JP2006508970A - イミダゾ[1,5a]ピリジン誘導体およびアルデステロンにより仲介される疾患の処置方法 - Google Patents

イミダゾ[1,5a]ピリジン誘導体およびアルデステロンにより仲介される疾患の処置方法 Download PDF

Info

Publication number
JP2006508970A
JP2006508970A JP2004552632A JP2004552632A JP2006508970A JP 2006508970 A JP2006508970 A JP 2006508970A JP 2004552632 A JP2004552632 A JP 2004552632A JP 2004552632 A JP2004552632 A JP 2004552632A JP 2006508970 A JP2006508970 A JP 2006508970A
Authority
JP
Japan
Prior art keywords
compound
hydrogen
optionally substituted
alkoxy
trifluoromethyl
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.)
Pending
Application number
JP2004552632A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006508970A5 (enExample
Inventor
ファリボーズ・フィルーズニア
Original Assignee
ノバルティス アクチエンゲゼルシャフト
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 ノバルティス アクチエンゲゼルシャフト filed Critical ノバルティス アクチエンゲゼルシャフト
Publication of JP2006508970A publication Critical patent/JP2006508970A/ja
Publication of JP2006508970A5 publication Critical patent/JP2006508970A5/ja
Pending legal-status Critical Current

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
    • A61P13/12—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
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity 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
    • 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
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • 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
    • 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
    • A61P9/12—Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2004552632A 2002-11-18 2003-11-17 イミダゾ[1,5a]ピリジン誘導体およびアルデステロンにより仲介される疾患の処置方法 Pending JP2006508970A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US42732502P 2002-11-18 2002-11-18
PCT/EP2003/012851 WO2004046145A1 (en) 2002-11-18 2003-11-17 Imidazo[1, 5a]pyridine derivatives and methods for treating aldosterone mediated diseases

Publications (2)

Publication Number Publication Date
JP2006508970A true JP2006508970A (ja) 2006-03-16
JP2006508970A5 JP2006508970A5 (enExample) 2006-12-28

Family

ID=32326521

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004552632A Pending JP2006508970A (ja) 2002-11-18 2003-11-17 イミダゾ[1,5a]ピリジン誘導体およびアルデステロンにより仲介される疾患の処置方法

Country Status (12)

Country Link
US (2) US7223866B2 (enExample)
EP (1) EP1565463B1 (enExample)
JP (1) JP2006508970A (enExample)
CN (1) CN100447142C (enExample)
AT (1) ATE398124T1 (enExample)
AU (1) AU2003292039A1 (enExample)
BR (1) BR0316306A (enExample)
CA (1) CA2505752A1 (enExample)
DE (1) DE60321593D1 (enExample)
ES (1) ES2305520T3 (enExample)
PT (1) PT1565463E (enExample)
WO (1) WO2004046145A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010520869A (ja) * 2007-03-09 2010-06-17 プロビオドルグ エージー グルタミニルシクラーゼ阻害剤としてのイミダゾ[1,5−a]ピリジン誘導体

