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PL3873884T3 - Pochodne 3-(chinolin-8-ylo)-1,4-dihydropirydo[3,4-d]pirymidyno-2,4-dionu jako inhibitory integryny alfa4beta7 do leczenia chorób zapalnych - Google Patents

Pochodne 3-(chinolin-8-ylo)-1,4-dihydropirydo[3,4-d]pirymidyno-2,4-dionu jako inhibitory integryny alfa4beta7 do leczenia chorób zapalnych

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Publication number
PL3873884T3
PL3873884T3 PL19805484.3T PL19805484T PL3873884T3 PL 3873884 T3 PL3873884 T3 PL 3873884T3 PL 19805484 T PL19805484 T PL 19805484T PL 3873884 T3 PL3873884 T3 PL 3873884T3
Authority
PL
Poland
Prior art keywords
dihydropyrido
quinolin
pyrimidin
treatment
inflammatory diseases
Prior art date
Application number
PL19805484.3T
Other languages
English (en)
Inventor
Peter A. Blomgren
Taryn CAMPBELL
Jayaraman Chandrasekhar
Christopher T. Clark
Julian A. Codelli
Kevin S. Currie
Jeffrey E. Kropf
Yasamin MOAZAMI
Nicole NAVA
Leena Patel
Stephane Perreault
Jason K. Perry
Kassandra F. Sedillo
Natalie SEEGER
Kirk L. Stevens
Jennifer Anne Treiberg
Suet C. YEUNG
Zhongdong Zhao
Original Assignee
Gilead Sciences, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Gilead Sciences, Inc. filed Critical Gilead Sciences, Inc.
Publication of PL3873884T3 publication Critical patent/PL3873884T3/pl

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Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3773573A4 (en) 2018-04-12 2022-04-06 Morphic Therapeutic, Inc. ANTAGONISTS OF HUMAN INTEGRIN (ALPHA4) (BETA7)
WO2020092394A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
EP3873897B1 (en) 2018-10-30 2024-08-14 Gilead Sciences, Inc. N-benzoyl-phenylalanine derivatives as alpha4beta7 integrin inhibitors for treating inflammatory diseases
DK3873884T3 (da) 2018-10-30 2025-02-17 Gilead Sciences Inc 3-(quinolin-8-yl)-1,4-dihydropyrido[3,4-d]pyrimidin-2,4-dion-derivater som alpha4beta7-integrinhæmmere til behandling af inflammatoriske sygdomme
PL3873605T3 (pl) 2018-10-30 2025-03-03 Gilead Sciences, Inc. Związki hamujące integrynę alfa4beta7
US11578069B2 (en) 2019-08-14 2023-02-14 Gilead Sciences, Inc. Compounds for inhibition of α4 β7 integrin
RS66976B1 (sr) 2019-10-16 2025-07-31 Morphic Therapeutic Inc Inhibiranje ljudskog integrina alfa4beta7
CN111518192A (zh) * 2020-05-26 2020-08-11 成都圣诺生物制药有限公司 一种Apraglutide的制备方法
CN112142661B (zh) * 2020-09-02 2022-04-12 苏州康润医药有限公司 3-氨基喹啉-5-羧酸甲酯的合成方法
WO2024249983A1 (en) * 2023-06-02 2024-12-05 Westol, Llc 2,8-dihydroxyquinoline glucuronide derivatives with enhanced properties for use as anticancer, antiviral, antimicrobial, and other therapeutic applications
WO2025106691A1 (en) * 2023-11-14 2025-05-22 Dice Molecules Sv, Inc. Alpha 4 beta 7 integrin modulators and uses thereof
WO2025106410A1 (en) * 2023-11-15 2025-05-22 Dice Molecules Sv, Inc. Alpha 4 beta 7 integrin modulators and uses thereof
WO2025117506A1 (en) * 2023-11-29 2025-06-05 Gilead Sciences, Inc. Therapies for the treatment of inflammatory bowel disease

Family Cites Families (235)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2150550A1 (en) 1992-12-01 1994-06-09 Melissa S. Egbertson Fibrinogen receptor antagonists
JPH10502349A (ja) 1994-06-29 1998-03-03 テキサス・バイオテクノロジー・コーポレイシヨン インテグリンα▲下4▼β▲下1▼のVCAM−1またはフィブロネクチンへの結合を阻害する方法
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
JPH11511137A (ja) 1995-08-08 1999-09-28 ファイブロゲン,インコーポレーテッド コラーゲンの過剰生産に関係した疾患を治療するためのc−プロテイナーゼ阻害剤
WO1998004247A1 (en) 1996-07-25 1998-02-05 Biogen, Inc. Cell adhesion inhibitors
WO1998042656A1 (en) 1997-03-21 1998-10-01 Cytel Corporation Novel compounds
EP0998282A4 (en) 1997-05-29 2000-08-30 Merck & Co Inc SULPHONAMIDES AS CELL ADHESION INHIBITORS
JP2001517245A (ja) 1997-05-29 2001-10-02 メルク エンド カンパニー インコーポレーテッド 細胞接着阻害薬としてのビアリールアルカン酸類
CA2291778A1 (en) 1997-05-29 1998-12-03 Merck & Co., Inc. Heterocyclic amide compounds as cell adhesion inhibitors
