AR117472A1 - Inhibidores de tienopiridina de ripk2 - Google Patents

Inhibidores de tienopiridina de ripk2

Info

Publication number
AR117472A1
AR117472A1 ARP190103805A ARP190103805A AR117472A1 AR 117472 A1 AR117472 A1 AR 117472A1 AR P190103805 A ARP190103805 A AR P190103805A AR P190103805 A ARP190103805 A AR P190103805A AR 117472 A1 AR117472 A1 AR 117472A1
Authority
AR
Argentina
Prior art keywords
nitrogen
sulfur
oxygen
heteroatoms
heterocyclic ring
Prior art date
Application number
ARP190103805A
Other languages
English (en)
Original Assignee
Celgene Corp
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 Celgene Corp filed Critical Celgene Corp
Publication of AR117472A1 publication Critical patent/AR117472A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Abstract

La presente proporciona compuestos, composiciones farmacéuticamente aceptables de estos y métodos para utilizarlos. Reivindicación 1: Un compuesto de la fórmula (1), o una sal farmacéuticamente aceptable de este, donde: R¹ es un anillo heterocíclico saturado o parcialmente no saturado monocíclico de 4 a 7 miembros que tiene de 1 a 3 heteroátomos que se seleccionan independientemente de nitrógeno, oxígeno, y azufre; un anillo heterocíclico bicíclico de 9 a 10 miembros que tiene de 1 a 3 heteroátomos que se seleccionan independientemente de nitrógeno, oxígeno y azufre; o un anillo heterocíclico fusionado con espirocíclico de 7 a 11 miembros que tiene de 1 a 3 heteroátomos que se seleccionan independientemente de nitrógeno, oxígeno y azufre, y donde R¹ está sustituido con (R²)ₚ; cada R² es independientemente halógeno, alifático C₁₋₆, opcionalmente sustituido, -OR, -N(R)₂, -C(O)R, -C(O)OR, -SO₂R, o un anillo heterocíclico saturado de 3 a 7 miembros opcionalmente sustituido que tiene de 1 a 2 heteroátomos que se seleccionan independientemente de nitrógeno, oxígeno y azufre; cada R es independientemente hidrógeno, alifático C₁₋₆ opcionalmente sustituido, o un anillo heterocíclico saturado de 4 a 6 miembros opcionalmente sustituido que tiene de 1 a 3 heteroátomos que se seleccionan independientemente de nitrógeno, oxígeno y azufre; o dos grupos R en un átomo de nitrógeno, junto con los átomos a los cuales se acopla, forma un anillo heterocíclico de 4 a 6 miembros que tiene de 1 a 2 heteroátomos adicionales que se seleccionan independientemente de nitrógeno, oxígeno o azufre; cada R³ es independientemente halógeno, CN, -N(R)₂, -OR, o alifático C₁₋₆ opcionalmente sustituido; X es hidrógeno o halógeno; p es 0 - 4; y q es 0 - 4.
ARP190103805A 2018-12-21 2019-12-20 Inhibidores de tienopiridina de ripk2 AR117472A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862783742P 2018-12-21 2018-12-21

Publications (1)

Publication Number Publication Date
AR117472A1 true AR117472A1 (es) 2021-08-11

Family

ID=71098055

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP190103805A AR117472A1 (es) 2018-12-21 2019-12-20 Inhibidores de tienopiridina de ripk2

Country Status (8)

Country Link
US (1) US11168093B2 (es)
EP (1) EP3897630B1 (es)
JP (1) JP7458406B2 (es)
KR (1) KR20210106506A (es)
CN (1) CN113874015A (es)
AR (1) AR117472A1 (es)
TW (1) TW202039481A (es)
WO (1) WO2020132384A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113874015A (zh) 2018-12-21 2021-12-31 细胞基因公司 Ripk2的噻吩并吡啶抑制剂
WO2021174024A1 (en) 2020-02-28 2021-09-02 First Wave Bio, Inc. Methods of treating iatrogenic autoimmune colitis
IT202000031778A1 (it) 2020-12-22 2022-06-22 Guala Closures Spa Chiusura con sigillo a strappo
CN114957280A (zh) * 2021-12-31 2022-08-30 成都赜灵生物医药科技有限公司 噻吩[2,3-d]嘧啶衍生物及其用途

