HRP20120202T1 - AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET - Google Patents

AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET Download PDF

Info

Publication number
HRP20120202T1
HRP20120202T1 HR20120202T HRP20120202T HRP20120202T1 HR P20120202 T1 HRP20120202 T1 HR P20120202T1 HR 20120202 T HR20120202 T HR 20120202T HR P20120202 T HRP20120202 T HR P20120202T HR P20120202 T1 HRP20120202 T1 HR P20120202T1
Authority
HR
Croatia
Prior art keywords
pharmaceutically acceptable
acceptable salt
methyl
compound according
cancer
Prior art date
Application number
HR20120202T
Other languages
English (en)
Croatian (hr)
Inventor
Li Tiechao
Andrew Pobanz Mark
Shih Chuan
Wu Zhipei
Jennifer Yang Wei
Zhong Boyu
Original Assignee
Eli Lilly & Company
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 Eli Lilly & Company filed Critical Eli Lilly & Company
Publication of HRP20120202T1 publication Critical patent/HRP20120202T1/hr

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)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
HR20120202T 2008-07-24 2009-07-15 AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET HRP20120202T1 (hr)

Applications Claiming Priority (4)

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
PCT/US2009/050640 WO2010011538A1 (en) 2008-07-24 2009-07-15 Amidophenoxyindazoles useful as inhibitors of c-met

Publications (1)

Publication Number Publication Date
HRP20120202T1 true HRP20120202T1 (hr) 2012-03-31

Family

ID=41010247

Family Applications (1)

Application Number Title Priority Date Filing Date
HR20120202T HRP20120202T1 (hr) 2008-07-24 2009-07-15 AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET

Country Status (35)

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

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2599458T3 (es) 2008-10-14 2017-02-01 Sunshine Lake Pharma Co., Ltd. Compuestos y métodos de uso
EP2408300B1 (en) 2009-03-21 2016-05-11 Sunshine Lake Pharma Co., Ltd. Amino ester derivatives, salts thereof and methods of use
RU2568258C2 (ru) 2011-02-28 2015-11-20 Саншайн Лейк Фарма Ко., Лтд Замещенные соединения хинолина и способы их использования
US8962623B2 (en) * 2011-03-04 2015-02-24 Locus Pharmaceuticals, Inc. Aminopyrazine compounds
KR20130118612A (ko) * 2012-04-20 2013-10-30 (주)네오믹스 신규한 아미노피리딘 유도체 및 이의 용도
WO2013169532A1 (en) * 2012-05-09 2013-11-14 Eli Lilly And Company Anti-c-met antibodies
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
US20150299219A1 (en) 2014-04-22 2015-10-22 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
US20190336599A1 (en) * 2016-04-15 2019-11-07 Eli Lilly And Company Combination of ramucirumab and merestinib for use in treatment of colorectal cancer
US11827688B2 (en) 2016-06-02 2023-11-28 Immunocore Limited Dosing regimen for GP100-specific TCR—anti-CD3 SCFV fusion protein
WO2018022438A1 (en) * 2016-07-29 2018-02-01 Eli Lilly And Company Combination therapy with merestinib and anti-pd-l1 or anti-pd-1 inhibitors for use in the treatment of cancer
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
JP6709340B2 (ja) 2016-11-16 2020-06-10 イーライ リリー アンド カンパニー エクソン14スキッピング変異(複数可)またはエクソン14スキッピング表現型を有するがんの併用療法
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
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
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
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
WO2019182274A1 (en) 2018-03-08 2019-09-26 Wellmarker Bio Co., Ltd. Thienopyridine derivatives and pharmaceutical composition comprising same
ES2985569T3 (es) * 2018-08-24 2024-11-06 Transthera Sciences Nanjing Inc Nuevo inhibidor de derivado de quinolina
JP7443373B2 (ja) * 2018-09-03 2024-03-05 タイリガンド バイオサイエンス(シャンハイ)リミテッド 抗がん性薬物としてのtrk阻害剤
EP3819300A4 (en) 2019-09-06 2021-11-24 Wellmarker Bio Co., Ltd. THERAPEUTIC COMPOSITION BASED ON BIOMARKERS
KR20220170766A (ko) * 2021-06-22 2022-12-30 주식회사 엘지화학 단백질 키나아제 억제제로서의 신규한 화합물
WO2023110936A1 (en) 2021-12-14 2023-06-22 Netherlands Translational Research Center Holding B.V Reversible macrocyclic kinase inhibitors

