SMT201500175B - Derivati di azaindoli come inibitori delle proteine chinasi abl e src - Google Patents

Derivati di azaindoli come inibitori delle proteine chinasi abl e src

Info

Publication number
SMT201500175B
SMT201500175B SM201500175T SM201500175T SMT201500175B SM T201500175 B SMT201500175 B SM T201500175B SM 201500175 T SM201500175 T SM 201500175T SM 201500175 T SM201500175 T SM 201500175T SM T201500175 B SMT201500175 B SM T201500175B
Authority
SM
San Marino
Prior art keywords
inhibitors
azaindole derivatives
src proteins
kinase abl
abl
Prior art date
Application number
SM201500175T
Other languages
English (en)
Italian (it)
Inventor
Abdelaziz Yasri
Gwenael Cheve
Cedric Bories
Louis Delon
Original Assignee
Oribase Pharma
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 Oribase Pharma filed Critical Oribase Pharma
Publication of SMT201500175B publication Critical patent/SMT201500175B/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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

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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SM201500175T 2009-02-12 2015-07-22 Derivati di azaindoli come inibitori delle proteine chinasi abl e src SMT201500175B (it)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US20227909P 2009-02-12 2009-02-12
FR0900631A FR2941948B1 (fr) 2009-02-12 2009-02-12 Derives d'azaindoles en tant qu'inhibiteur des proteines kinases abl et src
PCT/IB2010/000593 WO2010092489A1 (fr) 2009-02-12 2010-02-12 Dérivés d'azaindoles comme inhibiteurs des protéines kinases abl et src

Publications (1)

Publication Number Publication Date
SMT201500175B true SMT201500175B (it) 2015-09-07

Family

ID=40886859

Family Applications (1)

Application Number Title Priority Date Filing Date
SM201500175T SMT201500175B (it) 2009-02-12 2015-07-22 Derivati di azaindoli come inibitori delle proteine chinasi abl e src

Country Status (15)

Country Link
US (1) US8580815B2 (fr)
EP (1) EP2396325B1 (fr)
JP (1) JP5583698B2 (fr)
AU (1) AU2010212560B2 (fr)
CA (1) CA2751478A1 (fr)
DK (1) DK2396325T3 (fr)
ES (1) ES2540962T3 (fr)
FR (1) FR2941948B1 (fr)
HR (1) HRP20150697T8 (fr)
HU (1) HUE024989T2 (fr)
PL (1) PL2396325T3 (fr)
PT (1) PT2396325E (fr)
SI (1) SI2396325T1 (fr)
SM (1) SMT201500175B (fr)
WO (1) WO2010092489A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE036739T2 (hu) * 2012-12-21 2018-07-30 Plexxikon Inc Vegyületek és eljárások kináz modulációra, és azok indikációi
FR3000492B1 (fr) * 2012-12-28 2015-09-11 Oribase Pharma Nouveaux derives azaindole en tant qu'inhibiteurs multikinases
FR3000493A1 (fr) * 2012-12-28 2014-07-04 Oribase Pharma Nouveaux inhibiteurs de proteines kinases
FR3000494B1 (fr) * 2012-12-28 2015-08-21 Oribase Pharma Nouveaux derives d'azaindoles en tant qu'inhibiteurs de proteines kinases
US10722484B2 (en) 2016-03-09 2020-07-28 K-Gen, Inc. Methods of cancer treatment
MA49014A (fr) * 2017-03-21 2020-02-05 Arbutus Biopharma Corp Dihydroindène-4-carboxamides substitués, leurs analogues et procédés d'utilisation correspondant
CN111943947B (zh) * 2020-07-24 2021-04-30 重庆文理学院 1H-吡咯[2,3-b]吡啶衍生物及其合成方法与应用
JP2023545219A (ja) * 2020-10-05 2023-10-26 エンライブン インコーポレイテッド Bcr-ablチロシンキナーゼの阻害のための7-アザインドール化合物
US11767321B2 (en) 2020-10-05 2023-09-26 Enliven Inc. 5- and 6-azaindole compounds for inhibition of BCR-ABL tyrosine kinases

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0330043D0 (en) * 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions comprising them
GB0330042D0 (en) 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them
CA2570817A1 (fr) * 2004-06-17 2006-01-26 Plexxikon, Inc. Composes modulant l'activite de c-kit
EP2264033A1 (fr) 2004-07-27 2010-12-22 SGX Pharmaceuticals, Inc. DÉRIVÉS PYRROLO[2,3b]PYRIDINE, 3,5-DIPHÉNYL SUBSTITUÉS, EN TANT QU'INHIBITEURS DE KINASES
US7709645B2 (en) 2004-07-27 2010-05-04 Sgx Pharmaceuticals, Inc. Pyrrolo-pyridine kinase modulators
US7361764B2 (en) 2004-07-27 2008-04-22 Sgx Pharmaceuticals, Inc. Pyrrolo-pyridine kinase modulators
WO2006104971A1 (fr) * 2005-03-28 2006-10-05 Bristol-Myers Squibb Company Inhibiteurs de kinase exercant une action antiproliferative
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
WO2008060907A2 (fr) * 2006-11-10 2008-05-22 Bristol-Myers Squibb Company Nouveaux inhibiteurs de la kinase
WO2008144253A1 (fr) * 2007-05-14 2008-11-27 Irm Llc Inhibiteurs de la protéine kinase et procédé d'utilisation de ceux-ci
CL2009000447A1 (es) * 2008-02-29 2010-01-04 Array Biopharma Inc Y Genentech Inc Compuestos derivados de (1h-pirrolo{2,3-b}piridin-5-il)-sulfonamido-benzamida sustituida; procedimiento de preparacion; composicion farmaceutica; y su uso en el tratamiento del cancer, a travez de la inhibicion de raf.
CN102317283A (zh) * 2008-11-03 2012-01-11 辛塔佳股份有限公司 新型cc-1065类似物及其缀合物

Also Published As

Publication number Publication date
EP2396325B1 (fr) 2015-04-01
HRP20150697T1 (hr) 2015-08-14
SI2396325T1 (sl) 2015-08-31
JP2012517465A (ja) 2012-08-02
AU2010212560B2 (en) 2016-01-21
US8580815B2 (en) 2013-11-12
HRP20150697T8 (en) 2015-11-06
FR2941948B1 (fr) 2013-04-05
FR2941948A1 (fr) 2010-08-13
PT2396325E (pt) 2015-08-21
ES2540962T3 (es) 2015-07-15
HUE024989T2 (en) 2016-01-28
AU2010212560A1 (en) 2011-08-11
WO2010092489A1 (fr) 2010-08-19
CA2751478A1 (fr) 2010-08-19
JP5583698B2 (ja) 2014-09-03
US20110312959A1 (en) 2011-12-22
DK2396325T3 (en) 2015-06-29
PL2396325T3 (pl) 2015-10-30
EP2396325A1 (fr) 2011-12-21

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