Family Cites Families (200)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4659717A (en) 1985-08-21 1987-04-21 Eli Lilly And Company Dihydropyridines useful in the treatment of angina and stroke
CH681806A5 (es) 1991-03-19 1993-05-28 Ciba Geigy Ag
EP0682027B1 (de) 1994-05-03 1997-10-15 Novartis AG Pyrrolopyrimidinderivate mit antiproliferativer Wirkung
FR2732969B1 (fr) 1995-04-14 1997-05-16 Adir Nouveaux composes pyridiniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
SI9620103A (sl) 1995-07-06 1998-10-31 Novartis Ag Pirolopirimidini in postopki za njihovo pripravo
US5804585A (en) 1996-04-15 1998-09-08 Texas Biotechnology Corporation Thieno-pyridine sulfonamides derivatives thereof and related compounds that modulate the activity of endothelin
JP4242928B2 (ja) 1996-08-23 2009-03-25 ノバルティス アクチエンゲゼルシャフト 置換ピロロピリミジンおよびその製造方法
JP4166296B2 (ja) 1997-04-25 2008-10-15 塩野義製薬株式会社 ドーパミン受容体拮抗作用を有する化合物
US5939432A (en) 1997-10-29 1999-08-17 Medco Research, Inc. Thiophenes useful for modulating the adenosine receptor
CN1280580A (zh) 1997-11-11 2001-01-17 辉瑞产品公司 用作抗癌药的噻吩并嘧啶和噻吩并吡啶衍生物
SK18542000A3 (sk) 1998-06-04 2001-12-03 Abbott Laboratories Protizápalové zlúčeniny inhibujúce bunkovú adhéziu
JP3270834B2 (ja) 1999-01-27 2002-04-02 ファイザー・プロダクツ・インク 抗がん剤として有用なヘテロ芳香族二環式誘導体
EP1181296A1 (en) 1999-06-03 2002-02-27 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory compounds
CN1615873A (zh) 1999-12-24 2005-05-18 阿文蒂斯药物有限公司 氮杂吲哚类化合物
CZ20023199A3 (cs) 2000-02-25 2003-05-14 F. Hoffmann-La Roche Ag Modulátory receptoru adenosinu
WO2002051849A1 (fr) 2000-12-26 2002-07-04 Daiichi Pharmaceutical Co., Ltd. Inhibiteurs cdk4
WO2003000194A2 (en) 2001-06-21 2003-01-03 Pfizer Inc. Thienopyridine and thienopyrimidine anticancer agents
GB0115109D0 (en) 2001-06-21 2001-08-15 Aventis Pharma Ltd Chemical compounds
WO2003000690A1 (en) 2001-06-25 2003-01-03 Aventis Pharmaceuticals Inc. Synthesis of heterocyclic compounds employing microwave technology
GB0119249D0 (en) 2001-08-07 2001-10-03 Novartis Ag Organic compounds
EP1442028A4 (en) 2001-11-06 2009-11-04 Bristol Myers Squibb Co SUBSTITUTED ACID DERIVATIVES, WHICH APPRECIATE AS ANTIDIBILICS AND AGENTS AGAINST OBESITAS, AND METHODS
US7498349B2 (en) 2002-08-02 2009-03-03 Genesoft Pharmaceuticals, Inc. Biaryl compounds having anti-infective activity
US20050288299A1 (en) 2002-10-09 2005-12-29 Mavunkel Babu J Azaindole derivatives as inhibitors of p38 kinase
WO2004032874A2 (en) 2002-10-09 2004-04-22 Scios Inc. AZAINDOLE DERIVATIVES AS INHIBITORS OF p38 KINASE
US7384965B2 (en) 2003-01-06 2008-06-10 Eli Lilly And Company Fused heterocyclic derivatives as PPAR modulators
JP2006520796A (ja) 2003-03-17 2006-09-14 タケダ サン ディエゴ インコーポレイテッド ヒストンデアセチラーゼインヒビター
WO2004093812A2 (en) 2003-04-22 2004-11-04 Irm Llc Compounds that induce neuronal differentiation in embryonic stem cells
SE0301372D0 (sv) 2003-05-09 2003-05-09 Astrazeneca Ab Novel compounds
DE10337942A1 (de) 2003-08-18 2005-03-17 Merck Patent Gmbh Aminobenzimidazolderivate
JP2005194198A (ja) 2003-12-26 2005-07-21 Takeda Chem Ind Ltd チエノピリジン化合物
US20050165029A1 (en) 2004-01-13 2005-07-28 Ambit Biosciences Corporation Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases
WO2005080377A1 (ja) 2004-02-20 2005-09-01 Kirin Beer Kabushiki Kaisha TGFβ阻害活性を有する化合物およびそれを含んでなる医薬組成物
WO2005081960A2 (en) 2004-02-25 2005-09-09 Wyeth Inhibitors of protein tyrosine phosphatase 1b
GB0412467D0 (en) 2004-06-04 2004-07-07 Astrazeneca Ab Chemical compounds
WO2005121125A1 (en) 2004-06-09 2005-12-22 Pfizer Inc. Ether-linked heteroaryl compounds
US20060058339A1 (en) 2004-06-17 2006-03-16 Ibrahim Prabha N Compounds modulating c-kit activity and uses therefor
US20050288290A1 (en) 2004-06-28 2005-12-29 Borzilleri Robert M Fused heterocyclic kinase inhibitors
