HK1126488A1 - Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor - Google Patents

Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor

Info

Publication number
HK1126488A1
HK1126488A1 HK09105273.8A HK09105273A HK1126488A1 HK 1126488 A1 HK1126488 A1 HK 1126488A1 HK 09105273 A HK09105273 A HK 09105273A HK 1126488 A1 HK1126488 A1 HK 1126488A1
Authority
HK
Hong Kong
Prior art keywords
receptor
compounds
fused compounds
subtype
inhibit vanilloid
Prior art date
Application number
HK09105273.8A
Other languages
English (en)
Inventor
Arthur Gomtsyan
Erol K Bayburt
Chih-Hung Lee
John R Koenig
Robert Schmidt
Kirill Lukin
Gilles Chambournier
Margaret Hsu
Robert M 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=HK1126488(A1) "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
Publication of HK1126488A1 publication Critical patent/HK1126488A1/xx

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)
HK09105273.8A 2003-06-12 2006-11-14 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor HK1126488A1 (en)

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
HK06112524.4A HK1093727A1 (en) 2003-06-12 2006-11-14 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor

Publications (1)

Publication Number Publication Date
HK1126488A1 true HK1126488A1 (en) 2009-09-04

Family

ID=33555102

Family Applications (2)

Application Number Title Priority Date Filing Date
HK06112524.4A HK1093727A1 (en) 2003-06-12 2006-11-14 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor
HK09105273.8A HK1126488A1 (en) 2003-06-12 2006-11-14 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor

Family Applications Before (1)

Application Number Title Priority Date Filing Date
HK06112524.4A HK1093727A1 (en) 2003-06-12 2006-11-14 Fused compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor

Country Status (21)

Country Link
EP (2) EP2017265B1 (ko)
JP (2) JP4857113B2 (ko)
KR (2) KR101138216B1 (ko)
CN (1) CN102617464A (ko)
AT (2) ATE510824T1 (ko)
AU (2) AU2004247721C1 (ko)
BR (1) BRPI0411116A (ko)
CA (2) CA2526872C (ko)
CY (2) CY1108713T1 (ko)
DE (1) DE602004017329D1 (ko)
DK (2) DK1658269T3 (ko)
ES (1) ES2318308T3 (ko)
HK (2) HK1093727A1 (ko)
IL (4) IL172457A (ko)
MX (1) MXPA05013550A (ko)
NZ (3) NZ543713A (ko)
PL (2) PL2017265T3 (ko)
PT (2) PT1658269E (ko)
SI (2) SI1658269T1 (ko)
TW (3) TW201300361A (ko)
WO (1) WO2004111009A1 (ko)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2004228028B2 (en) 2003-04-03 2009-12-10 The Regents Of The University Of California Improved inhibitors for the soluble epoxide hydrolase
US20090018092A1 (en) 2004-03-16 2009-01-15 The Regents Of The University Of California Reducing Nephropathy with Inhibitors of Soluble Epoxide Hydrolase and Epoxyeicosanoids
US7662910B2 (en) 2004-10-20 2010-02-16 The Regents Of The University Of California Inhibitors for the soluble epoxide hydrolase
EP1824843A2 (en) 2004-12-07 2007-08-29 Locus Pharmaceuticals, Inc. Inhibitors of protein kinases
JP2008523071A (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 Ｍａｐキナーゼの尿素インヒビター
US7842703B2 (en) 2005-10-07 2010-11-30 Glenmark Pharmaceuticals S.A. Substituted benzofused derivatives and their use as vanilloid receptor ligands
EP1959926A1 (en) * 2005-10-25 2008-08-27 Abbott Laboratories Formulation comprising a drug of low water solubility and method of use thereof
CA2626593A1 (en) 2005-10-28 2007-05-03 Abbott Laboratories Indazole derivatives that inhibit trpv1 receptor
TW200808723A (en) 2006-03-13 2008-02-16 Univ California Conformationally restricted urea inhibitors of soluble epoxide hydrolase
KR20080111144A (ko) * 2006-04-18 2008-12-22 아보트 러보러터리즈 바닐로이드 수용체 서브타입 １(ｖｒ１)의 길항제 및 이의 용도
WO2009081222A1 (en) 2007-12-21 2009-07-02 Glenmark Pharmaceuticals, S.A. Substituted tricyclic pyridine or pyrimidine vanilloid receptor ligands
US8557872B2 (en) 2008-01-28 2013-10-15 Amorepacific Corporation Compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same
WO2010002209A2 (en) 2008-07-02 2010-01-07 Amorepacific Corporation Novel compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist and pharmaceutical compositions containing the same
TW201020236A (en) * 2008-10-17 2010-06-01 Abbott Lab TRPV1 antagonists
EP2528604B1 (en) 2010-01-29 2017-11-22 The Regents of the University of California Acyl piperidine inhibitors of soluble epoxide hydrolase
CN105130967B (zh) 2011-05-13 2018-04-17 阵列生物制药公司 作为trka激酶抑制剂的吡咯烷基脲和吡咯烷基硫脲化合物
JP6326043B2 (ja) * 2012-05-09 2018-05-16 バイエル・クロップサイエンス・アクチェンゲゼルシャフト ５−ハロゲノピラゾールインダニルカルボキサミド類
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
WO2014078331A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. N-(arylalkyl)-n'-pyrazolyl-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
RS55593B1 (sr) 2012-11-13 2017-06-30 Array Biopharma Inc Jedinjenja biciklične uree, tiouree, guanidina i cijanoguanidina korisna za lečenje bola
US9828360B2 (en) 2012-11-13 2017-11-28 Array Biopharma Inc. Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
MX365733B (es) 2012-11-13 2019-06-12 Array Biopharma Inc Compuestos de n-pirrolidinil, n' -pirazolil-urea, tiourea, guanidina y cianoguanidina como inhibidores de trka cinasa.
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
US9981959B2 (en) 2012-11-13 2018-05-29 Array Biopharma Inc. Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
US9822118B2 (en) 2012-11-13 2017-11-21 Array Biopharma Inc. Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
WO2014078417A1 (en) 2012-11-13 2014-05-22 Array Biopharma Inc. Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors
CR20160583A (es) 2014-05-15 2017-02-23 Array Biopharma Inc 1-((3s,4r)-4-(3-fluorofenil)-1-(2-metoxietil)pirrolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)urea como inhibidor de trka cinasa
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
US20040259875A1 (en) 2001-07-31 2004-12-23 Takeshi Yura Amine derivatives
JP2003192587A (ja) * 2001-12-26 2003-07-09 Bayer Ag 尿素誘導体
MXPA04008073A (es) * 2002-02-20 2004-11-26 Abbott Lab Compuestos azabiciclicos fusionados que inhiben el receptor de subtipo 1 (vr1) del receptor de vainilloide.
GB0206876D0 (en) * 2002-03-22 2002-05-01 Merck Sharp & Dohme Therapeutic agents
AU2003241453A1 (en) * 2002-05-17 2003-12-02 Janssen Pharmaceutica N.V. Aminotetralin-derived urea modulators of vanilloid vr1 receptor

