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MA38454A1 - Inhibiteurs de protéines kinases - Google Patents

Inhibiteurs de protéines kinases

Info

Publication number
MA38454A1
MA38454A1 MA38454A MA38454A MA38454A1 MA 38454 A1 MA38454 A1 MA 38454A1 MA 38454 A MA38454 A MA 38454A MA 38454 A MA38454 A MA 38454A MA 38454 A1 MA38454 A1 MA 38454A1
Authority
MA
Morocco
Prior art keywords
protein kinase
kinase inhibitors
useful
formula
fgfr
Prior art date
Application number
MA38454A
Other languages
English (en)
Other versions
MA38454B1 (fr
Inventor
Srinivasan Rajagopalan
Prasad Appukuttan
Arumugam Karthikeyan Narasingapuram
Ravi Kotrabasaiah Ujjinamatada
Shyla George
Tero Linnanen
Original Assignee
Orion Corp
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 Orion Corp filed Critical Orion Corp
Publication of MA38454A1 publication Critical patent/MA38454A1/fr
Publication of MA38454B1 publication Critical patent/MA38454B1/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
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Epidemiology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

L'invention concerne un composé de formule (i), dans laquelle r1 à r5, a, b, z, z1 et z2 étant tels que définis dans les revendications, et des sels pharmaceutiquement acceptables de celui-ci. Les composés de formule (i) selon l'invention sont utiles en tant qu'inhibiteurs de fgfr et sont utiles dans le traitement d'une affection où l'inhibition de la fgfr kinase est souhaitée, telle que le cancer.
MA38454A 2013-04-04 2014-04-03 Inhibiteurs de protéines kinases MA38454B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN382KO2013 2013-04-04
PCT/FI2014/000003 WO2014162039A1 (fr) 2013-04-04 2014-04-03 Inhibiteurs de protéines kinases

Publications (2)

Publication Number Publication Date
MA38454A1 true MA38454A1 (fr) 2018-02-28
MA38454B1 MA38454B1 (fr) 2018-11-30

Family

ID=50685938

Family Applications (1)

Application Number Title Priority Date Filing Date
MA38454A MA38454B1 (fr) 2013-04-04 2014-04-03 Inhibiteurs de protéines kinases

Country Status (33)

Country Link
US (1) US20160031855A1 (fr)
EP (1) EP2981533B1 (fr)
JP (1) JP6356782B2 (fr)
KR (1) KR20150138383A (fr)
CN (1) CN105073733B (fr)
AR (1) AR095781A1 (fr)
AU (1) AU2014246961B2 (fr)
BR (1) BR112015025413A2 (fr)
CA (1) CA2907855A1 (fr)
CL (1) CL2015002932A1 (fr)
CY (1) CY1120306T1 (fr)
DK (1) DK2981533T3 (fr)
EA (1) EA031076B1 (fr)
ES (1) ES2658183T3 (fr)
HR (1) HRP20180382T1 (fr)
HU (1) HUE036692T2 (fr)
LT (1) LT2981533T (fr)
MA (1) MA38454B1 (fr)
MX (1) MX2015013776A (fr)
MY (1) MY184528A (fr)
NO (1) NO2981533T3 (fr)
NZ (1) NZ713410A (fr)
PE (1) PE20160115A1 (fr)
PH (1) PH12015502284B1 (fr)
PL (1) PL2981533T3 (fr)
PT (1) PT2981533T (fr)
RS (1) RS56942B1 (fr)
SA (1) SA515361260B1 (fr)
SG (1) SG11201508125XA (fr)
SI (1) SI2981533T1 (fr)
TW (1) TWI628176B (fr)
UA (1) UA115176C2 (fr)
WO (1) WO2014162039A1 (fr)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
PE20190736A1 (es) 2012-06-13 2019-05-23 Incyte Holdings Corp Compuestos triciclicos sustituidos como inhibidores del receptor del factor de crecimiento de fibroblastos (fgfr)
WO2014026125A1 (fr) 2012-08-10 2014-02-13 Incyte Corporation Dérivés de pyrazine en tant qu'inhibiteurs de fgfr
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
AR094812A1 (es) 2013-02-20 2015-08-26 Eisai R&D Man Co Ltd Derivado de piridina monocíclico como inhibidor del fgfr
KR102269032B1 (ko) 2013-04-19 2021-06-24 인사이트 홀딩스 코포레이션 Fgfr 저해제로서 이환식 헤테로사이클
ES2914072T3 (es) 2014-08-18 2022-06-07 Eisai R&D Man Co Ltd Sal de derivado de piridina monocíclico y su cristal
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
US9580423B2 (en) 2015-02-20 2017-02-28 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
ES2895769T3 (es) 2015-02-20 2022-02-22 Incyte Corp Heterociclos bicíclicos como inhibidores de FGFR
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
EP3275442B1 (fr) 2015-03-25 2021-07-28 National Cancer Center Agent thérapeutique contre le cancer du canal cholédoque
RU2730503C2 (ru) 2015-12-17 2020-08-24 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Терапевтическое средство для лечения рака молочной железы
US10487863B2 (en) * 2017-02-17 2019-11-26 Ford Global Technologies, Llc Castellated joint for improved adhesive coverage when using mechanical fixings and adhesive in one joint
CN109963854B (zh) 2017-03-16 2022-04-12 江苏恒瑞医药股份有限公司 杂芳基并[4,3-c]嘧啶-5-胺类衍生物、其制备方法及其在医药上的应用
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
EP3777860A4 (fr) 2018-03-28 2021-12-15 Eisai R&D Management Co., Ltd. Agent thérapeutique pour le carcinome hépatocellulaire
SG11202010882XA (en) 2018-05-04 2020-11-27 Incyte Corp Salts of an fgfr inhibitor
SI3788047T1 (sl) 2018-05-04 2024-11-29 Incyte Corporation Trdne oblike inhibitorja fgfr in postopki priprave le-teh
WO2020185532A1 (fr) 2019-03-08 2020-09-17 Incyte Corporation Méthodes de traitement du cancer au moyen d'un inhibiteur de fgfr
AU2020242287A1 (en) 2019-03-21 2021-09-02 INSERM (Institut National de la Santé et de la Recherche Médicale) A Dbait molecule in combination with kinase inhibitor for the treatment of cancer
CA3141424C (fr) * 2019-06-14 2023-11-07 Zhengxia CHEN Compose cyclique fusionne en tant qu'inhibiteur double de fgfr et vegfr
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
JP7300057B2 (ja) * 2019-07-26 2023-06-28 シージーンテック (スーチョウ, チャイナ) カンパニー リミテッド Fgfrとvegfr二重阻害剤としてのピリジン誘導体
WO2021067374A1 (fr) 2019-10-01 2021-04-08 Incyte Corporation Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr
US11607416B2 (en) 2019-10-14 2023-03-21 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
KR20220098759A (ko) 2019-11-08 2022-07-12 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) 키나제 억제제에 대해 내성을 획득한 암의 치료 방법
WO2021113462A1 (fr) 2019-12-04 2021-06-10 Incyte Corporation Dérivés d'un inhibiteur de fgfr
EP4069696A1 (fr) 2019-12-04 2022-10-12 Incyte Corporation Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr
WO2021146424A1 (fr) 2020-01-15 2021-07-22 Incyte Corporation Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
CN116783192B (zh) * 2021-01-26 2025-10-31 盛世泰科生物医药技术(苏州)股份有限公司 甲基吡唑取代的吡啶并咪唑类化合物的晶型及其制备方法
WO2022203399A1 (fr) * 2021-03-26 2022-09-29 주식회사 스탠다임 Antagoniste du récepteur a2a de l'adénosine et son utilisation
WO2022221170A1 (fr) 2021-04-12 2022-10-20 Incyte Corporation Polythérapie comprenant un inhibiteur de fgfr et un agent de ciblage de nectine-4
WO2022261159A1 (fr) 2021-06-09 2022-12-15 Incyte Corporation Hétérocycles tricycliques utiles en tant qu'inhibiteurs de fgfr
WO2022261160A1 (fr) 2021-06-09 2022-12-15 Incyte Corporation Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1194152A4 (fr) * 1999-06-30 2002-11-06 Merck & Co Inc Composes inhibiteurs de la kinase src
US6329380B1 (en) * 1999-06-30 2001-12-11 Merck & Co., Inc. SRC kinase inhibitor compounds
US7521448B2 (en) * 2003-08-21 2009-04-21 Osi Pharmaceuticals, Inc. N-substituted benzimidazolyl c-Kit inhibitors
JP2010506879A (ja) * 2006-10-16 2010-03-04 ノバルティス アーゲー プロテインキナーゼ阻害剤として有用なフェニルアセトアミド
HRP20151398T1 (hr) * 2006-12-22 2016-02-12 Astex Therapeutics Limited Tricikliäśni derivati amina kao inhibitori protein tirozin kinaze
CN101679408B (zh) * 2006-12-22 2016-04-27 Astex治疗学有限公司 作为fgfr抑制剂的双环杂环化合物
GB0906472D0 (en) * 2009-04-15 2009-05-20 Astex Therapeutics Ltd New compounds
CN102216300B (zh) * 2009-09-30 2014-10-22 贝达药业股份有限公司 作为蛋白激酶抑制剂的化合物和组合物
UA111382C2 (uk) * 2011-10-10 2016-04-25 Оріон Корпорейшн Інгібітори протеїнкінази

Also Published As

Publication number Publication date
CL2015002932A1 (es) 2016-04-22
CY1120306T1 (el) 2019-07-10
NZ713410A (en) 2018-07-27
JP6356782B2 (ja) 2018-07-11
SI2981533T1 (en) 2018-04-30
HK1217198A1 (zh) 2016-12-30
MA38454B1 (fr) 2018-11-30
WO2014162039A1 (fr) 2014-10-09
PE20160115A1 (es) 2016-03-03
CN105073733A (zh) 2015-11-18
SG11201508125XA (en) 2015-10-29
UA115176C2 (uk) 2017-09-25
CA2907855A1 (fr) 2014-10-09
SA515361260B1 (ar) 2017-08-27
TW201524970A (zh) 2015-07-01
AU2014246961A1 (en) 2015-10-22
PL2981533T3 (pl) 2018-04-30
DK2981533T3 (en) 2018-02-12
ES2658183T3 (es) 2018-03-08
LT2981533T (lt) 2018-02-26
HRP20180382T1 (hr) 2018-04-06
TWI628176B (zh) 2018-07-01
AR095781A1 (es) 2015-11-11
US20160031855A1 (en) 2016-02-04
BR112015025413A2 (pt) 2017-07-18
NO2981533T3 (fr) 2018-05-05
MY184528A (en) 2021-04-01
KR20150138383A (ko) 2015-12-09
EP2981533B1 (fr) 2017-12-06
EA031076B1 (ru) 2018-11-30
EP2981533A1 (fr) 2016-02-10
PH12015502284A1 (en) 2016-02-01
EA201591913A1 (ru) 2016-03-31
RS56942B1 (sr) 2018-05-31
PH12015502284B1 (en) 2016-02-01
CN105073733B (zh) 2017-06-27
HUE036692T2 (hu) 2018-07-30
PT2981533T (pt) 2018-02-27
MX2015013776A (es) 2016-02-26
AU2014246961B2 (en) 2017-09-28
JP2016515604A (ja) 2016-05-30

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