WO2006014325A2 (en) 2004-07-02 2006-02-09 Exelixis, Inc. C-met modulators and method of use
FR2873694B1 (fr) 2004-07-27 2006-12-08 Merck Sante Soc Par Actions Si Nouveaux aza-indoles inhibiteurs de la mtp et apob
JP5096142B2 (ja) 2004-07-30 2012-12-12 メチルジーン インコーポレイテッド Vegfレセプターおよびhgfレセプターシグナル伝達の阻害剤
US7465726B2 (en) 2004-08-02 2008-12-16 Osi Pharmaceuticals, Inc. Substituted pyrrolo[2.3-B]pyridines
GB0420719D0 (en) 2004-09-17 2004-10-20 Addex Pharmaceuticals Sa Novel allosteric modulators
EP1802305A2 (en) 2004-10-19 2007-07-04 The Regents of The University of California Compositions and methods for disruption of brca2-rad51 interaction
JP2008517896A (ja) 2004-10-21 2008-05-29 ファイザー・インク C型肝炎ウイルスプロテアーゼの阻害剤並びにそれを用いた組成物及び治療
CN101072759B (zh) 2004-11-18 2013-06-19 Synta医药公司 调节hsp90活性的***化合物
AR054416A1 (es) 2004-12-22 2007-06-27 Incyte Corp Pirrolo [2,3-b]piridin-4-il-aminas y pirrolo [2,3-b]pirimidin-4-il-aminas como inhibidores de las quinasas janus. composiciones farmaceuticas.
US20060183758A1 (en) 2005-02-17 2006-08-17 Cb Research And Development, Inc. Method for synthesis of AZA-annelated pyrroles, thiophenes, and furans
WO2006092430A1 (de) 2005-03-03 2006-09-08 Universität des Saarlandes Selektive hemmstoffe humaner corticoidsynthasen
US7557103B2 (en) 2005-04-05 2009-07-07 Eli Lilly And Company Imidazopyridazine compounds
ATE524467T1 (de) 2005-04-25 2011-09-15 Merck Patent Gmbh Neuartige aza-heterozyklen als kinase-inhibitoren
WO2006124874A2 (en) 2005-05-12 2006-11-23 Kalypsys, Inc. Inhibitors of b-raf kinase
ES2473341T3 (es) 2005-05-20 2014-07-04 Methylgene Inc Inhibidores de la se�alizaci�n del receptor del VEGF y del receptor del HGF
ES2623221T3 (es) 2005-05-20 2017-07-10 Methylgene Inc Inhibidores de la señalización del receptor de VEGF y del receptor de HGF
KR100546041B1 (ko) 2005-05-31 2006-01-26 가야에이엠에이 주식회사 로터리 킬른형 노를 사용한 탄화티타늄 분말의 제조방법
US20060281768A1 (en) 2005-06-10 2006-12-14 Gaul Michael D Thienopyrimidine and thienopyridine kinase modulators
US20060281769A1 (en) 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators
WO2007028145A2 (en) 2005-09-02 2007-03-08 Dara Biosciences, Inc. Agents and methods for reducing protein tyrosine phosphatase 1b activity in the central nervous system
WO2007035428A1 (en) 2005-09-15 2007-03-29 Bristol-Myers Squibb Company Met kinase inhibitors
AR056200A1 (es) 2005-09-27 2007-09-26 Wyeth Corp Tieno [2,3-b]piridin-5-carbonitrilos como inhibidores de proteina quinasa
WO2007064861A2 (en) 2005-12-02 2007-06-07 Brandeis University Asymmetric friedel-crafts alkylations catalyzed by byfunctional cinchona alkaloids
EP1963320A1 (en) 2005-12-07 2008-09-03 OSI Pharmaceuticals, Inc. Pyrrolopyridine kinase inhibiting compounds
AR060061A1 (es) 2006-03-22 2008-05-21 Methylgene Inc Inhibidores de la actividad de la proteina tirosina quinasa
WO2007120726A2 (en) 2006-04-11 2007-10-25 The Regents Of The University Of California Compositions and methods related to rad51 inactivation in the treatment of neoplastic diseases, and especially cml
EP2040546A4 (en) 2006-06-22 2009-12-23 Merck & Co Inc TYROSINE KINASE INHIBITORS
PE20121506A1 (es) 2006-07-14 2012-11-26 Amgen Inc Compuestos triazolopiridinas como inhibidores de c-met
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
US20080021217A1 (en) 2006-07-20 2008-01-24 Allen Borchardt Heterocyclic inhibitors of rho kinase
ZA200900670B (en) 2006-08-08 2010-04-28 Millennium Pharm Inc Heteroaryl compounds useful as inhititors of E1 activating enzymes
AU2007284537B2 (en) 2006-08-17 2012-04-12 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
WO2008049855A2 (en) 2006-10-27 2008-05-02 Glaxo Group Limited 7-azaindole derivatives as c-met kinase inhibitors
JP2010510177A (ja) 2006-11-17 2010-04-02 クイーンズ ユニバーシティ アット キングストン タンパク質フォールディング障害を治療するための化合物および方法