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2508618C (en) * 2002-12-06 2012-02-21 Bayer Healthcare Ag Tetrahydro-naphthalene derivatives
AU2003288200A1 (en) * 2002-12-09 2004-06-30 Bayer Healthcare Ag Tetrahydro-naphthalene derivatives as vanilloid receptor antagonists
EP1853261B1 (de) * 2005-03-03 2017-01-11 Universität des Saarlandes Selektive hemmstoffe humaner corticoidsynthasen
TW200716105A (en) * 2005-05-31 2007-05-01 Speedel Experimenta Ag Imidazole compounds
TW200716634A (en) * 2005-05-31 2007-05-01 Speedel Experimenta Ag Heterocyclic spiro-compounds
TW200716636A (en) * 2005-05-31 2007-05-01 Speedel Experimenta Ag Heterocyclic spiro-compounds
GT200600381A (es) * 2005-08-25 2007-03-28 Compuestos organicos
EP1842543A1 (en) 2006-04-05 2007-10-10 Speedel Pharma AG Pharmaceutical composition coprising an aldosterone synthase inhibitor and a mineralcorticoid receptor antagonist
JP2011503081A (ja) 2007-11-01 2011-01-27 ブリストル−マイヤーズ スクイブ カンパニー グルココルチコイド受容体、AP−1および/またはNF−κB活性の調節剤として有用な非ステロイド性化合物、並びにその使用
EP2095819A1 (en) 2008-02-28 2009-09-02 Maastricht University N-benzyl imidazole derivatives and their use as aldosterone synthase inhibitors
PL2435409T3 (pl) 2009-05-28 2015-01-30 Novartis Ag Podstawione pochodne aminopropionowe jako inhibitory neprylizyny
CA2763565A1 (en) 2009-05-28 2010-12-02 Novartis Ag Substituted aminobutyric derivatives as neprilysin inhibitors
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
EP2507234B1 (en) * 2009-11-30 2014-03-12 Novartis AG Imidazole derivatives as aldosterone synthase inhibitors
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
CN103648495A (zh) 2011-07-08 2014-03-19 诺华股份有限公司 在高甘油三酯对象中治疗动脉粥样硬化的方法
EP2757883B1 (en) 2011-09-22 2021-01-13 Merck Sharp & Dohme Corp. Triazolopyridyl compounds as aldosterone synthase inhibitors
US9351973B2 (en) 2011-09-22 2016-05-31 Merck Sharp & Dohme Corp. Pyrazolopyridyl compounds as aldosterone synthase inhibitors
WO2013043518A1 (en) * 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Imidazopyridyl compounds as aldosterone synthase inhibitors
AU2013209952B2 (en) 2012-01-17 2016-09-01 Recordati Ag New forms and salts of a dihydropyrrolo(1,2-c)imidazolyl aldosterone synthase or aromatase inhibitor
UY35144A (es) 2012-11-20 2014-06-30 Novartis Ag Miméticos lineales sintéticos de apelina para el tratamiento de insuficiencia cardiaca
SG11201506018PA (en) 2013-02-14 2015-08-28 Novartis Ag Substituted bisphenyl butanoic phosphonic acid derivatives as nep (neutral endopeptidase) inhibitors
EP3024845A1 (en) 2013-07-25 2016-06-01 Novartis AG Cyclic polypeptides for the treatment of heart failure
WO2015013169A2 (en) 2013-07-25 2015-01-29 Novartis Ag Bioconjugates of synthetic apelin polypeptides
SG11201704758XA (en) 2015-01-23 2017-08-30 Novartis Ag Synthetic apelin fatty acid conjugates with improved half-life
GB201511790D0 (en) * 2015-07-06 2015-08-19 Iomet Pharma Ltd Pharmaceutical compound
JOP20190086A1 (ar) 2016-10-21 2019-04-18 Novartis Ag مشتقات نافثيريدينون جديدة واستخدامها في معالجة عدم انتظام ضربات القلب
UY38072A (es) 2018-02-07 2019-10-01 Novartis Ag Compuestos derivados de éster butanoico sustituido con bisfenilo como inhibidores de nep, composiciones y combinaciones de los mismos
UY38485A (es) 2018-11-27 2020-06-30 Novartis Ag Compuestos tetrámeros cíclicos como inhibidores de proproteína convertasa subtilisina/kexina tipo 9 (pcsk9), método de tratamiento, uso y su preparación
WO2020110008A1 (en) 2018-11-27 2020-06-04 Novartis Ag Cyclic pentamer compounds as proprotein convertase subtilisin/kexin type 9 (pcsk9) inhibitors for the treatment of metabolic disorder
JP7657151B2 (ja) 2018-11-27 2025-04-04 ノバルティス アーゲー 代謝性障害の処置のためのプロタンパク質コンバターゼスブチリシン/ケキシン9型(pcsk9)阻害剤としての環状ペプチド
WO2023084449A1 (en) 2021-11-12 2023-05-19 Novartis Ag Diaminocyclopentylpyridine derivatives for the treatment of a disease or disorder
AR127698A1 (es) 2021-11-23 2024-02-21 Novartis Ag Derivados de naftiridinona para el tratamiento de una enfermedad o un trastorno
IL324432A (en) 2023-05-24 2026-01-01 Novartis Ag Naphthyridinone derivatives for the treatment of a disease or disorder

