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WO2008153129A1 - Agent for lowering uric acid level - Google Patents

Agent for lowering uric acid level Download PDF

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Publication number
WO2008153129A1
WO2008153129A1 PCT/JP2008/060845 JP2008060845W WO2008153129A1 WO 2008153129 A1 WO2008153129 A1 WO 2008153129A1 JP 2008060845 W JP2008060845 W JP 2008060845W WO 2008153129 A1 WO2008153129 A1 WO 2008153129A1
Authority
WO
WIPO (PCT)
Prior art keywords
agent
uric acid
acid level
lowering
lowering uric
Prior art date
Application number
PCT/JP2008/060845
Other languages
French (fr)
Japanese (ja)
Inventor
Satoshi Oda
Kazutaka Shiobara
Yasuhito Yasogi
Kaori Uchino
Nobuko Toyota
Kisaburou Isobe
Tsuyoshi Mizuno
Kumiko Hase
Shin Umeda
Naoki Yajima
Original Assignee
Teijin Pharma Limited
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 Teijin Pharma Limited filed Critical Teijin Pharma Limited
Publication of WO2008153129A1 publication Critical patent/WO2008153129A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • A61P13/04—Drugs for disorders of the urinary system for urolithiasis
    • 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
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • 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
    • 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
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • C07D403/04—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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Vascular Medicine (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Disclosed is a novel agent for lowering an uric acid level or the like. Specifically disclosed is an agent for lowering an uric acid level or the like, which comprises a nitrogenated aromatic ring derivative represented by the formula (I) or a salt thereof as an active ingredient.
PCT/JP2008/060845 2007-06-14 2008-06-13 Agent for lowering uric acid level WO2008153129A1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2007157336 2007-06-14
JP2007-157336 2007-06-14
JP2007-259870 2007-10-03
JP2007259870 2007-10-03
JP2007-315718 2007-12-06
JP2007315718 2007-12-06

Publications (1)

Publication Number Publication Date
WO2008153129A1 true WO2008153129A1 (en) 2008-12-18

Family

ID=40129732

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/060845 WO2008153129A1 (en) 2007-06-14 2008-06-13 Agent for lowering uric acid level

Country Status (2)

Country Link
TW (1) TW200916098A (en)
WO (1) WO2008153129A1 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010147133A1 (en) 2009-06-17 2010-12-23 小野薬品工業株式会社 Novel imidazopyridine compound
WO2014183555A1 (en) 2013-05-13 2014-11-20 上海恒瑞医药有限公司 Cycloalkyl acid derivative, preparation method thereof, and pharmaceutical application thereof
US8952177B2 (en) 2013-03-15 2015-02-10 Janssen Pharmaceutica Nv 1,2,6-substituted benzimidazoles as FLAP modulators
US9067917B2 (en) 2013-03-15 2015-06-30 Janssen Pharmaceutica Nv 1,2,5-substituted benzimidazoles as FLAP modulators
US9173887B2 (en) 2010-12-22 2015-11-03 Abbvie Inc. Hepatitis C inhibitors and uses thereof
CN108084153A (en) * 2017-12-20 2018-05-29 广东赛烽医药科技有限公司 Pyridylthio acetic acid compound, composition and its application
CN110885318A (en) * 2019-11-28 2020-03-17 苏州大学 Benzoxazole derivatives and preparation method and application thereof
CN111943957A (en) * 2019-05-17 2020-11-17 中国医学科学院药物研究所 Quinoline carboxamide compounds and preparation method and use thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107987006B (en) * 2017-12-20 2021-06-01 华润赛科药业有限责任公司 Indole or azaindole derivatives, preparation method and application thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5262278A (en) * 1975-11-13 1977-05-23 Hoechst Ag Production of novel imidazole compound and pharmaceutical agent
JPH04211020A (en) * 1990-02-22 1992-08-03 Ciba Geigy Ag Method for reducing serum uric acid and/or increasing uric acid clearance of rectum using thromboxanesynthe inhibitor and/or thromboxane receptor antagonist or combination thereof
JPH05155858A (en) * 1990-02-16 1993-06-22 Lab Up Sa Novel benzimidazole and azabenzimidazole derivatives that are thromboxane acceptor antagonists, preparation thereof, and synthetic intermediate and medicinal composition containing same
WO2000003997A1 (en) * 1998-07-15 2000-01-27 Teijin Limited Thiobenzimidazole derivatives
WO2001053291A1 (en) * 2000-01-17 2001-07-26 Teijin Limited Benzimidazole derivatives
WO2001089519A1 (en) * 2000-05-22 2001-11-29 Nitromed, Inc. Thromboxane inhibitors, compositions and methods of use related applications
WO2007068621A1 (en) * 2005-12-15 2007-06-21 F. Hoffmann-La Roche Ag Novel fused pyrrole derivatives
WO2008045688A1 (en) * 2006-10-06 2008-04-17 Boehringer Ingelheim International Gmbh Chymase inhibitors