PT991619E (pt) 1997-06-23 2004-02-27 Upjohn Co Inibidores da adesao celular mediada pela alfa4beta1
IL133640A0 (en) 1997-07-31 2001-04-30 Elan Pharm Inc Substituted phenylalanine type compounds which inhibit leukocyte adhesion mediated by vla-4
CA2291473A1 (en) 1997-07-31 1999-02-11 Elan Pharmaceuticals, Inc. Benzyl compounds which inhibit leukocyte adhesion mediated by vla-4
DE69834642T2 (de) 1997-07-31 2007-05-03 Elan Pharmaceuticals, Inc., South San Francisco Verbindungen mit einer 4-amino-phenylalaningruppe, die die vla-4 vermittelte adhäsion von leukozyten inhibieren
AU8823498A (en) 1997-07-31 1999-02-22 American Home Products Corporation Sulfonylated dipeptide compounds which inhibit leukocyte adhesion mediated by vla-4
WO1999013898A1 (en) 1997-08-15 1999-03-25 Stefan Niewiarowski EC-3, AN INHIBITOR OF α4β1 AND α4β7 INTEGRINS
RU2220950C2 (ru) 1997-08-22 2004-01-10 Ф.Хоффманн-Ля Рош Аг N-алканоилфенилаланиновые производные
JP3727536B2 (ja) 1997-08-22 2005-12-14 エフ.ホフマン−ラ ロシュ アーゲー N−アルカノイルフェニルアラニン誘導体
WO1999025731A1 (fr) 1997-11-13 1999-05-27 Toray Industries, Inc. Peptides cycliques et leur utilisation medicinale
EP1034164B1 (en) 1997-11-24 2004-05-19 Merck & Co., Inc. Substituted beta-alanine derivatives as cell adhesion inhibitors
CA2309338A1 (en) 1997-11-24 1999-06-03 Merck & Co., Inc. Cyclic amino acid derivatives as cell adhesion inhibitors
US6645939B1 (en) 1997-11-24 2003-11-11 Merck & Co., Inc. Substituted β-alanine derivatives as cell adhesion inhibitors
DE69830806T2 (de) 1997-12-17 2006-04-27 Merck & Co., Inc. Integrinrezeptor antagonisten
MY153569A (en) * 1998-01-20 2015-02-27 Mitsubishi Tanabe Pharma Corp Inhibitors of ?4 mediated cell adhesion
JP4949552B2 (ja) 1998-04-16 2012-06-13 エンサイシブ・フアーマシユーテイカルズ,インコーポレイテツド インテグリンのそれの受容体への結合を阻害するn,n−ジ置換アミド
PT1082302E (pt) 1998-05-28 2004-04-30 Biogen Inc Um inibidor de amt-4: omepupa-v
GB9811969D0 (en) 1998-06-03 1998-07-29 Celltech Therapeutics Ltd Chemical compounds
AU8059598A (en) 1998-06-11 1999-12-30 Merck & Co., Inc. Heterocyclic amide compounds as cell adhesion inhibitors
TW591026B (en) 1998-06-23 2004-06-11 Upjohn Co Inhibitors of alpha4beta1 mediated cell adhesion
WO2000002903A1 (en) 1998-07-10 2000-01-20 Cytel Corporation Cs-1 peptidomimetics, compositions and methods of using the same
WO2000005223A2 (en) 1998-07-23 2000-02-03 Astrazeneca Ab Heterocyclic derivatives and their use as integrin inhibitors
DE69934238T2 (de) 1998-08-26 2007-06-21 Aventis Pharma Ltd., West Malling Azabicyclo-verbindungen welche die inhibition der zell adhesion modulieren
BR9916211A (pt) 1998-12-14 2001-09-11 American Home Prod Derivados de 3,4-diamino-3-ciclobuteno-1,2-diona que inibem adesão de leucócito mediada por vla-4
GB9828074D0 (en) 1998-12-18 1999-02-17 Glaxo Group Ltd Therapeutically useful compounds
WO2000043372A1 (en) 1999-01-22 2000-07-27 Elan Pharmaceuticals, Inc. Acyl derivatives which treat vla-4 related disorders
DE60021251D1 (de) 1999-01-22 2005-08-18 Elan Pharm Inc Multizyklische verbindungen zur hemmung der durch vla-4 vermittelten leukozytenadhäsion
EP1147091A2 (en) 1999-01-22 2001-10-24 Elan Pharmaceuticals, Inc. Fused ring heteroaryl and heterocyclic compounds which inhibit leukocyte adhesion mediated by vla-4
CN1195773C (zh) 1999-01-26 2005-04-06 依兰制药公司 可以抑制由vla-4介导的白细胞粘着的焦谷氨酸衍生物及相关化合物
SI1154993T1 (en) 1999-02-18 2004-12-31 F. Hoffmann-La Roche Ag Thioamide derivatives
EP1161416B1 (en) 1999-03-01 2004-04-14 Elan Pharmaceuticals, Inc. Alpha-aminoacetic acid derivatives useful as alpha 4 beta 7 - receptor antagonists
US6265572B1 (en) 1999-04-20 2001-07-24 Hoffmann-La Roche Inc. Pyrrolidincarbonylamino cyclic disulfide anti-inflammatory agents
GB9909409D0 (en) 1999-04-24 1999-06-23 Zeneca Ltd Chemical compounds
MXPA01011340A (es) 1999-05-07 2003-08-01 Texas Biotechnology Corp Derivados de acido carboxilico que inhiben la union de las integrinas a sus receptores.
