CN101282965A - 基于烷氧基吲哚酮的蛋白激酶抑制剂 - Google Patents

基于烷氧基吲哚酮的蛋白激酶抑制剂 Download PDF

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Publication number
CN101282965A
CN101282965A CNA2006800352235A CN200680035223A CN101282965A CN 101282965 A CN101282965 A CN 101282965A CN A2006800352235 A CNA2006800352235 A CN A2006800352235A CN 200680035223 A CN200680035223 A CN 200680035223A CN 101282965 A CN101282965 A CN 101282965A
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compound
salt
isomer
represented
prodrug according
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CNA2006800352235A
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English (en)
Chinese (zh)
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梁丛薪
冯扬波
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Scripps Research Institute
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Scripps Research Institute
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    • 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
    • C07D403/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D401/14Heterocyclic 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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
CNA2006800352235A 2005-09-22 2006-09-21 基于烷氧基吲哚酮的蛋白激酶抑制剂 Pending CN101282965A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71947405P 2005-09-22 2005-09-22
US60/719,474 2005-09-22

Publications (1)

Publication Number Publication Date
CN101282965A true CN101282965A (zh) 2008-10-08

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ID=37900093

Family Applications (1)

Application Number Title Priority Date Filing Date
CNA2006800352235A Pending CN101282965A (zh) 2005-09-22 2006-09-21 基于烷氧基吲哚酮的蛋白激酶抑制剂

Country Status (10)

Country Link
US (2) US7629339B2 (enExample)
EP (1) EP1926725A4 (enExample)
JP (1) JP2009508971A (enExample)
KR (1) KR20080046701A (enExample)
CN (1) CN101282965A (enExample)
AU (1) AU2006294600A1 (enExample)
BR (1) BRPI0616378A2 (enExample)
CA (1) CA2621809A1 (enExample)
RU (1) RU2008110083A (enExample)
WO (1) WO2007038251A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110016052A (zh) * 2018-01-08 2019-07-16 四川海思科制药有限公司 N-去乙基舒尼替尼的磷酰胺衍生物及其制备方法

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0616378A2 (pt) * 2005-09-22 2011-06-21 Scripps Research Inst inibidores de proteìna cinase baseados em alcóxi indolinona e métodos para modulação da atividade catalìtica
EP2061758A4 (en) * 2006-09-11 2011-11-30 Curis Inc A ZINC BINDING GROUP CONTAINING SUBSTITUTED 2-INDOLINONE AS PTK INHIBITORS
WO2008033562A2 (en) 2006-09-15 2008-03-20 Xcovery, Inc. Kinase inhibitor compounds
IN2014MN02105A (enExample) 2012-04-20 2015-09-11 Annji Pharm Co Ltd
ES2714110T3 (es) 2014-03-07 2019-05-27 Hoffmann La Roche Heteroarildihidropirimidinas 6-fusionadas novedosas para el tratamiento y profilaxis de la infección por el virus de la hepatitis B
SG11201706835WA (en) 2015-03-16 2017-09-28 Hoffmann La Roche Combined treatment with a tlr7 agonist and an hbv capsid assembly inhibitor
CN109715214B (zh) 2016-09-13 2022-03-04 豪夫迈·罗氏有限公司 Tlr7激动剂和hbv衣壳组装抑制剂的组合治疗
CA3130596A1 (en) 2019-03-25 2020-10-01 F. Hoffmann-La Roche Ag Solid forms of a compound of hbv core protein allosteric modifier

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US72934A (en) * 1867-12-31 Improvement in marking-gauge fob sswim-mgohines
AR042586A1 (es) * 2001-02-15 2005-06-29 Sugen Inc 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa
TWI259081B (en) * 2001-10-26 2006-08-01 Sugen Inc Treatment of acute myeloid leukemia with indolinone compounds
MXPA06006049A (es) * 2003-11-26 2007-05-24 Scripps Research Inst Inhibidores de proteina quinasa avanzados a base de indolinona.
BRPI0616378A2 (pt) * 2005-09-22 2011-06-21 Scripps Research Inst inibidores de proteìna cinase baseados em alcóxi indolinona e métodos para modulação da atividade catalìtica

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110016052A (zh) * 2018-01-08 2019-07-16 四川海思科制药有限公司 N-去乙基舒尼替尼的磷酰胺衍生物及其制备方法
CN110016052B (zh) * 2018-01-08 2021-09-28 四川海思科制药有限公司 N-去乙基舒尼替尼的磷酰胺衍生物及其制备方法

Also Published As

Publication number Publication date
EP1926725A1 (en) 2008-06-04
EP1926725A4 (en) 2010-10-06
WO2007038251A1 (en) 2007-04-05
RU2008110083A (ru) 2009-10-27
CA2621809A1 (en) 2007-04-05
AU2006294600A1 (en) 2007-04-05
JP2009508971A (ja) 2009-03-05
KR20080046701A (ko) 2008-05-27
US20070072934A1 (en) 2007-03-29
US20090305382A1 (en) 2009-12-10
BRPI0616378A2 (pt) 2011-06-21
US7629339B2 (en) 2009-12-08

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Open date: 20081008