[go: up one dir, main page]

MA32272B1 - Inhibiteurs de raf de pyrazole [3,4-b]pyridine - Google Patents

Inhibiteurs de raf de pyrazole [3,4-b]pyridine

Info

Publication number
MA32272B1
MA32272B1 MA33203A MA33203A MA32272B1 MA 32272 B1 MA32272 B1 MA 32272B1 MA 33203 A MA33203 A MA 33203A MA 33203 A MA33203 A MA 33203A MA 32272 B1 MA32272 B1 MA 32272B1
Authority
MA
Morocco
Prior art keywords
raf
pyrazole
pyridine
inhibitors
compounds
Prior art date
Application number
MA33203A
Other languages
Arabic (ar)
English (en)
Inventor
Meese Jason De
Kateri A Ahrendt
Alexandre J Buckmelter
Jonas Grina
Joshua D Hansen
Ellen R Laird
Paul Lunghofer
David Moreno
Brad Newhouse
Li Ren
Jeongbeob Seo
Hongqi Tian
Steven Mark Wenglowsky
Bainian Feng
Janet Gunzner
Kim Malesky
Simon Mathieu
Joachim Rudolph
Zhaoyang Wen
Wendy B Young
Original Assignee
Array Biopharma Inc
Genentech 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 Array Biopharma Inc, Genentech Inc filed Critical Array Biopharma Inc
Publication of MA32272B1 publication Critical patent/MA32272B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La présente invention concerne des composés de formule i qui sont utiles pour l'inhibition de kinases raf. La présente invention concerne des procédés d'utilisation de composés de formule i et des stéréo-isomères, tautomères, promédicaments et sels pharmaceutiquement acceptables de ceux-ci, pour le diagnostic, la prévention ou le traitement in vitro, in situ, et in vivo de tels troubles dans des cellules de mammifère, ou des états pathologiques associés.
MA33203A 2008-02-29 2010-09-24 Inhibiteurs de raf de pyrazole [3,4-b]pyridine MA32272B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3281308P 2008-02-29 2008-02-29
PCT/US2009/035381 WO2009111279A1 (fr) 2008-02-29 2009-02-27 Inhibiteurs de raf de pyrazole[3,4-b]pyridine

Publications (1)

Publication Number Publication Date
MA32272B1 true MA32272B1 (fr) 2011-05-02

Family

ID=40677552

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33203A MA32272B1 (fr) 2008-02-29 2010-09-24 Inhibiteurs de raf de pyrazole [3,4-b]pyridine

Country Status (19)

Country Link
US (1) US8394795B2 (fr)
EP (1) EP2265610B1 (fr)
JP (1) JP2011513331A (fr)
KR (1) KR20100117686A (fr)
CN (1) CN102149712A (fr)
AR (1) AR072657A1 (fr)
AU (1) AU2009222144A1 (fr)
BR (1) BRPI0908268A2 (fr)
CA (1) CA2716952A1 (fr)
CL (1) CL2009000448A1 (fr)
CR (1) CR11690A (fr)
EC (1) ECSP10010507A (fr)
ES (1) ES2400202T3 (fr)
IL (1) IL207845A0 (fr)
MA (1) MA32272B1 (fr)
MX (1) MX2010009411A (fr)
PE (1) PE20091623A1 (fr)
TW (1) TW200940539A (fr)
WO (1) WO2009111279A1 (fr)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008063888A2 (fr) 2006-11-22 2008-05-29 Plexxikon, Inc. Composés modulant l'activité de c-fms et/ou de c-kit et utilisations associées
SG183036A1 (en) 2007-07-17 2012-08-30 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
ES2426092T3 (es) 2008-01-09 2013-10-21 Array Biopharma, Inc. 5H-Ciclopenta[d]pirimidinas como inhibidores de proteínas cinasas AKT
MX2010009410A (es) * 2008-02-29 2010-11-30 Array Biopharma Inc Compuestos del inhibidor de raf y métodos de uso de los mismos.
US20110003809A1 (en) * 2008-02-29 2011-01-06 Array Biopharma Inc. Imidazo [4,5-b] pyridine derivatives used as raf inhibitors
JP2011513332A (ja) * 2008-02-29 2011-04-28 アレイ バイオファーマ、インコーポレイテッド 癌の治療のためのｒａｆ阻害剤としてのｎ−（６−アミノピリジン−３−イル）−３−（スルホンアミド）ベンズアミド誘導体
EA022924B1 (ru) 2009-04-03 2016-03-31 Ф.Хоффманн-Ля Рош Аг ТВЁРДАЯ ФОРМА {3-[5-(4-ХЛОРФЕНИЛ)-1Н-ПИРРОЛО[2,3-b]ПИРИДИН-3-КАРБОНИЛ]-2,4-ДИФТОРФЕНИЛ}АМИДА ПРОПАН-1-СУЛЬФОНОВОЙ КИСЛОТЫ И ЕЁ ПРИМЕНЕНИЕ
US8329724B2 (en) 2009-08-03 2012-12-11 Hoffmann-La Roche Inc. Process for the manufacture of pharmaceutically active compounds
DK2462118T3 (da) * 2009-08-03 2014-08-25 Acraf Fremgangsmåde til fremstilling af 1-benzyl-3-hydroxymethyl-1H-indazol og dets derivater og nødvendige magnesiummellemprodukter
US20130018033A1 (en) * 2009-08-28 2013-01-17 Array Biopharma Inc. Raf inhibitor compounds and methods of use thereof
EP2470532A1 (fr) * 2009-08-28 2012-07-04 Array Biopharma, Inc. Composés 1h-pyrazolo[3,4-b]pyridines pour l'inhibition des raf kinases
MA33975B1 (fr) 2009-11-06 2013-02-01 Plexxikon Inc Composés et méthodes de modulation des kinases et leurs indications d'emploi
WO2012094451A1 (fr) 2011-01-06 2012-07-12 Beta Pharma Canada Inc. Nouvelles urées pour le traitement et la prévention du cancer
JP5941069B2 (ja) 2011-02-07 2016-06-29 プレキシコン インコーポレーテッドＰｌｅｘｘｉｋｏｎ Ｉｎｃ． キナーゼ調節のための化合物および方法、ならびにそれに対する適応症
TWI558702B (zh) 2011-02-21 2016-11-21 普雷辛肯公司 醫藥活性物質的固態形式
BR122022000334B1 (pt) 2011-08-01 2023-03-21 Genentech, Inc Composição farmacêutica compreendendo um antagonista de ligação ao eixo pd-1 e um inibidor de mek
KR20140064971A (ko) 2011-09-19 2014-05-28 제넨테크, 인크. c-met 길항제 및 B-raf 길항제를 포함하는 조합 치료
CN102491974B (zh) 2011-12-12 2013-08-07 南京药石药物研发有限公司 1-（2-氟苄基）-1H-吡唑并[3，4-b]吡啶-3-甲脒盐酸盐的合成方法
WO2013127268A1 (fr) * 2012-03-02 2013-09-06 Genentech,Inc. Dérivés sulfonamides et sulfones amido-benzyliques
US9394315B2 (en) * 2012-05-08 2016-07-19 Lycera Corporation Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
HK1206605A1 (en) 2012-08-17 2016-01-15 霍夫曼-拉罗奇有限公司 Combination therapies for melanoma comprising administering cobimetinib and vemurafinib
