[go: up one dir, main page]

MA29915B1 - Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases - Google Patents

Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases

Info

Publication number
MA29915B1
MA29915B1 MA30737A MA30737A MA29915B1 MA 29915 B1 MA29915 B1 MA 29915B1 MA 30737 A MA30737 A MA 30737A MA 30737 A MA30737 A MA 30737A MA 29915 B1 MA29915 B1 MA 29915B1
Authority
MA
Morocco
Prior art keywords
compositions
new
kinase inhibitors
inhibiting
compounds
Prior art date
Application number
MA30737A
Other languages
English (en)
Inventor
Mina E Aikawa
Payman Amiri
Jeffrey H Dove
Barry Haskell Levine
Christopher Mcbride
Teresa E Pick
Daniel J Poon
Savithri Ramurthy
Paul A Renhowe
Cynthia Shafer
Darrin Stuart
Sharadha Subramanian
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of MA29915B1 publication Critical patent/MA29915B1/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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

CETTE INVENTION CONCERNE DES NOUVEAUX COMPOSÉS BENZIMIDAZOLES SUBSTITUÉS REPRÉSENTÉS PAR LA FORMULE (I). L'INVENTION CONCERNE ÉGALEMENT DES COMPOSITIONS, ET DES PROCÉDÉS PERMETTANT D'INHIBER L'ACTIVITÉ DES KINASES ASSOCIÉE À LA TUMORIGÉNÈSE CHEZ UN SUJET HUMAIN OU ANIMAL. DANS CERTAINS MODES DE RÉALISATION, LES COMPOSÉS ET LES COMPOSITIONS SONT EFFICACES POUR INHIBER L'ACTIVITÉ D'AU MOINS UNE SÉRINE/THRÉONINE KINASE OU UN RÉCEPTEUR TYROSINE KINASE. LES NOUVEAUX COMPOSÉS ET LES NOUVELLES COMPOSITIONS DE CETTE INVENTION PEUVENT ÊTRE UTILISÉS SEULS OU COMBINÉS AVEC AU MOINS UN AGENT SUPPLÉMENTAIRE POUR LE TRAITEMENT D'UN TROUBLE INDUIT PAR UNE SÉRINE/THRÉONINE KINASE OU PAR UN RÉCEPTEUR TYROSINE KINASE, TEL QUE LE CANCER.
MA30737A 2005-08-30 2008-03-11 Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases MA29915B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US71253905P 2005-08-30 2005-08-30
US71310805P 2005-08-30 2005-08-30
US73159105P 2005-10-27 2005-10-27
US77468406P 2006-02-17 2006-02-17

Publications (1)

Publication Number Publication Date
MA29915B1 true MA29915B1 (fr) 2008-11-03

Family

ID=37434025

Family Applications (2)

Application Number Title Priority Date Filing Date
MA30737A MA29915B1 (fr) 2005-08-30 2008-03-11 Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases
MA30738A MA29772B1 (fr) 2005-08-30 2008-03-11 Benzimidazoles substitues et procedes de preparation

Family Applications After (1)

Application Number Title Priority Date Filing Date
MA30738A MA29772B1 (fr) 2005-08-30 2008-03-11 Benzimidazoles substitues et procedes de preparation

Country Status (37)

Country Link
US (6) US20070049622A1 (fr)
EP (2) EP1924577B1 (fr)
JP (4) JP5210866B2 (fr)
KR (2) KR20080039965A (fr)
AR (2) AR057109A1 (fr)
AT (2) ATE503751T1 (fr)
AU (2) AU2006287688B2 (fr)
BR (2) BRPI0615314A2 (fr)
CA (2) CA2620472C (fr)
CR (1) CR9716A (fr)
CU (1) CU23784B7 (fr)
CY (2) CY1111871T1 (fr)
DE (1) DE602006021036D1 (fr)
DK (2) DK1924577T3 (fr)
EA (1) EA014230B1 (fr)
EC (2) ECSP088210A (fr)
ES (1) ES2374451T3 (fr)
GE (1) GEP20105004B (fr)
GT (1) GT200600394A (fr)
HK (2) HK1117519A1 (fr)
HN (1) HN2008000317A (fr)
HR (2) HRP20110312T1 (fr)
IL (2) IL189080A (fr)
MA (2) MA29915B1 (fr)
MY (2) MY163886A (fr)
NI (1) NI200800060A (fr)
NO (1) NO20081476L (fr)
NZ (2) NZ565451A (fr)
PE (2) PE20070427A1 (fr)
PL (2) PL1926722T3 (fr)
PT (2) PT1924577E (fr)
RS (1) RS52099B (fr)
SI (2) SI1924577T1 (fr)
SM (1) SMAP200800022A (fr)
TN (2) TNSN08088A1 (fr)
TW (2) TWI387592B (fr)
WO (2) WO2007030377A1 (fr)