US8076350B2 (en) 2006-12-22 2011-12-13 Abbott Laboratories Spirocyclic azaadamantane derivatives and methods of use
WO2008086053A1 (en) 2007-01-03 2008-07-17 Virobay, Inc. Hcv inhibitors
US20080194557A1 (en) 2007-01-18 2008-08-14 Joseph Barbosa Methods and compositions for the treatment of pain, inflammation and cancer
WO2008089310A2 (en) 2007-01-18 2008-07-24 Lexicon Pharmaceuticals, Inc. Delta 5 desaturase inhibitors for the treatment of obesity
EP2137158A4 (en) 2007-02-28 2012-04-18 Methylgene Inc LOW-MOLECULAR INHIBITORS OF PROTEINARGININE METHYLTRANSFERASES (PRMTS)
EP2134682B1 (en) 2007-04-13 2011-12-14 Sanofi A transition metal catalyzed synthesis of n-aminoindoles
WO2008135232A1 (en) 2007-05-02 2008-11-13 Riccardo Cortese Use and compositions of purine derivatives for the treatment of proliferative disorders
JP2008308448A (ja) 2007-06-15 2008-12-25 Sankyo Agro Kk (3−硫黄原子置換フェニル)へテロアリール誘導体
DE102007027800A1 (de) 2007-06-16 2008-12-18 Bayer Healthcare Ag Substituierte bicyclische Heteroaryl-Verbindungen und ihre Verwendung
CA2694218A1 (en) 2007-07-31 2009-02-05 Schering Corporation Anti-mitotic agent and aurora kinase inhibitor combination as anti-cancer treatment
WO2009027732A1 (en) 2007-08-24 2009-03-05 Astrazeneca Ab 5-6-bicyclic heteroaromatic compounds with antibacterial activity
DE102007048716A1 (de) 2007-10-11 2009-04-23 Merck Patent Gmbh Imidazo[1,2-a]pyrimidinderivate
EP2328586A2 (en) 2008-05-20 2011-06-08 Cephalon, Inc. Substituted pyridazinone derivatives as histamine-3 (h3) receptor ligands
CA2728559A1 (en) 2008-07-03 2010-01-07 Exelixis Inc. Cdk modulators
UY31982A (es) 2008-07-16 2010-02-26 Boehringer Ingelheim Int Derivados de 1,2-dihidropiridin-3-carboxamidas n-sustituidas
UY31984A (es) 2008-07-16 2010-02-26 Boehringer Ingelheim Int DERIVADOS DE 1-(3,4-difluorobencil)-6-oxo-1,6-dihidropirimidin-5-carboxamidas N-sustituidas y de 2-(3,4-difluorobencil)-3-oxo-2,3-dihidro-1H-pirazol-4-carboxamidas N-sustituidas.
US20110218211A1 (en) 2008-08-16 2011-09-08 Genentech, Inc. Azaindole inhibitors of iap
WO2010021686A1 (en) 2008-08-18 2010-02-25 Promega Corporation Luminogenic compounds and methods to detect cytochrome p450 3a enzymes
WO2010020000A1 (en) 2008-08-19 2010-02-25 The University Of Sydney Novel compounds and their uses in diagnosis
AR073739A1 (es) 2008-09-10 2010-12-01 Kalypsys Inc Aminopirimidinas como inhibidores de los receptores de histamina
CN102232071B (zh) 2008-09-26 2016-03-23 财团法人卫生研究院 作为蛋白激酶抑制剂的稠合多环化合物
US8293897B2 (en) 2008-10-14 2012-10-23 Ning Xi Compounds comprising a spiro-ring and methods of use
KR100961410B1 (ko) 2008-10-14 2010-06-09 (주)네오팜 단백질 키나제 억제제로서 헤테로사이클릭 화합물
WO2010054285A2 (en) 2008-11-10 2010-05-14 National Health Research Institutes Fused bicyclic and tricyclic pyrimidine compounds as tyrosine kinase inhibitors
GB2465405A (en) 2008-11-10 2010-05-19 Univ Basel Triazine, pyrimidine and pyridine analogues and their use in therapy
TW201028399A (en) 2008-11-27 2010-08-01 Shionogi & Co Pyrimidine derivative and pyridine derivative both having pi3k inhibitory activity
AU2009330131B2 (en) 2008-12-23 2015-09-03 Aquilus Pharmaceuticals, Inc Compounds and methods for the treatment of pain and other diseases
WO2010104306A2 (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
AR075858A1 (es) 2009-03-18 2011-05-04 Schering Corp Compuestos biciclicos como inhibidores de diacilglicerol aciltransferasa
EP2411057B1 (en) 2009-03-23 2020-05-06 Eli Lilly and Company Imaging agents for detecting neurological disorders
EP2417133A1 (en) 2009-04-06 2012-02-15 PTC Therapeutics, Inc. Compounds and methods for antiviral treatment
KR101070223B1 (ko) 2009-05-14 2011-10-06 덕산하이메탈(주) 아릴아미노 구조를 포함하는 화합물 및 이를 이용한 유기전기소자, 그 단말
