[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

TNSN07071A1 - Composes aminohetero-aryliques a substituant pyrazole servant d'inhibiteurs de proteine-kinases - Google Patents

Composes aminohetero-aryliques a substituant pyrazole servant d'inhibiteurs de proteine-kinases

Info

Publication number
TNSN07071A1
TNSN07071A1 TNP2007000071A TNSN07071A TNSN07071A1 TN SN07071 A1 TNSN07071 A1 TN SN07071A1 TN P2007000071 A TNP2007000071 A TN P2007000071A TN SN07071 A TNSN07071 A TN SN07071A TN SN07071 A1 TNSN07071 A1 TN SN07071A1
Authority
TN
Tunisia
Prior art keywords
inhibitors
aminohetero
kinases
pyrazole
protein
Prior art date
Application number
TNP2007000071A
Other languages
English (en)
Inventor
Jingrong Jean Cui
Lee Andrew Funk
Lei Jia
Pei-Pei Kung
Jerry Jialun Meng
Mitchell David Nambu
Mason Alan Pairish
Hong Shen
Michelle Bich Tran-Dube
Original Assignee
Pfizer
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35677463&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TNSN07071(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of TNSN07071A1 publication Critical patent/TNSN07071A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pyridine Compounds (AREA)

Abstract

Il est proposé des composés de formule (I), Ainsi que des procédés pour leur synthèse et leur utilisation. Les composés préférés sont de puissants inhibiteurs de la protéine-kinase c-Met et sont utiles dans le traitement de troubles comportant une croissance cellulaire anormale, tels que les cancers.
TNP2007000071A 2004-08-26 2007-02-23 Composes aminohetero-aryliques a substituant pyrazole servant d'inhibiteurs de proteine-kinases TNSN07071A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US60524404P 2004-08-26 2004-08-26
US69080305P 2005-06-14 2005-06-14
PCT/IB2005/002695 WO2006021881A2 (fr) 2004-08-26 2005-08-15 Composes aminoheteroaryle a substitution pyrazole servant d'inhibiteurs de proteine kinase

Publications (1)

Publication Number Publication Date
TNSN07071A1 true TNSN07071A1 (fr) 2008-06-02

Family

ID=35677463

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2007000071A TNSN07071A1 (fr) 2004-08-26 2007-02-23 Composes aminohetero-aryliques a substituant pyrazole servant d'inhibiteurs de proteine-kinases

Country Status (44)

Country Link
US (1) US20060128724A1 (fr)
EP (1) EP1784396B8 (fr)
JP (1) JP4167295B2 (fr)
KR (1) KR100869393B1 (fr)
CN (1) CN101018780B (fr)
AP (1) AP2332A (fr)
AR (1) AR050529A1 (fr)
AT (1) ATE492544T1 (fr)
AU (1) AU2005276132B2 (fr)
BR (1) BRPI0514537B8 (fr)
CA (1) CA2577937C (fr)
CR (2) CR8938A (fr)
CY (1) CY1111138T1 (fr)
DE (1) DE602005025499D1 (fr)
DK (1) DK1784396T3 (fr)
EA (1) EA011725B1 (fr)
EC (1) ECSP077278A (fr)
ES (1) ES2355923T3 (fr)
GE (1) GEP20094845B (fr)
GT (1) GT200500226A (fr)
HK (1) HK1105415A1 (fr)
HN (1) HN2005000477A (fr)
HR (1) HRP20110116T1 (fr)
IL (1) IL181045A0 (fr)
MA (1) MA28827B1 (fr)
ME (1) ME01309B (fr)
MX (1) MX2007002310A (fr)
MY (1) MY139942A (fr)
NI (1) NI200700058A (fr)
NL (1) NL1029809C2 (fr)
NO (1) NO338656B1 (fr)
NZ (1) NZ552946A (fr)
PA (1) PA8643201A1 (fr)
PE (1) PE20060651A1 (fr)
PL (1) PL1784396T3 (fr)
PT (1) PT1784396E (fr)
RS (1) RS51601B (fr)
SI (1) SI1784396T1 (fr)
SV (1) SV2006002208A (fr)
TN (1) TNSN07071A1 (fr)
TW (1) TWI300411B (fr)
UY (1) UY29080A1 (fr)
WO (1) WO2006021881A2 (fr)
ZA (1) ZA200701281B (fr)