Families Citing this family (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20070427A1 (es) * 2005-08-30 2007-04-21 Novartis Ag Compuestos derivados de benzimidazoles sustituidos como inhibidores de tirosina quinasas
GB0609378D0 (en) * 2006-05-11 2006-06-21 Novartis Ag Organic compounds
DE602007005139D1 (de) * 2006-07-21 2010-04-15 Novartis Ag Formulierungen für benzimidazolylpyridylether
PE20130814A1 (es) * 2006-08-30 2013-08-08 Novartis Ag Sales de benzimidazolil piridil eteres y formulaciones que las contienen
MX2009002936A (es) * 2006-09-19 2009-04-01 Novartis Ag Biomarcadores de la modulacion de objetivo, eficacia, diagnostico, y/o pronostico para los inhibidores de raf.
CN101679372A (zh) * 2007-03-02 2010-03-24 诺瓦提斯公司 Raf激酶抑制剂的固体形式
NZ580592A (en) * 2007-05-23 2012-02-24 Novartis Ag Raf inhibitors, such as benzimidazole derivatives, for the treatment of thyroid cancer
TW200904816A (en) 2007-06-05 2009-02-01 Takeda Pharmaceutical Fused heterocycle derivatives and use thereof
US8324395B2 (en) 2007-08-23 2012-12-04 Takeda Pharmaceutical Company Limited Heterocyclic compound and use thereof
JP5350247B2 (ja) * 2007-08-29 2013-11-27 武田薬品工業株式会社 複素環化合物およびその用途
RU2011100106A (ru) * 2008-06-13 2012-10-27 Новартис АГ (CH) Замещенные бензимидазолы для лечения нейрофиброматоза
JP2011527703A (ja) * 2008-07-11 2011-11-04 ノバルティス アーゲー (a)ホスホイノシタイド3−キナーゼ阻害剤および(b)Ras/Raf/Mek経路のモジュレーターの配合物
WO2010051176A1 (fr) * 2008-10-29 2010-05-06 Merck Sharp & Dohme Corp. Nouveaux agents antidiabétiques utiles avec des dérivés de benzimidazole cycliques
EP2399921B1 (fr) 2008-12-01 2015-08-12 Takeda Pharmaceutical Company Limited Composé hétérocyclique et applications
JO3101B1 (ar) 2008-12-02 2017-09-20 Takeda Pharmaceuticals Co مشتقات بنزوثيازول كعوامل مضادة للسرطان
JP2011020936A (ja) * 2009-07-14 2011-02-03 Lotte Co Ltd 口臭除去剤
JO3002B1 (ar) 2009-08-28 2016-09-05 Irm Llc مركبات و تركيبات كمثبطات كيناز بروتين
WO2011044072A1 (fr) 2009-10-05 2011-04-14 Novartis Ag Combinaison de raf-265 et d'un activateur d'ampk destinée à être utilisée dans le traitement d'une maladie proliférative
MX2013005668A (es) * 2010-11-19 2013-11-04 Glaxosmithkline Ip No 2 Ltd Metodo de tratamiento con inhibidor de braf.
KR101762999B1 (ko) 2011-04-18 2017-07-28 에자이 알앤드디 매니지먼트 가부시키가이샤 종양 치료제
WO2012145503A1 (fr) 2011-04-21 2012-10-26 Novartis Ag Combinaisons pharmaceutiques
CN103764144B (zh) 2011-08-31 2016-07-20 诺华股份有限公司 Pi3k抑制剂与mek抑制剂的协同组合
ES2709003T3 (es) * 2011-11-09 2019-04-12 Cancer Research Tech Ltd Compuestos de 5-(piridin-2-il-amino)-pirazina-2-carbonitrilo y su uso terapéutico
CN108542906A (zh) 2011-11-11 2018-09-18 诺华股份有限公司 治疗增生性疾病的方法
MY172729A (en) 2011-11-23 2019-12-11 Array Biopharma Inc Pharmaceutical formulations
PL2855448T3 (pl) 2012-05-15 2017-09-29 Cancer Research Technology Ltd 5-[[4-[[morfolino-2-ilo]metyloamino]-5-(trifluorometylo)-2-pirydylo]amino]pirazyno-2-karbonitryl i jego zastosowanie terapeutyczne
AU2013343425A1 (en) 2012-11-08 2015-06-11 Novartis Ag Pharmaceutical combination comprising a B-Raf inhibitor and a histone deacetylase inhibitor and their use in the treatment of proliferative diseases
MX2015013466A (es) 2013-03-21 2016-06-21 Novartis Ag Terapia de combinacion que comprende un inhibidor deb-raf y un segundo inhibidor.
WO2015041534A1 (fr) 2013-09-20 2015-03-26 Stichting Het Nederlands Kanker Instituut P90rsk en combinaison avec raf/erk/mek
US9629851B2 (en) 2013-09-20 2017-04-25 Stitching Het Nederlands Kanker Institut—Antoni Van Leeuwenhoek Ziekenhuis ROCK in combination with MAPK pathway
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
JOP20200096A1 (ar) 2014-01-31 2017-06-16 Children’S Medical Center Corp جزيئات جسم مضاد لـ tim-3 واستخداماتها