AR035011A1 (es) 1999-06-30 2004-04-14 Daiichi Seiyaku Co Compuestos inhibidores de vla-4
JP3795305B2 (ja) 1999-07-19 2006-07-12 田辺製薬株式会社 医薬組成物
WO2001007400A1 (en) 1999-07-26 2001-02-01 Toray Industries, Inc. Carboxylic acid derivatives and adhesion molecule inhibitors containing the same as the active ingredient
KR100720907B1 (ko) 1999-08-13 2007-05-25 바이오겐 아이덱 엠에이 인코포레이티드 세포 유착 억제제
US6420418B1 (en) 1999-08-16 2002-07-16 Merck & Co., Inc. Heterocycle amides as cell adhesion inhibitors
AU6909300A (en) 1999-08-20 2001-03-19 Merck & Co., Inc. Substituted ureas as cell adhesion inhibitors
PT1214292E (pt) 1999-09-24 2007-09-14 Genentech Inc Derivados de tirosina
AU7961200A (en) 1999-10-29 2001-05-14 Kaken Pharmaceutical Co., Ltd. Urea derivative, process for producing the same, and medicine containing the urea derivative
ATE355269T1 (de) 1999-11-18 2006-03-15 Ajinomoto Kk Phenylalaninderivate
MXPA02005564A (es) 1999-12-06 2002-09-02 Hoffmann La Roche 4-pirimidinil-n-acil-l.fenilalaninas.
NZ518888A (en) 1999-12-06 2004-02-27 F 4-pyridinyl-N-acyl-L-phenylalanines
DE60043308D1 (de) 1999-12-16 2009-12-24 Biogen Idec Inc Verfahren zur behandlung der schädigung des zentralnervensystems durch ischämie oder durch hämorrhagie mit antagonisten von alpha4 integrin
DE19962936A1 (de) 1999-12-24 2001-06-28 Bayer Ag Neue beta-Aminosäureverbindungen als Integrinantagonisten
AU2224901A (en) 1999-12-28 2001-07-09 Ajinomoto Co., Inc. Novel phenylalanine derivatives
GB0001348D0 (en) 2000-01-21 2000-03-08 Astrazeneca Uk Ltd Chemical compounds
GB0001346D0 (en) 2000-01-21 2000-03-08 Astrazeneca Uk Ltd Chemical compounds
WO2001055121A1 (en) 2000-01-28 2001-08-02 Kaken Pharmaceutical Co., Ltd. Azepine derivatives
ES2341843T3 (es) 2000-02-03 2010-06-29 EISAI R&D MANAGEMENT CO., LTD. Inhibidores de la expresion de integrina.
WO2001056994A1 (en) 2000-02-04 2001-08-09 Biogen, Inc. Integrin antagonists
WO2001068586A2 (en) 2000-03-14 2001-09-20 Novartis Ag α4β1 AND α4β7 INTEGRIN INHIBITORS
WO2001070670A1 (en) 2000-03-23 2001-09-27 Ajinomoto Co., Inc. Novel phenylalanine derivative
US6960597B2 (en) 2000-06-30 2005-11-01 Orth-Mcneil Pharmaceutical, Inc. Aza-bridged-bicyclic amino acid derivatives as α4 integrin antagonists
PE20020384A1 (es) 2000-07-21 2002-05-28 Schering Corp PEPTIDOS COMO INHIBIDORES DE LA PROTEASA SERINA NS3/NS4a DEL VIRUS DE LA HEPATITIS C
WO2002008206A1 (en) 2000-07-21 2002-01-31 Elan Pharmaceuticals, Inc. 3-amino-2-(4-aminocarbonyloxy)phenyl-propionic acid derivatives as alpha-4- integrin inhibitors
US6794506B2 (en) 2000-07-21 2004-09-21 Elan Pharmaceuticals, Inc. 3-(heteroaryl) alanine derivatives-inhibitors of leukocyte adhesion mediated by VLA-4
CA2419008A1 (en) 2000-08-11 2003-02-11 Kaken Pharmaceutical Co., Ltd. 2,3-diphenylpropionic acid derivatives or their salts, medicines or cell adhesion inhibitors containing the same, and their usage
WO2002016313A2 (en) 2000-08-18 2002-02-28 Genentech, Inc. Integrin receptor inhibitors
NZ524122A (en) 2000-08-18 2005-02-25 Ajinomoto Kk Phenylalanine derivatives useful as pharmaceutical agents
MY129000A (en) 2000-08-31 2007-03-30 Tanabe Seiyaku Co INHIBITORS OF a4 MEDIATED CELL ADHESION
JPWO2002022563A1 (ja) 2000-09-14 2004-01-22 東レ株式会社 ウレア誘導体及びそれを有効成分とする接着分子阻害剤
EP1329451B1 (en) 2000-09-25 2006-08-23 Toray Industries, Inc. Spiro compounds and adhesion molecule inhibitors containing the same as the active ingredient
JP4895067B2 (ja) 2000-09-29 2012-03-14 味の素株式会社 新規フェニルアラニン誘導体
US7157487B2 (en) 2000-12-28 2007-01-02 Daiichi Pharmaceutical Co., Ltd. Vla-4 inhibitors
ES2200617B1 (es) 2001-01-19 2005-05-01 Almirall Prodesfarma, S.A. Derivados de urea como antagonistas de integrinas alfa 4.