Also Published As

Publication number Publication date
TWI366461B (en) 2012-06-21
EP1658269A1 (en) 2006-05-24
IL207335A (en) 2012-02-29
DK1658269T3 (da) 2009-01-12
AU2010257277A1 (en) 2011-01-13
SI1658269T1 (sl) 2009-04-30
CA2526872A1 (en) 2004-12-23
AU2004247721C1 (en) 2011-12-22
TWI394569B (zh) 2013-05-01
EP1658269B1 (en) 2008-10-22
AU2004247721B2 (en) 2011-01-20
PL2017265T3 (pl) 2011-11-30
NZ578264A (en) 2011-02-25
WO2004111009A1 (en) 2004-12-23
CA2756058A1 (en) 2004-12-23
JP4857113B2 (ja) 2012-01-18
BRPI0411116A (pt) 2006-07-18
TW201038269A (en) 2010-11-01
IL172457A0 (en) 2006-04-10
DK2017265T3 (da) 2011-09-19
JP2011153148A (ja) 2011-08-11
NZ590234A (en) 2012-07-27
JP2007500753A (ja) 2007-01-18
KR20110089464A (ko) 2011-08-08
CY1108713T1 (el) 2014-04-09
MXPA05013550A (es) 2006-04-05
IL215997A0 (en) 2011-12-29
ES2318308T3 (es) 2009-05-01
HK1093727A1 (en) 2007-03-09
IL207335A0 (en) 2010-12-30
CA2526872C (en) 2013-02-05
PT1658269E (pt) 2009-01-09
ATE510824T1 (de) 2011-06-15
SI2017265T1 (sl) 2011-09-30
IL172457A (en) 2011-12-29
EP2017265A1 (en) 2009-01-21
PL1658269T3 (pl) 2009-08-31
EP2017265B1 (en) 2011-05-25
CY1111945T1 (el) 2015-11-04
TW200509926A (en) 2005-03-16
AU2010257277B2 (en) 2011-08-18
IL216046A0 (en) 2011-12-29
AU2004247721A1 (en) 2004-12-23
KR101138216B1 (ko) 2012-09-05
CN102617464A (zh) 2012-08-01
KR101150324B1 (ko) 2012-06-13
DE602004017329D1 (de) 2008-12-04
ATE411982T1 (de) 2008-11-15
KR20060058769A (ko) 2006-05-30
TW201300361A (zh) 2013-01-01
PT2017265E (pt) 2011-07-29
NZ543713A (en) 2009-08-28

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Legal Events

Date Code Title Description
CORR Corrigendum

Free format text: CORRECTED DATA OF SECTION 20 TO JOURNAL OF : [72] GOMTSYAN, ARTHUR - BAYBURT, EROL, K. - LEE, CHIH-HUNG - KOENIG, JOHN, R. - SCHMIDT, ROBERT - LUKIN, KIRILL - CHAMBOURNIER, GILLES - HSU, MARGARET - LEANNA, ROBERT, M. - CINK, RUSSEL, D. - THE FOLLOWING ITEMS IN BOLD SHOW THE CORRECTED DATA OF THE NOTICE OF GRANTED - DATED 2.10.2009

PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20150610