AU2003206068A1 - Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents - Google Patents

Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents

Info

Publication number
AU2003206068A1
AU2003206068A1 AU2003206068A AU2003206068A AU2003206068A1 AU 2003206068 A1 AU2003206068 A1 AU 2003206068A1 AU 2003206068 A AU2003206068 A AU 2003206068A AU 2003206068 A AU2003206068 A AU 2003206068A AU 2003206068 A1 AU2003206068 A1 AU 2003206068A1
Authority
AU
Australia
Prior art keywords
indolyl
urea derivatives
angiogenic agents
thienopyridines
useful
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
AU2003206068A
Other languages
English (en)
Other versions
AU2003206068A8 (en
Inventor
Stephan James Cripps
Mingying He
Robert Steven Kania
Jihong Lou
William Henry Romines Iii
Ru Zhou
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Inc
Original Assignee
PFIZER
Pfizer Inc
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 PFIZER, Pfizer Inc filed Critical PFIZER
Publication of AU2003206068A1 publication Critical patent/AU2003206068A1/en
Publication of AU2003206068A8 publication Critical patent/AU2003206068A8/xx
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (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)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
AU2003206068A 2002-03-01 2003-02-17 Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents Abandoned AU2003206068A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US36095202P 2002-03-01 2002-03-01
US60/360,952 2002-03-01
PCT/IB2003/000740 WO2003074529A2 (en) 2002-03-01 2003-02-17 iNDOLYL-UREA DERIVATIVES OF THIENOPYRIDINES USEFUL AS ANTI-ANGIOGENIC AGENTS

Publications (2)

Publication Number Publication Date
AU2003206068A1 true AU2003206068A1 (en) 2003-09-16
AU2003206068A8 AU2003206068A8 (en) 2003-09-16

Family

ID=27789048

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2003206068A Abandoned AU2003206068A1 (en) 2002-03-01 2003-02-17 Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents

Country Status (15)

Country Link
US (1) US6833456B2 (https=)
EP (1) EP1483268A2 (https=)
JP (1) JP2005527511A (https=)
AR (1) AR040398A1 (https=)
AU (1) AU2003206068A1 (https=)
BR (1) BR0308162A (https=)
CA (1) CA2478050A1 (https=)
GT (1) GT200300046A (https=)
HN (1) HN2003000080A (https=)
MX (1) MXPA04008403A (https=)
PA (1) PA8568101A1 (https=)
PE (1) PE20030944A1 (https=)
TW (1) TW200306193A (https=)
UY (1) UY27685A1 (https=)
WO (1) WO2003074529A2 (https=)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA77303C2 (en) 2002-06-14 2006-11-15 Pfizer Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use
TW200503994A (en) * 2003-01-24 2005-02-01 Novartis Ag Organic compounds
AU2004309166B2 (en) * 2003-12-23 2008-02-21 Pfizer Inc. Novel quinoline derivatives
AU2008202205B2 (en) * 2003-12-23 2009-09-10 Pfizer Inc. Novel quinoline derivatives
EP1698621A4 (en) * 2003-12-26 2008-11-19 Daiichi Seiyaku Co PROCESS FOR PREPARING A PYRROLIDINE DERIVATIVE
GB0412467D0 (en) * 2004-06-04 2004-07-07 Astrazeneca Ab Chemical compounds
ES2438017T3 (es) 2004-07-30 2014-01-15 Methylgene Inc. Inhibidores de la señalización del receptor del VEGF y del receptor del HGF
KR101378716B1 (ko) 2005-05-20 2014-04-10 메틸진 인코포레이티드 Vegf 수용체 및 hgf 수용체 신호전달의 억제제
AU2006313456B2 (en) 2005-05-20 2011-06-23 Methylgene Inc. Inhibitors of VEGF receptor and HGF receptor signaling
AU2006277742B2 (en) 2005-08-08 2010-08-26 Pfizer Inc. Salts and polymorphs of a VEGF-R inhibitor
JP2009526761A (ja) * 2006-01-30 2009-07-23 アレイ バイオファーマ、インコーポレイテッド ヘテロ二環式チオフェン化合物および使用の方法
AR060061A1 (es) * 2006-03-22 2008-05-21 Methylgene Inc Inhibidores de la actividad de la proteina tirosina quinasa
JP2009539878A (ja) * 2006-06-08 2009-11-19 アレイ バイオファーマ、インコーポレイテッド キノリン化合物および使用方法
NZ588355A (en) 2008-03-05 2012-03-30 Methylgene Inc Inhibitors of protein tyrosine kinase activity
KR101126736B1 (ko) * 2008-11-27 2012-04-12 주식회사 레고켐 바이오사이언스 티로신 키나아제 저해 화합물, 이의 이성질체 또는 이의 약학적으로 허용가능한 염 및 이를 포함하는 약학적 조성물
BR112013001721A2 (pt) 2010-07-29 2016-05-31 Bial Portela & Ca Sa processo de síntese de compostos de ureia substituída
AR088218A1 (es) 2011-07-19 2014-05-21 Infinity Pharmaceuticals Inc Compuestos heterociclicos utiles como inhibidores de pi3k
CA2929742C (en) 2013-12-04 2022-09-20 Evotec International Gmbh Sulfoximine substituted quinazolines for pharmaceutical compositions
WO2015162515A1 (en) 2014-04-25 2015-10-29 Pfizer Inc. Heteroaromatic compounds and their use as dopamine d1 ligands
CN115746017B (zh) * 2022-11-30 2024-06-07 英维沃化工科技(广州)有限公司 一种噻吩并嘧啶类化合物及其制备方法和应用
CN116082214A (zh) * 2023-02-24 2023-05-09 常州大学 一种2-芳基-3-叔丁基吲哚类化合物、制备方法及其应用

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
US6177401B1 (en) 1992-11-13 2001-01-23 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
RU2137762C1 (ru) 1994-02-23 1999-09-20 Пфайзер Инк. 4-гетероциклил-замещенные производные хиназолина, фармацевтическая композиция
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
DE69536015D1 (de) 1995-03-30 2009-12-10 Pfizer Prod Inc Chinazolinone Derivate
ES2153031T4 (es) 1995-04-20 2001-05-16 Pfizer Derivados del acido arilsulfonil hidroxamico como inhibidores de mmp y tnf.
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
JP3290666B2 (ja) 1995-06-07 2002-06-10 ファイザー・インコーポレーテッド 複素環式の縮合環ピリミジン誘導体
AR004010A1 (es) 1995-10-11 1998-09-30 Glaxo Group Ltd Compuestos heterociclicos
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
NZ331191A (en) 1996-03-05 2000-03-27 Zeneca Ltd 4-anilinoquinazoline derivatives and pharmaceutical compositions thereof
CA2258548C (en) 1996-06-24 2005-07-26 Pfizer Inc. Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases
WO1997049700A1 (en) * 1996-06-27 1997-12-31 Pfizer Inc. Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one and their use as farnesyl protein transferase inhibitors
EA199900021A1 (ru) 1996-07-13 1999-08-26 Глаксо, Груп Лимитед Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
KR20000067904A (ko) 1996-07-18 2000-11-25 디. 제이. 우드, 스피겔 알렌 제이 매트릭스 메탈로프로테아제의 포스피네이트계 억제제
KR20000068248A (ko) 1996-08-23 2000-11-25 디. 제이. 우드, 스피겔 알렌 제이 아릴설포닐아미노 하이드록삼산 유도체
WO1998023613A1 (en) 1996-11-27 1998-06-04 Pfizer Inc. Fused bicyclic pyrimidine derivatives
JP3338064B2 (ja) 1997-01-06 2002-10-28 ファイザー・インク 環状スルホン誘導体
NZ336840A (en) 1997-02-03 2001-01-26 Pfizer Prod Inc Arylsulfonylamino hydroxamic acid derivatives useful in the treatment of tumor necrosis factor and matrix metalloproteinase mediated diseases
JP2000507975A (ja) 1997-02-07 2000-06-27 ファイザー・インク N−ヒドロキシ−β−スルホニルプロピオンアミド誘導体類及びそれらのマトリックスメタロプロテイナーゼ阻害薬としての使用
EP0960098A1 (en) 1997-02-11 1999-12-01 Pfizer Inc. Arylsulfonyl hydroxamic acid derivatives
JP2002501532A (ja) 1997-05-30 2002-01-15 メルク エンド カンパニー インコーポレーテッド 新規血管形成阻害薬
ES2289791T3 (es) 1997-08-22 2008-02-01 Astrazeneca Ab Derivados de oxindolilquinazolina como inhibidores de la angiogenesis.
AU744939B2 (en) 1997-09-26 2002-03-07 Merck & Co., Inc. Novel angiogenesis inhibitors
PA8469501A1 (es) 1998-04-10 2000-09-29 Pfizer Prod Inc Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
PA8469401A1 (es) 1998-04-10 2000-05-24 Pfizer Prod Inc Derivados biciclicos del acido hidroxamico
SK287132B6 (sk) 1998-05-29 2009-12-07 Sugen, Inc. Farmaceutická kompozícia obsahujúca pyrolom substituovaný 2-indolinón, súprava obsahujúca uvedenú kompozíciu a použitie pyrolom substituovaného 2-indolinónu
AU2592600A (en) 1998-12-23 2000-07-31 G.D. Searle & Co. Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia
BR0111377A (pt) * 2000-06-06 2003-06-03 Pfizer Prod Inc Derivados de tiofeno úteis como agentes anticancerìgenos
WO2003000194A2 (en) * 2001-06-21 2003-01-03 Pfizer Inc. Thienopyridine and thienopyrimidine anticancer agents

