GB0130393D0 - Compounds - Google Patents

Compounds

Info

Publication number
GB0130393D0
GB0130393D0 GBGB0130393.2A GB0130393A GB0130393D0 GB 0130393 D0 GB0130393 D0 GB 0130393D0 GB 0130393 A GB0130393 A GB 0130393A GB 0130393 D0 GB0130393 D0 GB 0130393D0
Authority
GB
United Kingdom
Prior art keywords
compounds
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.)
Ceased
Application number
GBGB0130393.2A
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.)
SmithKline Beecham Ltd
Original Assignee
SmithKline Beecham Ltd
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 SmithKline Beecham Ltd filed Critical SmithKline Beecham Ltd
Priority to GBGB0130393.2A priority Critical patent/GB0130393D0/en
Publication of GB0130393D0 publication Critical patent/GB0130393D0/en
Priority to PCT/GB2002/005676 priority patent/WO2003051873A1/en
Priority to AU2002352389A priority patent/AU2002352389A1/en
Ceased legal-status Critical Current

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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
GBGB0130393.2A 2001-12-19 2001-12-19 Compounds Ceased GB0130393D0 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GBGB0130393.2A GB0130393D0 (en) 2001-12-19 2001-12-19 Compounds
PCT/GB2002/005676 WO2003051873A1 (en) 2001-12-19 2002-12-13 Piperazine compounds and their phamaceutical use
AU2002352389A AU2002352389A1 (en) 2001-12-19 2002-12-13 Piperazine compounds and their phamaceutical use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0130393.2A GB0130393D0 (en) 2001-12-19 2001-12-19 Compounds

Publications (1)

Publication Number Publication Date
GB0130393D0 true GB0130393D0 (en) 2002-02-06

Family

ID=9927958

Family Applications (1)

Application Number Title Priority Date Filing Date
GBGB0130393.2A Ceased GB0130393D0 (en) 2001-12-19 2001-12-19 Compounds

Country Status (3)