WO2015138920A1 (fr) 2014-03-14 2015-09-17 Novartis Ag Molécules d'anticorps anti-lag-3 et leurs utilisations
US20170027940A1 (en) 2014-04-10 2017-02-02 Stichting Het Nederlands Kanker Instituut Method for treating cancer
WO2015178770A1 (fr) 2014-05-19 2015-11-26 Stichting Het Nederlands Kanker Instituut Compositions pour le traitement du cancer
WO2015196072A2 (fr) 2014-06-19 2015-12-23 Whitehead Institute For Biomedical Research Utilisations d'inhibiteurs de kinase pour l'induction et le maintien de la pluripotence
MA41044A (fr) 2014-10-08 2017-08-15 Novartis Ag Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer
CR20170143A (es) 2014-10-14 2017-06-19 Dana Farber Cancer Inst Inc Moléculas de anticuerpo que se unen a pd-l1 y usos de las mismas
US20170340733A1 (en) 2014-12-19 2017-11-30 Novartis Ag Combination therapies
US10449211B2 (en) 2015-03-10 2019-10-22 Aduro Biotech, Inc. Compositions and methods for activating “stimulator of interferon gene”—dependent signalling
US9890187B2 (en) 2015-06-26 2018-02-13 Epos-Iasis Research And Development, Ltd. Prototype systems of theranostic biomarkers for in vivo molecular management of cancer
EP3316857B1 (fr) 2015-06-30 2021-08-04 Sequessome Technology Holdings Limited Compositions multiphasiques
US20180207273A1 (en) 2015-07-29 2018-07-26 Novartis Ag Combination therapies comprising antibody molecules to tim-3
US20180222982A1 (en) 2015-07-29 2018-08-09 Novartis Ag Combination therapies comprising antibody molecules to pd-1
ES2878188T3 (es) 2015-07-29 2021-11-18 Novartis Ag Terapias de combinación que comprenden moléculas de anticuerpos contra LAG-3
LT3370768T (lt) 2015-11-03 2022-05-25 Janssen Biotech, Inc. Antikūnai, specifiškai surišantys pd-1, ir jų panaudojimas
CN105481944B (zh) * 2015-12-10 2019-01-08 华南农业大学 一种苯并咪唑衍生物二肽铜配合物及其制备方法和应用
BR112018012138A2 (pt) 2015-12-17 2018-12-04 Novartis Ag moléculas de anticorpo para pd-1 e usos das mesmas
WO2018009466A1 (fr) 2016-07-05 2018-01-11 Aduro Biotech, Inc. Composés dinucléotidiques cycliques d'acide nucléique bloqué et leurs utilisations
EP3579872A1 (fr) 2017-02-10 2019-12-18 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
JP7094942B2 (ja) * 2017-03-15 2022-07-04 住友ファーマ株式会社 ベンズイミダゾール誘導体の製造方法
JP7110232B2 (ja) 2017-04-18 2022-08-01 イーライ リリー アンド カンパニー フェニル-2-ヒドロキシ-アセチルアミノ-2-メチル-フェニル化合物
UY37695A (es) 2017-04-28 2018-11-30 Novartis Ag Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
WO2018237173A1 (fr) 2017-06-22 2018-12-27 Novartis Ag Molécules d'anticorps dirigées contre cd73 et utilisations correspondantes
MX2019015885A (es) 2017-06-22 2020-09-10 Novartis Ag Moleculas de anticuerpo que se unen a cd73 y usos de las mismas.
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
AR126019A1 (es) 2018-05-30 2023-09-06 Novartis Ag Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación
WO2019232244A2 (fr) 2018-05-31 2019-12-05 Novartis Ag Molécules d'anticorps anti-cd73 et leurs utilisations
EP3876930A4 (fr) * 2018-11-07 2022-07-20 Dana-Farber Cancer Institute, Inc. Dérivés de benzimidazole et dérivés d'aza-benzimidazole en tant qu'inhibiteurs de janus kinase 2 et leurs utilisations
AU2020206036A1 (en) 2019-01-11 2021-08-05 Naegis Pharmaceuticals Inc. Leukotriene synthesis inhibitors
JP2022548881A (ja) 2019-09-18 2022-11-22 ノバルティス アーゲー Entpd2抗体、組合せ療法並びに抗体及び組合せ療法を使用する方法
CA3181537A1 (fr) 2020-05-06 2021-11-11 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2
WO2022140527A1 (fr) 2020-12-23 2022-06-30 Ajax Therapeutics, Inc. 6-hétéroaryloxy benzimidazoles et azabenzimidazoles utilisés en tant qu'inhibiteurs de jak2
WO2023086320A1 (fr) 2021-11-09 2023-05-19 Ajax Therapeutics, Inc. Formes et compositions d'inhibiteurs de jak2
TW202334139A (zh) 2021-11-09 2023-09-01 美商雅捷可斯治療公司 作為jak2抑制劑之6-雜芳氧基苯并咪唑及氮雜苯并咪唑