US20120172369A1 (en) 2009-09-14 2012-07-05 Ting Pauline C Inhibitors of diacylglycerol acyltransferase
US9095596B2 (en) 2009-10-15 2015-08-04 Southern Research Institute Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
EP2490530A4 (en) 2009-10-22 2014-01-22 Univ Washington COMPOUNDS AND METHOD FOR THE TREATMENT OF BACTERIAL INFECTIONS
US9062076B2 (en) 2009-10-22 2015-06-23 Fibrotech Therapeutics Pty Ltd Fused ring analogues of anti-fibrotic agents
GB0919380D0 (en) 2009-11-04 2009-12-23 Almac Discovery Ltd Pharmaceutical compouds
EA022458B1 (ru) 2009-12-28 2016-01-29 Дженерал Инкорпорейтед Ассошиэйшн Фарма Вэлли Проджект Саппортинг Организейшн 1,3,4-оксадиазол-2-карбоксамидное соединение
MX2012009377A (es) 2010-02-11 2012-09-12 Univ Vanderbilt Benzotiazoles y azabenzotiazoles como potenciadores alostericos mglur4, composiciones y metodos para tratar la disfuncion neurologica.
UY33304A (es) 2010-04-02 2011-10-31 Amgen Inc Compuestos heterocíclicos y sus usos
US20110312996A1 (en) 2010-05-17 2011-12-22 Intermune, Inc. Novel inhibitors of hepatitis c virus replication
WO2011149827A1 (en) 2010-05-24 2011-12-01 Glaxosmithkline Llc Compounds and methods
ES2526124T3 (es) 2010-06-16 2015-01-07 Cymabay Therapeutics, Inc. Agonistas del receptor GPR120 y sus usos
FR2963268B1 (fr) 2010-07-27 2015-03-13 Areva Nc Dispositif d'avivage de meule de travail et son utilisation dans une rectifieuse sans centre de pastilles de combustible nucleaire
DE102010033548A1 (de) 2010-08-05 2012-02-09 Merck Patent Gmbh Materialien für elektronische Vorrichtungen
WO2012024670A2 (en) 2010-08-20 2012-02-23 University Of Washington Through Its Center For Commercialization Composition and methods for treating glioblastoma
US20130317045A1 (en) * 2010-09-01 2013-11-28 Ambit Biosciences Corporation Thienopyridine and thienopyrimidine compounds and methods of use thereof
EP2426202A1 (en) 2010-09-03 2012-03-07 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Kinases as targets for anti-diabetic therapy
TW201219401A (en) 2010-09-14 2012-05-16 Lexicon Pharmaceuticals Inc Bicyclic inhibitors of Notum Pectinacetylesterase and methods of their use
CN102399233B (zh) 2010-09-15 2014-08-13 山东轩竹医药科技有限公司 PI3K和mTOR双重抑制剂类化合物
US10005750B2 (en) 2010-10-06 2018-06-26 J-Pharma Co., Ltd. Developing potent urate transporter inhibitors: compounds designed for their uricosuric action
CN103221048A (zh) 2010-11-18 2013-07-24 卡斯纳莱拉创新药物私人有限公司 取代的4-(硒吩-2(或3)-基氨基)嘧啶化合物及其使用方法
JP5720253B2 (ja) 2011-01-06 2015-05-20 コニカミノルタ株式会社 有機エレクトロニクス素子、それを具備した表示装置及び照明装置
US8759386B2 (en) 2011-01-24 2014-06-24 Boehringer Ingelheim International Gmbh Pyrazole compounds as CRTH2 antagonists
ES2734878T3 (es) 2011-02-01 2019-12-12 Univ Illinois Derivados de N-hidroxibenzamida como inhibidores de HDAC y métodos terapéuticos que utilizan los mismos
BR112013020329A2 (pt) 2011-02-09 2016-08-02 Hoffmann La Roche compostos heterocíclicos como inibidores da pi3-quinase
WO2012130829A1 (en) 2011-03-29 2012-10-04 Biolog Life Science Institute Forschungslabor Und Biochemica-Vertrieb Gmbh New boranophosphate analogues of cyclic nucleotides
KR20120119932A (ko) 2011-04-21 2012-11-01 (주)네오팜 Pi3 키나제 억제제로서 헤테로고리 화합물
WO2012154888A1 (en) 2011-05-09 2012-11-15 Proteostasis Therapeutics, Inc. Compounds for treating protein folding disorders
EP2710018B8 (en) 2011-05-19 2022-02-23 Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) Macrocyclic compounds as protein kinase inhibitors
DE102011111400A1 (de) 2011-08-23 2013-02-28 Merck Patent Gmbh Bicyclische heteroaromatische Verbindungen
WO2013033981A1 (zh) 2011-09-06 2013-03-14 江苏先声药物研究有限公司 一类2,7-萘啶衍生物及其制备方法和应用
US20130096136A1 (en) 2011-09-30 2013-04-18 Methylgene Inc. Inhibitors of Protein Tyrosine Kinase Activity
