PA8525701A1 - Compuestos con nucleos heterociclico-hidroximino-fluoreno y las composiciones farmaceuticas para la inhibicion de las proteinas cinasas y los metodos para su uso - Google Patents

Compuestos con nucleos heterociclico-hidroximino-fluoreno y las composiciones farmaceuticas para la inhibicion de las proteinas cinasas y los metodos para su uso

Info

Publication number
PA8525701A1
PA8525701A1 PA20018525701A PA8525701A PA8525701A1 PA 8525701 A1 PA8525701 A1 PA 8525701A1 PA 20018525701 A PA20018525701 A PA 20018525701A PA 8525701 A PA8525701 A PA 8525701A PA 8525701 A1 PA8525701 A1 PA 8525701A1
Authority
PA
Panama
Prior art keywords
compounds
pharmaceutical compositions
heterociclic
methods
fluorene
Prior art date
Application number
PA20018525701A
Other languages
English (en)
Inventor
Wesley Kwan Mung Chong
Rohit Kumar Duvadie
Original Assignee
Agouron 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
Application filed by Agouron Pharma filed Critical Agouron Pharma
Publication of PA8525701A1 publication Critical patent/PA8525701A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/16Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/12Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D285/00Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/14Thiadiazoles; Hydrogenated thiadiazoles condensed with carbocyclic rings or ring systems

Abstract

SE DESCRIBEN LOS COMPUESTOS DE NUCLEOS HETEROCICLICOS-HIDROXIIMINO-FLUORENO QUE MODULAN Y/O INHIBEN LA ACTIVIDAD DE LAS PROTEINAS CINASAS. ESTOS COMPUESTOS Y LAS COMPOSICIONES FARMACEUTICAS QUE LOS CONTIENEN, SON CAPACES DE MEDIAR LA TRANSDUCCION DE LA SEÑAL DE LA TIROSINA CINASA PARA MODULAR Y/O INHIBIR LA PROLIFERACION DE LAS CELULAS INDESEABLES. LA INVENCION TAMBIEN SE DIRIGE AL USO TERAPEUTICO O PROFILACTICO DE LAS COMPOSICIONES FARMACEUTICAS QUE CONTIENEN DICHOS COMPUESTOS Y A LOS METODOS, MEDIANTE LA ADMINISTRACION DE UNA CANTIDAD EFICAZ DE DICHOS COMPUESTOS, PARA EL TRATAMIENTO DEL CANCER Y LAS OTRAS ENFERMEDADES ASOCIADAS CON LA ANGIOGENESIS Y/O PROLIFERACION CELULAR INDESEABLE, TALES COMO RETINOPATIA DIABETICA, EL GLAUCOMA NEOVASCULAR, LA ARTRITIS REUMATOIDE Y LA SORIASIS.
PA20018525701A 2000-08-18 2001-08-17 Compuestos con nucleos heterociclico-hidroximino-fluoreno y las composiciones farmaceuticas para la inhibicion de las proteinas cinasas y los metodos para su uso PA8525701A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US22480500P 2000-08-18 2000-08-18

Publications (1)

Publication Number Publication Date
PA8525701A1 true PA8525701A1 (es) 2002-04-25

Family

ID=22842288

Family Applications (1)

Application Number Title Priority Date Filing Date
PA20018525701A PA8525701A1 (es) 2000-08-18 2001-08-17 Compuestos con nucleos heterociclico-hidroximino-fluoreno y las composiciones farmaceuticas para la inhibicion de las proteinas cinasas y los metodos para su uso

Country Status (16)

Country Link
US (1) US6462060B2 (es)
EP (1) EP1309563B1 (es)
JP (1) JP2004506720A (es)
AR (1) AR032891A1 (es)
AT (1) ATE295354T1 (es)
AU (1) AU2001279090A1 (es)
BR (1) BR0113258A (es)
CA (1) CA2411924A1 (es)
DE (1) DE60110802T2 (es)
ES (1) ES2238463T3 (es)
GT (1) GT200100170A (es)
MX (1) MXPA03001452A (es)
PA (1) PA8525701A1 (es)
PE (1) PE20020289A1 (es)
SV (1) SV2003000603A (es)
WO (1) WO2002016326A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6770652B2 (en) * 2001-10-18 2004-08-03 Duquesne University Of The Holy Ghost Multiple acting anti-angiogenic and cytotoxic compounds and methods for using the same
JP4502641B2 (ja) * 2002-01-24 2010-07-14 ティルタン ファーマ リミテッド 抗癌組み合わせおよびその使用方法
CA2542638A1 (en) * 2003-10-16 2005-04-28 Imclone Systems Incorporated Fibroblast growth factor receptor-1 inhibitors and methods of treatment thereof
WO2006056889A2 (en) * 2004-10-06 2006-06-01 Tiltan Pharma Ltd Method and composition for enhancing anti-angiogenic therapy
ES2356068T3 (es) 2005-03-29 2011-04-04 Icos Corporation Derivados de heteroaril urea utiles para inhibir chk1.
WO2007026720A1 (ja) * 2005-08-31 2007-03-08 Taisho Pharmaceutical Co., Ltd. 縮環ピラゾール誘導体