Family Cites Families (131)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3894037A (en) 1971-05-24 1975-07-08 Ciba Geigy Corp Certain isothiocyanobenzimidazoles
CH634306A5 (de) 1977-04-12 1983-01-31 Ciba Geigy Ag Benzimidazolderivate, verfahren zu ihrer herstellung und anthelmintische mittel enthaltend diese verbindungen als wirkstoffe.
US4319039A (en) 1979-06-15 1982-03-09 Merck & Co., Inc. Preparation of ammonium salt of hypocholesteremic fermentation product
US4231938A (en) 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4294926A (en) 1979-06-15 1981-10-13 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4444784A (en) 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
DK149080C (da) 1980-06-06 1986-07-28 Sankyo Co Fremgangsmaade til fremstilling af derivater af ml-236b-carboxylsyre
JPS5889191A (ja) 1981-11-20 1983-05-27 Sankyo Co Ltd 3−ヒドロキシ−ml−236b誘導体の製造法
US4430502A (en) 1982-08-13 1984-02-07 The Upjohn Company Pyridinyl substituted benzimidazoles and quinoxalines
US5354772A (en) 1982-11-22 1994-10-11 Sandoz Pharm. Corp. Indole analogs of mevalonolactone and derivatives thereof
US4911165A (en) 1983-01-12 1990-03-27 Ethicon, Inc. Pliabilized polypropylene surgical filaments
GB8307865D0 (en) 1983-03-22 1983-04-27 Fujisawa Pharmaceutical Co Benzimidazole derivatives
US4681893A (en) 1986-05-30 1987-07-21 Warner-Lambert Company Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis
US4782084A (en) 1987-06-29 1988-11-01 Merck & Co., Inc. HMG-COA reductase inhibitors
US4885314A (en) 1987-06-29 1989-12-05 Merck & Co., Inc. Novel HMG-CoA reductase inhibitors
US4820850A (en) 1987-07-10 1989-04-11 Merck & Co., Inc. Process for α-C-alkylation of the 8-acyl group on mevinolin and analogs thereof
US5180589A (en) 1988-03-31 1993-01-19 E. R. Squibb & Sons, Inc. Pravastatin pharmaceuatical compositions having good stability
US5030447A (en) 1988-03-31 1991-07-09 E. R. Squibb & Sons, Inc. Pharmaceutical compositions having good stability
US4916239A (en) 1988-07-19 1990-04-10 Merck & Co., Inc. Process for the lactonization of mevinic acids and analogs thereof
US5118853A (en) 1988-10-13 1992-06-02 Sandoz Ltd. Processes for the synthesis of 3-disubstituted aminoacroleins
US5290946A (en) 1988-10-13 1994-03-01 Sandoz Ltd. Processes for the synthesis of 3-(substituted indolyl-2-yl)propenaldehydes
US4929437A (en) 1989-02-02 1990-05-29 Merck & Co., Inc. Coenzyme Q10 with HMG-CoA reductase inhibitors
US5189164A (en) 1989-05-22 1993-02-23 Sandoz Ltd. Processes for the synthesis of syn-(E)-3,5-dihydroxy-7-substituted hept-6-enoic and heptanoic acids and derivatives and intermediates thereof
FI94339C (fi) 1989-07-21 1995-08-25 Warner Lambert Co Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi
JPH06759B2 (ja) 1989-09-22 1994-01-05 ファイザー製薬株式会社 新規なベンゾイミダゾール化合物
PH27357A (en) 1989-09-22 1993-06-21 Fujisawa Pharmaceutical Co Pyrazole derivatives and pharmaceutical compositions comprising the same
US5420245A (en) 1990-04-18 1995-05-30 Board Of Regents, The University Of Texas Tetrapeptide-based inhibitors of farnesyl transferase
US5041453A (en) 1990-05-30 1991-08-20 Rhone-Poulenc Rorer Pharmaceuticals Inc. Quinolinyl-benzoheterobicyclic derivatives as antagonists of leukotriene D4
FR2677020B1 (fr) 1991-05-31 1993-08-27 Cird Galderma Composes derives de benzimidazole, leur procede de preparation et leur utilisation dans les domaines therapeutique et cosmetique.
HU217629B (hu) 1991-12-12 2000-03-28 Novartis Ag. Eljárás fluvasztatint tartalmazó stabilizált gyógyszerkészítmények előállítására
US5612360A (en) 1992-06-03 1997-03-18 Eli Lilly And Company Angiotensin II antagonists
US5604260A (en) 1992-12-11 1997-02-18 Merck Frosst Canada Inc. 5-methanesulfonamido-1-indanones as an inhibitor of cyclooxygenase-2
CA2111902A1 (fr) 1992-12-21 1994-06-22 Jack Beuford Campbell Compositions antitumorales et methodes therapeutiques
US5298627A (en) 1993-03-03 1994-03-29 Warner-Lambert Company Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis
US5409944A (en) 1993-03-12 1995-04-25 Merck Frosst Canada, Inc. Alkanesulfonamido-1-indanone derivatives as inhibitors of cyclooxygenase
CA2118985A1 (fr) 1993-04-02 1994-10-03 Dinesh V. Patel Inhibiteurs heterocycliques de la farnesyl proteine transferase
US5843941A (en) 1993-05-14 1998-12-01 Genentech, Inc. Ras farnesyl transferase inhibitors
US5602098A (en) 1993-05-18 1997-02-11 University Of Pittsburgh Inhibition of farnesyltransferase
US5380738A (en) 1993-05-21 1995-01-10 Monsanto Company 2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents
US5436265A (en) 1993-11-12 1995-07-25 Merck Frosst Canada, Inc. 1-aroyl-3-indolyl alkanoic acids and derivatives thereof useful as anti-inflammatory agents
GB9602877D0 (en) 1996-02-13 1996-04-10 Merck Frosst Canada Inc 3,4-Diaryl-2-hydroxy-2,5- dihydrofurans as prodrugs to cox-2 inhibitors
US5474995A (en) 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
EP0639573A1 (fr) 1993-08-03 1995-02-22 Hoechst Aktiengesellschaft Hétérocycles à cinq chaînons benzocondensés, procédé pour leur préparation, leur utilisation comme médicament et comme diagnostique aussi bien que les produits pharmaceutiques le contenant
US5852046A (en) 1993-08-03 1998-12-22 Hoechst Aktiengesellschaft Benzo-fused heterocyclic compounds having a 5-membered ring processes for their preparation their use as medicaments their use as diagnostic agents and medicaments containing them
US5661152A (en) 1993-10-15 1997-08-26 Schering Corporation Tricyclic sulfonamide compounds useful for inhibition of G-protein function and for treatment of proliferative diseases
US5344991A (en) 1993-10-29 1994-09-06 G.D. Searle & Co. 1,2 diarylcyclopentenyl compounds for the treatment of inflammation
US5466823A (en) 1993-11-30 1995-11-14 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides
US5484799A (en) 1993-12-09 1996-01-16 Abbott Laboratories Antifungal dorrigocin derivatives
US5393790A (en) 1994-02-10 1995-02-28 G.D. Searle & Co. Substituted spiro compounds for the treatment of inflammation
AU1615895A (en) 1994-03-31 1995-10-12 Bristol-Myers Squibb Company Imidazole-containing inhibitors of farnesyl protein transferase
US5523430A (en) 1994-04-14 1996-06-04 Bristol-Myers Squibb Company Protein farnesyl transferase inhibitors
US5510510A (en) 1994-05-10 1996-04-23 Bristol-Meyers Squibb Company Inhibitors of farnesyl protein transferase
US6391636B1 (en) 1994-05-31 2002-05-21 Isis Pharmaceuticals, Inc. Antisense oligonucleotide modulation of raf gene expression
US6358932B1 (en) 1994-05-31 2002-03-19 Isis Pharmaceticals, Inc. Antisense oligonucleotide inhibition of raf gene expression
US5571792A (en) 1994-06-30 1996-11-05 Warner-Lambert Company Histidine and homohistidine derivatives as inhibitors of protein farnesyltransferase
CA2155448A1 (fr) 1994-08-11 1996-02-12 Katerina Leftheris Inhibiteurs de la farnesyl-proteine-transferase
EP0701907A1 (fr) 1994-09-13 1996-03-20 Agfa-Gevaert N.V. Elément donneur de colorant pour utilisation dans un procédé de transfert thermique de colorant
US6037136A (en) 1994-10-24 2000-03-14 Cold Spring Harbor Laboratory Interactions between RaF proto-oncogenes and CDC25 phosphatases, and uses related thereto
US5741789A (en) 1995-01-17 1998-04-21 Eli Lilly And Company Compounds having effects on serotonin-related systems
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
US6001866A (en) 1995-10-05 1999-12-14 Warner-Lambert Company Method for treating and preventing inflammation and atherosclerosis
US5717100A (en) 1995-10-06 1998-02-10 Merck & Co., Inc. Substituted imidazoles having anti-cancer and cytokine inhibitory activity
US6020343A (en) 1995-10-13 2000-02-01 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
PT903348E (pt) 1995-11-17 2002-11-29 Biotechnolog Forschung Mbh Gbf Derivados do epotilone e sua preparacao
JP3063162B2 (ja) 1995-12-28 2000-07-12 藤沢薬品工業株式会社 ベンズイミダゾール誘導体
GB9602029D0 (en) 1996-02-01 1996-04-03 Fujisawa Pharmaceutical Co New heterocyclic compounds
SI22713B (sl) 1996-04-12 2009-12-31 Searle & Co Substituirani benzensulfonamidni derivati kot predzdravila COX-2 inhibitorjev