JP5741373B2 (ja) 2011-10-25 2015-07-01 コニカミノルタ株式会社 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置、並びに照明装置
AR090037A1 (es) 2011-11-15 2014-10-15 Xention Ltd Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio
WO2013078254A1 (en) 2011-11-22 2013-05-30 Array Biopharma Inc. Bicyclic heteroaryl derivatives as kinase inhibitors
GB201120993D0 (en) 2011-12-06 2012-01-18 Imp Innovations Ltd Novel compounds and their use in therapy
WO2013085339A2 (ko) 2011-12-07 2013-06-13 주식회사 두산 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자
TW201728592A (zh) 2012-01-10 2017-08-16 林伯士艾瑞斯公司 Irak抑制劑及其用途
KR20150003767A (ko) 2012-04-26 2015-01-09 브리스톨-마이어스 스큅 컴퍼니 혈소판 응집을 치료하기 위한 프로테아제 활성화 수용체 4 (par4) 억제제로서의 이미다조티아디아졸 유도체
WO2013165898A2 (en) 2012-05-01 2013-11-07 The Trustees Of The University Of Pennsylvania Compositions and methods for inhibiting resolvases
KR101537436B1 (ko) 2012-08-17 2015-07-17 주식회사 두산 신규 화합물 및 이를 포함하는 유기 전계 발광 소자
CN103626783B (zh) 2012-08-22 2016-06-08 中国科学院上海药物研究所 双环稠杂环化合物及其用途和药物组合物
RU2769516C2 (ru) 2012-10-02 2022-04-01 Кэлифорниа Инститьют Оф Текнолоджи Восстановительное расщепление ароматических связей c-s активированными силанами
CN104822690B (zh) 2012-10-02 2017-08-25 加州理工学院 芳族化合物的无过渡金属的甲硅烷基化
US9556135B2 (en) 2012-10-12 2017-01-31 Amgen, Inc. Amino-dihydrothiazine and amino-dioxido dihydrothiazine compounds as beta-secretase antagonists and methods of use
KR101547623B1 (ko) 2012-10-24 2015-08-26 주식회사 두산 유기 전계 발광 소자
CN103833753B (zh) 2012-11-22 2017-02-01 广东东阳光药业有限公司 炔基化合物及其使用方法和用途
US20140148492A1 (en) 2012-11-23 2014-05-29 Boehringer Ingelheim International Gmbh Bicyclosubstituted pyrazole compounds for treating hair loss
WO2014089280A1 (en) 2012-12-07 2014-06-12 Calitor Sciences, Llc Alkynyl compounds and methods of use
CN103012428A (zh) 2013-01-08 2013-04-03 中国药科大学 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途
US9725430B2 (en) 2013-01-16 2017-08-08 Children's Hospital Medical Center Use of small molecule inhibitors targeting EYA tyrosine phosphatase
US9505781B2 (en) 2013-03-13 2016-11-29 The Regents Of The University Of Michigan Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof
US9499534B2 (en) * 2013-04-26 2016-11-22 Merck Sharp & Dohme Corp. Thiazole-substituted aminopyrimidines as spleen tyrosine kinase inhibitors
CN104119331B (zh) 2013-04-26 2018-02-06 广东东阳光药业有限公司 烯基化合物及其使用方法和用途
US9351494B2 (en) 2013-05-03 2016-05-31 Inscent, Inc. Honeybee repellents and uses thereof
WO2014179785A1 (en) 2013-05-03 2014-11-06 Inscent, Inc. Improved honeybee repellents and uses thereof
WO2014193647A2 (en) 2013-05-26 2014-12-04 Calitor Sciences, Llc Alkenyl compounds and methods of use
WO2014194242A2 (en) 2013-05-31 2014-12-04 Nimbus Iris, Inc. Flt3 inhibitors and uses thereof
WO2014194245A2 (en) 2013-05-31 2014-12-04 Nimbus Iris, Inc. Cdk8 inhibitors and uses thereof
EP2818472A1 (en) 2013-06-27 2014-12-31 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Imidazo[4,5-c]pyridine and pyrrolo[3,2-c]pyridine compounds as G-protein-coupled receptor kinase 5 (GRK5) modulators
WO2015042078A2 (en) 2013-09-22 2015-03-26 Calitor Sciences, Llc Substituted aminopyrimidine compounds and methods of use
KR20160076519A (ko) 2013-10-10 2016-06-30 아락세스 파마 엘엘씨 Kras g12c 억제제
SG11201602982YA (en) 2013-10-17 2016-05-30 Abbvie Deutschland Aminochromane, aminothiochromane and amino-1,2,3,4-tetrahydroquinoline derivatives, pharmaceutical compositions containing them, and their use in therapy
EP3444251B1 (en) 2013-12-11 2023-06-07 Biogen MA Inc. Biaryl compounds useful for the treatment of human diseases in oncology, neurology and immunology
JP2017514866A (ja) 2014-05-06 2017-06-08 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア Braf阻害剤を使用する創傷治癒
KR101713530B1 (ko) 2014-05-16 2017-03-08 (주)피엔에이치테크 유기발광 화합물 및 이를 포함하는 유기전계발광소자
