ZA200207273B - Indol-3-yl-derivatives and their use as integrin inhibitors. - Google Patents

Indol-3-yl-derivatives and their use as integrin inhibitors. Download PDF

Info

Publication number
ZA200207273B
ZA200207273B ZA200207273A ZA200207273A ZA200207273B ZA 200207273 B ZA200207273 B ZA 200207273B ZA 200207273 A ZA200207273 A ZA 200207273A ZA 200207273 A ZA200207273 A ZA 200207273A ZA 200207273 B ZA200207273 B ZA 200207273B
Authority
ZA
South Africa
Prior art keywords
formula
het
pyridin
propionic acid
ylamino
Prior art date
Application number
ZA200207273A
Other languages
English (en)
Inventor
Simon Goodman
Matthias Wiesner
Rudolf Gottschlich
Original Assignee
Merck Patent Gmbh
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 Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of ZA200207273B publication Critical patent/ZA200207273B/en

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
    • 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • C07D403/12Heterocyclic 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Communicable Diseases (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Ophthalmology & Optometry (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
ZA200207273A 2000-02-11 2002-09-10 Indol-3-yl-derivatives and their use as integrin inhibitors. ZA200207273B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE10006139A DE10006139A1 (de) 2000-02-11 2000-02-11 Indol-3-yl-Derivate

Publications (1)

Publication Number Publication Date
ZA200207273B true ZA200207273B (en) 2003-12-10

Family

ID=7630611

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA200207273A ZA200207273B (en) 2000-02-11 2002-09-10 Indol-3-yl-derivatives and their use as integrin inhibitors.

Country Status (28)