WO1997044058A1 (fr) 1996-05-23 1997-11-27 Applied Research Systems Ars Holding N.V. Composes inhibant la liaison de proteines raf-1 ou 14-3-3 a la chaine beta du recepteur d'il-2, et compositions pharmaceutiques les contenant
US5861419A (en) 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors
FR2751649B1 (fr) 1996-07-26 1998-08-28 Adir Nouveaux derives de benzimidazole, de benzoxazole et de benzothiazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
EP1386922B1 (fr) 1996-12-03 2012-04-11 Sloan-Kettering Institute For Cancer Research Synthèse d'épitholones, intermédiaires, analogues et leur utilisation
US6127380A (en) 1997-02-18 2000-10-03 American Home Products Corporation 4-aminoalkoxy-1H-benzoimidazoles
DE69816280T2 (de) 1997-03-14 2004-05-27 Vertex Pharmaceuticals Inc., Cambridge Inhibitoren des impdh-enzyms
US5932600A (en) 1997-03-14 1999-08-03 Vertex Pharmaceuticals Incorporated Inhibitors of IMPDH enzyme
AR012634A1 (es) 1997-05-02 2000-11-08 Sugen Inc Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
BR9810651A (pt) 1997-07-03 2000-10-03 Neurogen Corp Certos derivados de diarilimidazol; uma nova classe de ligantes npy especìficos
SI9700186B (sl) * 1997-07-14 2006-10-31 Lek, Tovarna Farmacevtskih In Kemicnih Izdelkov, D.D. Nova farmacevtska oblika z nadzorovanim sproscanjem zdravilnih ucinkovin
FR2766822B1 (fr) 1997-07-30 2001-02-23 Adir Nouveaux derives de benzimidazole, de benzoxazole et de benzothiazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
US6022884A (en) 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
US6204467B1 (en) 1998-03-24 2001-03-20 Ford Global Technologies, Inc. Method and apparatus for resistive welding
KR20010025087A (ko) 1998-05-22 2001-03-26 스튜어트 알. 수터 신규한 2-알킬 치환된 이미다졸 화합물
US6420555B1 (en) 1998-06-16 2002-07-16 Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S. Imidazolyl derivatives
FR2780973B1 (fr) 1998-07-09 2001-10-05 Hoechst Marion Roussel Inc Procede de preparation du 4-(3-pyridinyl)-1h-imidazole, et les intermediaires mis en oeuvre
DE19834751A1 (de) 1998-08-01 2000-02-03 Boehringer Ingelheim Pharma Disubstituierte bicyclische Heterocyclen, ihre Herstellung und ihre Verwendung als Arzneimittel
US6211177B1 (en) 1998-11-24 2001-04-03 Cell Pathways, Inc. Method for treating neoplasia by exposure to substituted 2-aryl-benzimidazole derivatives
US7351834B1 (en) 1999-01-13 2008-04-01 Bayer Pharmaceuticals Corporation ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
IL145748A0 (en) 1999-04-12 2002-07-25 Aventis Pharma Ltd Substituted bicyclic heteroaryl compounds as integrin antagonists
AU777275B2 (en) 1999-07-02 2004-10-07 Stuart A. Lipton Method of reducing neuronal injury or apoptosis
ATE266022T1 (de) 2000-03-06 2004-05-15 Smithkline Beecham Plc Imidazol derivate als raf kinase inhibitoren
WO2001072708A2 (fr) 2000-03-24 2001-10-04 Cor Therapeutics, Inc. INHIBITEURS D'OXINIDOLE DU FACTEUR Xa
EP1268432A1 (fr) 2000-03-24 2003-01-02 Millenium Pharmaceuticals, Inc. Inhibiteurs du facteur xa sous forme d'isoquinolone
JP2001322903A (ja) 2000-05-15 2001-11-20 Kumiai Chem Ind Co Ltd 農園芸用殺菌剤組成物
WO2002009761A2 (fr) * 2000-07-27 2002-02-07 Pharmacia Corporation Polytherapie par antagoniste d'aldosterone epoxy-steroidien et inhibiteur calcique pour le traitement de l'insuffisance cardiaque congestive
WO2002018654A1 (fr) 2000-08-30 2002-03-07 The Board Of Trustees Of The University Of Arkansas Induction de l'expression du recepteur ldl par erk-1/2, kinase regulee par un signal extracellulaire
JP4734705B2 (ja) 2000-10-31 2011-07-27 三菱化学株式会社 リチウム二次電池用正極材料、リチウム二次電池用正極及びリチウム二次電池
DE10060292A1 (de) * 2000-12-05 2002-06-20 Aventis Pharma Gmbh Verwendung substituierter Benzimidazole zur Herstellung eines Medikaments zur Behandlung von Krankheiten, welche durch Inhibierung des Na+/H+-Austauschers beeinflusst werden können und sie enthaltendes Medikament
EP1341769B1 (fr) 2000-12-15 2007-10-17 Vertex Pharmaceuticals Incorporated Inhibiteurs de la gyrase bactérienne et utilisations associees