KR101998435B1 (ko) 2014-06-09 2019-07-09 주식회사 두산 유기 전계 발광 소자
WO2016022446A1 (en) 2014-08-08 2016-02-11 Merck Sharp & Dohme Corp. [5,6]-fused bicyclic antidiabetic compounds
HRP20211778T1 (hr) 2014-08-29 2022-03-18 Chdi Foundation, Inc. Kontrastna sredstva za slikovnu dijagnostiku huntingtin proteina
US10246464B2 (en) 2014-09-09 2019-04-02 The Regents Of The University Of Michigan Thienopyrimidine and thienopyridine compounds and methods of use thereof
KR101708097B1 (ko) 2014-10-22 2017-02-17 주식회사 두산 유기 전계 발광 소자
PT3209655T (pt) 2014-10-24 2020-11-13 Landos Biopharma Inc Produtos terapêuticos à base da lancl2
CA2964282C (en) * 2014-10-27 2023-03-07 University Health Network Ripk2 inhibitors and method of treating cancer with same
CN105712998B (zh) 2014-12-05 2019-12-13 上海润诺生物科技有限公司 氮杂吲哚类衍生物、其制备方法及其在医药上的应用
ES2746839T3 (es) 2014-12-18 2020-03-09 Pfizer Derivados de pirimidina y triazina y su uso como inhibidores de AXL
JP6038111B2 (ja) 2014-12-27 2016-12-07 ヤマサ醤油株式会社 多置換7−デアザプリン誘導体合成のための2,6−ジクロロ−8−ヨード−7−デアザプリン
WO2016115360A1 (en) 2015-01-14 2016-07-21 Coferon, Inc. C-myc ligands capable of dimerizing in an aqueous solution, and methods of using same
BR112017019371A2 (pt) 2015-03-12 2018-07-03 Syngenta Participations Ag derivados tetracíclicos ativos em termos pesticidas com substituintes contendo enxofre
JP6070756B2 (ja) 2015-04-15 2017-02-01 コニカミノルタ株式会社 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子の製造方法、表示装置、並びに照明装置
EP3307798B1 (en) 2015-06-12 2020-08-05 Transitions Optical, Inc. Alignment compounds
EP3322711B1 (en) 2015-06-25 2021-03-10 University Health Network Hpk1 inhibitors and methods of using same
JP2018524337A (ja) 2015-07-01 2018-08-30 シンジェンタ パーティシペーションズ アーゲー 硫黄含有置換基を有する有害生物防除に活性な四環式誘導体
EP3319940B1 (en) 2015-07-10 2019-05-29 Technische Universität Braunschweig New indole compounds having antiprotozoal activity and its use as well as methods for producing the same
DE102015008860A1 (de) 2015-07-14 2017-01-19 Voxeljet Ag Vorrichtung zum Justieren eines Druckkopfes
US20170010630A1 (en) 2015-07-22 2017-01-12 Boe Technology Group Co., Ltd. Touch Display Screen, Method for Preparing Touch Display Screen and Attaching Adhesive Jig
GB201521767D0 (en) 2015-12-10 2016-01-27 Ucb Biopharma Sprl And Katholieke Universiteit Leuven K U Leuven R&D Therapeutic agents
MX2018007703A (es) 2015-12-22 2018-11-09 Vitae Pharmaceuticals Inc Inhibidores de la interaccion de menina-linaje leucemico mixto.
WO2017133664A1 (en) 2016-02-05 2017-08-10 Savira Pharmaceuticals Gmbh Bicyclic pyridine and pyrimidine derivatives and their use in the treatment, amelioration or prevention of influenza
ES2883450T3 (es) 2016-02-17 2021-12-07 Global Blood Therapeutics Inc Inhibidores de histona metiltransferasa
WO2017144341A1 (de) 2016-02-23 2017-08-31 Bayer Cropscience Aktiengesellschaft Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel
CN107151240A (zh) 2016-03-04 2017-09-12 中国科学院上海药物研究所 一类多取代喹诺酮类化合物及其制备方法和用途
KR102646115B1 (ko) 2016-03-11 2024-03-12 에이씨 이뮨 에스에이 진단 및 치료를 위한 바이사이클릭 화합물
US11332729B2 (en) 2016-08-24 2022-05-17 California Institute Of Technology Engineered synthase for production of tryptophan derivatives and intransigent substrates
UA123287C2 (uk) * 2016-09-15 2021-03-10 Бьорінгер Інгельхайм Інтернаціональ Гмбх Гетероарилкарбоксамідні сполуки як інгібітори ripk2
US10138222B2 (en) * 2016-09-15 2018-11-27 Boehringer Ingelheim International Gmbh Substituted benzamides as RIPK2 inhibitors
WO2018213219A1 (en) 2017-05-15 2018-11-22 University Of Houston System Pyrido[2,3-d]pyrimidin-7ones and related compounds as inhibitors of protein kinases
US20190002460A1 (en) 2017-06-28 2019-01-03 The Regents Of The University Of Michigan Small molecule inhibitors of egfr and pi3k
CN113874015A (zh) 2018-12-21 2021-12-31 细胞基因公司 Ripk2的噻吩并吡啶抑制剂

