GB2396613A - Five-membered heterocyclic compounds in the treatment of chronic and acute pain - Google Patents

Five-membered heterocyclic compounds in the treatment of chronic and acute pain Download PDF

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Publication number
GB2396613A
GB2396613A GB0406869A GB0406869A GB2396613A GB 2396613 A GB2396613 A GB 2396613A GB 0406869 A GB0406869 A GB 0406869A GB 0406869 A GB0406869 A GB 0406869A GB 2396613 A GB2396613 A GB 2396613A
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United Kingdom
Prior art keywords
chronic
treatment
acute pain
membered heterocyclic
heterocyclic compounds
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Withdrawn
Application number
GB0406869A
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GB0406869D0 (en
Inventor
Lars Jacob Stray Knutsen
Christopher John Hobbbs
Fleur Radford
Andrea Fiumana
Christopher Geoffrey Earnshaw
Sarah Louise Mellor
Nichola Jane Smith
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Ionix Pharmaceuticals Ltd
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Ionix Pharmaceuticals Ltd
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Priority claimed from GB0219721A external-priority patent/GB0219721D0/en
Priority claimed from GB0219719A external-priority patent/GB0219719D0/en
Application filed by Ionix Pharmaceuticals Ltd filed Critical Ionix Pharmaceuticals Ltd
Publication of GB0406869D0 publication Critical patent/GB0406869D0/en
Publication of GB2396613A publication Critical patent/GB2396613A/en
Withdrawn legal-status Critical Current

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    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/341Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
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    • A61K31/381Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/427Thiazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4425Pyridinium derivatives, e.g. pralidoxime, pyridostigmine
    • AHUMAN NECESSITIES
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4436Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Toxicology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

Compounds of formula (I) are found to antagonise N-type calcium channels F(I) wherein R<1>, R<2> and R<4> are organic residues, Y is a linker and R<3> is aryl, heteroaryl, carbocyclyl a heterocyclyl are N-type calcium channel antagonists and are therefore useful in the treatment of both chronic and acute pain.

Description

GB 2396613 A continuation (72) cont (56) cont Fleur Radford Asian Journal
of Chemistry, 2002, Vol. 14(21, pages Andrea Fiumana 718-722 Christopher Geoffrey Earnshaw Sarah Louise Mellor (58) Field of Search by ISA:
Nichola Jane Smith INT CLOT A61K Other: EPO-lnternal, CHEW ABS Data, EMBASE, BIOSIS (74) Agent and/or Address for Service: J A Kemp & Co. 14 South Square, Gray's Inn, LONDON, WC1R 5JJ, United Kingdom
GB0406869A 2002-08-23 2003-08-22 Five-membered heterocyclic compounds in the treatment of chronic and acute pain Withdrawn GB2396613A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0219721A GB0219721D0 (en) 2002-08-23 2002-08-23 Therapeutic compounds
GB0219719A GB0219719D0 (en) 2002-08-23 2002-08-23 Chemical compounds
PCT/GB2003/003674 WO2004017966A1 (en) 2002-08-23 2003-08-22 Five-membered heterocyclic compounds in the treatment of chronic and acute pain

Publications (2)

Publication Number Publication Date
GB0406869D0 GB0406869D0 (en) 2004-04-28
GB2396613A true GB2396613A (en) 2004-06-30

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GB0406869A Withdrawn GB2396613A (en) 2002-08-23 2003-08-22 Five-membered heterocyclic compounds in the treatment of chronic and acute pain

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AU (2) AU2003255843A1 (en)
GB (1) GB2396613A (en)
TW (1) TW200412948A (en)
WO (2) WO2004017965A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7834000B2 (en) * 2006-06-13 2010-11-16 Vertex Pharmaceuticals Incorporated CGRP receptor antagonists
MX2008015906A (en) * 2006-06-13 2009-03-06 Vertex Pharma Cgrp receptor antagonists.
US8163737B2 (en) 2006-06-13 2012-04-24 Vertex Pharmaceuticals Incorporated CGRP receptor antagonists
WO2008090356A1 (en) * 2007-01-25 2008-07-31 Betagenon Ab Thiazolidinone derivatives useful in the treatment of cancer and disorders caused by excess adiposity
WO2008099615A1 (en) 2007-02-16 2008-08-21 Aska Pharmaceutical Co., Ltd. Pharmaceutical composition containing fine particle oil-based suspension
WO2008132139A2 (en) * 2007-04-27 2008-11-06 Ucb Pharma S.A. New heterocyclic derivatives useful for the treatment of cns disorders
KR20120023767A (en) * 2009-05-12 2012-03-13 액테리온 파마슈티칼 리미티드 Thiazolidin-4-one and [1,3]-thiazinan-4-one compounds as orexin receptor antagonists

