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PE20160115A1 - Compuestos derivados de imidazol como inhibidores de protein quinasa - Google Patents

Compuestos derivados de imidazol como inhibidores de protein quinasa

Info

Publication number
PE20160115A1
PE20160115A1 PE2015002104A PE2015002104A PE20160115A1 PE 20160115 A1 PE20160115 A1 PE 20160115A1 PE 2015002104 A PE2015002104 A PE 2015002104A PE 2015002104 A PE2015002104 A PE 2015002104A PE 20160115 A1 PE20160115 A1 PE 20160115A1
Authority
PE
Peru
Prior art keywords
protein kinase
kinase inhibitors
derived compounds
pyrazol
halogen
Prior art date
Application number
PE2015002104A
Other languages
English (en)
Inventor
Prasad Appukuttan
Shyla George
Ravi Kotrabasaiah Ujjinamatada
Arumugan Karthikeyan Narasingapuram
Srinivasan Rajagopalan
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 PE20160115A1 publication Critical patent/PE20160115A1/es

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

Se describe un compuesto de la formula (I), util en el tratamiento del cancer; donde Z1 es N; Z2 es CH o Z1 es CH y Z2 es N o Z1 y Z2 son N; Z es CH o N; A es anillo fenilo, etc. R1 es alquilo C1-C7, etc. R2 es H, halogeno, etc. B es anillo heterociclico, etc. R3 es H, halogeno, etc. R4 es H, halogeno, etc. R5 es H etc. Los compuestos preferidos son: 4-(2,4-difluorofenil)-N-(1-metil-1H-pirazol-3-il)-6-(5-(1-metil-1H-pirazol-4-il)-1H-benzo[d]imidazol-1-il)piridin-2-amina; N-(4-(2,4-difluorofenil)-6-(5-(1-metil-1H-pirazol-4-il)-1H-benzo[d]imidazol-1-il)piridin-2-il)ciclopropansulfonamida
PE2015002104A 2013-04-04 2014-04-03 Compuestos derivados de imidazol como inhibidores de protein quinasa PE20160115A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN382KO2013 2013-04-04

Publications (1)

Publication Number Publication Date
PE20160115A1 true PE20160115A1 (es) 2016-03-03

Family

ID=50685938

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2015002104A PE20160115A1 (es) 2013-04-04 2014-04-03 Compuestos derivados de imidazol como inhibidores de protein quinasa

Country Status (33)

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

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HUE042374T2 (hu) 2012-06-13 2019-06-28 Incyte Holdings Corp Szubsztituált triciklusos vegyületek mint FGFR inhibitorok
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
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
KR102469849B1 (ko) 2013-04-19 2022-11-23 인사이트 홀딩스 코포레이션 Fgfr 저해제로서 이환식 헤테로사이클
KR102344105B1 (ko) 2014-08-18 2021-12-29 에자이 알앤드디 매니지먼트 가부시키가이샤 모노시클릭 피리딘 유도체의 염 및 이의 결정
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
AU2016219822B2 (en) 2015-02-20 2020-07-09 Incyte Holdings Corporation Bicyclic heterocycles as FGFR inhibitors
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
CN114984013A (zh) 2015-03-25 2022-09-02 国立癌症研究中心 胆管癌治疗剂
WO2017104739A1 (ja) 2015-12-17 2017-06-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 乳がん治療剤
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UA125592C2 (uk) 2017-03-16 2022-04-27 Джянгсу Хенгруй Медісін Ко., Лтд. ПОХІДНА ГЕТЕРОАРИЛ[4,3-c]ПІРИМІДИН-5-АМІНУ, СПОСІБ ЇЇ ОТРИМАННЯ ТА ЇЇ МЕДИЧНІ ЗАСТОСУВАННЯ
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
SG11202007591RA (en) 2018-03-28 2020-09-29 Eisai R&D Man Co Ltd Therapeutic agent for hepatocellular carcinoma
EP4309737A3 (en) 2018-05-04 2024-03-27 Incyte Corporation Solid forms of an fgfr inhibitor and processes for preparing the same
EP3788046B1 (en) 2018-05-04 2025-12-10 Incyte Corporation Salts of an fgfr inhibitor
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
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
WO2020249096A1 (zh) 2019-06-14 2020-12-17 南京明德新药研发有限公司 作为fgfr和vegfr双重抑制剂的并环类化合物
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
WO2021018047A1 (zh) 2019-07-26 2021-02-04 南京明德新药研发有限公司 作为fgfr和vegfr双重抑制剂的吡啶衍生物
US12122767B2 (en) 2019-10-01 2024-10-22 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
WO2021076602A1 (en) 2019-10-14 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
WO2021076728A1 (en) 2019-10-16 2021-04-22 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
JP7720840B2 (ja) 2019-12-04 2025-08-08 インサイト・コーポレイション Fgfr阻害剤としての三環式複素環
KR20220131900A (ko) 2019-12-04 2022-09-29 인사이트 코포레이션 Fgfr 억제제의 유도체
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
EP4286382A4 (en) * 2021-01-26 2025-01-08 CGeneTech (Suzhou, China) Co., Ltd. CRYSTAL FORM OF A METHYLPYRAZOLE-SUBSTITUTED PYRIDOIMIDAZOLE COMPOUND AND METHOD FOR PREPARING THE SAME
WO2022203399A1 (ko) * 2021-03-26 2022-09-29 주식회사 스탠다임 아데노신 a2a 수용체 길항제 및 이의 용도
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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
DK2981533T3 (en) 2018-02-12
MA38454A1 (fr) 2018-02-28
AR095781A1 (es) 2015-11-11
JP2016515604A (ja) 2016-05-30
PH12015502284A1 (en) 2016-02-01
CY1120306T1 (el) 2019-07-10
NZ713410A (en) 2018-07-27
EP2981533B1 (en) 2017-12-06
BR112015025413A2 (pt) 2017-07-18
PL2981533T3 (pl) 2018-04-30
JP6356782B2 (ja) 2018-07-11
CN105073733B (zh) 2017-06-27
SG11201508125XA (en) 2015-10-29
HUE036692T2 (hu) 2018-07-30
TW201524970A (zh) 2015-07-01
MY184528A (en) 2021-04-01
HK1217198A1 (zh) 2016-12-30
CA2907855A1 (en) 2014-10-09
SI2981533T1 (en) 2018-04-30
ES2658183T3 (es) 2018-03-08
PT2981533T (pt) 2018-02-27
NO2981533T3 (es) 2018-05-05
US20160031855A1 (en) 2016-02-04
EA201591913A1 (ru) 2016-03-31
MX2015013776A (es) 2016-02-26
UA115176C2 (uk) 2017-09-25
WO2014162039A1 (en) 2014-10-09
EA031076B1 (ru) 2018-11-30
SA515361260B1 (ar) 2017-08-27
RS56942B1 (sr) 2018-05-31
HRP20180382T1 (hr) 2018-04-06
EP2981533A1 (en) 2016-02-10
LT2981533T (lt) 2018-02-26
MA38454B1 (fr) 2018-11-30
PH12015502284B1 (en) 2016-02-01
CN105073733A (zh) 2015-11-18
TWI628176B (zh) 2018-07-01
KR20150138383A (ko) 2015-12-09
CL2015002932A1 (es) 2016-04-22
AU2014246961A1 (en) 2015-10-22
AU2014246961B2 (en) 2017-09-28

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