Also Published As

Publication number Publication date
JP7458406B2 (ja) 2024-03-29
EP3897630B1 (en) 2024-01-10
TW202039481A (zh) 2020-11-01
EP3897630A4 (en) 2022-09-07
CN113874015A (zh) 2021-12-31
WO2020132384A1 (en) 2020-06-25
JP2022515406A (ja) 2022-02-18
US20200199148A1 (en) 2020-06-25
US11168093B2 (en) 2021-11-09
KR20210106506A (ko) 2021-08-30
EP3897630A1 (en) 2021-10-27

Similar Documents

Publication Publication Date Title
AR117472A1 (es) Inhibidores de tienopiridina de ripk2
AR116604A1 (es) Inhibidores de kras g12c
AR107519A1 (es) Compuestos de piperidina sustituido y su uso
AR109349A1 (es) Compuestos y usos
AR106806A1 (es) Inhibidores triazol de acc y usos de los mismos
AR102177A1 (es) Compuestos de heteroarilo como inhibidores de btk y usos de los mismos
AR111407A1 (es) Compuestos inhibidores de ask1 y usos de los mismos
AR106472A1 (es) Inhibidores de acc y usos de los mismos
AR095192A1 (es) Quinolina y quinazolinamidas como modulares de canales de sodio
AR105459A1 (es) Derivados de pirrolo[2,1-f][1,2,4]triazina útiles para tratar trastornos relacionados con kit y pdfgr
AR098721A1 (es) Inhibidores de biarilo de tirosina quinasa de bruton
AR091273A1 (es) Inhibidores de pirimidinil tirosina quinasa
AR106798A1 (es) Inhibidores pirazol de acc y usos de los mismos
AR103833A1 (es) Compuestos bicíclicos de sulfonamida cetona
AR107030A1 (es) Inhibidores aza-bencimidazol de pad4
AR108387A1 (es) Compuestos de tipo tetrahidropirimidodiazepina y dihidropiridodiazepina para tratar el dolor y afecciones relacionadas con el dolor
AR100033A1 (es) Compuestos y composiciones para inhibir la actividad de shp2
AR100809A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR103990A1 (es) Ureas cíclicas como inhibidoras de rock
AR114496A1 (es) Compuestos antiproliferación y usos de los mismos
AR092306A1 (es) Antibacterianos de fenicol
AR088828A1 (es) DERIVADOS DE CICLOHEXILAMINA QUE TIENEN ACTIVIDAD COMO AGONISTAS ADRENERGICOS b2 Y COMO ANTAGONISTAS MUSCARINICOS M3
AR110298A1 (es) Compuestos de heterociclo tetracíclicos útiles como inhibidores de la integrasa del vih
AR094496A1 (es) Compuestos tetracíclicos sustituidos con heterociclo y métodos de uso de los mismos para el tratamiento de enfermedades víricas
AR109296A1 (es) Derivados de oxadiazolopiridina para el uso como inhibidores de ghrelin o-aciltransferasa (goat)

Legal Events

Date Code Title Description
FB Suspension of granting procedure