Families Citing this family (105)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT2476667E (pt) * 2003-02-26 2014-09-18 Sugen Inc Compostos de aminoheteroarilo como inibidores da proteína quinase
MX2007002312A (es) * 2004-08-26 2007-04-16 Pfizer Compuestos de aminoheteroarilo enantiomericamente puros como inhibidores de proteina quinasa.
US20070072908A1 (en) * 2005-06-08 2007-03-29 Japan Tobacco Inc. Heterocyclic compounds
DK1959955T3 (da) * 2005-12-05 2011-02-07 Pfizer Prod Inc Fremgangsmåde til behandling af abnorm cellevækst
WO2007066185A2 (fr) * 2005-12-05 2007-06-14 Pfizer Products Inc. Polymorphes d'un inhibiteur de c-met/hgfr
CA2667428A1 (fr) 2006-10-23 2008-05-02 Sgx Pharmaceuticals, Inc. Triazoles bicycliques en tant que modulateurs de proteine kinase
GB0621607D0 (en) * 2006-10-31 2006-12-06 Chroma Therapeutics Ltd Inhibitors of c-Met
EP2121608B1 (fr) 2006-12-14 2012-11-14 Bayer Intellectual Property GmbH Dérivés de dihydropyridine utiles en tant qu'inhibiteurs de la protéine kinase
EP2120578B1 (fr) * 2007-01-19 2014-11-19 Xcovery, INC. Composés inhibiteurs de kinase
WO2008127710A2 (fr) 2007-04-13 2008-10-23 Dana Farber Cancer Institute Méthodes de traitement d'un cancer résistant à des agents thérapeutiques anti-erbb
US8263585B2 (en) 2007-05-04 2012-09-11 Novartis Ag Organic compounds
DE102007026341A1 (de) 2007-06-06 2008-12-11 Merck Patent Gmbh Benzoxazolonderivate
US8748143B2 (en) 2007-09-13 2014-06-10 Codexis, Inc. Ketoreductase polypeptides for the reduction of acetophenones
JP2011500778A (ja) 2007-10-25 2011-01-06 アストラゼネカ・アクチエボラーグ ピリジン及びピラジン誘導体−083
JP2011511005A (ja) 2008-02-04 2011-04-07 オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド 2−アミノピリジン系キナーゼ阻害薬
AR070317A1 (es) 2008-02-06 2010-03-31 Osi Pharm Inc Furo (3,2-c) piridina y tieno (3,2-c) piridinas
US8268834B2 (en) 2008-03-19 2012-09-18 Novartis Ag Pyrazine derivatives that inhibit phosphatidylinositol 3-kinase enzyme
KR20100134693A (ko) 2008-04-23 2010-12-23 교와 핫꼬 기린 가부시키가이샤 2-아미노퀴나졸린 유도체
KR101034351B1 (ko) * 2008-05-14 2011-05-16 한국화학연구원 신규 벤즈옥사졸로 치환된 피리딘 유도체 또는 이의약학적으로 허용가능한 염, 이의 제조방법 및 이를유효성분으로 함유하는 이상세포 성장 질환의 예방 및치료용 약학적 조성물
BRPI0914305B8 (pt) 2008-06-19 2021-05-25 Xcovery Holding Co Llc compostos de piridazina carboxamida substituída como compostos inibidores da quinase, uso dos compostos e uso de uma composição compreendendo os compostos
US8592448B2 (en) * 2008-11-20 2013-11-26 OSI Pharmaceuticals, LLC Substituted pyrrolo[2,3-b]-pyridines and -pyrazines
DE102009003975A1 (de) 2009-01-07 2010-07-08 Merck Patent Gmbh Benzothiazolonderivate
US8269012B2 (en) * 2009-05-28 2012-09-18 Vertex Pharmaceuticals Incorporated Aminopyrazole triazolothiadiazole inhibitors of c-met protein kinase
CA2987503C (fr) 2009-07-07 2019-02-26 Mei Pharma, Inc. Pyrimidinyl et 1,3,5-triazinyl benzimidazoles et leur utilisation dans le traitement du cancer
DE102009056886A1 (de) 2009-12-03 2011-06-09 Bayer Schering Pharma Aktiengesellschaft cMet-Inhibitoren zur Behandlung der Endometriose
CA2780922A1 (fr) * 2010-02-11 2011-08-18 OSI Pharmaceuticals, LLC Derives de la 7-aminofuropyridine
CA2790692A1 (fr) * 2010-02-22 2011-08-25 Glaxosmithkline Llc Triazolones utilisees comme inhibiteurs d'acides gras synthase
WO2011109593A1 (fr) 2010-03-03 2011-09-09 OSI Pharmaceuticals, LLC 5-aminopyrrolo/pyrazolopyridines substituées
JP2013525476A (ja) * 2010-05-04 2013-06-20 ファイザー・インク Alk阻害剤としての複素環式誘導体
US8513238B2 (en) * 2010-05-10 2013-08-20 Hoffmann-La Roche Inc. Heteroaryl-cyclohexyl-tetraazabenzo[E]azulenes
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
JP2013526570A (ja) 2010-05-14 2013-06-24 オーエスアイ・ファーマシューティカルズ,エルエルシー 縮合二環式キナーゼ阻害剤
KR101871436B1 (ko) 2010-05-17 2018-06-27 인코젠 쎄라퓨틱스 프라이빗 리미티드 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물
CN101857594B (zh) * 2010-06-18 2013-04-03 南方医科大学 一种四氢吡啶并吲哚类化合物及其制备方法和应用
EP2588107A1 (fr) 2010-07-01 2013-05-08 Takeda Pharmaceutical Company Limited Combinaison d'un inhibiteur de cmet et d'un anticorps dirigé contre hgf et/ou cmet
EP2590982B1 (fr) * 2010-07-09 2017-08-23 The Walter and Eliza Hall Institute of Medical Research Inhibiteur de protéine kinases et méthodes de traitement
CN101967140A (zh) * 2010-09-14 2011-02-09 郑州泰基鸿诺药物科技有限公司 氘代克里唑蒂尼及其衍生物、制备方法和应用
PL2625176T3 (pl) 2010-10-08 2017-08-31 Xcovery Holding Company Llc Podstawione związki 6-amino-pirydazyn-3-ylo-karboksyamidu jako modulatory kinazy białkowej
US9145390B2 (en) 2011-03-03 2015-09-29 Concert Pharmaceuticals, Inc. Derivatives of pyrazole-substituted amino-heteroaryl compounds
JP6042406B2 (ja) 2011-03-28 2016-12-14 メイ プハルマ,インコーポレーテッド (α−置換アラルキルアミノ及びヘテロアリールアルキルアミノ)ピリミジニル及び1,3,5−トリアジニルベンズイミダゾール、それらを含む医薬組成物、並びに増殖性疾患の治療で使用するためのこれらの化合物
WO2012158658A1 (fr) 2011-05-16 2012-11-22 OSI Pharmaceuticals, LLC Inhibiteurs de kinases bicycliques fusionnés
CN102850328B (zh) * 2011-07-01 2014-12-24 苏州东南药业股份有限公司 吡啶类化合物、其制备方法、包含该化合物的药物组合物及其用途
US9226923B2 (en) 2011-07-27 2016-01-05 Nanjing Allgen Pharma Co. Ltd. Spirocyclic molecules as protein kinase inhibitors
US20160206608A1 (en) 2011-08-02 2016-07-21 Pfizer Inc. Crizotinib for use in the treatment of cancer
EP2758387A4 (fr) * 2011-09-21 2015-03-11 Teligene Ltd Composés de pyridine comme inhibiteurs de kinases
CN103087050A (zh) * 2011-10-28 2013-05-08 山东轩竹医药科技有限公司 芳基激酶抑制剂
ES2621220T3 (es) 2012-03-06 2017-07-03 Pfizer Inc. Derivados macrocíclicos para el tratamiento de enfermedades proliferativas
CN103304552B (zh) * 2012-03-09 2016-12-28 广东东阳光药业有限公司 取代的吡啶化合物及其使用方法和用途
WO2013138210A1 (fr) * 2012-03-14 2013-09-19 Ning Xi Composés cycliques substitués et procédés d'utilisation
JP6134376B2 (ja) 2012-03-16 2017-05-24 アクシキン ファーマシューティカルズ インコーポレーテッド 3,5−ジアミノピラゾールキナーゼ阻害剤
CN103319468B (zh) * 2012-03-21 2016-07-13 广东东阳光药业有限公司 取代的螺双环化合物及其使用方法和用途
WO2013144191A1 (fr) 2012-03-29 2013-10-03 Bayer Intellectual Property Gmbh 2-amino-3-cyanopyridines substituées utilisées comme inhibiteurs de l'échange sodium-calcium et leurs utilisations dans le cas de maladies cardiovasculaires