TW593278B (en) 2001-01-23 2004-06-21 Wyeth Corp 1-aryl-or 1-alkylsulfonylbenzazole derivatives as 5-hydroxytryptamine-6 ligands
AU2002237298B2 (en) * 2001-02-08 2006-08-03 Karo Bio Ab Phenoxy substituted benzocondensed heteroaryl derivatives as thyroid receptor ligands
JP2004525140A (ja) * 2001-03-26 2004-08-19 ユニサーチ リミテッド ガンの治療方法及び該治療方法に使用する組成物
EP1432690A2 (fr) * 2001-04-16 2004-06-30 Tanabe Seiyaku Co., Ltd. Substance d'ouverture du canal k activee par le calcium a grande conductance
US6855714B2 (en) 2001-07-06 2005-02-15 Schering Aktiengesellschaft 1-alkyl-2-aryl-benzimidazole derivatives, their use for the production of pharmaceutical agents as well as pharmaceutical preparations that contain these derivatives
US6740649B2 (en) 2001-09-17 2004-05-25 Bristol-Myers Squibb Company Cyclic hydroxamic acids as inhibitors of matrix metalloproteinases and/or TNF- α converting enzyme (TACE)
ATE511840T1 (de) 2001-10-09 2011-06-15 Amgen Inc Imidazolderivate als entzündungshemmende mittel
US7039413B2 (en) * 2001-10-24 2006-05-02 Ntt Docomo, Inc. Mobile station transfer control system, cell transfer control method, mobile station, cell transfer control method at mobile station, cell transfer control program, control apparatus, and allocating method of communication resources
TW200300140A (en) 2001-11-14 2003-05-16 Novartis Ag Organic compounds
TW200303742A (en) 2001-11-21 2003-09-16 Novartis Ag Organic compounds
UA83620C2 (ru) * 2001-12-05 2008-08-11 Уайт Замещенные бензоксазолы и их аналоги как эстрогенные агенты
JP4136395B2 (ja) 2002-02-22 2008-08-20 クミアイ化学工業株式会社 農園芸用殺菌剤組成物
US8299108B2 (en) * 2002-03-29 2012-10-30 Novartis Ag Substituted benzazoles and methods of their use as inhibitors of raf kinase
ATE447404T1 (de) * 2002-03-29 2009-11-15 Novartis Vaccines & Diagnostic Substituierte benzazole und ihre verwendung als raf-kinase-hemmer
JP4429738B2 (ja) 2002-04-25 2010-03-10 帝人株式会社 Ccr3拮抗作用を有する4,4−二置換ピペリジン誘導体
TW200400816A (en) * 2002-06-26 2004-01-16 Lilly Co Eli Tricyclic steroid hormone nuclear receptor modulators
EP1529045A2 (fr) 2002-08-09 2005-05-11 Astra Zeneca AB Nouveaux composes
OA12928A (en) * 2002-09-18 2006-10-13 Pfizer Prod Inc Novel imidazole compounds as transforming growth factor (TGF) inhibitors.
WO2004035056A1 (fr) 2002-10-13 2004-04-29 Neurosearch A/S Utilisation de medicaments bloquant les canaux skca pour lutter contre la maladie de parkinson
JP4768265B2 (ja) 2002-10-15 2011-09-07 シンタ ファーマシューティカルズ コーポレーション 新規化合物
US20050054705A1 (en) * 2003-02-04 2005-03-10 Aventis Pharma Deutschland Gmbh N-substituted (benzoimidazol-2-yl) phenylamines, process for their preparation, their use as medicament or diagnostic aid, and medicament comprising them
US7531553B2 (en) * 2003-03-21 2009-05-12 Amgen Inc. Heterocyclic compounds and methods of use
CA2520124A1 (fr) 2003-03-28 2004-10-14 Chiron Corporation Utilisation de composes de benzazole pour l' immunostimulation
CN1795193B (zh) 2003-05-20 2010-08-18 诺瓦提斯公司 用作过氧化物酶体增殖物激活受体的配体的n-酰基含氮杂环化合物
EP1626725A4 (fr) 2003-05-29 2006-06-14 Synta Pharmaceuticals Corp Composes heterocycliques permettant de prevenir et de traiter des troubles associes a une perte osseuse excessive
AU2004255342C1 (en) 2003-07-08 2009-05-14 Novartis Ag Benzenesulfonylamino compounds and pharmaceutical compositions containing these compounds
WO2005016914A1 (fr) 2003-08-14 2005-02-24 Smithkline Beecham Corporation Composes chimiques
PT2210607E (pt) 2003-09-26 2012-01-31 Exelixis Inc N-[3-fluoro-4-({6-(metiloxi)-7-[(3-morfolina-4-ilpropil)oxi]quinolina-4-il}oxi)fenil]-n'-(4-fluorofenil)ciclopropano-1,1-dicarboxamida para o tratamento do cancro
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
US7626030B2 (en) 2004-01-23 2009-12-01 Amgen Inc. Compounds and methods of use
PE20070427A1 (es) * 2005-08-30 2007-04-21 Novartis Ag Compuestos derivados de benzimidazoles sustituidos como inhibidores de tirosina quinasas
DE602007005139D1 (de) * 2006-07-21 2010-04-15 Novartis Ag Formulierungen für benzimidazolylpyridylether

