MX343894B - Síntesis y uso de inhibidores de cinasa. - Google Patents

Síntesis y uso de inhibidores de cinasa.

Info

Publication number
MX343894B
MX343894B MX2012014986A MX2012014986A MX343894B MX 343894 B MX343894 B MX 343894B MX 2012014986 A MX2012014986 A MX 2012014986A MX 2012014986 A MX2012014986 A MX 2012014986A MX 343894 B MX343894 B MX 343894B
Authority
MX
Mexico
Prior art keywords
synthesis
fak
based catalyst
kinase inhibitors
reactions
Prior art date
Application number
MX2012014986A
Other languages
English (en)
Spanish (es)
Other versions
MX2012014986A (es
Inventor
Lei Yixiong
Henry Behrens Carl
Li Hui-Yin
L Sun Connie
Original Assignee
Poniard Pharmaceuticals 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 Poniard Pharmaceuticals Inc * filed Critical Poniard Pharmaceuticals Inc *
Publication of MX2012014986A publication Critical patent/MX2012014986A/es
Publication of MX343894B publication Critical patent/MX343894B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • C07D279/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D279/101,4-Thiazines; Hydrogenated 1,4-thiazines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
MX2012014986A 2010-06-30 2011-06-28 Síntesis y uso de inhibidores de cinasa. MX343894B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US35994210P 2010-06-30 2010-06-30
PCT/US2011/042169 WO2012012139A1 (en) 2010-06-30 2011-06-28 Synthesis and use of kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2012014986A MX2012014986A (es) 2013-07-03
MX343894B true MX343894B (es) 2016-11-28

Family

ID=45497129

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2012014986A MX343894B (es) 2010-06-30 2011-06-28 Síntesis y uso de inhibidores de cinasa.

Country Status (10)

Country Link
US (1) US9505719B2 (https=)
EP (1) EP2588476A4 (https=)
JP (1) JP5923499B2 (https=)
CN (1) CN103168037A (https=)
AU (1) AU2011280031B2 (https=)
CA (1) CA2803005A1 (https=)
MX (1) MX343894B (https=)
NZ (1) NZ604801A (https=)
WO (1) WO2012012139A1 (https=)
ZA (1) ZA201300012B (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2675793B1 (en) 2011-02-17 2018-08-08 Cancer Therapeutics Crc Pty Limited Fak inhibitors
JP5937112B2 (ja) 2011-02-17 2016-06-22 カンサー・セラピューティクス・シーアールシー・プロプライエタリー・リミテッドCancer Therapeutics Crc Pty Limited 選択的fak阻害剤
WO2019117813A1 (en) * 2017-12-15 2019-06-20 National University Of Singapore Focal adhesion kinase targeted therapeutics for the treatment of glaucoma and fibrosis

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4656182A (en) * 1983-12-06 1987-04-07 Warner-Lambert Company Substituted trans-1,2-diaminocyclohexyl amide compounds
US20040006005A1 (en) 2002-07-02 2004-01-08 Sanjay Bhanot Use of integrin-linked kinase inhibitors for treating insulin resistance, hyperglycemia and diabetes
GB9828511D0 (en) 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
GB0004887D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
BR0114814A (pt) 2000-10-11 2005-01-25 Cephalon Inc Composições compreendendo composto de modafinila e seu uso
AR040456A1 (es) * 2002-06-27 2005-04-06 Bristol Myers Squibb Co Piridina n-oxidos 2,4 -disubstituidos utiles como inhibidores de transcriptasa inversa del virus de inmunodeficiencia humana
US20080119515A1 (en) 2003-03-10 2008-05-22 M Arshad Siddiqui Heterocyclic Kinase Inhibitors: Methods of Use and Synthesis
GT200500310A (es) 2004-11-19 2006-06-19 Compuestos organicos
ES2533258T3 (es) 2005-02-18 2015-04-08 Janssen Sciences Ireland Uc Derivados de óxido de 2-(4-cianofenilamino)pirimidina que inhiben el VIH
WO2007050574A1 (en) 2005-10-25 2007-05-03 Abbott Laboratories Formulation comprising a drug of low water solubility and method of use thereof
EP2012753A2 (en) * 2006-04-28 2009-01-14 Schering Corporation Process for the precipitation and isolation of 6,6-dimethyl-3-aza-bicyclo [3.1.0]hexane-amide compounds by controlled precipitation and pharmaceutical formulations containing same
CN101495095B (zh) * 2006-04-28 2013-05-29 默沙东公司 通过受控的沉淀来沉淀和分离6,6-二甲基-3-氮杂-双环[3.1.0]己烷-酰胺化合物的方法和含有其的药学制剂
EP2046292B1 (en) 2006-07-21 2010-03-03 Novartis AG Formulations for benzimidazolyl pyridyl ethers
DK2134689T3 (da) * 2007-03-16 2014-06-30 Scripps Research Inst Inhibitorer af fokal adhæsionskinase
WO2009100176A2 (en) 2008-02-07 2009-08-13 Abbott Laboratories Pharmaceutical dosage form for oral administration of tyrosine kinase inhibitor
WO2009105498A1 (en) * 2008-02-19 2009-08-27 Smithkline Beecham Corporation Anilinopyridines as inhibitors of fak
MX2010014057A (es) * 2008-06-17 2011-03-21 Astrazeneca Ab Compuestos de piridina.
CN102648197A (zh) 2009-08-12 2012-08-22 铂雅制药公司 促进细胞凋亡和抑制转移的方法
WO2011133668A2 (en) 2010-04-20 2011-10-27 President And Fellows Of Harvard College Methods and compositions for the treatment of cancer