HK1211235A1 (en) 2013-02-22 2016-05-20 霍夫曼-拉罗奇有限公司 Methods of treating cancer and preventing drug resistance
EP2968537A1 (fr) 2013-03-15 2016-01-20 Genentech, Inc. Procédés de traitement d'un cancer et de prévention de la résistance médicamenteuse d'un cancer
KR102178606B1 (ko) * 2013-03-15 2020-11-13 자임워크스 인코포레이티드 세포독성 및 유사분열-억제 화합물, 및 이를 사용하는 방법
BR112015028845A2 (pt) * 2013-05-30 2017-07-25 Plexxikon Inc compostos para a modulação da quinase e indicações da mesma
CN105531279A (zh) * 2013-07-08 2016-04-27 拜耳制药股份公司 取代的吡唑并吡啶胺
MX2016002626A (es) 2013-08-30 2016-06-06 Ambit Biosciences Corp Compuestos de biarilacetamida y metodos de uso de los mismos.
JP2017517552A (ja) 2014-06-13 2017-06-29 ジェネンテック， インコーポレイテッド 抗癌剤耐性の治療及び防止方法
US20170114323A1 (en) 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
CA2954508A1 (fr) 2014-07-15 2016-01-21 Genentech, Inc. Compositions de traitement du cancer a l'aide d'antagonistes de liaison a l'axe pd-1 et d'inhibiteurs de mek
EP3191478B1 (fr) * 2014-09-12 2019-05-08 Novartis AG Composés et compositions comme inhibiteurs de la kinase raf
KR102702851B1 (ko) 2015-11-19 2024-09-05 제넨테크, 인크. B-raf 억제제 및 면역 체크포인트 억제제를 사용하여 암을 치료하는 방법
WO2018146253A1 (fr) 2017-02-10 2018-08-16 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés et compositions pharmaceutiques pour le traitement de cancers associés à l'activation de la voie mapk
US20210086176A1 (en) * 2017-11-01 2021-03-25 The Board Of Trustees Of The Leland Stanford Junior University Analyte Detection method
US11725185B2 (en) 2017-12-28 2023-08-15 University Of Houston System Stem cell culture systems for columnar epithelial stem cells, and uses related thereto
CN111171019A (zh) * 2018-11-13 2020-05-19 上海轶诺药业有限公司 一类五元并六元杂环化合物及其作为蛋白受体激酶抑制剂的用途
KR20210142154A (ko) 2019-03-21 2021-11-24 옹쎄오 암 치료를 위한 키나제 억제제와 조합된 dbait 분자
CN110627691B (zh) * 2019-08-20 2022-03-25 中船(邯郸)派瑞特种气体股份有限公司 一种制备n-苯基-双(全氟烷基磺酰)亚胺的方法
CN114761006A (zh) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) 对激酶抑制剂产生耐药性的癌症的治疗方法
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
US12371667B2 (en) 2021-05-13 2025-07-29 Washington University Enhanced methods for inducing and maintaining naive human pluripotent stem cells
WO2024229406A1 (fr) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Polythérapie pour une maladie ou un trouble lié à ras
WO2025034702A1 (fr) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 destiné à être utilisé dans le traitement d'une maladie ou d'un trouble lié à une protéine ras
WO2025073765A1 (fr) 2023-10-03 2025-04-10 Institut National de la Santé et de la Recherche Médicale Méthodes de pronostic et de traitement de patients souffrant de mélanome
TW202530228A (zh) 2023-10-12 2025-08-01 美商銳新醫藥公司 Ｒａｓ抑制劑
WO2025171296A1 (fr) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025240847A1 (fr) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025255438A1 (fr) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Procédés de traitement d'une maladie ou d'un trouble lié à la protéine ras