Also Published As

Publication number Publication date
US20070049622A1 (en) 2007-03-01
AU2006287688A1 (en) 2007-03-15
DE602006021036D1 (de) 2011-05-12
PL1924577T3 (pl) 2011-09-30
US7767820B2 (en) 2010-08-03
TNSN08088A1 (en) 2009-07-14
JP5210867B2 (ja) 2013-06-12
BRPI0615314A2 (pt) 2011-05-17
CR9716A (es) 2008-04-16
SMP200800022B (it) 2008-04-02
CY1111871T1 (el) 2015-11-04
SMAP200800022A (it) 2008-04-02
WO2007027950A1 (fr) 2007-03-08
JP2009507026A (ja) 2009-02-19
IL189080A (en) 2013-05-30
HRP20110939T1 (hr) 2012-01-31
EP1924577A1 (fr) 2008-05-28
NZ565450A (en) 2011-04-29
US7482367B2 (en) 2009-01-27
PT1924577E (pt) 2011-07-04
TW200804346A (en) 2008-01-16
NI200800060A (es) 2009-03-03
SI1924577T1 (sl) 2011-07-29
CA2620472C (fr) 2013-12-24
ECSP088218A (es) 2008-03-26
IL189194A (en) 2013-09-30
HRP20110312T1 (hr) 2011-08-31
NO20081476L (no) 2008-03-26
EP1926722A1 (fr) 2008-06-04
JP2013060457A (ja) 2013-04-04
AU2006284666A1 (en) 2007-03-08
TWI387592B (zh) 2013-03-01
SI1926722T1 (sl) 2012-01-31
PE20070427A1 (es) 2007-04-21
TW200804345A (en) 2008-01-16
GEP20105004B (en) 2010-06-10
US20090170904A1 (en) 2009-07-02
ES2374451T3 (es) 2012-02-16
DK1924577T3 (da) 2011-05-16
IL189080A0 (en) 2008-08-07
TNSN08089A1 (en) 2009-07-14
AR057109A1 (es) 2007-11-14
WO2007030377A1 (fr) 2007-03-15
HK1117519A1 (en) 2009-01-16
MY148694A (en) 2013-05-31
IL189194A0 (en) 2008-06-05
GT200600394A (es) 2008-03-17
JP2009507794A (ja) 2009-02-26
AU2006287688B2 (en) 2010-08-19
RS52099B (en) 2012-06-30
BRPI0615309B1 (pt) 2021-07-27
AU2006284666B2 (en) 2011-04-28
CA2619966A1 (fr) 2007-03-08
ATE526325T1 (de) 2011-10-15
AR055622A1 (es) 2007-08-29
PE20070335A1 (es) 2007-04-21
ATE503751T1 (de) 2011-04-15
US20100256375A1 (en) 2010-10-07
CA2620472A1 (fr) 2007-03-15
CU23784B7 (es) 2012-02-15
CY1112157T1 (el) 2015-12-09
MA29772B1 (fr) 2008-09-01
HK1117523A1 (en) 2009-01-16
US7732465B2 (en) 2010-06-08
BRPI0615309A2 (pt) 2011-05-17
MY163886A (en) 2017-11-15
US20100234394A1 (en) 2010-09-16
NZ565451A (en) 2011-05-27
EP1926722B1 (fr) 2011-09-28
PT1926722E (pt) 2012-01-11
JP2013060458A (ja) 2013-04-04
KR20080039964A (ko) 2008-05-07
EP1924577B1 (fr) 2011-03-30
US20070161680A1 (en) 2007-07-12
EA200800441A1 (ru) 2008-08-29
JP5210866B2 (ja) 2013-06-12
US8592459B2 (en) 2013-11-26
CU20080027A7 (es) 2010-12-08
PL1926722T3 (pl) 2012-02-29
HN2008000317A (es) 2011-02-16
ECSP088210A (es) 2008-03-26
US20080287682A1 (en) 2008-11-20
EA014230B1 (ru) 2010-10-29
KR20080039965A (ko) 2008-05-07
DK1926722T3 (da) 2011-12-19

Similar Documents

Publication Publication Date Title
MA29915B1 (fr) Benzimidazoles substitues utilises en tant qu'inhibiteurs de kinases
MA32684B1 (fr) Dérivés de picolinamide en tant qu'inhibiteurs de kinase
MA27565A1 (fr) Derives de 4-tetrazolyl-4-phenylpiperidine utilises pour le traitement de la douleur
MA32232B1 (fr) Nouveaux compoés hétérocycliques et leurs utilisations
ATE516803T1 (de) Aryl-spirohydantoin-cgrp-rezeptor-antagonisten
MA29160B1 (fr) Derives de triazole substitues, servant d'antagonistes d'ocytocine
ATE394400T1 (de) Bicyclische anilidspirohydantoine als cgrp- rezeptorantagonisten
MA33811B1 (fr) Composés et méthodes utilisés pour la modulation kinases et indications à cet effet
ATE556060T1 (de) Monocyclische anilidspirohydantoine als cgrp- rezeptorantagonisten
DE602005023963D1 (de) Weitere heteropolycyclische verbindungen und deren verwendung als antagonisten des metabotropen glutamatrezeptors
TNSN04111A1 (fr) Derives de quinazoline pour le traitement d'une croissance cellulaire anormale
BRPI0515532A (pt) composto, composição farmacêutica, métodos de inibir a ligação de ligandos endógenos ao receptor de crth-2 em uma célula, de tratar, melhorar ou prevenir um distúrbio responsivo à inibição da ligação de ligandos endógenos ao receptor de crt-2 e de preparar um composto, e, kit
MA30655B1 (fr) Composes organiques.
MA29797B1 (fr) DERIVES DE LA PYRROLOPYRIMIDINE INHIBITEURS DE LA Syk
MA29723B1 (fr) Composes
MA52492B1 (fr) Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés
TW200505903A (en) CGRP receptor antagonists
EA200600048A1 (ru) Производные бензазепина, используемые для лечения заболеваний, ассоциированных с 5-ht-рецептором
ATE535514T1 (de) Carboxamid-spirohydantoin-cgrp-rezeptor- antagonisten
EA200501504A1 (ru) Лиганды каннабиноидных рецепторов и их применение
MA31766B1 (fr) Composés organiques
MA34300B1 (fr) Composés azotés hétérocycliques convenant comme inhibiteurs de la pde10
TNSN07305A1 (fr) Agonistes de pyy et leurs utilisations
MA30333B1 (fr) Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete.
BRPI0412231A (pt) derivados de pentanol substituìdos heterociclicamente, processos para a sua preparação e sua aplicação como inibidores de inflamação