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ECSP11010778A - Amidofenoxiindazoles útiles como inhibidores de c-met - Google Patents

Amidofenoxiindazoles útiles como inhibidores de c-met

Info

Publication number
ECSP11010778A
ECSP11010778A EC2011010778A ECSP11010778A ECSP11010778A EC SP11010778 A ECSP11010778 A EC SP11010778A EC 2011010778 A EC2011010778 A EC 2011010778A EC SP11010778 A ECSP11010778 A EC SP11010778A EC SP11010778 A ECSP11010778 A EC SP11010778A
Authority
EC
Ecuador
Prior art keywords
useful
amidophenoxyindazols
met inhibitors
inhibitors
met
Prior art date
Application number
EC2011010778A
Other languages
English (en)
Inventor
Boyu Zhong
Mark Andrew Pobanz
Chuan Shih
Tiechao Li
Zhipei Wu
Wei Jennifer Yang
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of ECSP11010778A publication Critical patent/ECSP11010778A/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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La presente invención se refiere a compuestos de amidofenoxiindazol útiles en el tratamiento de cáncer.
EC2011010778A 2008-07-24 2011-01-21 Amidofenoxiindazoles útiles como inhibidores de c-met ECSP11010778A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US8329408P 2008-07-24 2008-07-24
US8508208P 2008-07-31 2008-07-31
US10865908P 2008-10-27 2008-10-27

Publications (1)

Publication Number Publication Date
ECSP11010778A true ECSP11010778A (es) 2011-02-28

Family

ID=41010247

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2011010778A ECSP11010778A (es) 2008-07-24 2011-01-21 Amidofenoxiindazoles útiles como inhibidores de c-met

Country Status (35)

Country Link
US (2) US8030302B2 (es)
EP (1) EP2310382B1 (es)
JP (1) JP5414794B2 (es)
KR (1) KR101334456B1 (es)
CN (1) CN102105462B (es)
AR (1) AR074632A1 (es)
AT (1) ATE546444T1 (es)
AU (1) AU2009274256B2 (es)
BR (1) BRPI0916286B8 (es)
CA (1) CA2731773C (es)
CL (1) CL2011000134A1 (es)
CO (1) CO6351737A2 (es)
CR (1) CR20110046A (es)
CY (1) CY1112595T1 (es)
DK (1) DK2310382T3 (es)
DO (1) DOP2011000009A (es)
EA (1) EA018385B1 (es)
EC (1) ECSP11010778A (es)
ES (1) ES2379587T3 (es)
HR (1) HRP20120202T1 (es)
IL (1) IL210490A (es)
JO (1) JO2788B1 (es)
MA (1) MA32594B1 (es)
MX (1) MX2011000925A (es)
MY (1) MY163852A (es)
NZ (1) NZ590013A (es)
PE (1) PE20110150A1 (es)
PL (1) PL2310382T3 (es)
PT (1) PT2310382E (es)
RS (1) RS52261B (es)
SI (1) SI2310382T1 (es)
SV (1) SV2011003816A (es)
TW (1) TWI365185B (es)
WO (1) WO2010011538A1 (es)
ZA (1) ZA201100219B (es)

