NI200700311A - Derivados de tienopirimidina y tienopiridina como inhibidores de la cinasa de flt-3 - Google Patents

Derivados de tienopirimidina y tienopiridina como inhibidores de la cinasa de flt-3

Info

Publication number
NI200700311A
NI200700311A NI200700311A NI200700311A NI200700311A NI 200700311 A NI200700311 A NI 200700311A NI 200700311 A NI200700311 A NI 200700311A NI 200700311 A NI200700311 A NI 200700311A NI 200700311 A NI200700311 A NI 200700311A
Authority
NI
Nicaragua
Prior art keywords
compounds
kinase
inhibitors
tienopirimidine
tienopiridine
Prior art date
Application number
NI200700311A
Other languages
English (en)
Inventor
David Gaul Michael
Douglas Kreutter Kevin
Andrew Baumann Christian
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 filed Critical
Publication of NI200700311A publication Critical patent/NI200700311A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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

Abstract

La invención se refiere a compuestos de tienopirimidinas y tienopiridinas de Fórmula I y Fórmula II: donde R1, R3, B, Z, Q, p, q, y X son como se definen en presente documento, el uso de tales compuestos como moduladores de la proteína de tirosina cinasa, en particular inhibidores de FLT3, el uso de tales compuestos para reducir o inhibir la actividad de la cinasa de FLT3 en una célula o en un sujeto, y el uso de tales compuestos para prevenir o tratar en un sujeto un trastorno prolífero de célua y/o trastornos relacionados a FLT3. La presente invención también se refiere a composiciones farmacéuticas que comprenden los compuestos de la presente invención y a métodos para tratar condiciones tales como canceres y otros trastornos prolíferos de células.
NI200700311A 2005-06-10 2006-06-07 Derivados de tienopirimidina y tienopiridina como inhibidores de la cinasa de flt-3 NI200700311A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US68971005P 2005-06-10 2005-06-10
US74694106P 2006-05-10 2006-05-10

Publications (1)

Publication Number Publication Date
NI200700311A true NI200700311A (es) 2009-03-03

Family

ID=37074647

Family Applications (1)

Application Number Title Priority Date Filing Date
NI200700311A NI200700311A (es) 2005-06-10 2006-06-07 Derivados de tienopirimidina y tienopiridina como inhibidores de la cinasa de flt-3

Country Status (19)

Country Link
US (3) US20060281768A1 (es)
EP (1) EP1899355A1 (es)
JP (1) JP2008543759A (es)
KR (1) KR20080021126A (es)
AR (1) AR057063A1 (es)
AU (1) AU2006258049A1 (es)
BR (1) BRPI0613644A2 (es)
CA (1) CA2611587A1 (es)
CR (1) CR9650A (es)
EA (1) EA200800011A1 (es)
EC (1) ECSP077992A (es)
IL (1) IL187689A0 (es)
MX (1) MX2007015741A (es)
NI (1) NI200700311A (es)
NO (1) NO20080162L (es)
PE (1) PE20070070A1 (es)
TW (1) TW200716651A (es)
UY (1) UY29590A1 (es)
WO (1) WO2006135639A1 (es)

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MY179032A (en) 2004-10-25 2020-10-26 Cancer Research Tech Ltd Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors
EP2013206A1 (en) * 2006-04-25 2009-01-14 Astex Therapeutics Limited Pharmaceutical compounds
EP2043655A2 (en) 2006-04-25 2009-04-08 Astex Therapeutics Limited Purine and deazapurine derivatives as pharmaceutical compounds
JP2010504362A (ja) * 2006-09-25 2010-02-12 アレテ セラピューティクス, インコーポレイテッド 可溶性エポキシドヒドロラーゼ阻害剤
AU2008301897B2 (en) * 2007-09-14 2013-08-01 Janssen Pharmaceutica N.V. Thieno-and furo-pyrimidine modulators of the histamine H4 receptor
RS53552B1 (en) 2007-10-11 2015-02-27 Astrazeneca Ab DERIVATI PIROLO [2,3-D] PIRIMIDINA KAO INHIBITORI PROTEIN KINAZE B
WO2012131399A1 (en) 2011-04-01 2012-10-04 Astrazeneca Ab Therapeutic treatment
CN105130967B (zh) 2011-05-13 2018-04-17 阵列生物制药公司 作为trka激酶抑制剂的吡咯烷基脲和吡咯烷基硫脲化合物
AR090037A1 (es) * 2011-11-15 2014-10-15 Xention Ltd Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio
PT2785349T (pt) 2011-11-30 2019-12-11 Astrazeneca Ab Tratamento combinado de cancro
AU2013204533B2 (en) 2012-04-17 2017-02-02 Astrazeneca Ab Crystalline forms
LT3154959T (lt) 2014-05-15 2019-09-25 Array Biopharma, Inc. 1-((3s,4r)-4-(3-fluorfenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)karbamidas kaip trka kinazės inhibitorius
WO2018118598A1 (en) * 2016-12-23 2018-06-28 Arvinas, Inc. Compounds and methods for the targeted degradation of fetal liver kinase polypeptides
WO2020132384A1 (en) 2018-12-21 2020-06-25 Celgene Corporation Thienopyridine inhibitors of ripk2