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5262278A (en) * 1975-11-13 1977-05-23 Hoechst Ag Production of novel imidazole compound and pharmaceutical agent
JPH05155858A (en) * 1990-02-16 1993-06-22 Lab Up Sa Novel benzimidazole and azabenzimidazole derivatives that are thromboxane acceptor antagonists, preparation thereof, and synthetic intermediate and medicinal composition containing same
JPH04211020A (en) * 1990-02-22 1992-08-03 Ciba Geigy Ag Method for reducing serum uric acid and/or increasing uric acid clearance of rectum using thromboxanesynthe inhibitor and/or thromboxane receptor antagonist or combination thereof
WO2000003997A1 (en) * 1998-07-15 2000-01-27 Teijin Limited Thiobenzimidazole derivatives
WO2001053291A1 (en) * 2000-01-17 2001-07-26 Teijin Limited Benzimidazole derivatives
WO2001089519A1 (en) * 2000-05-22 2001-11-29 Nitromed, Inc. Thromboxane inhibitors, compositions and methods of use related applications
WO2007068621A1 (en) * 2005-12-15 2007-06-21 F. Hoffmann-La Roche Ag Novel fused pyrrole derivatives
WO2008045688A1 (en) * 2006-10-06 2008-04-17 Boehringer Ingelheim International Gmbh Chymase inhibitors

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2444401A1 (en) * 2009-06-17 2012-04-25 ONO Pharmaceutical Co., Ltd. Novel imidazopyridine compound
EP2444401A4 (en) * 2009-06-17 2012-11-07 Ono Pharmaceutical Co Novel imidazopyridine compound
US8569504B2 (en) 2009-06-17 2013-10-29 Ono Pharmaceutical Co., Ltd. Imidazopyridine compound
JP5621771B2 (en) * 2009-06-17 2014-11-12 小野薬品工業株式会社 New imidazopyridine compounds
WO2010147133A1 (en) 2009-06-17 2010-12-23 小野薬品工業株式会社 Novel imidazopyridine compound
US9173887B2 (en) 2010-12-22 2015-11-03 Abbvie Inc. Hepatitis C inhibitors and uses thereof
US9567355B2 (en) 2010-12-22 2017-02-14 Abbvie Inc. Hepatitis C inhibitors and uses thereof
US9453007B2 (en) 2010-12-22 2016-09-27 Abbvie Inc. Hepatitis C inhibitors and uses thereof
US9682971B2 (en) 2013-03-15 2017-06-20 Janssen Pharmaceutica Nv 1,2,5-Substituted benzimidazoles as flap modulators
US9089569B2 (en) 2013-03-15 2015-07-28 Janssen Pharmaceutica Nv 1,2,6-substituted benzimidazoles as flap modulators
US9265770B2 (en) 2013-03-15 2016-02-23 Janssen Pharmaceutica Nv 1,2,5-substituted benzimidazoles as FLAP modulators
US9067917B2 (en) 2013-03-15 2015-06-30 Janssen Pharmaceutica Nv 1,2,5-substituted benzimidazoles as FLAP modulators
US8952177B2 (en) 2013-03-15 2015-02-10 Janssen Pharmaceutica Nv 1,2,6-substituted benzimidazoles as FLAP modulators
US9682972B2 (en) 2013-03-15 2017-06-20 Janssen Pharmaceutica Nv 1,2,5-substituted benzimidazoles as flap modulators
US9695149B2 (en) 2013-03-15 2017-07-04 Janssen Pharmaceutica Nv 1,2,6-substituted benzimidazoles as flap modulators
US9637484B2 (en) 2013-05-13 2017-05-02 Shanghai Hengrui Pharmaceutical Co., Ltd. Cycloalkyl acid derivative, preparation method thereof, and pharmaceutical application thereof
WO2014183555A1 (en) 2013-05-13 2014-11-20 上海恒瑞医药有限公司 Cycloalkyl acid derivative, preparation method thereof, and pharmaceutical application thereof
CN108084153A (en) * 2017-12-20 2018-05-29 广东赛烽医药科技有限公司 Pyridylthio acetic acid compound, composition and its application
CN111943957A (en) * 2019-05-17 2020-11-17 中国医学科学院药物研究所 Quinoline carboxamide compounds and preparation method and use thereof
CN110885318A (en) * 2019-11-28 2020-03-17 苏州大学 Benzoxazole derivatives and preparation method and application thereof
CN110885318B (en) * 2019-11-28 2022-12-23 苏州大学 Benzoxazole derivative and preparation method and application thereof

Also Published As

Publication number Publication date
TW200916098A (en) 2009-04-16

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