SE0100568D0 - Compounds - Google Patents

Compounds

Info

Publication number
SE0100568D0
SE0100568D0 SE0100568A SE0100568A SE0100568D0 SE 0100568 D0 SE0100568 D0 SE 0100568D0 SE 0100568 A SE0100568 A SE 0100568A SE 0100568 A SE0100568 A SE 0100568A SE 0100568 D0 SE0100568 D0 SE 0100568D0
Authority
SE
Sweden
Prior art keywords
compounds
compound
relates
present
gnrh
Prior art date
Application number
SE0100568A
Other languages
Swedish (sv)
Inventor
Alexander Dossetter
Peter Kenny
Darren Mckerrecher
Michael Wardleworth
Original Assignee
Astrazeneca 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 Astrazeneca Ab filed Critical Astrazeneca Ab
Priority to SE0100568A priority Critical patent/SE0100568D0/en
Publication of SE0100568D0 publication Critical patent/SE0100568D0/en
Priority to PCT/GB2002/000677 priority patent/WO2002066478A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

The present invention relates to compounds of formula I which are antagonists of gonadotropin releasing hormone (GnRH) activity. The invention also relates to pharmaceutical formulations, the use of a compound of the present invention in the manufacture of a medicament, a method of therapeutic treatment using such a compound and processes for producing the compounds.
SE0100568A 2001-02-20 2001-02-20 Compounds SE0100568D0 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SE0100568A SE0100568D0 (en) 2001-02-20 2001-02-20 Compounds
PCT/GB2002/000677 WO2002066478A1 (en) 2001-02-20 2002-02-15 Antagonists of gonadotropin releasing hormone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE0100568A SE0100568D0 (en) 2001-02-20 2001-02-20 Compounds

Publications (1)

Publication Number Publication Date
SE0100568D0 true SE0100568D0 (en) 2001-02-20

Family

ID=20283058

Family Applications (1)

Application Number Title Priority Date Filing Date
SE0100568A SE0100568D0 (en) 2001-02-20 2001-02-20 Compounds

Country Status (2)

Country Link
SE (1) SE0100568D0 (en)
WO (1) WO2002066478A1 (en)

Families Citing this family (55)