EA026412B1 (ru) 2012-03-30 2017-04-28 Ризен Фармасьютикалз Са НОВЫЕ СОЕДИНЕНИЯ 3,5-ДИЗАМЕЩЕННОГО-3H-ИМИДАЗО[4,5-b]ПИРИДИНА И 3,5-ДИЗАМЕЩЕННОГО-3H-[1,2,3]ТРИАЗОЛО[4,5-b]ПИРИДИНА КАК МОДУЛЯТОРЫ c-MET ПРОТЕИНКИНАЗ
WO2013152252A1 (fr) 2012-04-06 2013-10-10 OSI Pharmaceuticals, LLC Polythérapie antinéoplasique
CN106349222B (zh) * 2012-04-22 2019-03-05 东南大学 克里唑替尼前药及其制备方法与用途
KR101582852B1 (ko) 2012-05-24 2016-01-07 서울대학교 산학협력단 타우 단백질 매개 신경 퇴행성 질환 치료제
WO2013181251A1 (fr) 2012-05-29 2013-12-05 Ratiopharm Gmbh Sel de chlorhydrate de crizotinib sous forme cristalline
GB201211310D0 (en) * 2012-06-26 2012-08-08 Chroma Therapeutics Ltd CSF-1R kinase inhibitors
WO2014020467A2 (fr) 2012-07-30 2014-02-06 Fresenius Kabi Oncology Ltd Procédé de préparation de composés d'aminohétéroaryle à substitution pyrazole
JO3215B1 (ar) 2012-08-09 2018-03-08 Phenex Pharmaceuticals Ag حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy
US9446039B2 (en) 2012-08-27 2016-09-20 Cemm Forschungszentrum Für Molekulare Medizin Gmbh Aminoheteroaryl compounds as MTH1 inhibitors
CN103720691A (zh) * 2012-10-11 2014-04-16 韩冰 一类治疗脑性瘫痪的化合物及其用途
WO2014060381A1 (fr) 2012-10-18 2014-04-24 Bayer Cropscience Ag Composés hétérocycliques pour la lutte contre les nuisibles
WO2014081816A1 (fr) * 2012-11-21 2014-05-30 Concert Pharmaceuticals, Inc. Dérivés fluorés de composés amino-hétéroaryle substitués par pyrazole
JP6199991B2 (ja) * 2013-01-18 2017-09-20 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 3置換ピラゾール及びdlk阻害剤としての使用
US9708295B2 (en) * 2013-02-02 2017-07-18 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Substituted 2-aminopyridine protein kinase inhibitor
CN103992307B (zh) 2013-02-16 2017-07-14 浙江九洲药物科技有限公司 一种克里唑替尼的制备方法
WO2014139391A1 (fr) * 2013-03-11 2014-09-18 Teligene Ltd Utilisation de composés de pyridine substituée en tant qu'inhibiteurs de kinases
WO2014153172A1 (fr) 2013-03-14 2014-09-25 Epizyme, Inc. Dérivés de pyrazole en tant qu'inhibiteurs de prmt1 et leurs utilisations
US9120757B2 (en) 2013-03-14 2015-09-01 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
WO2014153235A2 (fr) 2013-03-14 2014-09-25 Epizyme, Inc. Inhibiteurs de l'arginine méthyltransférase et utilisations de ceux-ci
US20160031839A1 (en) 2013-03-14 2016-02-04 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
AU2014260433A1 (en) 2013-03-14 2015-09-10 Epizyme, Inc. Pyrazole derivatives as arginine methyltransferase inhibitors and uses thereof
SI2970132T1 (sl) 2013-03-14 2021-02-26 Epizyme, Inc. Inhibitorji argininmetiltransferaze in njihove uporabe
EP2970181B1 (fr) 2013-03-14 2017-06-07 Epizyme, Inc. Inhibiteurs d'arginine méthyltransférase et leurs utilisations
WO2014153214A1 (fr) 2013-03-14 2014-09-25 Epizyme, Inc. Inhibteurs de l'arginine méthyltransférase et utilisations de ceux-ci
US9023883B2 (en) 2013-03-14 2015-05-05 Epizyme, Inc. PRMT1 inhibitors and uses thereof
CN104059054B (zh) * 2013-03-19 2018-11-20 浙江导明医药科技有限公司 用于治疗癌症的三级环状胺alk激酶抑制剂
