AU2002212895A1 - N-type calcium channel antagonists for the treatment of pain - Google Patents

N-type calcium channel antagonists for the treatment of pain

Info

Publication number
AU2002212895A1
AU2002212895A1 AU2002212895A AU1289502A AU2002212895A1 AU 2002212895 A1 AU2002212895 A1 AU 2002212895A1 AU 2002212895 A AU2002212895 A AU 2002212895A AU 1289502 A AU1289502 A AU 1289502A AU 2002212895 A1 AU2002212895 A1 AU 2002212895A1
Authority
AU
Australia
Prior art keywords
pain
treatment
calcium channel
type calcium
channel antagonists
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
AU2002212895A
Inventor
Marc Chapdelaine
Lucius Kemp
John Mccauley
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.)
AstraZeneca AB
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
Publication of AU2002212895A1 publication Critical patent/AU2002212895A1/en
Abandoned 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic 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
    • A61K31/47064-Aminoquinolines; 8-Aminoquinolines, e.g. chloroquine, primaquine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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 chain containing hetero atoms as chain links
AU2002212895A 2000-11-06 2001-10-31 N-type calcium channel antagonists for the treatment of pain Abandoned AU2002212895A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE0004054 2000-11-06
SE0004054A SE0004054D0 (en) 2000-11-06 2000-11-06 N-type calcium channel antagonists for the treatment of pain
PCT/SE2001/002389 WO2002036567A1 (en) 2000-11-06 2001-10-31 N-type calcium channel antagonists for the treatment of pain

Publications (1)

Publication Number Publication Date
AU2002212895A1 true AU2002212895A1 (en) 2002-05-15

Family

ID=20281714

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002212895A Abandoned AU2002212895A1 (en) 2000-11-06 2001-10-31 N-type calcium channel antagonists for the treatment of pain

Country Status (6)

Country Link
US (2) US7189714B2 (en)
EP (1) EP1339688A1 (en)
JP (1) JP2004513116A (en)
AU (1) AU2002212895A1 (en)
SE (1) SE0004054D0 (en)
WO (1) WO2002036567A1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020121638A1 (en) * 2000-06-30 2002-09-05 Vladimir Grushin Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds
US6900226B2 (en) * 2000-09-06 2005-05-31 Hoffman-La Roche Inc. Neuropeptide Y antagonists
DE10316659A1 (en) * 2003-04-11 2004-10-28 Boehringer Ingelheim Pharma Gmbh & Co. Kg Tricyclic heteroaromatic compounds
WO2005000285A2 (en) * 2003-06-13 2005-01-06 Dynogen Pharmaceuticals, Inc. METHODS OF TREATING NON-INFLAMMATORY GASTROINTESTINAL TRACT DISORDERS USING Cav2.2 SUBUNIT CALCIUM CHANNEL MODULATORS
RU2440991C2 (en) * 2004-09-02 2012-01-27 Вертекс Фармасьютикалз Инкорпорейтед Quinazoline effective as ion channel modulators
US8084260B2 (en) * 2004-11-24 2011-12-27 Applied Biosystems, Llc Spectral calibration method and system for multiple instruments
ATE453638T1 (en) * 2006-07-31 2010-01-15 Rottapharm Spa AMIDENE DERIVATIVES OF 2-HETEROARYLQUINAZOLINES AND QUINOLINES; EFFECTIVE ANALGESICS AND ANTI-INFLAMMATORY AGENTS
US8987301B2 (en) 2009-11-07 2015-03-24 Merck Patent Gmbh Heteroarylaminoquinolines as TGF-beta receptor kinase inhibitors
EP2549872B1 (en) * 2010-03-23 2015-11-25 GlaxoSmithKline LLC Trpv4 antagonists
WO2011119693A1 (en) * 2010-03-23 2011-09-29 Glaxosmithkline Llc Trpv4 antagonists
AU2011321310B2 (en) * 2010-10-29 2016-02-11 Clino Ltd. Tau imaging probe
CA2922542A1 (en) * 2013-11-22 2015-05-28 University Of Kentucky Research Foundation Arylquinoline and analog compounds and use thereof to treat cancer
CA3227251A1 (en) * 2021-08-09 2023-02-16 Jianguang HAN Ferroptosis modulators, preparations, and uses thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2568778A (en) * 1948-05-28 1951-09-25 Sterling Drug Inc Tertiary-aminoalkyl-alpha-arylalpha-(4-quinolyl) acetates and amides and their preparation
US2616889A (en) * 1948-07-05 1952-11-04 Roussel Uclaf Condensation products of the sugars with derivatives of esculetol and process
GB794043A (en) * 1955-06-03 1958-04-30 Ici Ltd New quinoline derivatives
US4816588A (en) * 1986-09-12 1989-03-28 American Cyanamid Company Method for the preparation of pyridine-2,3-dicarboxylic acids
HUP0101275A3 (en) * 1998-03-26 2002-12-28 Japan Tobacco Inc Amide derivatives and pharmaceutical compositions containing them as nociceptin antagonists
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
EP1147094A1 (en) 1999-01-15 2001-10-24 Novo Nordisk A/S Non-peptide glp-1 agonists
US6927214B1 (en) * 1999-01-15 2005-08-09 Novo Nordisk A/S Non-peptide GLP-1 agonists

Also Published As

Publication number Publication date
US20040077644A1 (en) 2004-04-22
US7348340B2 (en) 2008-03-25
US20070129363A1 (en) 2007-06-07
US7189714B2 (en) 2007-03-13
WO2002036567A1 (en) 2002-05-10
JP2004513116A (en) 2004-04-30
EP1339688A1 (en) 2003-09-03
SE0004054D0 (en) 2000-11-06

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