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58979A (ja) * 1981-06-22 1983-01-06 チバ−ガイギ−・アクチエンゲゼルシヤフト イミダゾ[1,5―a]ピリジン誘導体、その製法及びそれを含む医薬組成物
JPS59118784A (ja) * 1982-12-21 1984-07-09 チバ−ガイギ−・アクチエンゲゼルシヤフト 置換イミダゾ〔1,5−a〕ピリジン及びその製造方法,並びに該化合物を含有する医薬
JPS59118785A (ja) * 1982-12-21 1984-07-09 チバ−ガイギ−・アクチエンゲゼルシヤフト イミダゾ〔1,5−a〕ピリジン誘導体及びその製造方法,並びに該誘導体を含有する医薬
JPS615076A (ja) * 1984-06-19 1986-01-10 Toyama Chem Co Ltd 新規な1,4−ジヒドロピリジン誘導体およびその塩
JPS6112688A (ja) * 1984-06-20 1986-01-21 チバ・ガイギー・アクチエンゲゼルシヤフト 置換双環化合物、その製造方法およびその用途ならびにそれを含む医薬製剤
GB2174094A (en) * 1985-04-25 1986-10-29 Wyeth John & Brother Ltd Imidazo [1,5-a] pyridine derivatives
JPH0971586A (ja) * 1995-09-07 1997-03-18 Yamanouchi Pharmaceut Co Ltd 新規な二環性縮合イミダゾール誘導体

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4889861A (en) 1982-12-21 1989-12-26 Ciba-Geigy Corp. Substituted imidazo[1,5-a]pyridine derivatives and other substituted bicyclic derivatives and their use as aromatase inhibitors
US5428160A (en) * 1982-12-21 1995-06-27 Ciba-Geigy Corporation Substituted imidazo[5-a]pyridine derviatives and other substituted bicyclic derivatives
US5798364A (en) * 1992-03-26 1998-08-25 Merck Patent Gesellschaft Mit Beschrankter Haftung Imidazopyridines
US5529992A (en) 1992-04-21 1996-06-25 Curators Of The University Of Missouri Method for inhibiting myocardial fibrosis by administering an aldosterone antagonist which suppresses aldoster one receptors
US6150347A (en) 1992-04-21 2000-11-21 The Curators Of The University Of Missouri Use of aldosterone antagonists to inhibit myocardial fibrosis
DE19701257A1 (de) * 1997-01-17 1998-07-23 Hannecke Wolf D Kunststoff Säulenpräsentationssystem in Modulbauweise zur Schaustellung von Waren oder Prospektmaterial und insbesondere von dünnen Gegenständen
US6887870B1 (en) 1999-10-12 2005-05-03 Bristol-Myers Squibb Company Heterocyclic sodium/proton exchange inhibitors and method

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58979A (ja) * 1981-06-22 1983-01-06 チバ−ガイギ−・アクチエンゲゼルシヤフト イミダゾ[1,5―a]ピリジン誘導体、その製法及びそれを含む医薬組成物
JPS59118784A (ja) * 1982-12-21 1984-07-09 チバ−ガイギ−・アクチエンゲゼルシヤフト 置換イミダゾ〔1,5−a〕ピリジン及びその製造方法,並びに該化合物を含有する医薬
JPS59118785A (ja) * 1982-12-21 1984-07-09 チバ−ガイギ−・アクチエンゲゼルシヤフト イミダゾ〔1,5−a〕ピリジン誘導体及びその製造方法,並びに該誘導体を含有する医薬
JPS615076A (ja) * 1984-06-19 1986-01-10 Toyama Chem Co Ltd 新規な1,4−ジヒドロピリジン誘導体およびその塩
JPS6112688A (ja) * 1984-06-20 1986-01-21 チバ・ガイギー・アクチエンゲゼルシヤフト 置換双環化合物、その製造方法およびその用途ならびにそれを含む医薬製剤
GB2174094A (en) * 1985-04-25 1986-10-29 Wyeth John & Brother Ltd Imidazo [1,5-a] pyridine derivatives
JPH0971586A (ja) * 1995-09-07 1997-03-18 Yamanouchi Pharmaceut Co Ltd 新規な二環性縮合イミダゾール誘導体