Family Cites Families (97)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR6121M (fr) * 1966-01-12 1968-06-17
NZ186175A (en) * 1977-01-27 1980-03-05 Shionogi & Co Meta-sulphonamidobenzamide derivatives
US5800711A (en) * 1996-10-18 1998-09-01 Mdv Technologies, Inc. Process for the fractionation of polyoxyalkylene block copolymers
ATE355841T1 (de) 1997-12-13 2007-03-15 Bristol Myers Squibb Co Verwendung von pyrazolo ( 3,4-b) pyridin als cyclin-abhängige kinase hemmer
PL205321B1 (pl) 1997-12-22 2010-04-30 Bayer Corp Zastosowanie podstawionych heterocyklicznych moczników do wytwarzania leku do hamowania kinazy raf, podstawione heterocykliczne moczniki oraz kompozycja farmaceutyczna je zawierająca
TR200002617T2 (tr) 1997-12-22 2000-11-21 Bayer Corporation Aril ve heteroaril sübstitüentli heterosiklik üreler kullanılarak RAF kinazın inhibe edilmesi
CA2315646C (fr) 1997-12-22 2010-02-09 Bayer Corporation Inhibition de raf kinase au moyen de diphenylurees substituees symetriques et asymetriques
US8124630B2 (en) * 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7351834B1 (en) * 1999-01-13 2008-04-01 Bayer Pharmaceuticals Corporation ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7928239B2 (en) * 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
EP1140840B1 (fr) * 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf
ATE556713T1 (de) * 1999-01-13 2012-05-15 Bayer Healthcare Llc Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer
US6761824B2 (en) * 2000-08-17 2004-07-13 Reeve Lorraine E Process for the fractionation of polymers
US7235576B1 (en) * 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US20030207914A1 (en) * 2001-04-20 2003-11-06 Bayer Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
GB0112348D0 (en) 2001-05-19 2001-07-11 Smithkline Beecham Plc Compounds
US20020192289A1 (en) * 2001-06-18 2002-12-19 Ji Zheng Polymer gel for cancer treatment
GB0121490D0 (en) 2001-09-05 2001-10-24 Smithkline Beecham Plc Ciompounds
WO2003068773A1 (fr) 2002-02-12 2003-08-21 Glaxo Group Limited Derives de pyrazolopyridine
DK1499311T3 (da) * 2002-03-29 2010-03-08 Novartis Vaccines & Diagnostic Substituerede benzaboler og anvendelse deraf som RAF-kinaseinhibitorer
CN1794980A (zh) * 2003-03-24 2006-06-28 生物领域医疗公司 利用逆向热敏聚合物的暂时栓塞
JP2006527230A (ja) * 2003-06-13 2006-11-30 ノバルティス アクチエンゲゼルシャフト Ｒａｆキナーゼ阻害剤としての２−アミノピリミジン誘導体
JP5001650B2 (ja) * 2003-07-11 2012-08-15 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング ベンズイミダゾールカルボキサミド
EP1653951B1 (fr) * 2003-07-11 2011-12-28 Merck Patent GmbH Derives de benzimidazoles utilises comme inhibiteurs de kinase raf
WO2005009958A1 (fr) 2003-07-17 2005-02-03 Plexxikon, Inc. Composes ayant une activite sur des ppar
DE10337942A1 (de) * 2003-08-18 2005-03-17 Merck Patent Gmbh Aminobenzimidazolderivate
DE10344223A1 (de) * 2003-09-24 2005-04-21 Merck Patent Gmbh 1,3-Benzoxazolylderivate als Kinase-Inhibitoren
CA2542105C (fr) * 2003-10-08 2011-08-02 Irm Llc Composes et compositions convenant comme inhibiteurs de proteine-kinases
EP1682126B1 (fr) * 2003-10-16 2009-07-01 Novartis Vaccines and Diagnostics, Inc. Benzazoles substitues et leur utilisation en tant qu'inhibiteurs de la raf kinase
CN1882345A (zh) * 2003-10-16 2006-12-20 希龙公司 作为raf激酶抑制剂以治疗癌症的2,6－二取代的喹唑啉、喹喔啉、喹啉和异喹啉
ES2527118T3 (es) * 2003-12-19 2015-01-20 Plexxikon Inc. Compuestos y procedimientos de desarrollo de moduladores de Ret
DE102004009238A1 (de) * 2004-02-26 2005-09-08 Merck Patent Gmbh Arylamid-Derivate
TW200616974A (en) * 2004-07-01 2006-06-01 Astrazeneca Ab Chemical compounds
BRPI0514691A (pt) * 2004-08-31 2008-06-17 Astrazeneca Ab composto ou um sal farmaceuticamente aceitável do mesmo, processo para preparar o mesmo, composição farmacêutica, e, uso de um composto ou um sal farmaceuticamente aceitável do mesmo
