CO5680444A2 - Agonista a-2 no sedante 1-(2,3-dimetil-fenil)-etil-1,3-dihidro-imidazol-2-tiona - Google Patents

Agonista a-2 no sedante 1-(2,3-dimetil-fenil)-etil-1,3-dihidro-imidazol-2-tiona

Info

Publication number
CO5680444A2
CO5680444A2 CO06017219A CO06017219A CO5680444A2 CO 5680444 A2 CO5680444 A2 CO 5680444A2 CO 06017219 A CO06017219 A CO 06017219A CO 06017219 A CO06017219 A CO 06017219A CO 5680444 A2 CO5680444 A2 CO 5680444A2
Authority
CO
Colombia
Prior art keywords
agonist
sedante
etil
tiona
imidazol
Prior art date
Application number
CO06017219A
Other languages
English (en)
Inventor
Ken Chow
Original Assignee
Allergan Inc
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 Allergan Inc filed Critical Allergan Inc
Publication of CO5680444A2 publication Critical patent/CO5680444A2/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/4164—1,3-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/84—Sulfur atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Otolaryngology (AREA)
  • Hospice & Palliative Care (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1.- Un agonista selectivo a-2A/a-1A, que comprende un compuesto representado por o su sal farmacéuticamente aceptable, éster, amida, estereoisómero o mezcla racémica.2.- El agonista selectivo a-2A/a-1A de la reivindicación 1, en donde dicho agonista selectivo tiene una eficacia a-1A menor que la de la brimonidina o un índice de potencia a-1A/a-2A mayor que el de la brimonidina.3.- El agonista selectivo a-2A/a-1A de la reivindicación 1, que comprende un compuesto representado por
CO06017219A 2003-09-12 2006-02-21 Agonista a-2 no sedante 1-(2,3-dimetil-fenil)-etil-1,3-dihidro-imidazol-2-tiona CO5680444A2 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US50256203P 2003-09-12 2003-09-12
US10/891,953 US7141597B2 (en) 2003-09-12 2004-07-15 Nonsedating α-2 agonists

Publications (1)

Publication Number Publication Date
CO5680444A2 true CO5680444A2 (es) 2006-09-29

Family

ID=34278841

Family Applications (1)

Application Number Title Priority Date Filing Date
CO06017219A CO5680444A2 (es) 2003-09-12 2006-02-21 Agonista a-2 no sedante 1-(2,3-dimetil-fenil)-etil-1,3-dihidro-imidazol-2-tiona

Country Status (26)

Country Link
US (4) US7141597B2 (es)
EP (2) EP1800679B1 (es)
JP (1) JP4698591B2 (es)
KR (1) KR101145046B1 (es)
CN (1) CN100417379C (es)
AT (2) ATE487477T1 (es)
AU (1) AU2004279332B2 (es)
BR (1) BRPI0413719A (es)
CA (1) CA2537832C (es)
CO (1) CO5680444A2 (es)
CY (1) CY1107608T1 (es)
DE (2) DE602004030051D1 (es)
DK (2) DK1800679T3 (es)
ES (1) ES2285522T3 (es)
HK (2) HK1092704A1 (es)
IL (1) IL173530A (es)
MX (1) MXPA06002668A (es)
NO (1) NO20060667L (es)
NZ (1) NZ545181A (es)
PL (2) PL1663206T3 (es)
PT (1) PT1663206E (es)
RU (1) RU2345987C2 (es)
SI (1) SI1663206T1 (es)
TW (1) TWI337999B (es)
WO (1) WO2005034946A1 (es)
ZA (1) ZA200601002B (es)