CN101025419A (zh) 2001-02-21 2007-08-29 卫材R&D管理有限公司 测定通过抑制整联蛋白表达所介导的血管生成抑制剂的作用的方法
PL364142A1 (pl) 2001-02-22 2004-12-13 Celltech R & D Limited Pochodne fenyloalaninoenamidu
EP1441006B1 (en) 2001-06-20 2009-09-23 Asahi Kasei Kabushiki Kaisha Thermoplastic resin composition
JP2005022976A (ja) 2001-07-18 2005-01-27 Ajinomoto Co Inc カルボン酸誘導体
WO2003010135A1 (en) 2001-07-26 2003-02-06 Ajinomoto Co., Inc. Novel phenylpropionic acid derivatives
US7557130B2 (en) 2001-07-26 2009-07-07 Ucb Pharma, S.A. Bicyclic heteroaromatic alanines
JP2003048889A (ja) 2001-08-01 2003-02-21 Ajinomoto Co Inc 新規核酸系化合物
WO2003016907A1 (fr) 2001-08-17 2003-02-27 Eisai Co. Ltd. Reactif de dosage pour antigene de la laminine 5 dans un echantillon biologique et procede de dosage
JPWO2003024933A1 (ja) 2001-09-12 2004-12-24 科研製薬株式会社 2−フェニル−3−ヘテロアリールプロピオン酸誘導体またはその塩、それを用いた医薬
GB0127423D0 (en) 2001-11-15 2002-01-09 Glaxo Group Ltd Process
JP4452899B2 (ja) 2001-12-13 2010-04-21 味の素株式会社 新規フェニルアラニン誘導体
AU2003211560A1 (en) 2002-02-20 2003-09-09 Ajinomoto Co., Inc. Novel phenylalanine derivative
JP4233353B2 (ja) 2002-02-27 2009-03-04 田辺三菱製薬株式会社 医薬組成物
MY140707A (en) 2002-02-28 2010-01-15 Mitsubishi Tanabe Pharma Corp Process for preparing a phenylalanine derivative and intermediates thereof
AU2003227186A1 (en) 2002-03-22 2003-10-08 Toray Industries, Inc. Spiro derivatives and adhesion molecule inhibitors comprising the same as the active ingredient
JP2003277340A (ja) 2002-03-22 2003-10-02 Toray Ind Inc 接着分子阻害剤及び新規アミノ酸誘導体
WO2003089410A1 (en) 2002-04-19 2003-10-30 Kyowa Hakko Kogyo Co., Ltd. Phenylalanine derivative
EP1870402A1 (en) 2002-04-30 2007-12-26 UCB Pharma, S.A. 2,6-quinolinyl and 2,6-naphthyl derivatives, processes for preparing them and their uses as VLA-4 inhibitors
TWI281470B (en) 2002-05-24 2007-05-21 Elan Pharm Inc Heterocyclic compounds which inhibit leukocyte adhesion mediated by alpha4 integrins
TW200307671A (en) 2002-05-24 2003-12-16 Elan Pharm Inc Heteroaryl compounds which inhibit leukocyte adhesion mediated by α 4 integrins
GB0216568D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
GB0216574D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
GB0216571D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
PL374971A1 (pl) 2002-08-09 2005-11-14 Transtech Pharma, Inc. Związki arolo-i heteroarylowe oraz sposoby modulowania krzepnięcia
GB0218630D0 (en) 2002-08-10 2002-09-18 Tanabe Seiyaku Co Novel compounds
SG2012000667A (en) 2003-01-08 2015-03-30 Univ Washington Antibacterial agents
KR20050114212A (ko) 2003-01-24 2005-12-05 엘란 파마슈티칼스, 인크. 수초재생제의 투여에 의한 탈수초성 질환 및 마비의 치료및 조성물
ES2548419T3 (es) 2003-02-20 2015-10-16 Ajinomoto Co., Inc. Procedimiento para producir un derivado de fenilalanina que tiene esqueleto de quinazolindiona e intermedio para el mismo
JP2004277338A (ja) 2003-03-14 2004-10-07 Nippon Soda Co Ltd N−アシルアミノ酸類の製造方法
ES2219177B1 (es) 2003-05-05 2006-02-16 Almirall Prodesfarma, S.A. Derivados de n-(2-feniletil) sulfamida como antagonistas de la integrina alfa4.
