[go: up one dir, main page]

DE602004011578D1 - Tetrahydroisochinolin- und tetrahydrobenzazepin derivative als igf-1r inhibitoren - Google Patents

Tetrahydroisochinolin- und tetrahydrobenzazepin derivative als igf-1r inhibitoren

Info

Publication number
DE602004011578D1
DE602004011578D1 DE602004011578T DE602004011578T DE602004011578D1 DE 602004011578 D1 DE602004011578 D1 DE 602004011578D1 DE 602004011578 T DE602004011578 T DE 602004011578T DE 602004011578 T DE602004011578 T DE 602004011578T DE 602004011578 D1 DE602004011578 D1 DE 602004011578D1
Authority
DE
Germany
Prior art keywords
tetrahydroisochinoline
tetrahydrobenzazepine
igf
inhibitors
derivative
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.)
Expired - Lifetime
Application number
DE602004011578T
Other languages
English (en)
Other versions
DE602004011578T2 (de
Inventor
Jan Gunzinger
Kurt Leander
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.)
Analytecon SA
Original Assignee
Analytecon SA
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 Analytecon SA filed Critical Analytecon SA
Publication of DE602004011578D1 publication Critical patent/DE602004011578D1/de
Application granted granted Critical
Publication of DE602004011578T2 publication Critical patent/DE602004011578T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • 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
    • 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
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • 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
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/14Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
    • C07D217/16Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals substituted by oxygen atoms
    • 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

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)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Transplantation (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
DE602004011578T 2004-03-12 2004-03-12 Tetrahydroisochinolin- und tetrahydrobenzazepin derivative als igf-1r inhibitoren Expired - Lifetime DE602004011578T2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CH2004/000147 WO2005087743A1 (en) 2004-03-12 2004-03-12 Tetrahydroisoquinoline-and tetrahydrobenzazepine derivatives as igf-1r inhibitors

Publications (2)

Publication Number Publication Date
DE602004011578D1 true DE602004011578D1 (de) 2008-03-13
DE602004011578T2 DE602004011578T2 (de) 2009-02-19

Family

ID=34957074

Family Applications (1)

Application Number Title Priority Date Filing Date
DE602004011578T Expired - Lifetime DE602004011578T2 (de) 2004-03-12 2004-03-12 Tetrahydroisochinolin- und tetrahydrobenzazepin derivative als igf-1r inhibitoren

Country Status (21)

Country Link
US (1) US7875631B2 (de)
EP (1) EP1732898B1 (de)
JP (1) JP2007528877A (de)
CN (1) CN100590118C (de)
AR (1) AR049323A1 (de)
AT (1) ATE384700T1 (de)
AU (1) AU2004317166B2 (de)
BR (1) BRPI0418462A (de)
CA (1) CA2555745C (de)
DE (1) DE602004011578T2 (de)
DK (1) DK1732898T3 (de)
EA (1) EA200601687A1 (de)
ES (1) ES2299825T3 (de)
IL (1) IL177307A (de)
NO (1) NO20063794L (de)
PL (1) PL1732898T3 (de)
PT (1) PT1732898E (de)
SI (1) SI1732898T1 (de)
TW (1) TW200530213A (de)
WO (1) WO2005087743A1 (de)
ZA (1) ZA200607198B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1940796A1 (de) * 2005-09-09 2008-07-09 Analytecon S.A. Isochinolinderivate als igf-1r-inhibitoren
EP1931636B1 (de) * 2005-09-09 2011-04-13 Analytecon S.A. Isochinoline als igf-1r-inhibitoren
US8476297B2 (en) 2007-12-04 2013-07-02 Amgen Inc. TRP-M8 receptor ligands and their use in treatments
WO2011112666A1 (en) 2010-03-09 2011-09-15 OSI Pharmaceuticals, LLC Combination anti-cancer therapy
AU2011275417A1 (en) 2010-07-05 2013-02-21 Actelion Pharmaceuticals Ltd 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin D2 receptor modulators
JP2014510265A (ja) 2011-02-02 2014-04-24 アムジェン インコーポレイテッド Igf−1rの阻害に関する方法および組成物
US9700619B2 (en) 2011-11-11 2017-07-11 Duke University Combination drug therapy for the treatment of solid tumors
TW201331179A (zh) 2011-12-21 2013-08-01 Actelion Pharmaceuticals Ltd 雜環衍生物及其作為前列腺素d2受體調節劑之用途
CA2876808A1 (en) 2012-07-05 2014-01-09 Actelion Pharmaceuticals Ltd 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators
US8980259B2 (en) 2012-07-20 2015-03-17 Novartis Ag Combination therapy
CN104672136B (zh) * 2013-11-30 2017-01-25 沈阳药科大学 1‑取代菲基‑n‑烷基(酰基)‑6,7‑二甲氧基‑1,2,3,4‑四氢异喹啉衍生物及其制备方法和用途
WO2017129763A1 (en) 2016-01-28 2017-08-03 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of signet ring cell gastric cancer
CN112500345B (zh) * 2020-12-18 2022-06-21 西安石油大学 α-氰基季碳取代四氢异喹啉化合物的合成方法
WO2024067463A1 (zh) * 2022-09-27 2024-04-04 苏州阿尔脉生物科技有限公司 苯并[7]环烯类衍生物、包含其的药物组合物及其医药用途