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US5625031A (en) 1994-02-08 1997-04-29 Bristol-Myers Squibb Company Peptide inhibitors of the p33cdk2 and p34cdc2 cell cycle regulatory kinases and human papillomavirus E7 oncoprotein
US5631156A (en) 1994-06-21 1997-05-20 The University Of Michigan DNA encoding and 18 KD CDK6 inhibiting protein
ATE262902T1 (de) 1994-11-10 2004-04-15 Millennium Pharm Inc Verwendung von pyrazole verbindungen zur behandlung von glomerulonephritis, krebs, atherosklerose oder restenose
US5733920A (en) 1995-10-31 1998-03-31 Mitotix, Inc. Inhibitors of cyclin dependent kinases
EP0888310B1 (en) 1996-03-15 2005-09-07 AstraZeneca AB Cinnoline derivatives and use as medicine
US5849733A (en) 1996-05-10 1998-12-15 Bristol-Myers Squibb Co. 2-thio or 2-oxo flavopiridol analogs
CN1160309C (zh) * 1996-05-30 2004-08-04 赫彻斯特马里恩鲁斯公司 烷氧基氨基取代的芴酮以及它们作为蛋白激酶c抑制剂的用途
GB9621757D0 (en) 1996-10-18 1996-12-11 Ciba Geigy Ag Phenyl-substituted bicyclic heterocyclyl derivatives and their use
EP0964864B1 (en) 1997-02-05 2008-04-09 Warner-Lambert Company LLC Pyrido 2,3-d pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
CA2294244A1 (en) 1997-07-12 1999-01-21 Cancer Research Campaign Technology Limited Cyclin dependent kinase inhibiting purine derivatives
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
ES2206997T3 (es) 1997-10-06 2004-05-16 ABBOTT GMBH & CO. KG Derivados de indeno(1,2-c)-,de nafto(1,2-c),y de benzo(6,7)cicloepta(1,2-c)pirazol.
ES2267873T3 (es) 1997-10-27 2007-03-16 Agouron Pharmaceuticals, Inc. Derivados de 4-aminotiazol, su preparacion y uso como inhibidores de kinasas dependientes de ciclina.
ATE355841T1 (de) 1997-12-13 2007-03-15 Bristol Myers Squibb Co Verwendung von pyrazolo ( 3,4-b) pyridin als cyclin-abhängige kinase hemmer
US6479487B1 (en) 1998-02-26 2002-11-12 Aventis Pharmaceuticals Inc. 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
DK1056745T3 (da) 1998-02-26 2004-10-25 Aventis Pharma Inc 6,9-Disubstituerede 2-[trans-(4-aminocyklohexyl)amino]puriner
BR9909597A (pt) 1998-04-21 2001-10-02 Du Pont Pharm Co Composto, composição farmacêutica e método de tratamento de câncer e doenças proliferativas
UA60365C2 (uk) 1998-06-04 2003-10-15 Пфайзер Продактс Інк. Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця
DE69933680T2 (de) 1998-08-29 2007-08-23 Astrazeneca Ab Pyrimidine verbindungen
ATE336484T1 (de) 1998-08-29 2006-09-15 Astrazeneca Ab Pyrimidine verbindungen
US6316603B1 (en) * 1998-09-08 2001-11-13 Agouron Pharmaceuticals, Inc. Modifications of the VEGF receptor-2 protein and methods of use
PL348210A1 (en) * 1998-11-06 2002-05-06 Basf Ag Tricyclic pyrazole derivatives

Also Published As

Publication number Publication date
JP2004506720A (ja) 2004-03-04
MXPA03001452A (es) 2004-05-04
US20020049238A1 (en) 2002-04-25
DE60110802T2 (de) 2005-10-06
CA2411924A1 (en) 2002-02-28
GT200100170A (es) 2002-05-16
BR0113258A (pt) 2003-07-15
SV2003000603A (es) 2003-01-13
WO2002016326A1 (en) 2002-02-28
DE60110802D1 (de) 2005-06-16
AU2001279090A1 (en) 2002-03-04
ES2238463T3 (es) 2005-09-01
ATE295354T1 (de) 2005-05-15
PE20020289A1 (es) 2002-05-27
US6462060B2 (en) 2002-10-08
EP1309563A1 (en) 2003-05-14
AR032891A1 (es) 2003-12-03
EP1309563B1 (en) 2005-05-11

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