AU2004240940A1 (en) 2003-05-20 2004-12-02 Genentech, Inc. Thiocarbamate inhibitors of alpha-4 integrins
WO2005000244A2 (en) 2003-06-25 2005-01-06 Elan Pharmaceuticals, Inc. Methods and compositions for treating rheumatoid arthritis
MXPA06000850A (es) 2003-07-24 2006-03-30 Daiichi Seiyaku Co Compuesto de acido ciclohexancarboxilico.
WO2005014532A1 (en) 2003-08-08 2005-02-17 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions and methods of use
US20070099938A1 (en) 2003-10-24 2007-05-03 Ono Pharmaceutical Co., Ltd. Antistress drug and medical use thereof
US20050176755A1 (en) 2003-10-31 2005-08-11 Dyatkin Alexey B. Aza-bridged-bicyclic amino acid derivatives as alpha4 integrin antagonists
ATE551339T1 (de) 2003-11-05 2012-04-15 Sarcode Bioscience Inc Modulatoren der zellulären adhäsion
CN100563658C (zh) 2003-11-14 2009-12-02 味之素株式会社 苯丙氨酸衍生物的固体分散体或固体分散体医药制剂
EP3216449A1 (en) 2003-11-14 2017-09-13 EA Pharma Co., Ltd. Oral administration preparation of phenylalanine derivatives
CN1886385B (zh) 2003-11-27 2013-02-27 味之素株式会社 苯丙氨酸衍生物的结晶及其制造方法
GB0329584D0 (en) 2003-12-20 2004-01-28 Tanabe Seiyaku Co Novel compounds
WO2005061466A1 (ja) 2003-12-22 2005-07-07 Ajinomoto Co., Inc. 新規フェニルアラニン誘導体
MY140489A (en) 2003-12-26 2009-12-31 Eisai R&D Man Co Ltd 1,2-di (cyclic) substituted benzene compounds
EP1706399A1 (en) 2004-01-23 2006-10-04 Elan Pharmaceuticals, Inc. Polyethylene glycol conjugates of heterocycloalkyl carboxamido propanoic acids
EP1720839A1 (en) 2004-02-10 2006-11-15 Janssen Pharmaceutica N.V. Pyridazinones as antagonists of a4 integrins
KR20070001976A (ko) 2004-02-10 2007-01-04 얀센 파마슈티카 엔.브이. 알파4 인테그린의 길항제로서의 피리다지논 우레아
AU2005222074B2 (en) 2004-03-10 2011-02-17 Merck Sharp & Dohme Corp. VLA-4 antagonists
EP1763361A2 (en) 2004-04-01 2007-03-21 Elan Pharmaceuticals, Inc. Steroid sparing agents and their use
JP2007532681A (ja) 2004-04-16 2007-11-15 ジェネンテック・インコーポレーテッド B細胞の枯渇を増大させる方法
US7618981B2 (en) 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
TW200610754A (en) 2004-06-14 2006-04-01 Daiichi Seiyaku Co Vla-4 inhibitor
AR050425A1 (es) 2004-07-08 2006-10-25 Elan Pharm Inc Antagonistas multivalentes de vla-4 que comprende fracciones polimericas. composiciones farmaceuticas
US7196112B2 (en) 2004-07-16 2007-03-27 Biogen Idec Ma Inc. Cell adhesion inhibitors
CN101006097B (zh) 2004-08-16 2012-07-11 默沙东公司 Vla-4拮抗剂
JP2008512111A (ja) 2004-09-09 2008-04-24 オークランド ユニサービシズ リミテッド 炎症性疾患の治療のための新規ペプチド及び方法
US7618983B2 (en) 2004-11-10 2009-11-17 Janssen Pharmaceutica, N.V. Bicyclic triazole α4 integrin inhibitors
KR101274879B1 (ko) 2004-12-20 2013-06-14 에자이 알앤드디 매니지먼트 가부시키가이샤 1-시클로프로필메틸-4-[2-(3,3,5,5-테트라메틸시클로헥실)페닐]피페라진의 염 및 결정
WO2006066780A1 (en) 2004-12-22 2006-06-29 F. Hoffmann-La Roche Ag Combinations of valategrast and montelukast for treating asthma
DK1840121T3 (da) 2004-12-24 2012-11-26 Toray Industries Glycinderivat og anvendelse heraf
WO2006081986A1 (en) 2005-02-07 2006-08-10 F.Hoffmann-La Roche Ag Bambuterol and integrin inhibitor combination
WO2006090234A1 (en) 2005-02-22 2006-08-31 Ranbaxy Laboratories Limited Heterocyclic derivatives as cell adhesion inhibitors
US20060223846A1 (en) 2005-03-08 2006-10-05 Dyatkin Alexey B Aza-bridged-bicyclic amino acid derivatives as alpha4 integrin antagonists
JP2008536850A (ja) 2005-04-14 2008-09-11 メルク エンド カムパニー インコーポレーテッド Vla−4アンタゴニスト
WO2006112738A1 (en) 2005-04-19 2006-10-26 Auckland Uniservices Limited Novel peptides and methods for the treatment of inflammatory disorders
CN101163472A (zh) 2005-04-21 2008-04-16 默克公司 Vla-4拮抗剂