KR20070055575A (ko) * 2004-09-01 2007-05-30 아스트라제네카 아베 퀴나졸리논 유도체 및 이의 ｂ―ｒａｆ 억제제로서의 용도
US20070054916A1 (en) * 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
DE502005002697D1 (de) 2004-10-13 2008-03-13 Merck Patent Gmbh Als kinaseinhibitoren geeignete derivate des n,n'-diphenylharnstoffs
AU2005297531B2 (en) 2004-10-13 2011-06-23 Merck Patent Gmbh Phenylurea derivatives used as inhibitors of tyrosinkinase for treating tumors
MX2007004480A (es) * 2004-10-15 2007-05-08 Astrazeneca Ab Quinoxalinas como inhibidores b raf.
GB0423554D0 (en) * 2004-10-22 2004-11-24 Cancer Rec Tech Ltd Therapeutic compounds
CA2589773A1 (fr) 2004-12-22 2006-06-29 Astrazeneca Ab Derives de pyridinecarboxamide employes en tant qu'agents anticancereux
EP1833829A2 (fr) 2004-12-23 2007-09-19 F. Hoffmann-Roche AG Imidazo- et pyrrolo-pyridines à substitution benzamide comme inhibiteurs de protéine kinase
WO2006071940A2 (fr) * 2004-12-23 2006-07-06 Deciphera Pharmaceuticals, Llc Modulateurs d'enzymes et traitements
MX2007008924A (es) * 2005-01-25 2007-08-21 Astrazeneca Ab Compuestos quimicos.
US20090105250A1 (en) * 2005-01-26 2009-04-23 Irm Llc Compounds and compositions as protein kinase inhibitors
TW200639163A (en) * 2005-02-04 2006-11-16 Genentech Inc RAF inhibitor compounds and methods
JP2008533172A (ja) * 2005-03-17 2008-08-21 ノバルティス アクチエンゲゼルシャフト チロシン／スレオニンキナーゼ阻害剤、特にＢ−ＲＡＦキナーゼ阻害剤としての、Ｎ−［３−（１−アミノ−５，６，７，８−テトラヒドロ−２，４，４ｂ−トリアザフルオレン−９−イル）−フェニル］ベンズアミド
WO2006124780A2 (fr) 2005-05-12 2006-11-23 Kalypsys, Inc. Inhibiteurs de la b-raf kinase
WO2006124731A2 (fr) 2005-05-12 2006-11-23 Irm Llc Composes et compositions utilise(e)s en tant qu'inhibiteurs de proteines-kinases
EP1891066B1 (fr) * 2005-05-13 2010-12-22 Irm, Llc Composes et compositions convenant comme inhibiteurs de proteine kinase
NZ563444A (en) * 2005-05-17 2011-04-29 Plexxikon Inc Pyrrolo(2,3-b)pyridine derivatives as protein kinase inhibitors
MX2007014510A (es) * 2005-05-20 2008-02-05 Array Biopharma Inc Compuestos inhibidores de raf y metodos de uso de los mismos.
UA95244C2 (ru) 2005-06-22 2011-07-25 Плексикон, Инк. Соединения и способ модулирования активности киназ, и показания для их применения
EP1919910B1 (fr) 2005-07-29 2011-02-23 F. Hoffmann-La Roche AG Derives de l'azabenzimidazole, leur fabrication et leur utilisation en tant qu'agents anticancereux
CA2617359A1 (fr) * 2005-08-09 2007-02-22 Irm Llc Composes et compositions utiles comme inhibiteurs de proteines kinases
JP2009507024A (ja) * 2005-09-01 2009-02-19 アレイ バイオファーマ、インコーポレイテッド Ｒａｆ阻害剤化合物およびその使用方法
CA2621830C (fr) * 2005-09-15 2013-12-03 F. Hoffmann-La Roche Ag Derives d'acide 4-amino-thieno[3,2-c]pyridine-7-carboxylique
WO2007056625A2 (fr) * 2005-11-04 2007-05-18 Smithkline Beecham Corporation Inhibiteurs de thienopyridine b-raf kinase
BRPI0619514A2 (pt) * 2005-12-08 2011-10-04 Millennium Pharm Inc compostos bicìclicos com atividade inibidora cinase, composição farmacêutica contendo os mesmos e uso de ditos compostos
CA2633023C (fr) 2005-12-13 2015-11-24 Schering Corporation Derives polycycliques d'indazole inhibiteurs des erk
CN101341133A (zh) * 2005-12-22 2009-01-07 阿斯利康(瑞典)有限公司 喹唑啉衍生物，其制备方法及其作为抗癌药的用途
WO2007076460A2 (fr) 2005-12-23 2007-07-05 Kalypsys, Inc. Nouveaux thiazole-urees substitues utiles en tant qu'inhibiteurs de proteine-kinases
TW200804349A (en) * 2005-12-23 2008-01-16 Kalypsys Inc Novel substituted pyrimidinyloxy ureas as inhibitors of protein kinases
US20070155746A1 (en) * 2005-12-23 2007-07-05 Kalypsys, Inc. Novel substituted pyridinyloxy and pyrimidinyloxy amides useful as inhibitors of protein kinases
CN101415689A (zh) * 2006-04-05 2009-04-22 阿斯利康(瑞典)有限公司 具有抗癌活性的经取代的喹唑啉