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010520869A (ja) * 2007-03-09 2010-06-17 プロビオドルグ エージー グルタミニルシクラーゼ阻害剤としてのイミダゾ[1,5−a]ピリジン誘導体

Also Published As

Publication number Publication date
BR0316306A (pt) 2005-09-27
EP1565463A1 (en) 2005-08-24
ATE398124T1 (de) 2008-07-15
EP1565463B1 (en) 2008-06-11
CN100447142C (zh) 2008-12-31
HK1081540A1 (en) 2006-05-19
US20070197582A1 (en) 2007-08-23
US7223866B2 (en) 2007-05-29
US20060058342A1 (en) 2006-03-16
PT1565463E (pt) 2008-09-10
ES2305520T3 (es) 2008-11-01
WO2004046145A1 (en) 2004-06-03
CN1711262A (zh) 2005-12-21
DE60321593D1 (de) 2008-07-24
CA2505752A1 (en) 2004-06-03
US7713991B2 (en) 2010-05-11
AU2003292039A1 (en) 2004-06-15

Similar Documents

Publication Publication Date Title
US7713991B2 (en) Imidazo[[1, 5-A] pyridine derivatives and methods for treating aldosterone mediated diseases
JP4533139B2 (ja) アルドステロン介在性病状の処置用剤としての有機化合物
JP6665169B2 (ja) 新規化合物αvβ6インテグリンアンタゴニスト
KR101608927B1 (ko) 이온 채널 조절제로서의 융합 벤조옥사제피논
AU2004309390A1 (en) Imidazo[4,5-c]pyridine compounds and methods of antiviral treatment
JP5628902B2 (ja) フェノキシメチル複素環化合物
KR20170117030A (ko) 질환의 치료를 위한 융합된 비시클릭 화합물
TW201113269A (en) New compounds, pharmaceutical composition and methods relating thereto
TW201200133A (en) Substituted pyrimidines as prostaglandin D2 receptor antagonists
JPH06340647A (ja) N−ヘテロアリール−n′−フェニル尿素誘導体,その製法及びその用途
JP2018184408A (ja) 多発性硬化症を治療するためのレチノイン酸関連核内オーファン受容体拮抗剤である置換された2,3−ジヒドロ−1h−インデン−1−オン
US20090298872A1 (en) Compounds and compositions as modulators of steroidal receptors and calcium channel activities
CN111542522A (zh) 可用作激酶抑制剂的被取代的吡唑并嘧啶
CN103415506B (zh) 作为用于治疗糖尿病的hsl抑制剂的仲-羟基环己基衍生物
JP6052685B2 (ja) α2アドレナリン受容体の調節因子としてのN−(イミダゾリジン−2−イリデン)−ヘテロシクロペンタ[b]ピリジン誘導体
HK1081540B (en) Imidazo[1,5a]pyridine derivatives and methods for treating aldosterone mediated diseases
CN101115722A (zh) 作为类固醇激素核受体和钙通道活性调节剂的化合物和组合物
HK1080290B (en) Organic compounds as agents for the treatment of aldosterone mediated conditions
TW201910325A (zh) 吲哚衍生物及其用途
HK1260375A1 (en) Heterocyclic compounds for the treatment of disease

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20061108

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20061108

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100427

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100726

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20101116