DK1658269T3 - Kondenserede forbindelser som inhiberer vanilloidreceptorsubtype 1 (VR1)-receptoren - Google Patents

Kondenserede forbindelser som inhiberer vanilloidreceptorsubtype 1 (VR1)-receptoren

Info

Publication number
DK1658269T3
DK1658269T3 DK04754996T DK04754996T DK1658269T3 DK 1658269 T3 DK1658269 T3 DK 1658269T3 DK 04754996 T DK04754996 T DK 04754996T DK 04754996 T DK04754996 T DK 04754996T DK 1658269 T3 DK1658269 T3 DK 1658269T3
Authority
DK
Denmark
Prior art keywords
receptor
inhibit
compounds
condensed compounds
vanilloid
Prior art date
Application number
DK04754996T
Other languages
Danish (da)
English (en)
Inventor
Arthur Gomtsyan
Erol K Bayburt
Chih-Hung Lee
John R Koenig
Robert Schmidt
Kirill Lukin
Gilles Chambournier
Margaret Hsu
M Robert Leanna
Russel D Cink
Original Assignee
Abbott Lab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33555102&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK1658269(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US10/459,925 external-priority patent/US7015233B2/en
Priority claimed from US10/864,068 external-priority patent/US7375126B2/en
Application filed by Abbott Lab filed Critical Abbott Lab
Application granted granted Critical
Publication of DK1658269T3 publication Critical patent/DK1658269T3/da

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/06—Anti-spasmodics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • 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
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Materials For Photolithography (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
DK04754996T 2003-06-12 2004-06-10 Kondenserede forbindelser som inhiberer vanilloidreceptorsubtype 1 (VR1)-receptoren DK1658269T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10/459,925 US7015233B2 (en) 2003-06-12 2003-06-12 Fused compounds that inhibit vanilloid subtype 1 (VR1) receptor
US10/864,068 US7375126B2 (en) 2003-06-12 2004-06-09 Fused compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor
PCT/US2004/018590 WO2004111009A1 (en) 2003-06-12 2004-06-10 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor

Publications (1)

Publication Number Publication Date
DK1658269T3 true DK1658269T3 (da) 2009-01-12

Family

ID=33555102

Family Applications (2)

Application Number Title Priority Date Filing Date
DK08166079.7T DK2017265T3 (da) 2003-06-12 2004-06-10 Kondenserede forbindelser, som inhiberer vanilje-receptor-subtype-1 (VR1)
DK04754996T DK1658269T3 (da) 2003-06-12 2004-06-10 Kondenserede forbindelser som inhiberer vanilloidreceptorsubtype 1 (VR1)-receptoren

Family Applications Before (1)

Application Number Title Priority Date Filing Date
DK08166079.7T DK2017265T3 (da) 2003-06-12 2004-06-10 Kondenserede forbindelser, som inhiberer vanilje-receptor-subtype-1 (VR1)

Country Status (21)