Also Published As

Publication number Publication date
PA8568101A1 (es) 2003-11-12
PE20030944A1 (es) 2003-11-08
MXPA04008403A (es) 2004-11-26
HN2003000080A (es) 2004-05-05
BR0308162A (pt) 2004-12-07
AR040398A1 (es) 2005-04-06
TW200306193A (en) 2003-11-16
UY27685A1 (es) 2003-10-31
US6833456B2 (en) 2004-12-21
WO2003074529A3 (en) 2003-12-24
AU2003206068A8 (en) 2003-09-16
EP1483268A2 (en) 2004-12-08
GT200300046A (es) 2003-10-10
JP2005527511A (ja) 2005-09-15
US20040019065A1 (en) 2004-01-29
WO2003074529A2 (en) 2003-09-12
CA2478050A1 (en) 2003-09-12

Similar Documents

Publication Publication Date Title
AU2003206068A1 (en) Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents
AU2003255376A1 (en) Piperidine-derivatives as pde4 inhibitors
AU2003218758A1 (en) Derivatives of 1-phenyl-3-phenylpyrazole as herbicides
AP2005003343A0 (en) Substituted pyrrolo-pyrazole derivatives as kinaseinhibitors
AU2003286711A1 (en) Indazolinone compositions useful as kinase inhibitors
AU2002363005A1 (en) Derivatives of uk-2a
EP1682493B8 (en) Amidoacetonitrile derivatives
AU2003293356A1 (en) Dihydropyridinone derivatives as hne inhibitors
EP1606277B8 (en) Imidazol-4-yl-ethynyl-pyridine derivatives
AU2003901815A0 (en) Phosphate derivatives
PL371344A1 (en) Benzenesulfonamide derivatives as antipsychotic agents
AU2003269140A1 (en) Clopidogrel
EP1706373B8 (en) Amidoacetonitrile derivatives
AU2003214609A1 (en) Derivatives of isoflavones
AU2003215635A1 (en) Thiazol-2-yl-imine compounds as pde-7 inhibitors
AU2003282510A1 (en) Hexahydro-benzimidazolone compounds useful as anti-inflammatory agents
AU2003267781A1 (en) Laser modification of complex objects
AU2003245183A1 (en) Derivatives of rifabutine useful as antimicrobial agents
AU2003273169A1 (en) 7-phenylsulfonyl-tetrahydro-3-benzazepine derivatives as antipsychotic agents
AU2003232362A1 (en) 4-pyrazol-phenylalanine derivatives as ace-nep inhibitors
AU2003304151A1 (en) Heteroaryl-ethanolamine derivatives as antiviral agents
AU2003284704A1 (en) Substituted 1h-pyridine-2-one derivatives
AU2003265385A1 (en) Aryl-ethanolamine derivatives as antiviral agents
AU2003244821A1 (en) Articles of wear
AU2003904235A0 (en) Packaging of elongate articles

Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase