[go: up one dir, main page]

AR025752A1 - Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis - Google Patents

Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis

Info

Publication number
AR025752A1
AR025752A1 ARP000104981A ARP000104981A AR025752A1 AR 025752 A1 AR025752 A1 AR 025752A1 AR P000104981 A ARP000104981 A AR P000104981A AR P000104981 A ARP000104981 A AR P000104981A AR 025752 A1 AR025752 A1 AR 025752A1
Authority
AR
Argentina
Prior art keywords
inhibition activity
ring
piridacines
piridines
replaced
Prior art date
Application number
ARP000104981A
Other languages
English (en)
Original Assignee
Bayer Corp
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 Bayer Corp filed Critical Bayer Corp
Publication of AR025752A1 publication Critical patent/AR025752A1/es

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
    • C07D401/02Heterocyclic 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
    • 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
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • A61P31/22Antivirals for DNA viruses for herpes viruses
    • 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
    • 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
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Vascular Medicine (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)

Abstract

Piridinas y piridacinas sustituidas que tienen actividad de inhibicion de angiogénesis y la formula estructural generalizada (1), donde el anillo quecontiene A, B, D, E, y L es fenilo o un heterociclo que contiene nitrogeno; los grupos X e Y pueden ser cualquiera de una variedad de unidades de enlace; R1 yR2 pueden ser sustituyentes independientes definidos o juntos pueden ser un puente que define un anillo; el anillo J puede ser un grupo arilo, piridilo ocicloalquilo; y los grupos G pueden sercualquiera de una variedad de sustituyentes definidos. También se describen composiciones farmacéuticas que contienenestos materiales y los métodos de tratamiento de un mamífero que tiene un trastorno caracterizado por procesos de angiogénesis e hiperpermeabilidad anormalesmediante el uso de estos materiales.
ARP000104981A 1999-09-28 2000-09-22 Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis AR025752A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US40760099A 1999-09-28 1999-09-28

Publications (1)

Publication Number Publication Date
AR025752A1 true AR025752A1 (es) 2002-12-11

Family

ID=23612752

Family Applications (3)

Application Number Title Priority Date Filing Date
ARP000104981A AR025752A1 (es) 1999-09-28 2000-09-22 Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis
ARP110102558A AR082231A2 (es) 1999-09-28 2011-07-15 Piridinas y piridazinas sustituidas con actividad de inhibicion de angiogenesis, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento
ARP110102559A AR082232A2 (es) 1999-09-28 2011-07-15 Piridinas y piridazinas sustituidas con actividad de inhibicion de angiogenesis, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento

Family Applications After (2)

Application Number Title Priority Date Filing Date
ARP110102558A AR082231A2 (es) 1999-09-28 2011-07-15 Piridinas y piridazinas sustituidas con actividad de inhibicion de angiogenesis, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento
ARP110102559A AR082232A2 (es) 1999-09-28 2011-07-15 Piridinas y piridazinas sustituidas con actividad de inhibicion de angiogenesis, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento

Country Status (36)

Country Link
EP (1) EP1228063B1 (es)
JP (1) JP4919567B2 (es)
KR (3) KR100895572B1 (es)
CN (3) CN100374435C (es)
AR (3) AR025752A1 (es)
AT (1) ATE422494T1 (es)
AU (1) AU782820B2 (es)
BG (1) BG65860B1 (es)
BR (1) BRPI0014382B8 (es)
CA (1) CA2385817C (es)
CO (1) CO5200835A1 (es)
CZ (1) CZ304767B6 (es)
DE (1) DE60041548D1 (es)
DO (1) DOP2000000070A (es)
EE (1) EE05258B1 (es)
ES (1) ES2320525T3 (es)
GT (1) GT200000158A (es)
HK (2) HK1091819A1 (es)
HR (1) HRP20020308A2 (es)
HU (1) HU230223B1 (es)
IL (3) IL148880A0 (es)
MA (1) MA25563A1 (es)
MX (1) MXPA02003156A (es)
MY (3) MY143580A (es)
NO (1) NO20021520L (es)
NZ (1) NZ518589A (es)
PA (1) PA8503201A1 (es)
PE (1) PE20010607A1 (es)
PL (1) PL205957B1 (es)
RS (1) RS50369B (es)
RU (1) RU2260008C2 (es)
SK (1) SK287417B6 (es)
TW (1) TW593315B (es)
UA (1) UA75053C2 (es)
WO (1) WO2001023375A2 (es)
ZA (1) ZA200202760B (es)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL154034A0 (en) * 2000-08-09 2003-07-31 Astrazeneca Ab Indole, azaindole and indazole derivatives, processes for their preparation, pharmaceutical compositions containing them and use thereof in the manufacture of medicaments for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals
CN101029022B (zh) 2000-10-20 2011-01-12 卫材R&D管理有限公司 含氮芳环衍生物的制备方法
WO2003059354A2 (en) * 2001-12-21 2003-07-24 Bayer Pharmaceuticals Corporation Anti-angiogenesis combination therapies comprising pyridazine or pyridine derivatives
TWI299664B (en) 2003-01-06 2008-08-11 Osi Pharm Inc (2-carboxamido)(3-amino)thiophene compounds
TW200501955A (en) * 2003-03-11 2005-01-16 Novartis Ag Method of treatment
WO2004089412A1 (ja) * 2003-04-08 2004-10-21 Mitsubishi Pharma Corporation 特異的nad(p)hオキシダーゼ抑制剤
CN100450998C (zh) 2003-11-11 2009-01-14 卫材R&D管理有限公司 脲衍生物的制备方法
KR100553398B1 (ko) * 2004-03-12 2006-02-16 한미약품 주식회사 티에노[3,2-c]피리딘 유도체의 제조 방법 및 이에사용되는 중간체
EP1797877A4 (en) 2004-09-13 2010-12-15 Eisai Co Ltd JOINT USE OF A SULFONAMIDE-BASED COMPOUND AND AN ANGIOGENESIS INHIBITOR
US8772269B2 (en) 2004-09-13 2014-07-08 Eisai R&D Management Co., Ltd. Use of sulfonamide-including compounds in combination with angiogenesis inhibitors
ATE428421T1 (de) 2004-09-17 2009-05-15 Eisai R&D Man Co Ltd Medizinische zusammensetzung mit verbesserter stabilität und reduzierten gelierungseigenschaften
US9006240B2 (en) 2005-08-02 2015-04-14 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
EP2010173A1 (en) 2006-04-15 2009-01-07 Bayer HealthCare AG Compounds for treating pulmonary hypertension
EP2036557B1 (en) 2006-05-18 2015-10-21 Eisai R&D Management Co., Ltd. Antitumor agent for thyroid cancer
US8865737B2 (en) 2006-08-28 2014-10-21 Eisai R&D Management Co., Ltd. Antitumor agent for undifferentiated gastric cancer
CN101600694A (zh) 2007-01-29 2009-12-09 卫材R&D管理有限公司 未分化型胃癌治疗用组合物
CA2704000C (en) 2007-11-09 2016-12-13 Eisai R&D Management Co., Ltd. Combination of anti-angiogenic substance and anti-tumor platinum complex
CN101481380B (zh) * 2008-01-08 2012-10-17 浙江医药股份有限公司新昌制药厂 噻吩并哒嗪类化合物及其制备方法、药物组合物及其用途
WO2011162343A1 (ja) 2010-06-25 2011-12-29 エーザイ・アール・アンド・ディー・マネジメント株式会社 キナーゼ阻害作用を有する化合物の併用による抗腫瘍剤
US8962650B2 (en) 2011-04-18 2015-02-24 Eisai R&D Management Co., Ltd. Therapeutic agent for tumor
JP6038128B2 (ja) 2011-06-03 2016-12-07 エーザイ・アール・アンド・ディー・マネジメント株式会社 レンバチニブ化合物に対する甲状腺癌対象及び腎臓癌対象の反応性を予測及び評価するためのバイオマーカー
KR20150098605A (ko) 2012-12-21 2015-08-28 에자이 알앤드디 매니지먼트 가부시키가이샤 퀴놀린 유도체의 비정질 형태 및 그의 제조방법
NZ714049A (en) 2013-05-14 2020-05-29 Eisai R&D Man Co Ltd Biomarkers for predicting and assessing responsiveness of endometrial cancer subjects to lenvatinib compounds
CN103396361B (zh) * 2013-07-24 2016-05-04 中国人民解放军第二军医大学 3,4-二氢异喹啉类抗肿瘤化合物及其制备方法与应用
RS63559B1 (sr) 2014-08-28 2022-10-31 Eisai R&D Man Co Ltd Derivat hinolina velike čistoće i postupak za njegovu proizvodnju
PL3263106T3 (pl) 2015-02-25 2024-04-02 Eisai R&D Management Co., Ltd. Sposób tłumienia goryczy pochodnej chinoliny
AU2015384801B2 (en) 2015-03-04 2022-01-06 Eisai R&D Management Co., Ltd. Combination of a PD-1 antagonist and a VEGFR/FGFR/RET tyrosine kinase inhibitor for treating cancer
CN104804008B (zh) * 2015-03-27 2016-03-23 亿腾药业(泰州)有限公司 一种工业化生产甲磺酸特拉替尼的方法
RU2729936C2 (ru) 2015-06-16 2020-08-13 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Противораковое средство
RU2718048C2 (ru) 2015-08-20 2020-03-30 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Противоопухолевое терапевтическое средство
CN107129502B (zh) * 2017-04-13 2022-08-05 泰州亿腾景昂药业股份有限公司 EOC315 Mod.I晶型化合物及其制备方法
KR20200013644A (ko) 2017-05-16 2020-02-07 에자이 알앤드디 매니지먼트 가부시키가이샤 간세포 암종의 치료
JP7624404B2 (ja) * 2019-04-22 2025-01-30 ミラティ セラピューティクス,インク. Prc2阻害剤としてのナフチリジン誘導体
CN112830932B (zh) * 2020-12-25 2022-04-08 泰州亿腾景昂药业股份有限公司 特拉替尼的游离碱晶型及其制备方法与用途
JP2024540411A (ja) 2021-11-08 2024-10-31 プロジェントス・セラピューティクス・インコーポレイテッド 血小板由来成長因子受容体(pdgfr)アルファ阻害剤及びその使用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1453897A (fr) * 1965-06-16 1966-07-22 Dérivés du thiophène et de thiéno pyridazines
GB1094044A (en) * 1965-07-12 1967-12-06 Vantorex Ltd Phthalazine derivatives
FR1516777A (fr) * 1966-08-02 1968-02-05 Innothera Lab Sa Dérivés du thiazole ainsi que de la thiazolo [4,5-d] pyridazine et leur préparation
GB1293565A (en) * 1969-05-03 1972-10-18 Aspro Nicholas Ltd Aminophthalazines and pharmaceutical compositions thereof
JPH03106875A (ja) * 1989-09-20 1991-05-07 Morishita Pharmaceut Co Ltd 1―(3―ピリジルメチル)フタラジン誘導体
NZ290952A (en) * 1994-08-09 1998-05-27 Eisai Co Ltd Phthalazine derivatives optionally substituted in position-1 by (generally benzyl) amino groups
CO4950519A1 (es) * 1997-02-13 2000-09-01 Novartis Ag Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion
ES2342240T3 (es) * 1998-08-11 2010-07-02 Novartis Ag Derivados de isoquinolina con actividad que inhibe la angiogenia.
ES2265929T3 (es) * 1999-03-30 2007-03-01 Novartis Ag Derivados de ftalazina para el tratamiento de enfermedades inflamatorias.
AR025068A1 (es) * 1999-08-10 2002-11-06 Bayer Corp Pirazinas sustituidas y piridazinas fusionadas, composicion farmaceutica que las comprenden, uso de dichos compuestos para la manufactura de un medicamentocon actividad inhibidora de angiogenesis
AU2001231710A1 (en) * 2000-02-09 2001-08-20 Novartis Ag Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase

Also Published As

Publication number Publication date
KR20080086547A (ko) 2008-09-25
WO2001023375A3 (en) 2002-05-02
SK5912002A3 (en) 2003-01-09
BG106637A (bg) 2003-02-28
MY135058A (en) 2008-01-31
RS50369B (sr) 2009-11-10
GT200000158A (es) 2002-03-16
IL193368A0 (en) 2009-02-11
MXPA02003156A (es) 2002-09-30
ATE422494T1 (de) 2009-02-15
AR082232A2 (es) 2012-11-21
RU2260008C2 (ru) 2005-09-10
EE05258B1 (et) 2010-02-15
HK1091818A1 (en) 2007-01-26
CN1420879A (zh) 2003-05-28
IL193368A (en) 2011-05-31
IL193367A0 (en) 2009-02-11
EP1228063B1 (en) 2009-02-11
MY143377A (en) 2011-05-13
CN100374435C (zh) 2008-03-12
KR100895571B1 (ko) 2009-04-29
UA75053C2 (en) 2006-03-15
BR0014382A (pt) 2003-06-24
NZ518589A (en) 2005-03-24
CZ304767B6 (cs) 2014-10-08
CN100422173C (zh) 2008-10-01
KR20080091505A (ko) 2008-10-13
IL148880A0 (en) 2002-09-12
BG65860B1 (bg) 2010-03-31
CZ20021444A3 (cs) 2002-08-14
EE200200161A (et) 2003-08-15
JP4919567B2 (ja) 2012-04-18
CN1769282A (zh) 2006-05-10
EP1228063A2 (en) 2002-08-07
HRP20020308A2 (en) 2004-06-30
PA8503201A1 (es) 2002-08-26
BRPI0014382B8 (pt) 2021-05-25
KR20020038775A (ko) 2002-05-23
HUP0202704A2 (hu) 2002-12-28
MA25563A1 (fr) 2002-10-01
BR0014382B1 (pt) 2014-04-01
AR082231A2 (es) 2012-11-21
AU782820B2 (en) 2005-09-01
CN100422172C (zh) 2008-10-01
KR100890473B1 (ko) 2009-03-26
DOP2000000070A (es) 2002-02-28
KR100895572B1 (ko) 2009-04-29
TW593315B (en) 2004-06-21
HRP20020308B1 (es) 2013-01-31
PL205957B1 (pl) 2010-06-30
HK1091819A1 (en) 2007-01-26
CO5200835A1 (es) 2002-09-27
CA2385817A1 (en) 2001-04-05
DE60041548D1 (de) 2009-03-26
AU1569601A (en) 2001-04-30
MY143580A (en) 2011-05-31
WO2001023375A2 (en) 2001-04-05
SK287417B6 (sk) 2010-09-07
CA2385817C (en) 2010-05-04
IL193367A (en) 2011-03-31
PE20010607A1 (es) 2001-07-12
YU22902A (sh) 2004-12-31
NO20021520D0 (no) 2002-03-26
HU230223B1 (en) 2015-10-28
HUP0202704A3 (en) 2003-12-29
ZA200202760B (en) 2003-10-29
NO20021520L (no) 2002-05-23
CN1769283A (zh) 2006-05-10
PL366342A1 (en) 2005-01-24
ES2320525T3 (es) 2009-05-25
JP2003526632A (ja) 2003-09-09

Similar Documents

Publication Publication Date Title
AR025752A1 (es) Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis
ES2117400T3 (es) Inhibidores de metaloproteinasas.
ES2188280T3 (es) Acetales heteroaril-ciclicos.
ES2185338T3 (es) Derivados de fumagilol y procedimientos para su fabricacion.
FI903215A0 (fi) Heteroarylamino- och heteroaryloxipyridinaminer och till desa hoerande foereningar, foerfarande foer deras framstaellning samt deras anvaendning som laekemedel.
ES2079576T3 (es) Derivados piranicos biciclicos y su uso como inhibidores de 5-lipoxigenasa.
ES2158109T3 (es) Nuevo derivado de indano fusionado y sal del mismo farmaceuticamente aceptable.
NO934718D0 (no) Nye HIV protease inhibitorer
DE69911935D1 (de) Granulatimide-derivate zur behandlung von krebs
SE8505715D0 (sv) Indolderivat
ES2039361T3 (es) Derivados de 3-vinil- y 3-etinil-beta-carbolinas, su preparacion y su utilizacion como medicamentos.
ATE172193T1 (de) Piperazinderivate
BR0013113A (pt) Piridazinas substituìdas e piridazinas fundidas com atividade inibidora da angiogênese
DK1717229T3 (da) Ny cyklisk forbindelse med 4-pyridylalkylthiogruppe med deri indført (u)substitueret amino
UY34283A (es) Piridacinas sustituidas con actividad de inhibición de angiogénesis
FI956300A0 (fi) Pyridatsinonijohdannaisia
ECSP003679A (es) Piridinas y piridacinas substituidas con actividad de inhibicion de angiogenesis
DK0736009T3 (da) N-oxider af 4-arylpiperaziner og 4-arylpiperidiner som antipsykotiske medikamenter
SE9401353D0 (sv) Novel antitumour compounds with antimitotic activity
DK0466662T3 (da) 6,7-Disubstituerede-2-aminotetraliner, der er aktive som immunmodulatorer, samt farmaceutiske præparater indeholdende sådanne forbindelser
MX9303753A (es) Dihidropiridinas anilladas y composiciones farmaceuticas que las contienen.
DE69622065D1 (de) 4-Alkylthio-Pyrimidin-5-ylessigsäure Derivate
DK517486A (da) 3-imino-pyridazinderivater, fremgangsmaade til fremstilling deraf og farmaceutiske midler der indeholder dem
GB2299334A (en) Metalloproteinase inhibitors
IT1217900B (it) Composti eterociclici azotati ad azione antifungina

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed, e.g., due to non-payment of fee