Country Link
EP (2) EP2017265B1 (xx)
JP (2) JP4857113B2 (xx)
KR (2) KR101150324B1 (xx)
CN (1) CN102617464A (xx)
AT (2) ATE411982T1 (xx)
AU (2) AU2004247721C1 (xx)
BR (1) BRPI0411116A (xx)
CA (2) CA2526872C (xx)
CY (2) CY1108713T1 (xx)
DE (1) DE602004017329D1 (xx)
DK (2) DK2017265T3 (xx)
ES (1) ES2318308T3 (xx)
HK (2) HK1126488A1 (xx)
IL (4) IL172457A (xx)
MX (1) MXPA05013550A (xx)
NZ (3) NZ590234A (xx)
PL (2) PL1658269T3 (xx)
PT (2) PT2017265E (xx)
SI (2) SI1658269T1 (xx)
TW (3) TW201300361A (xx)
WO (1) WO2004111009A1 (xx)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004089296A2 (en) 2003-04-03 2004-10-21 The Regents Of The University Of California Improved inhibitors for the soluble epoxide hydrolase
EP1765311A4 (en) 2004-03-16 2009-04-29 Univ California REDUCTION OF NEPHROPATHY WITH INHIBITORS OF SOLUBLE EPOXY HYDROLASE AND EPOXYEICOSANOIDS
NZ554555A (en) 2004-10-20 2011-09-30 Univ California Cyclohexyl-urea derivatives as improved inhibitors for the soluble epoxide hydrolase
EP1828169A2 (en) 2004-12-07 2007-09-05 Locus Pharmaceuticals, Inc. Urea inhibitors of map kinases
JP2008523072A (ja) 2004-12-07 2008-07-03 ルーカス ファーマシューティカルズ， インコーポレイテッド タンパク質キナーゼの阻害剤
AR057543A1 (es) 2005-10-07 2007-12-05 Glenmark Pharmaceuticals Sa Derivados de benzofusionado sustituido utilizables como ligandos receptores de vainiloide
US20070104780A1 (en) * 2005-10-25 2007-05-10 Lipari John M Formulation comprising a drug of low water solubility and method of use thereof
RU2008121205A (ru) 2005-10-28 2009-12-10 Абботт Лаборэтриз (Us) Производные индазола (варианты), включающая их фармацевтическая композиция и способ лечения или предупреждения заболеваний, чувствительных к ингибированию рецептора trpv1 (варианты)
TW200808723A (en) * 2006-03-13 2008-02-16 Univ California Conformationally restricted urea inhibitors of soluble epoxide hydrolase
MY144307A (en) * 2006-04-18 2011-08-29 Abbott Lab Antagonists of the vanilloid receptor subtype 1 (vr1) and uses thereof
WO2009081222A1 (en) 2007-12-21 2009-07-02 Glenmark Pharmaceuticals, S.A. Substituted tricyclic pyridine or pyrimidine vanilloid receptor ligands
EP2238105B1 (en) 2008-01-28 2014-04-16 Amorepacific Corporation Novel compounds as vanilloid receptor antagonists
US8691855B2 (en) 2008-07-02 2014-04-08 Amorepacific Corporation Compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist and pharmaceutical compositions containing the same
JP2012505907A (ja) * 2008-10-17 2012-03-08 アボット・ラボラトリーズ Ｔｒｐｖ１拮抗薬
US9296693B2 (en) 2010-01-29 2016-03-29 The Regents Of The University Of California Acyl piperidine inhibitors of soluble epoxide hydrolase
NZ618795A (en) 2011-05-13 2015-07-31 Array Biopharma Inc Pyrrolidinyl urea, pyrrolidinyl thiourea and pyrrolidinyl guanidine compounds as trka kinase inhibitors
US9375005B2 (en) * 2012-05-09 2016-06-28 Bayer Cropscience Ag 5-halogenopyrazole indanyl carboxamides
DK2922844T3 (en) 2012-11-13 2018-03-05 Array Biopharma Inc N-PYRROLIDINYL, N'-PYRAZOLYL-URINE, THIOURINE, GUANIDINE AND CYANOGUANIDE COMPOUNDS AS TRKA-KINASE INHIBITORS
WO2014078408A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
WO2014078378A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
WO2014078322A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
US9790178B2 (en) 2012-11-13 2017-10-17 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
LT2920166T (lt) 2012-11-13 2016-12-12 Array Biopharma, Inc. Bicikliniai karbamido, tiokarbamido, guanidino ir cianoguanidino junginiai, tinkami naudoti skausmo gydymui
US9546156B2 (en) 2012-11-13 2017-01-17 Array Biopharma Inc. N-bicyclic aryl,N'-pyrazolyl urea, thiourea, guanidine cyanoguanidine compounds as TrkA kinase inhibitors
US9969694B2 (en) 2012-11-13 2018-05-15 Array Biopharma Inc. N-(arylalkyl)-N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
US9809578B2 (en) 2012-11-13 2017-11-07 Array Biopharma Inc. Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors
WO2014078325A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. N-(monocyclic aryl),n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
LT3154959T (lt) 2014-05-15 2019-09-25 Array Biopharma, Inc. 1-((3s,4r)-4-(3-fluorfenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)karbamidas kaip trka kinazės inhibitorius
DE102022104759A1 (de) 2022-02-28 2023-08-31 SCi Kontor GmbH Co-Kristall-Screening Verfahren, insbesondere zur Herstellung von Co-Kristallen

