[go: up one dir, main page]

WO2003035614A3 - Inhibiteurs de la tyrosine kinase - Google Patents

Inhibiteurs de la tyrosine kinase Download PDF

Info

Publication number
WO2003035614A3
WO2003035614A3 PCT/US2002/033919 US0233919W WO03035614A3 WO 2003035614 A3 WO2003035614 A3 WO 2003035614A3 US 0233919 W US0233919 W US 0233919W WO 03035614 A3 WO03035614 A3 WO 03035614A3
Authority
WO
WIPO (PCT)
Prior art keywords
compounds
tyrosine kinase
kinase inhibitors
present
receptor
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/US2002/033919
Other languages
English (en)
Other versions
WO2003035614A2 (fr
Inventor
B Wesley Trotter
Ian M Bell
C Blair Zartman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck and Co Inc
Original Assignee
Merck and Co 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 Merck and Co Inc filed Critical Merck and Co Inc
Priority to AU2002348393A priority Critical patent/AU2002348393A1/en
Publication of WO2003035614A2 publication Critical patent/WO2003035614A2/fr
Publication of WO2003035614A3 publication Critical patent/WO2003035614A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne des composés capables d'inhiber, moduler et/ou réguler la transduction des signaux des tyrosine kinases de type récepteurs et de type non récepteurs. Les composés de l'invention possèdent une structure centrale qui contient un 2-carboxy-5-formyl pyrrole. Par ailleurs, l'invention concerne des sels acceptables sur le plan pharmaceutique, des hydrates et des stéréo-isomères de ces composés.
PCT/US2002/033919 2001-10-25 2002-10-21 Inhibiteurs de la tyrosine kinase Ceased WO2003035614A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2002348393A AU2002348393A1 (en) 2001-10-25 2002-10-21 Tyrosine kinase inhibitors

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US34290201P 2001-10-25 2001-10-25
US60/342,902 2001-10-25

Publications (2)

Publication Number Publication Date
WO2003035614A2 WO2003035614A2 (fr) 2003-05-01
WO2003035614A3 true WO2003035614A3 (fr) 2004-03-18

Family

ID=23343779

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2002/033919 Ceased WO2003035614A2 (fr) 2001-10-25 2002-10-21 Inhibiteurs de la tyrosine kinase

Country Status (2)

Country Link
AU (1) AU2002348393A1 (fr)
WO (1) WO2003035614A2 (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2004258963A1 (en) * 2003-07-24 2005-02-03 Merck & Co., Inc. Tyrosine kinase inhibitors
CA2623125A1 (fr) 2005-09-20 2007-03-29 Osi Pharmaceuticals, Inc. Marqueurs biologiques predictifs d'une reaction anticancereuse aux inhibiteurs kinase du recepteur du facteur de croissance 1 analogue a l'insuline
US20120189641A1 (en) 2009-02-25 2012-07-26 OSI Pharmaceuticals, LLC Combination anti-cancer therapy
JP2012519170A (ja) 2009-02-26 2012-08-23 オーエスアイ・ファーマシューティカルズ,エルエルシー 生体内の腫瘍細胞のemtステータスをモニターするためのinsitu法
EP2401613A2 (fr) 2009-02-27 2012-01-04 OSI Pharmaceuticals, LLC Méthodes d'identification d'agents qui inhibent les cellules cancéreuses mésenchymateuses ou leur formation
WO2010099138A2 (fr) 2009-02-27 2010-09-02 Osi Pharmaceuticals, Inc. Procédés pour l'identification d'agents qui inhibent les cellules tumorales de type mésenchymateuses ou leur formation
EP2401614A1 (fr) 2009-02-27 2012-01-04 OSI Pharmaceuticals, LLC Méthodes d'identification d'agents qui inhibent les cellules cancéreuses mésenchymateuses ou leur formation
WO2010146059A2 (fr) 2009-06-16 2010-12-23 F. Hoffmann-La Roche Ag Biomarqueurs pour une thérapie par inhibiteur d'igf-1r
EP2542893A2 (fr) 2010-03-03 2013-01-09 OSI Pharmaceuticals, LLC Marqueurs biologiques prédictifs d'une réponse anticancéreuse aux inhibiteurs de kinase du récepteur du facteur de croissance insulinique 1
JP2013527748A (ja) 2010-03-03 2013-07-04 オーエスアイ・ファーマシューティカルズ,エルエルシー インスリン様増殖因子1受容体キナーゼ阻害剤に対する抗癌反応の予測に役立つ生物学的マーカー
WO2011112666A1 (fr) 2010-03-09 2011-09-15 OSI Pharmaceuticals, LLC Thérapie anticancéreuse combinatoire
US20120214830A1 (en) 2011-02-22 2012-08-23 OSI Pharmaceuticals, LLC Biological markers predictive of anti-cancer response to insulin-like growth factor-1 receptor kinase inhibitors in hepatocellular carcinoma
WO2012149014A1 (fr) 2011-04-25 2012-11-01 OSI Pharmaceuticals, LLC Utilisation de signatures de gènes de tem dans la découverte de médicaments contre le cancer, diagnostics et traitement du cancer
WO2013152252A1 (fr) 2012-04-06 2013-10-10 OSI Pharmaceuticals, LLC Polythérapie antinéoplasique
US9834575B2 (en) 2013-02-26 2017-12-05 Triact Therapeutics, Inc. Cancer therapy
EP3044593A4 (fr) 2013-09-09 2017-05-17 Triact Therapeutics, Inc. Traitement du cancer