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US6699493B2 (en) * 2000-11-29 2004-03-02 Oculex Pharmaceuticals, Inc. Method for reducing or preventing transplant rejection in the eye and intraocular implants for use therefor
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US7323485B2 (en) * 2002-05-21 2008-01-29 Allergan, Inc. 4-(substituted cycloalkylmethyl) imidazole-2-thiones, 4-(substituted cycloalkenylmethyl) imidazole-2-thiones, 4-(substituted cycloalkylmethyl) imidazol-2-ones and 4-(substituted cycloalkenylmethyl) imidazol-2-ones and related compounds
US7358269B2 (en) * 2002-05-21 2008-04-15 Allergan, Inc. 2-((2-Thioxo-2,3-dihydro-1H-imidazol-4-yl)methyl)-3,4-dihydronapthalen-1(2H)-one
US20050048099A1 (en) 2003-01-09 2005-03-03 Allergan, Inc. Ocular implant made by a double extrusion process
US7141597B2 (en) * 2003-09-12 2006-11-28 Allergan, Inc. Nonsedating α-2 agonists
US20050059664A1 (en) * 2003-09-12 2005-03-17 Allergan, Inc. Novel methods for identifying improved, non-sedating alpha-2 agonists
US20060293359A1 (en) * 2003-06-25 2006-12-28 Allergan, Inc. Methods and compositions for the treatment of diabetes
US7812049B2 (en) * 2004-01-22 2010-10-12 Vicept Therapeutics, Inc. Method and therapeutic/cosmetic topical compositions for the treatment of rosacea and skin erythema using α1-adrenoceptor agonists
US20050244469A1 (en) 2004-04-30 2005-11-03 Allergan, Inc. Extended therapeutic effect ocular implant treatments
EP1791833A2 (en) * 2004-09-24 2007-06-06 Allergan, Inc. 4-(condensed cyclicmethyl)-imidazole-2-thiones acting as alpha2 adrenergic agonists
EP1797043A1 (en) * 2004-09-24 2007-06-20 Allergan, Inc. 4-(phenylmethyl and substituted phenylmethyl)-imidazole-2-thiones acting as specific alpha2 adrenergic agonists
CA2603044A1 (en) * 2005-06-29 2007-01-11 Allergan, Inc. Alpha-2 adrenergic agonists for the treatment of pain
US20070203144A1 (en) * 2006-01-17 2007-08-30 Allergan, Inc. Use of Memantine and Brimonidine to Attenuate Vitreoretinal Vascular Endothelial Growth Factor (VEGF) Protein Levels in Animals
CA2648742A1 (en) * 2006-04-07 2007-10-18 Allergan, Inc. Compositions including relatively water insoluble/unwettable drugs and methods for using same
US20070298073A1 (en) * 2006-06-23 2007-12-27 Allergan, Inc. Steroid-containing sustained release intraocular implants and related methods
US8802128B2 (en) 2006-06-23 2014-08-12 Allergan, Inc. Steroid-containing sustained release intraocular implants and related methods
US20080153874A1 (en) * 2006-12-22 2008-06-26 Allergan Inc. Alpha-2b receptor agonist and anticonvulsant compositions for treating chronic pain
BRPI0811781A2 (pt) 2007-05-23 2014-11-11 Allergan Inc Compostos de ((fenil) imidazolil)metilquinolinila terapêuticos.
PL2155733T3 (pl) * 2007-05-23 2013-02-28 Allergan Inc Cykliczne laktamy do leczenia jaskry lub podwyższonego ciśnienia śródgałkowego
US20110028559A1 (en) * 2007-07-06 2011-02-03 Fang Wenkui K Substituted fluoroethyl ureas as alpha 2 adrenergic agents
CA2696315A1 (en) 2007-08-15 2009-02-19 Allergan, Inc. Heterocyclyl substituted fused carbocyles useful in the treatment of conditions such as glaucoma and pain
EP2188261A1 (en) * 2007-08-15 2010-05-26 Allergan, Inc. Therapeutic compounds
KR101642520B1 (ko) * 2007-08-15 2016-07-25 알러간, 인코포레이티드 아드레날린성 화합물
US20110269805A1 (en) * 2007-10-18 2011-11-03 Gil Daniel W Method of treating sensorimotor disorders with 4-(1-(2,3-dimethylphenyl)ethyl)-1h-imidazole-2(3h)-thione
US8455548B2 (en) * 2007-10-18 2013-06-04 Allergan, Inc. Method of treating sensorimotor disorders with alpha-2 adrenergic receptor agonists
WO2009052072A1 (en) * 2007-10-18 2009-04-23 Allergan, Inc. Treating motor disorders with 4-(1-(2,3-dimethylphenyl)ethyl)-1h-imidazole-2(3h)-thione
EP2242748A1 (en) * 2008-01-11 2010-10-27 Allergan, Inc. Therapeutic disulfide compounds for treating pain and diabetes
US8956641B2 (en) 2008-04-18 2015-02-17 Warsaw Orthopedic, Inc. Alpha adrenergic receptor agonists for treatment of inflammatory diseases
US9072727B2 (en) 2008-04-18 2015-07-07 Warsaw Orthopedic, Inc. Alpha adrenergic receptor agonists for treatment of degenerative disc disease
US8889173B2 (en) * 2008-04-18 2014-11-18 Warsaw Orthopedic, Inc. Alpha adrenergic receptor agonists for treatment of pain and/or inflammation
US20090264477A1 (en) * 2008-04-18 2009-10-22 Warsaw Orthopedic, Inc., An Indiana Corporation Beta adrenergic receptor agonists for treatment of pain and/or inflammation
USRE48948E1 (en) 2008-04-18 2022-03-01 Warsaw Orthopedic, Inc. Clonidine compounds in a biodegradable polymer
US8420114B2 (en) * 2008-04-18 2013-04-16 Warsaw Orthopedic, Inc. Alpha and beta adrenergic receptor agonists for treatment of pain and / or inflammation
US20090263451A1 (en) * 2008-04-18 2009-10-22 Warsaw Orthopedic, Inc. Anti-Inflammatory and/or Analgesic Agents for Treatment of Myofascial Pain
US20120136035A1 (en) 2009-02-13 2012-05-31 Allergan, Inc. 4-(1-(3-(hydroxymethyl)-2-methylphenyl)ethyl)-1h-imidazole-2(3h)-thione
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Also Published As

Publication number Publication date
CA2537832C (en) 2012-01-24
DE602004005720T2 (de) 2007-12-27
KR20060119970A (ko) 2006-11-24
US20110034525A1 (en) 2011-02-10
AU2004279332B2 (en) 2010-10-07
TW200526591A (en) 2005-08-16
US7312238B2 (en) 2007-12-25
CA2537832A1 (en) 2005-04-21
HK1104979A1 (en) 2008-02-01
NZ545181A (en) 2009-07-31
US20080176918A1 (en) 2008-07-24
ZA200601002B (en) 2007-04-25
NO20060667L (no) 2006-04-06
PL1663206T3 (pl) 2007-08-31
PT1663206E (pt) 2007-06-22
IL173530A (en) 2010-05-31
EP1663206A1 (en) 2006-06-07
PL379561A1 (pl) 2006-10-16
CN1849118A (zh) 2006-10-18
SI1663206T1 (sl) 2007-06-30
ES2285522T3 (es) 2007-11-16
MXPA06002668A (es) 2006-06-06
CN100417379C (zh) 2008-09-10
DE602004005720D1 (de) 2007-05-16
JP2007505111A (ja) 2007-03-08
BRPI0413719A (pt) 2006-10-17
HK1092704A1 (en) 2007-02-16
DK1800679T3 (da) 2011-02-07
WO2005034946A1 (en) 2005-04-21
ATE487477T1 (de) 2010-11-15
CY1107608T1 (el) 2013-03-13
EP1663206B1 (en) 2007-04-04
JP4698591B2 (ja) 2011-06-08
US8022226B2 (en) 2011-09-20
ATE358479T1 (de) 2007-04-15
US20050059721A1 (en) 2005-03-17
AU2004279332A1 (en) 2005-04-21
US7141597B2 (en) 2006-11-28
DE602004030051D1 (de) 2010-12-23
US20070004790A1 (en) 2007-01-04
EP1800679A2 (en) 2007-06-27
TWI337999B (en) 2011-03-01
DK1663206T3 (da) 2007-07-30
RU2345987C2 (ru) 2009-02-10
EP1800679B1 (en) 2010-11-10
KR101145046B1 (ko) 2012-05-21
EP1800679A3 (en) 2009-01-21
IL173530A0 (en) 2006-07-05
RU2006113600A (ru) 2007-11-10

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