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW536734B (en) * 2000-07-31 2003-06-11 Clariant Int Ltd Process for manufacturing a microelectronic device
JP2005501873A (ja) * 2001-07-31 2005-01-20 バイエル・ヘルスケア・アクチェンゲゼルシャフト アミン誘導体
JP2003192587A (ja) * 2001-12-26 2003-07-09 Bayer Ag 尿素誘導体
CA2476936A1 (en) * 2002-02-20 2003-08-28 Chih-Hung Lee Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor
GB0206876D0 (en) * 2002-03-22 2002-05-01 Merck Sharp & Dohme Therapeutic agents
EP1506166B1 (en) * 2002-05-17 2011-11-16 Janssen Pharmaceutica NV Aminotetralin-derived urea modulators of vanilloid vr1 receptor

Also Published As

Publication number Publication date
PT2017265E (pt) 2011-07-29
AU2004247721C1 (en) 2011-12-22
EP1658269A1 (en) 2006-05-24
EP1658269B1 (en) 2008-10-22
KR20110089464A (ko) 2011-08-08
ES2318308T3 (es) 2009-05-01
TW201038269A (en) 2010-11-01
IL207335A (en) 2012-02-29
TW201300361A (zh) 2013-01-01
KR20060058769A (ko) 2006-05-30
TW200509926A (en) 2005-03-16
NZ590234A (en) 2012-07-27
AU2004247721A1 (en) 2004-12-23
DE602004017329D1 (de) 2008-12-04
CY1108713T1 (el) 2014-04-09
HK1126488A1 (en) 2009-09-04
JP2011153148A (ja) 2011-08-11
AU2010257277B2 (en) 2011-08-18
SI1658269T1 (sl) 2009-04-30
IL216046A0 (en) 2011-12-29
AU2004247721B2 (en) 2011-01-20
CA2756058A1 (en) 2004-12-23
AU2010257277A1 (en) 2011-01-13
CA2526872C (en) 2013-02-05
PL2017265T3 (pl) 2011-11-30
JP2007500753A (ja) 2007-01-18
IL207335A0 (en) 2010-12-30
CY1111945T1 (el) 2015-11-04
NZ578264A (en) 2011-02-25
WO2004111009A1 (en) 2004-12-23
NZ543713A (en) 2009-08-28
ATE411982T1 (de) 2008-11-15
CA2526872A1 (en) 2004-12-23
PL1658269T3 (pl) 2009-08-31
DK2017265T3 (da) 2011-09-19
MXPA05013550A (es) 2006-04-05
CN102617464A (zh) 2012-08-01
IL172457A0 (en) 2006-04-10
EP2017265A1 (en) 2009-01-21
BRPI0411116A (pt) 2006-07-18
IL215997A0 (en) 2011-12-29
SI2017265T1 (sl) 2011-09-30
JP4857113B2 (ja) 2012-01-18
KR101150324B1 (ko) 2012-06-13
EP2017265B1 (en) 2011-05-25
KR101138216B1 (ko) 2012-09-05
HK1093727A1 (en) 2007-03-09
TWI366461B (en) 2012-06-21
TWI394569B (zh) 2013-05-01
IL172457A (en) 2011-12-29
ATE510824T1 (de) 2011-06-15
PT1658269E (pt) 2009-01-09

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