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

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth 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)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Hospice & Palliative Care (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
AU2003294748A1 (en) * 2002-12-06 2004-06-30 Bayer Healthcare Ag Tetrahydro-naphthalene derivatives
EP1572632B1 (en) * 2002-12-09 2008-08-13 Xention Limited Tetrahydro-naphthalene derivatives as vanilloid receptor antagonists
WO2006092430A1 (de) * 2005-03-03 2006-09-08 Universität des Saarlandes Selektive hemmstoffe humaner corticoidsynthasen
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
TW200716105A (en) * 2005-05-31 2007-05-01 Speedel Experimenta Ag Imidazole 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
CN101910171A (zh) 2007-11-01 2010-12-08 百时美施贵宝公司 可用作糖皮质激素受体AP-1和/或者NF-κB活性调节剂的非甾类化合物及其用途
EP2095819A1 (en) * 2008-02-28 2009-09-02 Maastricht University N-benzyl imidazole derivatives and their use as aldosterone synthase inhibitors
EP2594557B1 (en) 2009-05-28 2016-08-10 Novartis AG Substituted aminopropionic derivatives as neprilysin inhibitors
SG176010A1 (en) 2009-05-28 2011-12-29 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
JP5575913B2 (ja) * 2009-11-30 2014-08-20 ノバルティス アーゲー アルドステロン合成酵素阻害剤としてのイミダゾール誘導体
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
CA2841117A1 (en) 2011-07-08 2013-01-17 Novartis Ag 1,2-disubstituted-4-benzylamino-piperidinyl derivatives as cetp inhibitors useful for the treatment of atherosclerosis in high triglyceride subjects
EP2757882B1 (en) * 2011-09-22 2020-11-04 Merck Sharp & Dohme Corp. Imidazopyridyl compounds as aldosterone synthase inhibitors
WO2013043521A1 (en) * 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Pyrazolopyridyl compounds as aldosterone synthase inhibitors
US9193724B2 (en) 2011-09-22 2015-11-24 Merck Sharp & Dohme Corp. Triazolopyridyl compounds as aldosterone synthase inhibitors
PE20142358A1 (es) 2012-01-17 2015-01-30 Novartis Ag Nuevas formas y sales de un dihidropirrolo[1,2-c]imidazolilo, inhibidor de la aldosterona sintasa o aromatasa
UY35144A (es) 2012-11-20 2014-06-30 Novartis Ag Miméticos lineales sintéticos de apelina para el tratamiento de insuficiencia cardiaca
HRP20180958T1 (hr) 2013-02-14 2018-07-27 Novartis Ag Supstituirani derivati bisfenolbutanfosfonske kiseline kao inhibitori za nep (neutralnu endopeptidazu)
CN105705167A (zh) 2013-07-25 2016-06-22 诺华股份有限公司 合成的apelin多肽的生物缀合物
AU2014293386B2 (en) 2013-07-25 2016-11-17 Novartis Ag Cyclic polypeptides for the treatment of heart failure
MX2017009534A (es) 2015-01-23 2018-04-10 Novartis Ag Conjugados de acidos grasos y apelina sintetica con mayor vida media.
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
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
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
WO2020110011A1 (en) 2018-11-27 2020-06-04 Novartis Ag Cyclic peptides as proprotein convertase subtilisin/kexin type 9 (pcsk9) inhibitors for the treatment of metabolic disorders
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
US20240391941A1 (en) 2023-05-24 2024-11-28 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
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
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
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
US6150347A (en) 1992-04-21 2000-11-21 The Curators Of The University Of Missouri Use of aldosterone antagonists to inhibit myocardial fibrosis
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
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
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
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
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
ATE398124T1 (de) 2008-07-15
US7223866B2 (en) 2007-05-29
CN1711262A (zh) 2005-12-21
CN100447142C (zh) 2008-12-31
AU2003292039A1 (en) 2004-06-15
US20070197582A1 (en) 2007-08-23
DE60321593D1 (de) 2008-07-24
EP1565463A1 (en) 2005-08-24
US7713991B2 (en) 2010-05-11
EP1565463B1 (en) 2008-06-11
WO2004046145A1 (en) 2004-06-03
CA2505752A1 (en) 2004-06-03
BR0316306A (pt) 2005-09-27
PT1565463E (pt) 2008-09-10
HK1081540A1 (en) 2006-05-19
ES2305520T3 (es) 2008-11-01
US20060058342A1 (en) 2006-03-16

Similar Documents

Publication Publication Date Title
JP2006508970A (ja) 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
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
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