Citations (7)

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US4019892A (en) * 1975-12-31 1977-04-26 Shell Oil Company Herbicidal heterocyclic compounds
EP0325496A1 (en) * 1988-01-22 1989-07-26 Sumitomo Pharmaceuticals Company, Limited 2-Pyridyl thiazolidin-4-one derivatives as anti-ulcer agents
US5061720A (en) * 1989-09-13 1991-10-29 A. H. Robins Company, Inc. Substituted-4-thiazolidinone derivatives
WO1999062891A1 (en) * 1998-06-05 1999-12-09 Icagen, Inc. Potassium channel inhibitors
WO2000063197A1 (en) * 1999-04-19 2000-10-26 Sumitomo Pharmaceuticals Company, Limited Hydroxamic acid derivative
WO2002009706A1 (en) * 2000-07-27 2002-02-07 Smithkline Beecham Corporation Agonists of follicle stimulating hormone activity
WO2003008398A1 (en) * 2001-07-16 2003-01-30 Euro-Celtique S.A. Aryl substituted thiazolidinones and the use thereof

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JPS5785380A (en) * 1980-11-18 1982-05-28 Hisamitsu Pharmaceut Co Inc Thiazolidone derivative
JPH0387300A (en) * 1989-04-21 1991-04-12 Reiko Co Ltd Three-dimensional pattern transfer foil and base material therefor
JPH0734846B2 (en) * 1990-05-22 1995-04-19 日揮株式会社 Method and apparatus for supplying high humidity sanitized gas
EP0705816B1 (en) * 1993-06-23 2000-09-20 Chugai Seiyaku Kabushiki Kaisha Benzene derivative useful for ischemic diseases
JPH07304689A (en) * 1994-05-10 1995-11-21 Sumitomo Pharmaceut Co Ltd Treating medicine for fulminant hepatitis and acute hepatic insufficiency
CA2208508A1 (en) * 1994-12-22 1996-06-27 Chugai Seiyaku Kabushiki Kaisha Therapeutic agent for ischemic diseases

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4019892A (en) * 1975-12-31 1977-04-26 Shell Oil Company Herbicidal heterocyclic compounds
EP0325496A1 (en) * 1988-01-22 1989-07-26 Sumitomo Pharmaceuticals Company, Limited 2-Pyridyl thiazolidin-4-one derivatives as anti-ulcer agents
US5061720A (en) * 1989-09-13 1991-10-29 A. H. Robins Company, Inc. Substituted-4-thiazolidinone derivatives
WO1999062891A1 (en) * 1998-06-05 1999-12-09 Icagen, Inc. Potassium channel inhibitors
WO2000063197A1 (en) * 1999-04-19 2000-10-26 Sumitomo Pharmaceuticals Company, Limited Hydroxamic acid derivative
WO2002009706A1 (en) * 2000-07-27 2002-02-07 Smithkline Beecham Corporation Agonists of follicle stimulating hormone activity
WO2003008398A1 (en) * 2001-07-16 2003-01-30 Euro-Celtique S.A. Aryl substituted thiazolidinones and the use thereof

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Asian Journal of Chemistry, 2002, Vol. 14(2), pages 718-722 *
Bioorganic & Medicinal Chemistry Letters, 1996, Vol. 6(6), pages 707-712 *
Bioorganic & Medicinal Chemistry Letters, 2000, Vol. 10(8), pages 715-717 *
Tetrahedron Letters, 1998, Vol. 39(40), pages 7223-7226 *

Also Published As

Publication number Publication date
TW200412948A (en) 2004-08-01
AU2003255843A1 (en) 2004-03-11
WO2004017966A1 (en) 2004-03-04
AU2003255844A1 (en) 2004-03-11
WO2004017965A1 (en) 2004-03-04
GB0406869D0 (en) 2004-04-28

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