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4349472A (en) 1979-04-27 1982-09-14 Schering Corporation (S)-8(1-Adamantanecarbonyloxy)-7-chloro-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine
CA1330560C (en) * 1986-05-21 1994-07-05 Maurits E. A. Vandewalle Di- and tetrahydroisoquinoline derivatives
WO1990002119A1 (fr) * 1988-08-18 1990-03-08 Banyu Pharmaceutical Co., Ltd. Derives de 1,2,3,4-tetrahydro-isoquinoline
WO2000035455A1 (en) 1998-12-15 2000-06-22 Telik, Inc. Heteroaryl-aryl ureas as igf-1 receptor antagonists
EP1113007A1 (de) * 1999-12-24 2001-07-04 Pfizer Inc. Tetrahydroisochinolin-Verbindungen zur Verwendung als Östrogen-Agonisten/-Antagonisten
WO2002046164A1 (en) * 2000-12-07 2002-06-13 Astrazeneca Ab Therapeutic compounds
SE0102168D0 (sv) 2001-06-19 2001-06-19 Karolinska Innovations Ab New use and new compounds
SE0104140D0 (sv) * 2001-12-07 2001-12-07 Astrazeneca Ab Novel Compounds
GB0212303D0 (en) 2002-05-28 2002-07-10 Isis Innovation Molecular targetting of IGF-1 receptor

Also Published As

Publication number Publication date
CN1922147A (zh) 2007-02-28
US7875631B2 (en) 2011-01-25
EP1732898A1 (de) 2006-12-20
IL177307A (en) 2011-09-27
NO20063794L (no) 2006-12-12
DK1732898T3 (da) 2008-05-13
CA2555745A1 (en) 2005-09-22
ATE384700T1 (de) 2008-02-15
AR049323A1 (es) 2006-07-19
SI1732898T1 (sl) 2008-06-30
WO2005087743A1 (en) 2005-09-22
IL177307A0 (en) 2006-12-10
ZA200607198B (en) 2008-04-30
TW200530213A (en) 2005-09-16
PT1732898E (pt) 2008-04-07
AU2004317166A1 (en) 2005-09-22
CA2555745C (en) 2011-05-31
EA200601687A1 (ru) 2007-04-27
DE602004011578T2 (de) 2009-02-19
BRPI0418462A (pt) 2007-06-05
US20070129399A1 (en) 2007-06-07
EP1732898B1 (de) 2008-01-23
AU2004317166B2 (en) 2010-11-11
CN100590118C (zh) 2010-02-17
PL1732898T3 (pl) 2008-06-30
ES2299825T3 (es) 2008-06-01
JP2007528877A (ja) 2007-10-18

Similar Documents

Publication Publication Date Title
CY2022001I1 (el) Παραγωγα του uk-2a
ATE423121T1 (de) Diphenylimidazopyrimidin- und -imidazolamine als b-sekretase-inhibitoren
ATE400271T1 (de) Aryl-pyridinderivate als 11-beta-hsd1-hemmer
ATE540936T1 (de) Substituierte 2-alkyl-chinazolinonderivate als parp-hemmer
ATE420076T1 (de) Indozolonderivate als 11b-hsd1-inhibitoren
ATE520671T1 (de) Pyrimidin-harnstoff-derivate als kinase-hemmer
DE602005017215D1 (de) Thiadiazolidinone als GSK3-Inhibitoren
ATE452631T1 (de) N-2-adamantanyl-2-phenoxy-acetamid-derivate als 11-betahydroxysteroid-dehydrogenase-hemmer
PT1586571E (pt) Inibidores da dipeptidil-peptidase
ATE527240T1 (de) Polyzyklische indazol-derivate als erk-hemmer
ATE437876T1 (de) Hexahydropyridoisochinoline als dpp-iv- inhibitoren
DE602006011363D1 (de) Heteroaryl-substituierte piperidin-derivate als l-cpt1-hemmer
ATE485268T1 (de) Pyrrolidin-derivate als erk-hemmer
DK2253614T3 (da) IAP-inhibitorer
DK1778718T3 (da) Iap-inhibitorer
DE602007008837D1 (de) Als protein-kinase-inhibitoren nutzbare dyhydrodiazepine
ATE531705T1 (de) Substituierte 2-chinolyloxazole geeignet als pde4 inhibitoren
ZA200610771B (en) Quinazolinedolone derivatives as PARP inhibitors
ATE501138T1 (de) Thiophenderivate als chk-1-inhibitoren
ATE478868T1 (de) Pyrrolodihydroisochinoline als pde10- inhibitoren
ATE553079T1 (de) Heteroarylphenylharnstoffderivat
ATE509011T1 (de) Pyrimidinderivate als 11beta-hsd1-inhibitoren
ATE462692T1 (de) 3-amino-1-arylpropyl-indole als monoamin- wiederaufnahmehemmer
DE602004011578D1 (de) Tetrahydroisochinolin- und tetrahydrobenzazepin derivative als igf-1r inhibitoren
ATE433449T1 (de) Kinaseinhibitoren

Legal Events

Date Code Title Description
8364 No opposition during term of opposition