Family Cites Families (15)

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DE69332948T2 (de) * 1992-03-05 2003-11-27 Univ Texas Verwendung von Immunokonjugate zur Diagnose und/oder Therapie der vaskularisierten Tumoren
US5474765A (en) * 1992-03-23 1995-12-12 Ut Sw Medical Ctr At Dallas Preparation and use of steroid-polyanionic polymer-based conjugates targeted to vascular endothelial cells
US5932765A (en) * 1997-05-23 1999-08-03 Merck Patent Gesellschaft Mit Nitromethyl ketones, process for preparing them and compositions containing them
CN101328186A (zh) * 1997-11-11 2008-12-24 辉瑞产品公司 用作抗癌药的噻吩并嘧啶和噻吩并吡啶衍生物
EA200000768A1 (ru) * 1998-01-27 2001-06-25 Эвентис Фармасьютикалз Продактс Инк. ЗАМЕЩЕННЫЕ ОКСОАЗАГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ ФАКТОРА Ха
ES2223705T3 (es) * 1999-04-28 2005-03-01 Board Of Regents, The University Of Texas System Composiciones y metodos para el tratamiento de cancer mediante inhibi cion selectiva del vegf.
US6776796B2 (en) * 2000-05-12 2004-08-17 Cordis Corportation Antiinflammatory drug and delivery device
DE10110750A1 (de) * 2001-03-07 2002-09-12 Bayer Ag Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften
AR035885A1 (es) * 2001-05-14 2004-07-21 Novartis Ag Derivados de 4-amino-5-fenil-7-ciclobutilpirrolo (2,3-d)pirimidina, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos derivados para la preparacion de una composicion farmaceutica
US7105505B2 (en) * 2002-04-18 2006-09-12 Schering Corporation Benzimidazole derivatives useful as histamine H3 antagonists
MY141867A (en) * 2002-06-20 2010-07-16 Vertex Pharma Substituted pyrimidines useful as protein kinase inhibitors
MXPA05001631A (es) * 2002-08-12 2005-08-19 Takeda Pharmaceutical Derivado de benceno fusionado y su uso.
WO2004039782A1 (ja) * 2002-10-29 2004-05-13 Kirin Beer Kabushiki Kaisha Flt3自己リン酸化を阻害するキノリン誘導体およびキナゾリン誘導体並びにそれらを含有する医薬組成物
US20050026944A1 (en) * 2003-07-24 2005-02-03 Patrick Betschmann Thienopyridine and furopyridine kinase inhibitors
US20060281769A1 (en) * 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators

Also Published As

Publication number Publication date
TW200716651A (en) 2007-05-01
EP1899355A1 (en) 2008-03-19
MX2007015741A (es) 2008-04-29
CA2611587A1 (en) 2006-12-21
AU2006258049A8 (en) 2006-12-21
US20090143378A1 (en) 2009-06-04
BRPI0613644A2 (pt) 2011-01-25
WO2006135639A1 (en) 2006-12-21
KR20080021126A (ko) 2008-03-06
CR9650A (es) 2008-09-09
EA200800011A1 (ru) 2008-06-30
JP2008543759A (ja) 2008-12-04
AU2006258049A1 (en) 2006-12-21
NO20080162L (no) 2008-03-07
UY29590A1 (es) 2006-10-02
ECSP077992A (es) 2008-01-23
US20060281768A1 (en) 2006-12-14
IL187689A0 (en) 2008-08-07
AR057063A1 (es) 2007-11-14
PE20070070A1 (es) 2007-03-08
US20090163710A1 (en) 2009-06-25

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