WO2014203177A1 (fr) * 2013-06-18 2014-12-24 Shilpa Medicare Limited (r)-3-[1-(2,6-dichloro-3-fluorophényl)méthoxy]-5-[1-(pipéridin-4-yl)-1h-pyrazol-4-yl]pyridine-2-amine amorphe
CN104230890A (zh) * 2013-06-19 2014-12-24 信诺凯(北京)化工有限公司 吡啶-2-胺衍生物及其制法和药物组合物与用途
CN104650049B (zh) * 2013-08-28 2018-06-08 广东东阳光药业有限公司 取代的吡啶化合物及其使用方法和用途
KR101598664B1 (ko) 2013-09-04 2016-03-02 씨제이헬스케어 주식회사 피롤로피리다진 유도체를 포함하는 단백질 키나제 억제제
WO2015034729A1 (fr) * 2013-09-05 2015-03-12 Calitor Sciences, Llc Composés de pyridine substituée et leurs méthodes d'utilisation
NZ631142A (en) 2013-09-18 2016-03-31 Axikin Pharmaceuticals Inc Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors
BR112016006444B1 (pt) 2013-09-30 2021-01-19 Korea Research Institute Of Chemical Technology derivado de triazolopirazina e composições farmacêuticas compreendendo o mesmo
JP2017516458A (ja) 2014-03-24 2017-06-22 ジェネンテック, インコーポレイテッド c−met拮抗剤による癌治療及びc−met拮抗剤のHGF発現との相関
WO2015172747A1 (fr) * 2014-05-16 2015-11-19 Zhaoyin Wang Molécules spirocycliques servant d'inhibiteurs de mth1
US10695426B2 (en) 2014-08-25 2020-06-30 Pfizer Inc. Combination of a PD-1 antagonist and an ALK inhibitor for treating cancer
WO2016044576A1 (fr) * 2014-09-17 2016-03-24 Epizyme, Inc. Sels, co-cristaux, formes amorphes, et formes cristallines d'un inhibiteur d'arginine méthyltransférase
CN104402868B (zh) * 2014-11-04 2016-08-24 郑州泰基鸿诺医药股份有限公司 氘代克里唑蒂尼晶型及其制备方法
US10398774B2 (en) 2014-12-09 2019-09-03 INSERM (Institut National de la Santé et de la Recherche Médicale) Human monoclonal antibodies against AXL
AR103264A1 (es) 2014-12-23 2017-04-26 Axikin Pharmaceuticals Inc Derivados de 3,5-aminopirazol como inhibidores de quinasa rc
WO2016135041A1 (fr) 2015-02-26 2016-09-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Protéines de fusion et anticorps les contenant pour favoriser l'apoptose
WO2016145383A1 (fr) * 2015-03-11 2016-09-15 Board Of Regents, University Of Texas System Inhibiteurs de mth1 pour le traitement de maladies
CN111440189B (zh) 2015-04-24 2022-08-09 广州再极医药科技有限公司 稠环嘧啶氨基衍生物、其制备方法、中间体、药物组合物及应用
CN106279112A (zh) * 2015-06-12 2017-01-04 浙江九洲药业股份有限公司 一种克里唑替尼中间体及其制备方法和应用
US20180282415A1 (en) 2015-09-30 2018-10-04 Merck Patent Gmbh Combination of a PD-1 Axis Binding Antagonist and an ALK Inhibitor for Treating ALK-Negative Cancer
LT4019019T (lt) 2016-05-20 2024-06-25 Biohaven Therapeutics Ltd. Riluzolo, riluzolo provaistų arba riluzolo analogų naudojimas kartu su imunoterapijos rūšimis vėžio formų gydymui
TWI646094B (zh) 2016-06-01 2019-01-01 大陸商貝達藥業股份有限公司 Crystal form of inhibitory protein kinase active compound and application thereof
CN106632260B (zh) * 2016-09-29 2019-04-26 上海天慈生物谷生物工程有限公司 一种小分子激酶抑制剂的制备方法
WO2018217787A1 (fr) 2017-05-23 2018-11-29 Mei Pharma, Inc. Polythérapie
CN111212643A (zh) 2017-08-14 2020-05-29 梅制药公司 联合疗法
CN110372664A (zh) * 2018-04-13 2019-10-25 华东理工大学 选择性jak2抑制剂及其应用
KR102207608B1 (ko) 2019-04-24 2021-01-26 윤종오 카르복실산으로 유기화된 규소 이온 복합체 및 복합체의 제조방법과 이를 이용한 제품
WO2024009921A1 (fr) 2022-07-04 2024-01-11 中外製薬株式会社 Association médicamenteuse