Also Published As

Publication number Publication date
US20140235635A1 (en) 2014-08-21
JP5923499B2 (ja) 2016-05-24
CA2803005A1 (en) 2012-01-26
ZA201300012B (en) 2013-09-25
AU2011280031B2 (en) 2015-09-10
AU2011280031A1 (en) 2013-01-10
MX2012014986A (es) 2013-07-03
US9505719B2 (en) 2016-11-29
EP2588476A4 (en) 2014-07-23
NZ604801A (en) 2015-03-27
EP2588476A1 (en) 2013-05-08
JP2013529687A (ja) 2013-07-22
CN103168037A (zh) 2013-06-19
WO2012012139A1 (en) 2012-01-26

Similar Documents

Publication Publication Date Title
MX2015000667A (es) Proceso y sistema de reaccion para la preparacion de metanol.
WO2012054364A3 (en) Bicyclic diamines as janus kinase inhibitors
EP4223730A3 (en) Organo-catalytic biomass deconstruction
EP2538979A4 (en) ADHESIVE COMPOSITE KOAZERVATE MANUFACTURED FROM ELECTROSTATICALLY ASSOCIATED BLOCK COPOLYMERS AND METHOD FOR THE PRODUCTION AND USE THEREOF
MX2015000129A (es) Derivados de pirimidin pirazolilo.
WO2012135113A3 (en) Cyclopropylamines as lsd1 inhibitors
TN2014000138A1 (en) Substituted benzylindazoles for use as bub1 kinase inhibitors in the treatment of hyperproliferative diseases.
NZ701407A (en) Triazolone compounds as mpges-1 inhibitors
WO2011090949A3 (en) Methods and compositions for processing chemical reactions
MX2012003770A (es) Metodos para la modulacion de autofagia a traves de la modulacion de productos de genes que aumentan la autofagia.
WO2011113060A3 (en) Antiviral compounds and methods of use thereof
MX349801B (es) Sustratos de enzimas de ácido nucleico.
WO2011090694A8 (en) Orally administrable film dosage forms containing ondansetron
EP2382434A1 (de) Verfahren zur thermischen behandlung von zementrohmehl in einem reaktionsraum
IL286892B1 (en) Portable oxygen production system
MX343894B (es) Síntesis y uso de inhibidores de cinasa.
IN2012DN00459A (https=)
WO2010013498A1 (ja) 変形性関節症治療剤又は予防剤
AP2013007133A0 (en) Hydrocarbon synthesis reaction apparatus, start-upprocess thereof and hydrocarbon synthesis reactio n system
IN2015DN02588A (https=)
PH12017500270A1 (en) Use of 1-phenyl-3-dimethylaminopropane compounds for treating rheumatoid pain
WO2011113895A3 (en) Characterization and validation of inhibitors and ligands of dipeptidyl aminopeptidase iv (dp iv)
IT1397233B1 (it) Procedimento migliorativo per la sintesi del mono-acetil ganciclovir, intermedio chiave per la sintesi del valganciclovir.
WO2013184570A3 (en) Synthesis of 1,3-substituted aminouracils and other xanthine-related compounds
ZA201304841B (en) Use of the reaction product of a hydrocarbyl-substituted dicarboxylic acid and a nitrogen compound for reducing fuel consumption

Legal Events

Date Code Title Description
FG Grant or registration