US8030328B2 (en) 2005-05-20 2011-10-04 Elan Pharmaceuticals, Inc. Imidazolone phenylalanine derivatives
CN101146760A (zh) 2005-05-25 2008-03-19 卫材R&D管理有限公司 [2-(3,3,5,5-四甲基环己基)苯基]哌嗪化合物的制备中间体
CA2609255A1 (en) 2005-05-25 2006-11-30 Eisai R&D Management Co., Ltd. Intermediate in production of [2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine compound
BRPI0611243A2 (pt) 2005-06-09 2010-08-24 Ucb Pharma Sa composto, enanciâmeros, diastereoisâmeros do mesmo ou um sal farmaceuticamente aceitÁvel do mesmo, composiÇço farmacÊutica, e, uso de um composto
JP2007023029A (ja) 2005-06-17 2007-02-01 Tanabe Seiyaku Co Ltd 医薬組成物
JP5046188B2 (ja) 2005-06-21 2012-10-10 味の素株式会社 フェニルアラニン誘導体の結晶、その製造方法及びその使用
TW200726767A (en) 2005-07-04 2007-07-16 Astrazeneca Ab Chemical compounds 2
WO2007069635A1 (ja) 2005-12-13 2007-06-21 Daiichi Sankyo Company, Limited Vla-4阻害薬
DE602007005601D1 (de) 2006-01-18 2010-05-12 Hoffmann La Roche Pharmazeutische zusammensetzungen, enthaltend valatograst, und verfahren zu deren herstellung
MY151045A (en) 2006-02-27 2014-03-31 Elan Pharm Inc Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4
US8410115B2 (en) 2006-02-28 2013-04-02 Elan Pharmaceuticals, Inc. Methods of treating inflammatory and autoimmune diseases with alpha-4 inhibitory compounds
ATE549321T1 (de) 2006-11-22 2012-03-15 Ajinomoto Kk Verfahren zur herstellung von phenylalaninderivaten mit chinazolindiongerüsten, und zwischenprodukte für die herstellung
WO2008064830A1 (en) 2006-11-27 2008-06-05 Ucb Pharma, S.A. Bicyclic and heterobicyclic derivatives, processes for preparing them and their pharmaceutical uses
HUE029188T2 (en) 2007-03-12 2017-03-28 Ym Biosciences Australia Pty Phenylamino-pyrimidine compounds and their use
WO2008125210A1 (en) 2007-04-12 2008-10-23 Ucb Pharma, S.A. Quinoline and naphthalene derivatives, processes for their preparation and their use in treatment of inflammatory diseases
WO2008138591A2 (en) 2007-05-14 2008-11-20 Ucb Pharma, S.A. Bicyclic and heterobicyclic derivatives,processes for preparing them and their uses
WO2008154642A2 (en) 2007-06-12 2008-12-18 Achaogen, Inc. Antibacterial agents
CA2708262A1 (en) 2007-12-07 2009-06-18 Elan Pharmaceuticals, Inc. Methods and compositions for treating liquid tumors
WO2009124755A1 (en) 2008-04-08 2009-10-15 European Molecular Biology Laboratory (Embl) Compounds with novel medical uses and method of identifying such compounds
CA2724413C (en) 2008-05-15 2016-10-18 Duke University Compositions and methods relating to heat shock transcription factor activating compounds and targets thereof
PL2310509T3 (pl) 2008-07-21 2015-08-31 Apogenix Ag Jednołańcuchowe cząsteczki TNFSF
WO2010104307A2 (ko) 2009-03-07 2010-09-16 주식회사 메디젠텍 세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
CN102498124B (zh) 2009-03-16 2015-05-13 多伦多大学管理委员会 环状氨基酸分子及其制备方法
GB0905641D0 (en) 2009-04-01 2009-05-13 Serodus As Compounds
CN102459179A (zh) 2009-04-27 2012-05-16 艾伦药物公司 α-4整联蛋白的吡啶酮拮抗剂
EP2491006A1 (en) 2009-10-21 2012-08-29 Glaxo Group Limited Process for preparing a phenylalanine derivative
WO2011094890A1 (en) 2010-02-02 2011-08-11 Argusina Inc. Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
EP2554169B1 (en) 2010-03-29 2019-11-20 EA Pharma Co., Ltd. Pharmaceutical preparation comprising phenylalanine derivative
EP2554542B1 (en) 2010-03-29 2015-10-07 Ajinomoto Co., Inc. Phenylalanine derivative hydrochloride salt crystal
JP2013528374A (ja) 2010-05-10 2013-07-11 パーシード セラピューティクス リミテッド ライアビリティ カンパニー Vla4のポリペプチド阻害剤
WO2011150499A1 (en) 2010-05-31 2011-12-08 The Governing Council Of The University Of Toronto A method to insert molecular fragments into cyclic molecules