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO155316C (no) * 1982-04-23 1987-03-11 Sintef Fremgangsmaate for fremstilling av magnetiske polymerpartikler.
US5484681A (en) * 1994-10-31 1996-01-16 Xerox Corporation Conductive composite particles and processes for the preparation thereof
IL114149A0 (en) * 1995-06-14 1995-10-31 Yeda Res & Dev Modified avidin and streptavidin molecules and use thereof
US5747577A (en) * 1995-12-27 1998-05-05 Xerox Corporation Conductive particles containing carbon black and processes for the preparation thereof
DE10046029A1 (de) 2000-09-18 2002-03-28 Bayer Ag Indazole
ES2268015T3 (es) * 2001-05-18 2007-03-16 Srl, Inc. Procedimiento de inmunoensayo.
US6956084B2 (en) * 2001-10-04 2005-10-18 Bridgestone Corporation Nano-particle preparation and applications
JP2004067703A (ja) * 2002-04-24 2004-03-04 Japan Science & Technology Corp 架橋ポリマー、微粒子および製造方法
US7192780B2 (en) * 2002-10-23 2007-03-20 Evident Technologies Fluorescent lifetime biological detection and imaging using water-stable semiconductor nanocrystals
ES2273047T3 (es) 2002-10-28 2007-05-01 Bayer Healthcare Ag Fenilaminopirimidinas sustituidas con heteroariloxi como inhibidores de rho-cinasa.
US6986913B2 (en) * 2003-07-17 2006-01-17 Dynal Biotech Asa Process
US7163998B2 (en) * 2003-09-09 2007-01-16 Eastman Kodak Company Stabilized polymer beads and method of preparation
US7173031B2 (en) * 2004-06-28 2007-02-06 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US7439246B2 (en) * 2004-06-28 2008-10-21 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
HRP20170103T1 (hr) 2005-12-21 2017-03-24 Janssen Pharmaceutica N.V. Triazolopiridazini kao modulatori tirozin kinaze
WO2007103308A2 (en) * 2006-03-07 2007-09-13 Array Biopharma Inc. Heterobicyclic pyrazole compounds and methods of use
EP2038320B1 (en) * 2006-06-29 2014-03-12 Life Technologies AS Particles containing multi- block polymers
PE20080403A1 (es) 2006-07-14 2008-04-25 Amgen Inc Derivados heterociclicos fusionados y metodos de uso
BRPI0717320A2 (pt) 2006-10-23 2013-10-22 Sgx Pharmaceuticals Inc Triazóis bicíclicos como moduladores de proteína cinase
KR101550250B1 (ko) 2007-06-27 2015-09-04 알케마 인코포레이티드 하이드로플루오로올레핀의 제조 방법

Also Published As

Publication number Publication date
IL210490A0 (en) 2011-03-31
AR074632A1 (es) 2011-02-02
IL210490A (en) 2013-06-27
MX2011000925A (es) 2011-03-21
CR20110046A (es) 2011-04-27
HK1155172A1 (en) 2012-05-11
US20100022529A1 (en) 2010-01-28
CA2731773C (en) 2013-03-12
MA32594B1 (fr) 2011-09-01
PE20110150A1 (es) 2011-03-07
TWI365185B (en) 2012-06-01
ECSP11010778A (es) 2011-02-28
SV2011003816A (es) 2011-03-17
EA201170252A1 (ru) 2011-06-30
DOP2011000009A (es) 2011-03-31
ES2379587T3 (es) 2012-04-27
JP2011529054A (ja) 2011-12-01
MY163852A (en) 2017-10-31
KR20110022691A (ko) 2011-03-07
CA2731773A1 (en) 2010-01-28
PT2310382E (pt) 2012-04-11
JO2788B1 (en) 2014-03-15
PL2310382T3 (pl) 2012-07-31
JP5414794B2 (ja) 2014-02-12
BRPI0916286B8 (pt) 2021-05-25
CO6351737A2 (es) 2011-12-20
AU2009274256A1 (en) 2010-01-28
ATE546444T1 (de) 2012-03-15
USRE43878E1 (en) 2012-12-25
DK2310382T3 (da) 2012-03-26
CN102105462A (zh) 2011-06-22
RS52261B (sr) 2012-10-31
BRPI0916286B1 (pt) 2019-10-08
KR101334456B1 (ko) 2013-11-29
EP2310382A1 (en) 2011-04-20
EP2310382B1 (en) 2012-02-22
CN102105462B (zh) 2014-07-23
CY1112595T1 (el) 2016-02-10
US8030302B2 (en) 2011-10-04
CL2011000134A1 (es) 2011-07-08
EA018385B1 (ru) 2013-07-30
NZ590013A (en) 2012-06-29
WO2010011538A1 (en) 2010-01-28
SI2310382T1 (sl) 2012-04-30
TW201006817A (en) 2010-02-16
AU2009274256B2 (en) 2013-07-11
ZA201100219B (en) 2012-06-27

Similar Documents

Publication Publication Date Title
HRP20120202T1 (hr) AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET
JP2011529054A5 (da)
HRP20210949T1 (hr) Spojevi i sastavi za moduliranje aktivnosti egfr mutant kinaze
JP2014508811A5 (da)
JP2021523221A5 (da)
JP2015512435A5 (da)
UA115881C2 (uk) Алкоксипіразоли як активатори розчинної гуанілатциклази
JP2015518894A5 (da)
ME02684B (me) Jedinjenja i preparati protein kinaznih inhibitora
JP2016506369A5 (da)
PH12018500106A1 (en) Ethynyl derivatives as metabotropic glutamate receptor modulators
HRP20170352T1 (hr) Spojevi bis(fluroalkil)-1,4-benzodiazepinona kao notch inhibitori
MD20140084A2 (en) New indolizine derivatives, method for preparing same and pharmaceutical compositions containing same
HRP20210291T1 (hr) Imunoregulatorna sredstva
EA201491671A1 (ru) Гетероциклильные соединения
NZ607638A (en) Novel compounds and compositions for the inhibition of nampt
JP2015537020A5 (da)
RU2015121424A (ru) Комбинированная терапия
JP2013505969A5 (da)
CY1115175T1 (el) Ενωσεις 9-υποκατεστημενης-8-οξο-αδενινης ως ρυθμιστες υποδοχεων τυπου toll (tlr7)
JP2014506907A5 (da)
JP2016506960A5 (da)
JP2013525458A5 (da)
JP2013534245A5 (da)
JP2016501185A5 (da)