US20090170849A1 (en) * 2006-04-05 2009-07-02 Astrazeneca Ab Quinazolinone derivatives having b-raf inhibitory activity
EP2010504A1 (fr) * 2006-04-18 2009-01-07 AstraZeneca AB Derives de quinazolin-4-one, procede de fabrication de ces derives et compositions pharmaceutiques les contenant
US20070224169A1 (en) * 2006-07-18 2007-09-27 Sliwa John W Jr Selectively switched gels for surgery, therapy and maintenance
CN101511828A (zh) * 2006-09-06 2009-08-19 霍夫曼-拉罗奇有限公司 作为蛋白激酶抑制剂的杂芳基衍生物
US7897762B2 (en) * 2006-09-14 2011-03-01 Deciphera Pharmaceuticals, Llc Kinase inhibitors useful for the treatment of proliferative diseases
US8188113B2 (en) * 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
MX2009003456A (es) * 2006-10-02 2009-04-14 Irm Llc Compuestos y composiciones como inhibidores de proteina cinasa.
WO2008044688A1 (fr) 2006-10-11 2008-04-17 Daiichi Sankyo Company, Limited Dérivé de l'urée
EP1914234A1 (fr) * 2006-10-16 2008-04-23 GPC Biotech Inc. Pyrido[2,3-d]pyrimidines et leur utilisation comme inhibiteurs de kinases
CN105251035A (zh) * 2006-12-11 2016-01-20 健赞公司 灌注器官止血法
RU2009122670A (ru) * 2006-12-21 2011-01-27 Плекссикон, Инк. (Us) Соединения и способы для модуляции киназ и показания к их применению
WO2008079909A1 (fr) * 2006-12-21 2008-07-03 Plexxikon, Inc. Composés et méthodes de modulation des kinases, et indications connexes
PE20081581A1 (es) * 2006-12-21 2008-11-12 Plexxikon Inc COMPUESTOS PIRROLO[2,3-b]PIRIDINAS COMO MODULADORES DE QUINASA
WO2008112695A2 (fr) 2007-03-12 2008-09-18 Irm Llc Inhibiteurs de protéine kinase et procédés d'utilisation de ceux-ci
WO2008124393A1 (fr) 2007-04-04 2008-10-16 Irm Llc Derives de benzothiazole et leur utilisation en tant qu'inhibiteurs des proteines kinases
WO2008144253A1 (fr) 2007-05-14 2008-11-27 Irm Llc Inhibiteurs de la protéine kinase et procédé d'utilisation de ceux-ci
JP2010529990A (ja) * 2007-06-15 2010-09-02 アイアールエム・リミテッド・ライアビリティ・カンパニー タンパク質キナーゼ阻害剤およびそれを使用するための方法
KR20100035635A (ko) * 2007-06-21 2010-04-05 아이알엠 엘엘씨 단백질 키나제 억제제 및 그의 사용 방법
SG183036A1 (en) 2007-07-17 2012-08-30 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
WO2009025358A1 (fr) * 2007-08-23 2009-02-26 Takeda Pharmaceutical Company Limited Composé hétérocyclique et son utilisation
EP2184285B1 (fr) * 2007-08-29 2015-11-04 Takeda Pharmaceutical Company Limited Composé hétérocyclique et son utilisation
JP2011513332A (ja) * 2008-02-29 2011-04-28 アレイ バイオファーマ、インコーポレイテッド 癌の治療のためのｒａｆ阻害剤としてのｎ−（６−アミノピリジン−３−イル）−３−（スルホンアミド）ベンズアミド誘導体
US20110003809A1 (en) * 2008-02-29 2011-01-06 Array Biopharma Inc. Imidazo [4,5-b] pyridine derivatives used as raf inhibitors
MX2010009410A (es) * 2008-02-29 2010-11-30 Array Biopharma Inc Compuestos del inhibidor de raf y métodos de uso de los mismos.
PT2268623E (pt) * 2008-03-17 2015-09-17 Ambit Biosciences Corp Derivados de quinazolina como moduladores de cinase raf e métodos para utilização dos mesmos
GB0807609D0 (en) * 2008-04-25 2008-06-04 Cancer Rec Tech Ltd Therapeutic compounds and their use
UA103319C2 (en) * 2008-05-06 2013-10-10 Глаксосмитклайн Ллк Thiazole- and oxazole-benzene sulfonamide compounds
US8158636B2 (en) * 2008-05-19 2012-04-17 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
PE20091846A1 (es) * 2008-05-19 2009-12-16 Plexxikon Inc DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
EP2313411A1 (fr) * 2008-06-10 2011-04-27 Plexxikon, Inc. Dérivés 5h-pyrrolo-[2,3-b]-pyrazine destinés à la modulation de kinases, et des indications pour ceux-ci
WO2009152087A1 (fr) * 2008-06-10 2009-12-17 Plexxikon, Inc. Composés hétéroaryles bicycliques et procédés destinés à la modulation de kinases, et des indications pour celle-ci
KR101061599B1 (ko) * 2008-12-05 2011-09-02 한국과학기술연구원 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물