WO2011159781A2 (en) 2010-06-17 2011-12-22 Senomyx, Inc. Bitter taste modulators
EP2595957B1 (en) 2010-07-20 2014-08-13 Council of Scientific & Industrial Research Pyridin-2-yl sulfanyl acid esters and process for the preparation thereof
ES2677668T3 (es) 2010-11-16 2018-08-06 Texas Heart Institute Agonistas que mejoran la unión de células que expresan integrina a receptores de integrina
CA2825599C (en) 2011-02-01 2021-07-13 The Board Of Trustees Of The University Of Illinois 4-methyl-n-hydroxybenzamide compounds as histone deacetylase (hdac) inhibitors
US20140357654A1 (en) 2011-11-09 2014-12-04 Aestus Therapeutics, Inc. METHODS OF TREATING SCHIZOPHRENIA WITH PHENYLALANINE ENAMIDE DERIVATIVE INHIBITORS OF a4 INTEGRIN POSSESSING A CYCLOBUTENE GROUP
KR20140127234A (ko) 2012-01-27 2014-11-03 에프. 호프만-라 로슈 아게 Vla-4 발현 세포로의 표적화된 전달을 위한 인테그린 안타고니스트 접합체
DK2806896T3 (en) 2012-01-27 2018-03-05 Hoffmann La Roche Chitosan covalently bound to small molecule integrin antagonist for targeted delivery
WO2013148978A1 (en) 2012-03-30 2013-10-03 Lexicon Pharmaceuticals, Inc. Methods and compositions for the treatment of necrotizing enterocolitis
DK2842945T3 (en) 2012-04-24 2017-01-30 Ea Pharma Co Ltd Sulfonamide derivative and medical use thereof
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
EP2900228A1 (en) 2012-09-26 2015-08-05 KFLP Biotech, LLC Compounds for the treatment and prevention of retroviral infections
WO2014051056A1 (ja) 2012-09-28 2014-04-03 東レ株式会社 グリシン誘導体の結晶及びその医薬用途
US20150045435A1 (en) 2013-08-06 2015-02-12 Indiana University Research And Technology Corporation Compounds and methods for treating diabetes
JP6399874B2 (ja) 2013-09-20 2018-10-03 エーザイ・アール・アンド・ディー・マネジメント株式会社 化合物の抗炎症効果または免疫抑制効果を予測する方法
BR112016009515B1 (pt) 2013-10-29 2022-05-03 EA Pharma Co., Ltd Derivado de sulfonamida, composição farmacêutica, agente terapêutico ou um agente preventivo para doença inflamatória, e, inibidor de integrina a4ß7
US9994560B2 (en) 2014-03-14 2018-06-12 Aerpio Therapeutics, Inc. HPTP-β inhibitors
WO2015172196A1 (en) 2014-05-13 2015-11-19 Monash University Heterocyclic compounds and use of same
JP2016037467A (ja) 2014-08-07 2016-03-22 味の素株式会社 スルホンアミド誘導体及びその医薬用途
JP2016037468A (ja) 2014-08-07 2016-03-22 味の素株式会社 スルホンアミド誘導体及びその医薬用途
KR102496364B1 (ko) 2014-09-10 2023-02-06 에피자임, 인코포레이티드 Smyd 억제제
JP6580053B2 (ja) 2014-09-29 2019-09-25 Eaファーマ株式会社 潰瘍性大腸炎の治療用医薬組成物
US10383842B2 (en) 2015-02-13 2019-08-20 Global Biolife Inc. Method and composition for preventing and treating viral infections
WO2016145258A1 (en) 2015-03-10 2016-09-15 The Regents Of The University Of California Anti-alphavbeta1 integrin inhibitors and methods of use
HK1247120A1 (zh) 2015-07-08 2018-09-21 艾克瑟罗视觉股份有限公司 用於治疗眼部炎性病症含有整联蛋白α4拮抗剂的药物组合物
ES2941969T3 (es) 2015-10-23 2023-05-29 Navitor Pharm Inc Moduladores de la interacción de Sestrina-GATOR2 y sus usos
CN105483206B (zh) 2016-01-06 2019-09-13 北京汉氏联合生物技术股份有限公司 一种用vcam-1检测msc促内皮细胞增殖能力的方法
WO2017126637A1 (ja) 2016-01-20 2017-07-27 味の素株式会社 炎症性腸疾患抑制剤
CN106995439B (zh) 2016-01-26 2019-09-20 镇江圣安医药有限公司 氘取代3-(甲磺酰基)-l-苯丙氨酸衍生物及其药物组合物、药物制剂和用途
WO2017132620A1 (en) 2016-01-29 2017-08-03 La Jolla Institute For Allergy And Immunology Methods and compositions using integrin-based therapeutics
JP6820282B2 (ja) 2016-02-05 2021-01-27 Eaファーマ株式会社 スルホンアミド誘導体及びそれを含有する医薬組成物
TW201731824A (zh) 2016-02-05 2017-09-16 Ea Pharma Co Ltd α4β7整合蛋白抑制劑
TW201823208A (zh) 2016-09-07 2018-07-01 美商普萊恩醫療公司 N-醯基胺基酸化合物及其使用方法
AU2017336523B2 (en) 2016-09-28 2022-07-21 Blade Therapeutics, Inc. Calpain modulators and therapeutic uses thereof