Country Link
AU (1) AU2002352389A1 (en)
GB (1) GB0130393D0 (en)
WO (1) WO2003051873A1 (en)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60309481T2 (en) * 2002-09-18 2007-06-21 Glaxo Group Ltd., Greenford CYCLIC N-AROYLAMINES AS OREXINE RECEPTOR ANTAGONISTS
DE60335891D1 (en) 2002-10-11 2011-03-10 Actelion Pharmaceuticals Ltd SULPHONYLAMINE ACID DERIVATIVES AND THEIR USE AS OREXIN RECEPTOR ANTAGONIST
TW200505447A (en) 2003-02-07 2005-02-16 Daiichi Seiyaku Co Pyrazole derivative
ATE383345T1 (en) 2003-04-28 2008-01-15 Actelion Pharmaceuticals Ltd QUINOXALIN-3-ONE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS.
AU2005250077B2 (en) 2004-03-01 2011-06-09 Idorsia Pharmaceuticals Ltd Substituted 1,2,3,4-tetrahydroisoquinoline derivatives
US7501395B2 (en) 2005-04-25 2009-03-10 Eisai R & D Management Co., Ltd. Method of screening for antianxiety drugs
AU2007245037A1 (en) 2006-03-29 2007-11-08 Merck Sharp & Dohme Corp. Diazepan orexin receptor antagonists
WO2008008517A2 (en) 2006-07-14 2008-01-17 Merck & Co., Inc. Bridged diazepan orexin receptor antagonists
ATE481383T1 (en) * 2006-09-29 2010-10-15 Actelion Pharmaceuticals Ltd 3-AZA-BICYCLOÄ3.1.0ÜHEXANE DERIVATIVES
US8133901B2 (en) 2006-12-01 2012-03-13 Actelion Pharmaceuticals Ltd. 3-heteroaryl (amino or amido)-1-(biphenyl or phenylthiazolyl) carbonylpiperidine derivatives as orexin receptor inhibitors
PE20081229A1 (en) 2006-12-01 2008-08-28 Merck & Co Inc DIAZEPAM OREXIN RECEPTOR ANTAGONISTS REPLACED
AR064561A1 (en) * 2006-12-28 2009-04-08 Actelion Pharmaceuticals Ltd DERIVATIVES OF 2-AZA-BICYCLE [3.1.0] HEXANE AND ITS USE IN THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OF DISEASES RELATED TO GENERAL DYSFUNCTIONS OF THE OREXINE SYSTEM.
CL2008000836A1 (en) 2007-03-26 2008-11-07 Actelion Pharmaceuticals Ltd Thiazolidine derivative compounds, orexin receptor antagonists; pharmaceutical composition that includes them; and its use in the treatment of emotional neurosis, severe depression, psychotic disorders, Alzheimer's, parkinson's, pain, among others.
CA2688776A1 (en) 2007-05-18 2008-11-27 Merck & Co., Inc. Oxo bridged diazepan orexin receptor antagonists
CA2687230A1 (en) 2007-05-23 2008-12-11 Merck & Co., Inc. Cyclopropyl pyrrolidine orexin receptor antagonists
UA99620C2 (en) 2007-05-23 2012-09-10 Мерк Шарп Энд Доме Корп. Pyridyl piperidine orexin receptor antagonists
AU2008281399A1 (en) 2007-07-27 2009-02-05 Actelion Pharmaceuticals Ltd 2-aza-bicyclo[3.3.0]octane derivatives
CA2699328A1 (en) 2007-09-24 2009-04-02 Actelion Pharmaceuticals Ltd Pyrrolidines and piperidines as orexin receptor antagonists
ATE555107T1 (en) 2008-02-21 2012-05-15 Actelion Pharmaceuticals Ltd 2-AZA-BICYCLO-Ä2,2,1-ÜHEPTAN DERIVATIVES
EP2275421A1 (en) 2009-07-15 2011-01-19 Rottapharm S.p.A. Spiro amino compounds suitable for the treatment of inter alia sleep disorders and drug addiction
AR088352A1 (en) 2011-10-19 2014-05-28 Merck Sharp & Dohme ANTAGONISTS OF THE RECEIVER OF 2-PIRIDILOXI-4-NITRILE OREXINE
US9440982B2 (en) 2012-02-07 2016-09-13 Eolas Therapeutics, Inc. Substituted prolines/piperidines as orexin receptor antagonists
JP6346862B2 (en) 2012-02-07 2018-06-20 エオラス セラピューティクス, インコーポレイテッド Substituted proline / piperidine as an orexin receptor antagonist
ES2617863T3 (en) 2012-06-04 2017-06-20 Actelion Pharmaceuticals Ltd. Benzimidazole-proline derivatives
CA2885180C (en) 2012-10-10 2021-03-02 Actelion Pharmaceuticals Ltd Orexin receptor antagonists which are [ortho bi-(hetero-)aryl]-[2-(meta bi-(hetero-)aryl)-pyrrolidin-1-yl]-methanone derivatives
KR20150130413A (en) 2013-03-12 2015-11-23 액테리온 파마슈티칼 리미티드 Azetidine amide derivatives as orexin receptor antagonists
UA119151C2 (en) 2013-12-03 2019-05-10 Ідорсія Фармасьютікалз Лтд Crystalline salt form of (s)-(2-(6-chloro-7-methyl-1 h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone as orexin receptor antagonist
CN105793257B (en) 2013-12-03 2018-11-13 爱杜西亚药品有限公司 The crystalline form and application thereof of benzimidazole cycle compound
MX366642B (en) 2013-12-04 2019-07-17 Idorsia Pharmaceuticals Ltd Use of benzimidazole-proline derivatives.
TW201613902A (en) 2014-08-13 2016-04-16 Eolas Therapeutics Inc Difluoropyrrolidines as orexin receptor modulators
CN109219606B (en) 2016-02-12 2021-10-01 阿斯利康(瑞典)有限公司 Halogen substituted piperidines as orexin receptor modulators
US20190151304A1 (en) 2016-05-10 2019-05-23 Inserm (Institut National De La Santé Et De La Rechercjae Médicale Methods and pharmaceutical compositions for the treatment of autoimmune inflammatory
WO2020007964A1 (en) 2018-07-05 2020-01-09 Idorsia Pharmaceuticals Ltd 2-(2-azabicyclo[3.1.0]hexan-1-yl)-1h-benzimidazole derivatives
WO2020099511A1 (en) 2018-11-14 2020-05-22 Idorsia Pharmaceuticals Ltd Benzimidazole-2-methyl-morpholine derivatives
AR129309A1 (en) 2022-05-13 2024-08-07 Idorsia Pharmaceuticals Ltd DERIVATIVES OF HYDRAZINE-N-CARBOXAMIDE CYCLIC SUBSTITUTED WITH THIAZOLOARYL-METHYL

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR900018073A (en) * 1988-05-23 1990-12-20 추후보충 Piperazine Compounds

Also Published As

Publication number Publication date
AU2002352389A1 (en) 2003-06-30
WO2003051873A1 (en) 2003-06-26

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Legal Events

Date Code Title Description
AT Applications terminated before publication under section 16(1)