[go: up one dir, main page]

AU2003288857A1 - New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor - Google Patents

New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor

Info

Publication number
AU2003288857A1
AU2003288857A1 AU2003288857A AU2003288857A AU2003288857A1 AU 2003288857 A1 AU2003288857 A1 AU 2003288857A1 AU 2003288857 A AU2003288857 A AU 2003288857A AU 2003288857 A AU2003288857 A AU 2003288857A AU 2003288857 A1 AU2003288857 A1 AU 2003288857A1
Authority
AU
Australia
Prior art keywords
igf
inhibitors
receptor
phenyl
new substituted
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
AU2003288857A
Inventor
Magnus Axelson
Olle Larsson
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.)
Swedish Orphan Biovitrum AB
Original Assignee
Axelar AB
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 Axelar AB filed Critical Axelar AB
Publication of AU2003288857A1 publication Critical patent/AU2003288857A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/70Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with ring systems containing two or more relevant rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dermatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU2003288857A 2002-12-18 2003-12-18 New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor Abandoned AU2003288857A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE0203746-3 2002-12-18
SE0203746A SE0203746D0 (en) 2002-12-18 2002-12-18 New compounds
PCT/SE2003/002010 WO2004054996A1 (en) 2002-12-18 2003-12-18 New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor

Publications (1)

Publication Number Publication Date
AU2003288857A1 true AU2003288857A1 (en) 2004-07-09

Family

ID=20289899

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2003288857A Abandoned AU2003288857A1 (en) 2002-12-18 2003-12-18 New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor

Country Status (3)

Country Link
AU (1) AU2003288857A1 (en)
SE (1) SE0203746D0 (en)
WO (1) WO2004054996A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7625859B1 (en) 2000-02-16 2009-12-01 Oregon Health & Science University HER-2 binding antagonists
US8044067B2 (en) * 2005-09-09 2011-10-25 Analytecon S.A. Isoquinolines as IGF-1R inhibitors
BRPI0616731A2 (en) * 2005-09-09 2016-08-23 Analytecon Sa isoquinoline derivatives as igf-1r inhibitors
WO2009100349A1 (en) 2008-02-09 2009-08-13 The Trustees Of Columbia University In The City Of New York Analogues of (-)-picropodophyllin, synthesis and uses thereof
WO2011083391A2 (en) 2010-01-05 2011-07-14 Pfizer Inc. Biomarkers for anti-igf-ir cancer therapy

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU201672B (en) * 1984-12-28 1990-12-28 Conpharm Ab Process for producing pharmaceutical compositions comprising podophyllotoxin
SE0102168D0 (en) * 2001-06-19 2001-06-19 Karolinska Innovations Ab New use and new compounds

Also Published As

Publication number Publication date
WO2004054996A1 (en) 2004-07-01
SE0203746D0 (en) 2002-12-18

Similar Documents

Publication Publication Date Title
AU2003280188A1 (en) Benzoxazin-3-ones and derivatives thereof as inhibitors of pi3k
AU2003235676A1 (en) Tricyclic-bis-enone derivatives and methods of use thereof
AU2003303231A1 (en) Benzoxazines and derivatives thereof as inhibitors of pi3ks
AU2003303128A1 (en) Inhibitors and methods of use thereof
PL375877A1 (en) Hydantoine derivatives and their use as tace inhibitors
AU2003237987A1 (en) Novel sweetener compositions and methods of use
AU2003217870A1 (en) Pini-modulating compounds and methods of use thereof
AU2003225669A1 (en) Pin1-modulating compounds and methods of use thereof
AU2003225668A1 (en) Pin1-modulating compounds and methods of use thereof
AU2003259735A1 (en) Small-mer compositions and methods of use
AU2003251559A1 (en) Heterocyclic inhibitors of kinases
AU2003213673A1 (en) Pin1-modulating compounds and methods of use thereof
AU2003302919A1 (en) Pyridine derivatives as jnk inhibitors and their use
AU2003217105A1 (en) Novel of cytokine inhibitors
AU2003269364A1 (en) Use of piperazine derivatives as ccr1 antagonists
AU2003299441A1 (en) Nf-hev compositions and methods of use
AU2003301216A1 (en) Novel use of liver x receptor agonists
AU2003240668A1 (en) Attenuation of metapneumovirus
AU2003210983A1 (en) Kinase inhibitors and methods of use thereof
AU2003279841A1 (en) Uses of human zven antagonists
AU2002238103A1 (en) Use of beta-lactamase inhibitors as neuroprotectants
HUP0401641A3 (en) Use of substituted diazonine derivatives as phosphorodiesterase iv inhibitors
AU2002367730A1 (en) Use of leukotriene receptor antagonist for treatment of scarring
AU2003288857A1 (en) New substituted 1-phenyl-tetrahydronaphtalene derivatives and their use as inhibitors of igf-1 receptor
AU2003297612A1 (en) 2-substituted-3-propenamide derivatives and methods of using the same

Legal Events

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