WO2018085574A2 (en) 2016-11-02 2018-05-11 Washington University Compositions comprising an integrin inhibitor and agents which interact with a chemokine and methods of use thereof
WO2018085552A1 (en) 2016-11-02 2018-05-11 Saint Louis University Integrin antagonists
JP7220653B2 (ja) 2016-11-08 2023-02-10 ブリストル-マイヤーズ スクイブ カンパニー アルファvインテグリン阻害剤としてのピロールアミド
PL3538525T3 (pl) 2016-11-08 2022-09-12 Bristol-Myers Squibb Company 3-podstawione kwasy propionowe jako inhibitory integryny alfa v
BR112019009245A2 (pt) 2016-11-08 2019-07-16 Bristol-Myers Squibb Company azol amidas e aminas como inibidores de alfav integrina
BR112019009129A2 (pt) 2016-11-08 2019-07-16 Bristol-Myers Squibb Company compostos mono e espirocíclicos contendo ciclobutano e azetidina como inibidores de alfa v integrina
MA46745A (fr) 2016-11-08 2021-03-31 Bristol Myers Squibb Co Dérivés d'indazole en tant qu'antagonistes de l'intégrine alpha v
CN116283977A (zh) 2017-02-28 2023-06-23 莫菲克医疗股份有限公司 αvβ6整合蛋白的抑制剂
EP3589285A4 (en) 2017-02-28 2020-08-12 Morphic Therapeutic, Inc. INHIBITORS OF INTEGRIN (ALPHA-V) (BETA-6)
ES3040534T3 (en) 2017-04-26 2025-11-03 Navitor Pharm Inc Modulator of sestrin-gator2 interaction for use in the treatment of treatment-resistant depression
US10875875B2 (en) 2017-04-26 2020-12-29 Aviara Pharmaceuticals, Inc. Propionic acid derivatives and methods of use thereof
US10246451B2 (en) 2017-04-26 2019-04-02 Aviara Pharmaceuticals, Inc. Propionic acid derivatives and methods of use thereof
JP2019031449A (ja) 2017-08-04 2019-02-28 Eaファーマ株式会社 スルホンアミド誘導体及びそれを含有する医薬組成物
CN109721605B (zh) 2017-10-31 2022-03-11 维眸生物科技(上海)有限公司 一种免疫细胞迁徙抑制剂
AU2018365793A1 (en) 2017-11-07 2020-06-18 Bristol-Myers Squibb Company Pyrrolopyrazine derivatives as alpha V integrin inhibitors
PE20201502A1 (es) 2018-03-07 2020-12-29 Pliant Therapeutics Inc Compuestos de aminoacidos y metodos de uso
WO2019178248A1 (en) 2018-03-13 2019-09-19 The Regents Of The University Of California Inhibitors of integrin alpha 2 beta 1 and methods of use
EP3773573A4 (en) 2018-04-12 2022-04-06 Morphic Therapeutic, Inc. ANTAGONISTS OF HUMAN INTEGRIN (ALPHA4) (BETA7)
WO2019246455A1 (en) 2018-06-20 2019-12-26 Progenity, Inc. Treatment of a disease of the gastrointestinal tract with an integrin inhibitor
AU2019318538B2 (en) 2018-08-08 2025-02-06 The General Hospital Corporation Polypeptide integrin antagonists
CN112805284A (zh) 2018-08-17 2021-05-14 奥克斯润有限责任公司 整合素拮抗剂
SG11202101913PA (en) 2018-08-29 2021-03-30 Morphic Therapeutic Inc INHIBITING aV ß6 INTEGRIN
EP3843727A4 (en) 2018-08-29 2022-08-17 Morphic Therapeutic, Inc. INHIBITORS OF (ALPHA-V)(BETA-6) INTEGRIN
ES3027421T3 (en) 2018-08-29 2025-06-13 Morphic Therapeutic Inc Inhibitors of (alpha-v)(beta-6) integrin
EP3873897B1 (en) 2018-10-30 2024-08-14 Gilead Sciences, Inc. N-benzoyl-phenylalanine derivatives as alpha4beta7 integrin inhibitors for treating inflammatory diseases
PL3873605T3 (pl) 2018-10-30 2025-03-03 Gilead Sciences, Inc. Związki hamujące integrynę alfa4beta7
WO2020092394A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
DK3873884T3 (da) 2018-10-30 2025-02-17 Gilead Sciences Inc 3-(quinolin-8-yl)-1,4-dihydropyrido[3,4-d]pyrimidin-2,4-dion-derivater som alpha4beta7-integrinhæmmere til behandling af inflammatoriske sygdomme
US11578069B2 (en) 2019-08-14 2023-02-14 Gilead Sciences, Inc. Compounds for inhibition of α4 β7 integrin
RS66976B1 (sr) 2019-10-16 2025-07-31 Morphic Therapeutic Inc Inhibiranje ljudskog integrina alfa4beta7

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