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WO2014134313A1 (en) * 2013-02-27 2014-09-04 Array Biopharma Inc. Intermediates for use in the preparation of indazole derivatives and processes for the preparation thereof
CN104140393B (zh) * 2013-12-10 2016-09-21 郑州泰基鸿诺医药股份有限公司 一种芳环/芳杂环叔丁醇酯类化合物的制备方法
US9718841B2 (en) 2014-04-22 2017-08-01 Calitor Sciences, Llc Bicyclic pyrazolone compounds and methods of use
TW201716085A (zh) * 2015-08-12 2017-05-16 應克隆公司 癌症之組合療法
EP3442573A1 (en) * 2016-04-15 2019-02-20 Eli Lilly and Company Combination of ramucirumab and merestinib for use in treatment of colorectal cancer
FI3464380T3 (fi) 2016-06-02 2025-01-31 Immunocore Ltd Gp100-spesifisen tcr-anti-cd3 scfv-fuusioproteiinin annosteluohjelma
JP2019525934A (ja) * 2016-07-29 2019-09-12 イーライ リリー アンド カンパニー 癌の治療に使用するためのメレスチニブおよび抗pd−l1または抗pd−1阻害剤を用いた組み合わせ治療
CN108069938A (zh) * 2016-11-15 2018-05-25 中国药科大学 2,4-二取代吡啶类化合物及其制备方法和应用
WO2018093654A1 (en) 2016-11-16 2018-05-24 Eli Lilly And Company Treatment of cancer with exon 14 skipping mutation(s) or exon 14 skipping phenotype
ES2866348T3 (es) 2016-11-16 2021-10-19 Lilly Co Eli Terapia de combinación para el cáncer con mutación o mutaciones de omisión del exón 14 o fenotipo de omisión del exón 14
CN107382968A (zh) * 2017-07-06 2017-11-24 北京万全德众医药生物技术有限公司 一种吲哚类c‑Met抑制剂的制备方法
CN107311983A (zh) * 2017-07-06 2017-11-03 北京万全德众医药生物技术有限公司 吲哚类小分子c‑met抑制剂
US10180422B1 (en) 2017-08-22 2019-01-15 Scripps Health Methods of treating a neuroendocrine tumor
EP3480201A1 (en) 2017-11-06 2019-05-08 Oncostellae, S.L. New analogs as androgen receptor and glucocorticoid receptor modulators
US11623923B2 (en) 2017-11-24 2023-04-11 Medshine Discovery, Inc. Uracil compound as c-MET/AXL inhibitor
US20210177828A1 (en) * 2018-01-17 2021-06-17 Nanjing Transthera Biosciences Co., Ltd. Tam family kinase /and csf1r kinase inhibitor and use thereof
CN111295386B (zh) 2018-03-08 2022-09-06 伟迈可生物有限公司 噻吩并吡啶衍生物及含有该衍生物的药物组合物
SG11202101622VA (en) * 2018-08-24 2021-03-30 Nanjing Transthera Biosciences Co Ltd Novel quinoline derivative inhibitor
EP3848365A4 (en) 2018-09-03 2022-06-01 Tyligand Bioscience (Shanghai) Limited TRK INHIBITORS AS AN ANTI-CANCER AGENT
KR20220059386A (ko) 2019-09-06 2022-05-10 웰마커바이오 주식회사 바이오마커 기반 치료용 조성물
CN117355533A (zh) * 2021-06-22 2024-01-05 株式会社Lg化学 作为蛋白激酶抑制剂的新型化合物
WO2023110936A1 (en) 2021-12-14 2023-06-22 Netherlands Translational Research Center Holding B.V Reversible macrocyclic kinase inhibitors

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Also Published As

Publication number Publication date
BRPI0916286B1 (pt) 2019-10-08
KR20110022691A (ko) 2011-03-07
SI2310382T1 (sl) 2012-04-30
PE20110150A1 (es) 2011-03-07
IL210490A (en) 2013-06-27
US20100022529A1 (en) 2010-01-28
TWI365185B (en) 2012-06-01
EA201170252A1 (ru) 2011-06-30
MX2011000925A (es) 2011-03-21
CR20110046A (es) 2011-04-27
CA2731773C (en) 2013-03-12
CN102105462B (zh) 2014-07-23
MA32594B1 (fr) 2011-09-01
CA2731773A1 (en) 2010-01-28
TW201006817A (en) 2010-02-16
ZA201100219B (en) 2012-06-27
EP2310382B1 (en) 2012-02-22
AU2009274256A1 (en) 2010-01-28
MY163852A (en) 2017-10-31
JP5414794B2 (ja) 2014-02-12
WO2010011538A1 (en) 2010-01-28
JO2788B1 (en) 2014-03-15
RS52261B (sr) 2012-10-31
NZ590013A (en) 2012-06-29
CY1112595T1 (el) 2016-02-10
CL2011000134A1 (es) 2011-07-08
CO6351737A2 (es) 2011-12-20
SV2011003816A (es) 2011-03-17
PL2310382T3 (pl) 2012-07-31
AU2009274256B2 (en) 2013-07-11
EP2310382A1 (en) 2011-04-20
JP2011529054A (ja) 2011-12-01
DK2310382T3 (da) 2012-03-26
DOP2011000009A (es) 2011-03-31
ATE546444T1 (de) 2012-03-15
ES2379587T3 (es) 2012-04-27
HK1155172A1 (en) 2012-05-11
US8030302B2 (en) 2011-10-04
KR101334456B1 (ko) 2013-11-29
AR074632A1 (es) 2011-02-02
PT2310382E (pt) 2012-04-11
HRP20120202T1 (hr) 2012-03-31
USRE43878E1 (en) 2012-12-25
BRPI0916286B8 (pt) 2021-05-25
CN102105462A (zh) 2011-06-22
EA018385B1 (ru) 2013-07-30
IL210490A0 (en) 2011-03-31

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