Also Published As

Publication number Publication date
CR11690A (es) 2010-11-02
MX2010009411A (es) 2010-11-30
EP2265610A1 (fr) 2010-12-29
KR20100117686A (ko) 2010-11-03
ES2400202T3 (es) 2013-04-08
WO2009111279A1 (fr) 2009-09-11
IL207845A0 (en) 2010-12-30
BRPI0908268A2 (pt) 2018-10-30
AU2009222144A1 (en) 2009-09-11
US8394795B2 (en) 2013-03-12
EP2265610B1 (fr) 2012-12-12
TW200940539A (en) 2009-10-01
ECSP10010507A (es) 2010-10-30
PE20091623A1 (es) 2009-11-19
AR072657A1 (es) 2010-09-15
CL2009000448A1 (es) 2009-11-27
JP2011513331A (ja) 2011-04-28
CA2716952A1 (fr) 2009-09-11
CN102149712A (zh) 2011-08-10
US20110092479A1 (en) 2011-04-21

Similar Documents

Publication Publication Date Title
MA32272B1 (fr) Inhibiteurs de raf de pyrazole [3,4-b]pyridine
UA111933C2 (uk) Піролопіридини як інгібітори кінази
WO2009111278A3 (fr) Composés inhibiteurs de kinases raf et procédés d'utilisation
SG178899A1 (en) Raf inhibitor compounds and methods of use thereof
NZ609448A (en) Tricyclic pi3k inhibitor compounds and methods of use
EA201290957A1 (ru) Пиразол-4-илгетероциклилкарбоксамидные соединения и способы их применения
TW200942536A (en) PIM kinase inhibitors and methods of their use
MX2009012066A (es) Imidazopirinas sustituidas como inhibidoras de cinasa de lipido p13k.
NO20084418L (no) Azolopyridin-3-on derivater som inhibitorer av endoteliallipase
MX2010006241A (es) Derivados de aminotriazol como agonistas de alx.
MX340013B (es) Compuestos de benzoxazepina selectivos para fosfatidilinositol 3-cinasa (pi3k) p110 delta y metodos de uso.
UA116774C2 (uk) Інгібітори серин/треонінкінази
TN2011000611A1 (en) 1,3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
WO2014194245A3 (fr) Inhibiteurs de cdk8 et leurs utilisations
EP2595482A4 (fr) Inhibiteurs de l'aldostérone synthase
EA201590624A1 (ru) Циклические эфиры пиразол-4-ил-гетероциклил-карбоксамидных соединений и способы их применения
MX2014014828A (es) Compuestos de 5-azaindazol y metodos de uso.
WO2012016186A8 (fr) Inhibiteurs de kinases macrocycliques et leurs utilisations
MY147649A (en) Benzimidazole derivatives useful in treatment of vallinoid receptor trpv1 related disorders
EA201100358A1 (ru) Дабигатран для чрескожной хирургической катетеризации сердца
MX2009004623A (es) Imidazopiridazinas como inhibidores de la lipido cinasa pi3k.
UA109290C2 (uk) Спільні кристали і солі інгібіторів ccr3
NO20083708L (no) 4-Fenyl-tiazol-5-karboksylsyre og 4-fenyl-tiazol-5-karboksylmider som PLK1-inhibitorer
EA201100872A1 (ru) Производные хиназолинамида
WO2009094560A3 (fr) Thiénopyranones en tant qu'inhibiteurs de kinase