Country Link
US (1) US6743810B2 (fr)
EP (1) EP1254133B9 (fr)
JP (1) JP4938194B2 (fr)
KR (1) KR20020073585A (fr)
CN (1) CN1214026C (fr)
AR (1) AR027398A1 (fr)
AT (1) ATE293620T1 (fr)
AU (2) AU2001231664C1 (fr)
BR (1) BR0108154A (fr)
CA (1) CA2399813C (fr)
CO (1) CO5261548A1 (fr)
CZ (1) CZ20022616A3 (fr)
DE (2) DE10006139A1 (fr)
EC (1) ECSP013923A (fr)
ES (1) ES2240400T3 (fr)
HK (1) HK1051863A1 (fr)
HU (1) HUP0302671A2 (fr)
IL (1) IL151154A0 (fr)
MX (1) MXPA02007732A (fr)
NO (1) NO20023770D0 (fr)
NZ (1) NZ521260A (fr)
PE (1) PE20011125A1 (fr)
PL (1) PL356427A1 (fr)
PT (1) PT1254133E (fr)
RU (1) RU2257380C2 (fr)
SK (1) SK11152002A3 (fr)
WO (1) WO2001058893A2 (fr)
ZA (1) ZA200207273B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040063790A1 (en) * 1996-05-31 2004-04-01 The Scripps Research Institute Methods for inhibition of angiogenesis
US20040138284A1 (en) * 2000-02-11 2004-07-15 Matthias Wiesner Indol-3-yl derivatives
WO2002018377A1 (fr) * 2000-08-29 2002-03-07 Pharmacia Corporation Composes contenant un systeme de noyau bicyclique et utiles en tant qu'antagonistes de l'integrine alpha v beta 3
SI1381382T1 (sl) * 2000-11-01 2009-04-30 Merck Patent Gmbh Postopki in sestavki za zdravljenje oäśesnih bolezni
GB0028367D0 (en) * 2000-11-21 2001-01-03 Celltech Chiroscience Ltd Chemical compounds
JP4615826B2 (ja) * 2001-01-29 2011-01-19 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド 置換インドールおよびインテグリンアンタゴニストとしてのそれらの使用
US6872730B2 (en) 2001-04-27 2005-03-29 3-Dimensional Pharmaceuticals, Inc. Substituted benzofurans and benzothiophenes, methods of making and methods of use as integrin antagonists
EP1411926B1 (fr) * 2001-08-01 2005-06-01 MERCK PATENT GmbH Inhibiteurs de l'integrine pour le traitement de maladies des yeux
PL371281A1 (en) * 2002-02-14 2005-06-13 Merck Patent Gmbh Methods and compositions for the treatment of eye diseases
US20070208026A1 (en) * 2003-04-07 2007-09-06 Liu Kevin N-Containing Heteroaromatic Compounds As Modulators Of Ppars And Methods Of Treating Metabolic Disorders
CA2523245C (fr) * 2003-04-28 2012-03-06 Bayer Pharmaceuticals Corporation Derives d'acide indole acetique et leur utilisation en tant qu'agents pharmaceutiques
US7211588B2 (en) 2003-07-25 2007-05-01 Zentaris Gmbh N-substituted indolyl-3-glyoxylamides, their use as medicaments and process for their preparation
DE10337863A1 (de) * 2003-08-18 2005-03-17 Merck Patent Gmbh Verwendung von Chromen-4-on-Derivaten
CA2540730C (fr) * 2003-10-01 2012-08-21 Merck Patent Gmbh Antagonistes d'integrine alfavbeta3 et alfavbeta6 en tant qu'agents antifibrosants
JP2007536344A (ja) * 2004-05-04 2007-12-13 ノボ ノルディスク アクティーゼルスカブ 新規のインドール誘導体
EP1828144A2 (fr) * 2004-11-12 2007-09-05 OSI Pharmaceuticals, Inc. Antagonistes de l'integrine utiles en tant qu'agents anticancereux
US7777040B2 (en) 2005-05-03 2010-08-17 Cgi Pharmaceuticals, Inc. Certain substituted ureas, as modulators of kinase activity
CN102335168B (zh) * 2011-10-25 2014-04-02 合肥博太医药生物技术发展有限公司 吲哚-3-甲醇、二吲哚甲烷及其衍生物在制备治疗骨质疏松药物中的应用
AR094812A1 (es) * 2013-02-20 2015-08-26 Eisai R&D Man Co Ltd Derivado de piridina monocíclico como inhibidor del fgfr
CA2956270C (fr) 2014-08-18 2022-08-09 Eisai R&D Management Co., Ltd. Sel de derive de pyridine monocyclique et son cristal
JPWO2019189241A1 (ja) 2018-03-28 2021-03-18 エーザイ・アール・アンド・ディー・マネジメント株式会社 肝細胞癌治療剤

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT290523B (de) * 1962-01-05 1971-06-11 Merck & Co Inc Verfahren zur Herstellung neuer α-(3-Indolyl)-carbonsäuren
GB1148909A (en) * 1965-04-19 1969-04-16 Sumitomo Chemical Co Process for production of novel phenylhydrazone and phenylhydrazine derivatives
US4824850A (en) * 1982-05-18 1989-04-25 University Of Florida Brain-specific drug delivery
US4983615A (en) * 1989-06-28 1991-01-08 Hoechst-Roussel Pharmaceuticals Inc. Heteroarylamino- and heteroaryloxypyridinamine compounds which are useful in treating skin disorders
IT1244548B (it) * 1991-02-06 1994-07-15 Poli Ind Chimica Spa Derivati della 5-oxo-l-prolina e loro applicazioni farmaceutiche
GB9225141D0 (en) 1992-12-01 1993-01-20 Smithkline Beecham Corp Chemical compounds
JP2000508319A (ja) 1996-04-10 2000-07-04 メルク エンド カンパニー インコーポレーテッド αvβ3拮抗薬
PT923548E (pt) * 1996-08-27 2003-06-30 Wyeth Corp 4-aminoetoxi-indolos como agonistas d2 da dopaminae como ligandos da 5ht1a
AU1687699A (en) * 1997-12-25 1999-07-19 Yamanouchi Pharmaceutical Co., Ltd. Nitrogenous heterocyclic derivatives
MXPA00008216A (es) * 1998-02-23 2004-11-22 Univ South Alabama Acidos indol-3-propionicos, sales y esteres de los mismos utilizados como medicamentos.
AU765427B2 (en) * 1998-02-25 2003-09-18 Genetics Institute, Llc Inhibitors of phospholipase enzymes
AU3386299A (en) * 1998-04-08 1999-10-25 American Home Products Corporation N-aryloxyethylamine derivatives for the treatment of depression
AU3386199A (en) * 1998-04-08 1999-10-25 American Home Products Corporation N-aryloxyethyl-indoly-alkylamines for the treatment of depression (5-ht1a receptor active agents)
JP4425699B2 (ja) * 2004-05-17 2010-03-03 川崎重工業株式会社 小型滑走艇

