018-04-16 2019-10-24 C4 Therapeutics, Inc. Spirocyclic compounds
CN109053495B (zh) * 2018-07-23 2021-05-28 江苏宇田医药有限公司 一种lcz696中间体的合成方法
CN120698985A (zh) 2018-12-20 2025-09-26 C4医药公司 靶向蛋白降解
JP7687721B2 (ja) * 2020-12-25 2025-06-03 エムティックスバイオ カンパニ- リミテッド 新規なアミノアルカン酸にビフェニル基を導入した誘導体化合物およびそれを含む抗炎症用組成物

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2139588T3 (es) 1991-03-05 2000-02-16 Ajinomoto Kk Derivado de ciclopropano.
JPH10101656A (ja) 1996-10-01 1998-04-21 Sumitomo Chem Co Ltd オキサゾール化合物の製造法
JPH10101655A (ja) 1996-10-01 1998-04-21 Sumitomo Chem Co Ltd オキサゾリン類、その製造法およびそれを用いるスレオ−3−芳香族セリン類の製造法
HUP0004436A3 (en) 1997-09-09 2001-09-28 Procter & Gamble Aromatic c16-c20-substituted tetrahydro prostaglandins useful as fp agonists
US6239134B1 (en) 1999-03-03 2001-05-29 American Home Products Corp. Diazole derivatives as serotonergic agents
JP2002538152A (ja) 1999-03-03 2002-11-12 ワイス セロトニン作動薬としての新規なジアゾール誘導体
JP2005508355A (ja) 2001-10-19 2005-03-31 トランス テック ファーマ,インコーポレイテッド 治療薬としてのビス−ヘテロアリールアルカン
ITRM20020016A1 (it) 2002-01-15 2003-07-15 Sigma Tau Ind Farmaceuti Derivati di acidi fenil(alchil)carbossilici e derivati fenilalchileterociclici dionici, loro uso come medicamenti ad attivita' ipoglicemizza
US7109243B2 (en) 2003-03-24 2006-09-19 Irm Llc Inhibitors of cathepsin S
WO2005014532A1 (en) 2003-08-08 2005-02-17 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions and methods of use
JP2007501844A (ja) * 2003-08-08 2007-02-01 トランス テック ファーマ,インコーポレイテッド アリール及びヘテロアリール化合物、組成物並びに使用方法
RU2006112342A (ru) 2003-10-28 2007-12-10 Д-р Редди`с Лабораторис Лтд (IN) Новые соединения и их использование в медицине, способ их получения и содержащие их фармацетические композиции
US7618981B2 (en) * 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
US7795448B2 (en) * 2004-05-06 2010-09-14 Cytokinetics, Incorporated Imidazoyl-benzamide anti-cancer agents
WO2006015279A1 (en) 2004-07-28 2006-02-09 Neurogen Corporation Heterocyclic diamine compounds as ligands of the melanin concentrating hormone receptor useful for the treatment of obesity, diabetes, eating and sexual disorders
US7618983B2 (en) 2004-11-10 2009-11-17 Janssen Pharmaceutica, N.V. Bicyclic triazole α4 integrin inhibitors
US20080175795A1 (en) 2005-06-30 2008-07-24 Bexel Pharmaceuticals, Inc. Novel derivatives of amino acids for treatment of obesity and related disorders
US7399786B2 (en) 2005-06-30 2008-07-15 Bexel Pharmaceuticals, Inc. Derivatives of amino acids for treatment of obesity and related disorders
JP2009511589A (ja) 2005-10-12 2009-03-19 エラン ファーマシューティカルズ,インコーポレイテッド アリール−シクロプロピル誘導体のアスパルチルプロテアーゼ阻害剤を使用してアミロイドーシスを治療する方法
CA2629317A1 (en) 2005-11-16 2007-05-24 Merck & Co., Inc. Imidazolidinone compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease
WO2007083776A1 (ja) 2006-01-17 2007-07-26 Sumitomo Chemical Company, Limited 光学活性ビフェニルアラニン化合物またはその塩およびそのエステルの製造方法
US8980833B2 (en) * 2007-05-10 2015-03-17 R&D-Biopharmaceuticals Gmbh Tubulysine derivatives
RS51912B (sr) 2007-07-27 2012-02-29 Sanofi DERIVATI 1,2,3,4-TETRAHIDROPIROLO(1,2-a)PIRAZIN-6-KARBOKSAMIDA I 2,3,4,5-TETRAHIDROPIROLO(1,2-a)(1,4)-DIAZEPIN-7-KARBOKSAMIDA NJIHOVO DOBIJANJE I TERAPEUTSKA PRIMENA
EP2215065B1 (en) 2007-10-19 2012-07-11 Boehringer Ingelheim International GmbH Ccr10 antagonists
US20100022767A1 (en) 2008-07-25 2010-01-28 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. Development of a synthesis of syringolin a and b and derivatives thereof
JP2011529500A (ja) * 2008-07-28 2011-12-08 ジェンザイム コーポレーション 虚脱性糸球体症および他の糸球体疾患の処置のためのグルコシルセラミドシンターゼ阻害
DK2413693T3 (en) 2009-03-30 2015-11-16 Vtv Therapeutics Llc Substituted azoanthracenderivater, pharmaceutical compositions and methods for use thereof
CN101555211B (zh) 2009-05-13 2012-01-25 浙江九洲药业股份有限公司 2-酰基氨基-3-联苯基丙酸的化学合成方法
MX2011012628A (es) 2009-05-28 2011-12-14 Novartis Ag Derivados amino-propionicos sustituidos como inhibidores de neprilisina.
WO2011048091A1 (en) 2009-10-21 2011-04-28 Glaxo Group Limited Process for preparing a phenylalanine derivative
WO2011106721A1 (en) * 2010-02-26 2011-09-01 The Regents Of The University Of Colorado, A Body Corporate Flurbiprofen analogs and methods of use in treating cancer
JP5944921B2 (ja) 2010-12-15 2016-07-05 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤
CA2850987C (en) 2011-10-17 2019-10-15 Biotheryx, Inc. Substituted biaryl alkyl amides

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