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DE10247271A1 (en) * 2002-10-10 2004-08-26 Grünenthal GmbH Use of new and known 7-(methyl or trifluoromethyl)-imidazo-(1,2-a)-pyridines as nitrogen monoxide synthase inhibitors useful e.g. for treating migraine, neurodegenerative diseases, inflammatory pain, diabetes or cancer
GB0320806D0 (en) 2003-09-05 2003-10-08 Astrazeneca Ab Therapeutic treatment
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AR064491A1 (en) 2006-12-22 2009-04-08 Astex Therapeutics Ltd IMIDAZO DERIVATIVES [1, 2-A] PYRIMIDINE, A PROCESS FOR PREPARATION, A PHARMACEUTICAL COMPOSITION THAT INCLUDES THEM AND ITS USE IN THE TREATMENT OF DISEASES MEDIATED BY FGFR KINASES.
CA2672213C (en) 2006-12-22 2016-02-16 Astex Therapeutics Limited Bicyclic amine derivatives as protein tyrosine kinase inhibitors
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EP2180893B1 (en) 2007-08-09 2014-11-12 Urifer Ltd Pharmaceutical compositions and methods for the treatment of cancer
GB0720038D0 (en) 2007-10-12 2007-11-21 Astex Therapeutics Ltd New compounds
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EP2072516A1 (en) 2007-12-21 2009-06-24 Santhera Pharmaceuticals (Schweiz) AG Substituted imidazopyridine derivates as Melancortin-4 receptor antagonists
EP2103614A1 (en) 2008-03-18 2009-09-23 Santhera Pharmaceuticals (Schweiz) AG Substituted imidazopyrimidine, imidazopyrazine and imidazopyridazine derivatives as melanocortin-4 receptor modulators
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CA2796311A1 (en) 2010-04-14 2011-10-20 Incyte Corporation Fused derivatives as pi3k.delta. inhibitors
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
ES2764848T3 (en) 2010-12-20 2020-06-04 Incyte Holdings Corp N- (1- (substituted phenyl) ethyl) -9H-purine-6-amines as PI3K inhibitors
KR20140048079A (en) 2011-02-01 2014-04-23 교와 핫꼬 기린 가부시키가이샤 Ring-fused heterocyclic derivative
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
MX344600B (en) 2011-06-27 2016-12-20 Janssen Pharmaceutica Nv 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES.
US8883819B2 (en) 2011-09-01 2014-11-11 Irm Llc Bicyclic heterocycle derivatives for the treatment of pulmonary arterial hypertension
EP2751109B1 (en) 2011-09-02 2016-11-30 Incyte Holdings Corporation Heterocyclylamines as pi3k inhibitors
AR090548A1 (en) 2012-04-02 2014-11-19 Incyte Corp BICYCLIC AZAHETEROCICLOBENCILAMINS AS PI3K INHIBITORS
JP6426603B2 (en) 2012-06-26 2018-11-21 ヤンセン ファーマシューティカ エヌ．ベー． A PDE2 inhibitor such as a 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] -quinoxaline compound and a PDE10 inhibitor for use in the treatment of a neurological or metabolic disorder combination
BR112015000459B1 (en) 2012-07-09 2022-02-08 Janssen Pharmaceutica N.V. PHOSPHODIESTERASE 10 ENZYME INHIBITORS, THEIR USE, PHARMACEUTICAL COMPOSITION INCLUDING THEM, THEIR PREPARATION PROCESS AND PRODUCT
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US9073921B2 (en) 2013-03-01 2015-07-07 Novartis Ag Salt forms of bicyclic heterocyclic derivatives
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
EP3262046B1 (en) 2015-02-27 2020-11-04 Incyte Corporation Salts of pi3k inhibitor and processes for their preparation
WO2016183063A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Crystalline forms of a pi3k inhibitor
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
EP3386993A1 (en) 2015-12-10 2018-10-17 Bayer Pharma Aktiengesellschaft Substituted perhydropyrrolo[3,4-c]pyrrole derivatives and the use of same
EA201891374A1 (en) 2015-12-10 2018-11-30 Байер Фарма Акциенгезельшафт SUBSTITUTED 2-PHENYL-3- (PIPERAZINMETHIL) IMIDAZOPIRIDINES AND THEIR APPLICATION
US9926316B2 (en) * 2016-03-03 2018-03-27 The Cleveland Clinic Foundation Antitumor derivatives for differentiation therapy
JOP20190005A1 (en) 2016-07-20 2019-01-20 Bayer Ag Substituted diazahetero-bicyclic compounds and their use
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CA3073656C (en) 2017-09-22 2024-03-05 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
DK3697785T3 (en) 2017-10-18 2023-04-03 Jubilant Epipad LLC IMIDAZO-PYRIDINE COMPOUNDS AS PAD INHIBITORS
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US11459338B2 (en) 2017-11-24 2022-10-04 Jubilant Episcribe Llc Heterocyclic compounds as PRMT5 inhibitors
KR20200131845A (en) 2018-03-13 2020-11-24 주빌런트 프로델 엘엘씨 Bicyclic compounds as inhibitors of PD1/PD-L1 interaction/activation

Family Cites Families (2)

* Cited by examiner, † Cited by third party
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WO1999051596A1 (en) * 1998-04-02 1999-10-14 Merck & Co., Inc. Antagonists of gonadotropin releasing hormone
EP1171135A4 (en) * 1999-03-10 2002-05-15 Merck & Co Inc 6-azaindole compounds as antagonists of gonadotropin releasing hormone

Also Published As

Publication number Publication date
WO2002066478A1 (en) 2002-08-29

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