Also Published As

Publication number Publication date
CZ20022616A3 (cs) 2002-10-16
KR20020073585A (ko) 2002-09-27
AU2001231664C1 (en) 2006-10-05
BR0108154A (pt) 2003-01-21
RU2002123332A (ru) 2004-01-10
US6743810B2 (en) 2004-06-01
ECSP013923A (es) 2002-09-27
CN1398264A (zh) 2003-02-19
AU2001231664B2 (en) 2006-02-23
EP1254133B9 (fr) 2005-09-07
DE50105955D1 (de) 2005-05-25
PE20011125A1 (es) 2001-11-07
CA2399813A1 (fr) 2001-08-16
JP2003530319A (ja) 2003-10-14
WO2001058893A3 (fr) 2002-04-18
US20030045728A1 (en) 2003-03-06
WO2001058893A2 (fr) 2001-08-16
AU3166401A (en) 2001-08-20
PL356427A1 (en) 2004-06-28
CN1214026C (zh) 2005-08-10
HUP0302671A2 (hu) 2003-12-29
EP1254133B1 (fr) 2005-04-20
NO20023770L (no) 2002-08-09
JP4938194B2 (ja) 2012-05-23
ES2240400T3 (es) 2005-10-16
SK11152002A3 (sk) 2003-01-09
IL151154A0 (en) 2003-04-10
EP1254133A2 (fr) 2002-11-06
DE10006139A1 (de) 2001-08-16
CA2399813C (fr) 2010-03-09
NZ521260A (en) 2004-02-27
RU2257380C2 (ru) 2005-07-27
ATE293620T1 (de) 2005-05-15
CO5261548A1 (es) 2003-03-31
MXPA02007732A (es) 2002-10-11
PT1254133E (pt) 2005-09-30
AR027398A1 (es) 2003-03-26
NO20023770D0 (no) 2002-08-09
HK1051863A1 (en) 2003-08-22

Similar Documents

Publication Publication Date Title
ZA200207273B (en) Indol-3-yl-derivatives and their use as integrin inhibitors.
CA2259224A1 (fr) Derives de phenylalanine utilises comme inhibiteurs de l'integrine
US6559144B2 (en) Bicyclic amino acids
RU2187506C2 (ru) Бициклические ароматические аминокислоты
ZA200308024B (en) Inhibitors of integrin alphavbeta6.
RU2234505C2 (ru) Производные хроменона и хроманона в качестве ингибиторов интегринов
CA2431974C (fr) Derives d'uree and d'urethanne en tant qu'inhibiteurs de l'integrine
US6649613B1 (en) Diacylhydrazine derivatives
CZ20033000A3 (cs) Inhibitory integrinů a(v)B6
US20040138284A1 (en) Indol-3-yl derivatives
JP2003507458A (ja) 新規なインテグリンαvβ3阻害剤
UA55439C2 (uk) Похідні циклопептидів, спосіб їх одержання, фармацевтична композиція, спосіб її одержання
ZA200302253B (en) Biphenyl derivatives and the use thereof as integrin inhibitors.
JP2002542231A (ja) 血栓症、骨粗鬆症、動脈硬化症を処置するためのジベンゾアズレン誘導体
JP2003506439A (ja) フルオレン誘導体
Schadt et al. Inhibitors of integrin α ν β 6
DE19912187A1 (de) Tetrahydrofuranderivate