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5587458A (en) * 1991-10-07 1996-12-24 Aronex Pharmaceuticals, Inc. Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof
DE69334255D1 (de) * 1992-02-06 2009-02-12 Novartis Vaccines & Diagnostic Marker für Krebs und biosynthetisches Bindeprotein dafür
US5863949A (en) * 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
CA2218503C (fr) * 1995-04-20 2001-07-24 Pfizer Inc. Derives d'acide hydroxamique arylsufonyle en tant qu'inhibiteurs de mmp et de tnf
US5747498A (en) * 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
GB9518953D0 (en) * 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
JPH11512750A (ja) * 1996-06-27 1999-11-02 ファイザー インク. 2―(2―オキソ―エチリデン)―イミダゾリジン―4―オンの誘導体およびファルネシル蛋白質トランスフェラーゼ阻害物質としてのそれらの使用法
JPH11236333A (ja) * 1997-12-30 1999-08-31 Pfizer Prod Inc 抗ガン剤として有用なイミダゾリン−4−オン誘導体
AU4925499A (en) * 1998-08-27 2000-03-21 Pfizer Products Inc. Alkynyl-substituted quinolin-2-one derivatives useful as anticancer agents
DE69923849T2 (de) * 1998-08-27 2006-01-12 Pfizer Products Inc., Groton Quinolin-2-on-derivate verwendbar als antikrebsmittel
EP1006113A1 (fr) * 1998-12-02 2000-06-07 Pfizer Products Inc. Dérivés de 2-(2-oxo-éthylidène)-imidazolidin-4-one et leur utilisation pour inhiber la croissance anormale des cellules
US6682736B1 (en) * 1998-12-23 2004-01-27 Abgenix, Inc. Human monoclonal antibodies to CTLA-4
UA71945C2 (en) * 1999-01-27 2005-01-17 Pfizer Prod Inc Substituted bicyclic derivatives being used as anticancer agents
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
WO2000047574A1 (fr) * 1999-02-11 2000-08-17 Pfizer Products Inc. Derives de quinolin-2-one a substitution heteroaryle convenant comme anti-cancereux
US6586447B1 (en) * 1999-04-01 2003-07-01 Pfizer Inc 3,3-disubstituted-oxindole derivatives useful as anticancer agents
EP1081137A1 (fr) * 1999-08-12 2001-03-07 Pfizer Products Inc. Inhibiteurs sélectifs de l'aggrécanase pour le traitement de l'ostéoarthrite
PT1106612E (pt) * 1999-11-30 2004-06-30 Pfizer Prod Inc Derivados de quinolina uteis para inibir a farnesil-proteina-transferase
HN2000000266A (es) * 2000-01-21 2001-05-21 Pfizer Prod Inc Compuesto anticanceroso y metodo de separacion de enantiomeros util para sintetizar dicho compuesto.
US6844357B2 (en) * 2000-05-01 2005-01-18 Pfizer Inc. Substituted quinolin-2-one derivatives useful as antiproliferative agents
SE0102439D0 (sv) * 2001-07-05 2001-07-05 Astrazeneca Ab New compounds
SE0102438D0 (sv) * 2001-07-05 2001-07-05 Astrazeneca Ab New compounds
AU2003206109A1 (en) * 2002-02-06 2003-09-02 Yissum Research Development Company Of The Hebrew University Of Jerusalem Catechol bioisosteres
WO2004004720A1 (fr) * 2002-07-03 2004-01-15 Astex Technology Limited 3-(hetero) arylmethoxy pyridines et leurs analogues en tant qu'inhibiteurs de la p38 map kinase
AU2003247141A1 (en) * 2002-08-01 2004-02-23 Yissum Research Development Company Of The Hebrew University Of Jerusalem 4-anilido substituted quinazolines and use thereof as inhibitors of epidermal growth factor receptor kinases
SE0203754D0 (sv) * 2002-12-17 2002-12-17 Astrazeneca Ab New compounds
DE10307845A1 (de) * 2003-02-25 2004-09-02 Bayer Cropscience Gmbh Heterocyclische Amide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
PT2476667E (pt) * 2003-02-26 2014-09-18 Sugen Inc Compostos de aminoheteroarilo como inibidores da proteína quinase
MX2007002312A (es) * 2004-08-26 2007-04-16 Pfizer Compuestos de aminoheteroarilo enantiomericamente puros como inhibidores de proteina quinasa.

Also Published As

Publication number Publication date
CY1111138T1 (el) 2015-06-11
NO338656B1 (no) 2016-09-26
MX2007002310A (es) 2007-05-08
ATE492544T1 (de) 2011-01-15
TW200621751A (en) 2006-07-01
TWI300411B (en) 2008-09-01
EP1784396B8 (fr) 2011-04-20
CN101018780B (zh) 2012-01-11
EA011725B1 (ru) 2009-04-28
BRPI0514537B8 (pt) 2021-05-25
KR100869393B1 (ko) 2008-11-21
HK1105415A1 (en) 2008-04-03
CA2577937A1 (fr) 2006-03-02
BRPI0514537B1 (pt) 2020-05-12
ECSP077278A (es) 2007-03-29
JP2008510788A (ja) 2008-04-10
GEP20094845B (en) 2009-11-25
AP2332A (en) 2011-12-05
AR050529A1 (es) 2006-11-01
CR8938A (es) 2007-08-14
BRPI0514537A (pt) 2008-06-17
AP2007003906A0 (en) 2007-02-28
ZA200701281B (en) 2008-12-31
DK1784396T3 (da) 2011-02-14
RS51601B (en) 2011-08-31
AU2005276132B2 (en) 2011-09-29
NI200700058A (es) 2008-03-07
EP1784396B1 (fr) 2010-12-22
CN101018780A (zh) 2007-08-15
WO2006021881A2 (fr) 2006-03-02
SI1784396T1 (sl) 2011-03-31
HRP20110116T1 (hr) 2011-03-31
HN2005000477A (es) 2010-06-09
EP1784396A2 (fr) 2007-05-16
MY139942A (en) 2009-11-30
PL1784396T3 (pl) 2011-05-31
PE20060651A1 (es) 2006-07-19
JP4167295B2 (ja) 2008-10-15
NL1029809C2 (nl) 2006-10-17
WO2006021881A3 (fr) 2006-05-18
ME01309B (me) 2013-12-20
NZ552946A (en) 2010-09-30
ES2355923T3 (es) 2011-04-01
US20060128724A1 (en) 2006-06-15
GT200500226A (es) 2006-04-10
NO20071320L (no) 2007-05-29
EA200700321A1 (ru) 2007-08-31
PT1784396E (pt) 2011-01-27
MA28827B1 (fr) 2007-08-01
UY29080A1 (es) 2006-03-31
IL181045A0 (en) 2007-07-04
PA8643201A1 (es) 2006-06-02
NL1029809A1 (nl) 2006-02-28
KR20070038569A (ko) 2007-04-10
SV2006002208A (es) 2006-10-04
DE602005025499D1 (de) 2011-02-03
CR20120421A (es) 2012-09-14
AU2005276132A1 (en) 2006-03-02
CA2577937C (fr) 2010-12-21