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000038519A1 (fr) * 1998-12-31 2000-07-06 Sugen, Inc. Composes 3-heteroarylidenyl-2-indolinone utilises pour modulation de l'activite de la proteine kinase et dans la chimiotherapie du cancer

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000038519A1 (fr) * 1998-12-31 2000-07-06 Sugen, Inc. Composes 3-heteroarylidenyl-2-indolinone utilises pour modulation de l'activite de la proteine kinase et dans la chimiotherapie du cancer

Also Published As

Publication number Publication date
AU2002348393A1 (en) 2003-05-06
WO2003035614A2 (fr) 2003-05-01

Similar Documents

Publication Publication Date Title
WO2004014300A3 (fr) Inhibiteurs de la tyrosine kinase
WO2003035615A3 (fr) Inhibiteurs de tyrosine kinase
WO2004014851A3 (fr) Inhibiteurs de tyrosine kinases
WO2003035616A3 (fr) Inhibiteurs de la tyrosine kinase
WO2003035614A3 (fr) Inhibiteurs de la tyrosine kinase
WO2003035619A8 (fr) Inhibiteurs de la tyrosine kinase
WO2002046183A3 (fr) Composes de pyrroline substitues par l'indazolyle comme inhibiteurs de kinase
WO2004031401A3 (fr) Nouveaux inhibiteurs de tyrosine kinases
CA2400447A1 (fr) Inhibiteurs de kinases
AU2001241798A1 (en) 3-(pyrolyllactone)-2-indolinone compounds as kinase inhibitors
WO2001060814A3 (fr) Inhibiteurs de la proteine kinase 2-indolinone a substitution pyrrole
WO2004096795A3 (fr) Inhibiteurs de la kinase c-fms
WO2000043373A3 (fr) Inhibiteurs de kinase
AU2001288374A1 (en) Substituted oxindole derivatives as tyrosine kinase inhibitors
EP0766676A4 (fr) Composes et procede destines a inhiber la phosphodiesterase iv
AU9158498A (en) Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases
WO2006050109A3 (fr) Nouveaux inhibiteurs de kinase
WO2004009597A3 (fr) Pyrazolopyrimidines en tant qu'inhibiteurs de kinases
HK1053831A1 (zh) 作为治疗药物的激酶抑制剂
WO2000002576A3 (fr) Egf-genistein utilise pour la prevention de la restenose
WO2006047479A3 (fr) Inhibiteurs de c-fms kinase
WO2006047503A3 (fr) Inhibiteurs de la c-fms kinase
AU5215700A (en) Substituted indolinone as tyrosine kinase inhibitors
WO2002081728A3 (fr) Inhibiteurs quinoline des kinases hyak1 et hyak3
WO2005009373A3 (fr) Inhibiteurs de tyrosine kinase

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP