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NO20011477D0 - Nye substituerte indolinoner med inhiberende virkning pÕ forskjellige kinaser og cyclin/CDK-komplekser - Google Patents

Nye substituerte indolinoner med inhiberende virkning pÕ forskjellige kinaser og cyclin/CDK-komplekser

Info

Publication number
NO20011477D0
NO20011477D0 NO20011477A NO20011477A NO20011477D0 NO 20011477 D0 NO20011477 D0 NO 20011477D0 NO 20011477 A NO20011477 A NO 20011477A NO 20011477 A NO20011477 A NO 20011477A NO 20011477 D0 NO20011477 D0 NO 20011477D0
Authority
NO
Norway
Prior art keywords
cyclin
inhibitory effect
novel substituted
cdk complexes
various kinases
Prior art date
Application number
NO20011477A
Other languages
English (en)
Norwegian (no)
Other versions
NO20011477L (no
Inventor
Rainer Walter
Wolfgang Grell
Armin Heckel
Frank Himmelsbach
Wolfgang Eberlein
Gerald Roth
Jacobus C A Van Meel
Norbert Redemann
Walter Spevak
Ulrike Tontsch-Grunt
Thomas Von Rueden
Original Assignee
Boehringer Ingelheim Pharma
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
Priority claimed from DE19844003A external-priority patent/DE19844003A1/de
Priority claimed from DE19937496A external-priority patent/DE19937496A1/de
Application filed by Boehringer Ingelheim Pharma filed Critical Boehringer Ingelheim Pharma
Publication of NO20011477L publication Critical patent/NO20011477L/no
Publication of NO20011477D0 publication Critical patent/NO20011477D0/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32—Oxygen atoms
    • C07D209/34—Oxygen atoms in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
NO20011477A 1998-09-25 2001-03-22 Nye substituerte indolinoner med inhiberende virkning pÕ forskjellige kinaser og cyclin/CDK-komplekser NO20011477D0 (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19844003A DE19844003A1 (de) 1998-09-25 1998-09-25 Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
DE19937496A DE19937496A1 (de) 1999-08-07 1999-08-07 Neue substituierte Indolinone, ihre Herstellung und ihre Verwendung als Arzneimittel
PCT/EP1999/007040 WO2000018734A1 (fr) 1998-09-25 1999-09-22 Nouvelles indolinones substituees a effet inhibiteur sur differentes kinases et differents complexes cycline/cdk

Publications (2)

Publication Number Publication Date
NO20011477L NO20011477L (no) 2001-03-22
NO20011477D0 true NO20011477D0 (no) 2001-03-22

Family

ID=26049076

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20011477A NO20011477D0 (no) 1998-09-25 2001-03-22 Nye substituerte indolinoner med inhiberende virkning pÕ forskjellige kinaser og cyclin/CDK-komplekser

Country Status (28)

Country Link
US (1) US6855710B2 (fr)
EP (1) EP1115704B1 (fr)
JP (1) JP2002525356A (fr)
KR (1) KR20010085841A (fr)
CN (1) CN1319090A (fr)
AT (1) ATE243195T1 (fr)
AU (1) AU763361B2 (fr)
BG (1) BG105327A (fr)
BR (1) BR9914065A (fr)
CA (1) CA2342622A1 (fr)
DE (1) DE59906030D1 (fr)
DK (1) DK1115704T3 (fr)
EA (1) EA200100320A1 (fr)
EE (1) EE200100184A (fr)
ES (1) ES2196860T3 (fr)
HR (1) HRP20010216A2 (fr)
HU (1) HUP0104973A3 (fr)
ID (1) ID27757A (fr)
IL (1) IL141622A0 (fr)
NO (1) NO20011477D0 (fr)
NZ (1) NZ510845A (fr)
PL (1) PL346898A1 (fr)
PT (1) PT1115704E (fr)
SI (1) SI1115704T1 (fr)
SK (1) SK4032001A3 (fr)
TR (1) TR200100854T2 (fr)
WO (1) WO2000018734A1 (fr)
YU (1) YU21301A (fr)

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GB9904933D0 (en) * 1999-03-04 1999-04-28 Glaxo Group Ltd Compounds
CA2461812C (fr) * 2001-09-27 2011-09-20 Allergan, Inc. L'utilisation de 3-(arylamino)methylene-1, 3-dihydro-2h-indol-2-ones en tant qu'inhibiteurs de kinases
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
US6797825B2 (en) 2001-12-13 2004-09-28 Abbott Laboratories Protein kinase inhibitors
EA008830B1 (ru) 2002-03-26 2007-08-31 Бёрингер Ингельхайм Фармасьютиклз, Инк. Миметики глюкокортикоидов, способы их получения, фармацевтические композиции и их применение
US7169936B2 (en) 2002-07-23 2007-01-30 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments
DE10233366A1 (de) * 2002-07-23 2004-02-12 Boehringer Ingelheim Pharma Gmbh & Co. Kg In 6-Stellung substituierte Indolinonderivate, ihre Herstellung und ihre Verwendung als Arzneimittel
US7514468B2 (en) 2002-07-23 2009-04-07 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinone derivatives substituted in the 6 position, the preparation thereof and their use as pharmaceutical compositions
PE20040701A1 (es) * 2002-07-23 2004-11-30 Boehringer Ingelheim Pharma Derivados de indolinona sustituidos en posicion 6 y su preparacion como medicamentos
DE10237423A1 (de) 2002-08-16 2004-02-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verwendung von LCK-Inhibitoren für die Behandlung von immunologischen Erkrankungen
US20040204458A1 (en) 2002-08-16 2004-10-14 Boehringer Ingelheim Pharma Gmbh & Co. Kg Use of Lck inhibitors for treatment of immunologic diseases
NZ538932A (en) * 2002-08-29 2007-04-27 Boehringer Ingelheim Pharma 3-(sulfonamidoethyl)-indole derivatives for use as glucocorticoid mimetics in the treatment of inflammatory, allergic and proliferative disease
US7148249B2 (en) * 2002-09-12 2006-12-12 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinones substituted by heterocycles, the preparation thereof and their use as medicaments
JP4879492B2 (ja) * 2002-11-27 2012-02-22 アラーガン、インコーポレイテッド 疾患の治療のためのキナーゼ阻害剤
US20050043233A1 (en) 2003-04-29 2005-02-24 Boehringer Ingelheim International Gmbh Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis
UY28526A1 (es) 2003-09-24 2005-04-29 Boehringer Ingelheim Pharma Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos
JP4949845B2 (ja) * 2003-10-03 2012-06-13 ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド タンパク質キナーゼインヒビター結合アッセイにおける使用のための蛍光プローブ
KR101165863B1 (ko) 2004-03-11 2012-07-13 액테리온 파마슈티칼 리미티드 인돌-1-일-아세트산 유도체
US7795272B2 (en) 2004-03-13 2010-09-14 Boehringer Ingelheim Pharmaceutical, Inc. Glucocorticoid mimetics, methods of making them, pharmaceutical compositions and uses thereof
PE20061155A1 (es) * 2004-12-24 2006-12-16 Boehringer Ingelheim Int Derivados de indolinona como agentes para el tratamiento o la prevencion de enfermedades fibroticas
PE20060777A1 (es) 2004-12-24 2006-10-06 Boehringer Ingelheim Int Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
DE602005015027D1 (de) 2004-12-27 2009-07-30 Boehringer Ingelheim Pharma Glucocorticoid-mimetika, verfahren zu deren herstellung, pharmazeutische zusammensetzungen und deren verwendung
KR20080007645A (ko) * 2005-04-28 2008-01-22 베링거 인겔하임 인터내셔날 게엠베하 염증성 질환 치료용 신규 화합물
MX2009005264A (es) 2006-12-06 2009-05-28 Boehringer Ingelheim Int Mimeticos de glucocorticoides, metodos para su fabricacion, composiciones farmaceuticas y usos de los mismos.
MX2009006202A (es) * 2006-12-11 2009-06-22 Genentech Inc Composiciones y metodos para el tratamiento de neoplasma.
CN101273991B (zh) * 2007-03-28 2010-05-26 广东同德药业有限公司 四氢吲哚酮/四氢吲唑酮/四氢咔唑衍生物及其盐在制备抗病毒药物中的应用
PE20091445A1 (es) 2007-12-03 2009-10-19 Boehringer Ingelheim Int Derivados de indolinona y procedimiento para su fabricacion
NZ585799A (en) * 2007-12-03 2012-04-27 Boehringer Ingelheim Int Process for the manufacture of an indolinone derivative in particular 3-z-[1-(4-(n-((4-methyl-piperazin-1-yl)-methylcarbonyl)-n-methyl-amino)-anilino)-1-phenyl-methylene]-6-methoxycarbonyl-2-indolinone
ES2394239T3 (es) * 2008-01-25 2013-01-23 Boehringer Ingelheim International Gmbh Formas salinas de un derivado de 6-fluoro-1,2-dihidro-2-oxo-3H-indol-3-ilideno, procedimiento para su preparación y composiciones farmacéuticas que las contienen
PT2300472E (pt) 2008-06-06 2012-02-20 Boehringer Ingelheim Int Miméticos de glucocorticóides, métodos de os preparar, composições farmacêuticas e suas utilizações
EA201100254A1 (ru) 2008-07-29 2011-08-30 Бёрингер Ингельхайм Интернациональ Гмбх Новые соединения
WO2013137371A1 (fr) * 2012-03-15 2013-09-19 興和株式会社 Nouveau composé pyrimidine et médicament comprenant celui-ci
CN103664737A (zh) * 2012-09-25 2014-03-26 杨子娇 一类治疗房角狭窄的化合物及其用途
US11666888B2 (en) 2018-02-05 2023-06-06 Bio-Rad Laboratories, Inc. Chromatography resin having an anionic exchange-hydrophobic mixed mode ligand
CN114957084B (zh) * 2022-01-21 2023-05-09 九江学院 一种吲哚酮类化合物及其制备方法和应用
WO2025155711A1 (fr) * 2024-01-17 2025-07-24 The Board Of Trustees Of The Leland Stanford Junior University Inhibiteurs de lrrk2 et compositions et utilisations associées

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GB9501567D0 (en) * 1995-01-26 1995-03-15 Pharmacia Spa Hydrosoluble 3-arylidene-2-oxindole derivatives as tyrosine kinase inhibitors
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease

Also Published As

Publication number Publication date
US20040058978A1 (en) 2004-03-25
EA200100320A1 (ru) 2001-10-22
CN1319090A (zh) 2001-10-24
DE59906030D1 (de) 2003-07-24
ATE243195T1 (de) 2003-07-15
SK4032001A3 (en) 2001-11-06
KR20010085841A (ko) 2001-09-07
DK1115704T3 (da) 2003-09-29
ID27757A (id) 2001-04-26
HRP20010216A2 (en) 2002-04-30
EE200100184A (et) 2002-08-15
AU6086399A (en) 2000-04-17
WO2000018734A1 (fr) 2000-04-06
IL141622A0 (en) 2002-03-10
HUP0104973A2 (hu) 2002-04-29
TR200100854T2 (tr) 2001-12-21
NO20011477L (no) 2001-03-22
JP2002525356A (ja) 2002-08-13
EP1115704A1 (fr) 2001-07-18
NZ510845A (en) 2003-10-31
BG105327A (bg) 2001-12-29
EP1115704B1 (fr) 2003-06-18
US6855710B2 (en) 2005-02-15
HUP0104973A3 (en) 2002-06-28
PL346898A1 (en) 2002-03-11
AU763361B2 (en) 2003-07-17
PT1115704E (pt) 2003-11-28
YU21301A (sh) 2003-04-30
BR9914065A (pt) 2001-06-19
SI1115704T1 (sl) 2003-12-31
ES2196860T3 (es) 2003-12-16
CA2342622A1 (fr) 2000-04-06

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Legal Events

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FC2A Withdrawal, rejection or dismissal of laid open patent application