Similar Documents

Publication Publication Date Title
TNSN07071A1 (fr) Composes aminohetero-aryliques a substituant pyrazole servant d'inhibiteurs de proteine-kinases
TNSN07070A1 (fr) Composes aminoheteroaryliques enantiomeriquement purs servant d'inhibiteurs de proteine-kinases
MA30232B1 (fr) Inhibiteurs de kinase bases sur l'hydantoine
MXPA03009439A (es) Derivados de 4,5-dihidro-1h-pirazol que tienen una potente actividad antagonistica de cb1.
MA29772B1 (fr) Benzimidazoles substitues et procedes de preparation
MXPA04002583A (es) Derivados de 4,5-dihidro-1h-pirazol novedosos que tienen actividad antagonistica del canabinoide (cb1).
AP1649A (en) Triamide-substituted heterobicyclic compounds.
MA31949B1 (fr) Dérivés d'aminotriazole comme agonistes d'alx
MA27334A1 (fr) Utilisation d'inhibiteurs de l'ikb kinase dans le traitement de la douleur
TNSN05073A1 (fr) Quinazolinones spirocondensees nouvelles et leur utilisation comme inhibiteurs de phosphodiesterase
TN2009000551A1 (fr) Nouveaux composes chimiques
HK1047098A1 (en) Tri-aryl acid derivatives as ppar receptor ligands.
HUP0203509A2 (hu) Triciklusos pirazolkarbonsav-származékok, a vegyületek előállítása és a vegyületeket tartalmazó gyógyászati készítmények
SE9902987D0 (sv) Novel compounds
EA200700711A1 (ru) Производные бензимидазолуксусной кислоты, проявляющие антагонизм в отношении рецептора crth2, и их применение
JP2015527349A (ja) 免疫関連及び炎症性疾患の治療
MA26697A1 (fr) Composes nouveaux inhibiteurs de gsk-3 et compositions pharmaceutiques les contenant
HK1048990A1 (en) Novel compounds.
RS20060129A (en) /1,8/naphthyridin-2-ones and related compounds for the treatment of schizophrenia
HUP9800417A2 (hu) 5-Szubsztituált-3-(1,2,3,6-tetrahidro-piridin-4-il)-1H-indolok és 5-szubsztituált-3-(piridin-4-il)-1H-indolok, alkalmazásuk mint új 5-HT agonisták, a vegyületeket tartalmazó gyógyszerkészítmények
MA29170B1 (fr) Derives puriniques agissant comme des agonistes du recepteur a2a
TNSN07275A1 (fr) Derives de triazole substitues, servant d'antagonistes d'ocytocine
IS7965A (is) Þíenópýrimidíndíón og notkun þeirra í breytingu ásjálfsnæmissjúkdómi
MA30539B1 (fr) Derives de piperazinyle utiles dans le traitement de maladies induites par le recepteur gpr38.
TNSN99031A1 (fr) Composes heterocycliques nouveaux inhibiteurs de romatases, procede pour leur preparation et compositions pharmaceutiques les contenant