JP2009518365A5 - - Google Patents

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Publication number
JP2009518365A5
JP2009518365A5 JP2008543841A JP2008543841A JP2009518365A5 JP 2009518365 A5 JP2009518365 A5 JP 2009518365A5 JP 2008543841 A JP2008543841 A JP 2008543841A JP 2008543841 A JP2008543841 A JP 2008543841A JP 2009518365 A5 JP2009518365 A5 JP 2009518365A5
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JP
Japan
Prior art keywords
substituted
alkyl
unsubstituted
alkoxycarbonyl
alkoxy
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.)
Granted
Application number
JP2008543841A
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English (en)
Japanese (ja)
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JP2009518365A (ja
JP5258573B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/EP2006/069462 external-priority patent/WO2007065942A2/en
Publication of JP2009518365A publication Critical patent/JP2009518365A/ja
Publication of JP2009518365A5 publication Critical patent/JP2009518365A5/ja
Application granted granted Critical
Publication of JP5258573B2 publication Critical patent/JP5258573B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2008543841A 2005-12-09 2006-12-08 ビス−へテロ環式イミダゾリル化合物 Expired - Fee Related JP5258573B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP05111907.1 2005-12-09
EP05111907 2005-12-09
PCT/EP2006/069462 WO2007065942A2 (en) 2005-12-09 2006-12-08 Bis-heterocyclic imidazolyl compounds

Publications (3)

Publication Number Publication Date
JP2009518365A JP2009518365A (ja) 2009-05-07
JP2009518365A5 true JP2009518365A5 (US06894165-20050517-C00155.png) 2010-01-14
JP5258573B2 JP5258573B2 (ja) 2013-08-07

Family

ID=36284061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008543841A Expired - Fee Related JP5258573B2 (ja) 2005-12-09 2006-12-08 ビス−へテロ環式イミダゾリル化合物

Country Status (10)

Country Link
US (2) US8008334B2 (US06894165-20050517-C00155.png)
EP (1) EP1957489A2 (US06894165-20050517-C00155.png)
JP (1) JP5258573B2 (US06894165-20050517-C00155.png)
CN (2) CN101326184B (US06894165-20050517-C00155.png)
AR (1) AR056888A1 (US06894165-20050517-C00155.png)
BR (1) BRPI0619536A2 (US06894165-20050517-C00155.png)
CA (1) CA2629137A1 (US06894165-20050517-C00155.png)
IL (1) IL191844A0 (US06894165-20050517-C00155.png)
TW (1) TW200804378A (US06894165-20050517-C00155.png)
WO (1) WO2007065942A2 (US06894165-20050517-C00155.png)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR056888A1 (es) 2005-12-09 2007-10-31 Speedel Experimenta Ag Derivados de heterociclil imidazol
TW200808813A (en) * 2006-04-12 2008-02-16 Speedel Experimenta Ag Imidazo compounds
SG176010A1 (en) 2009-05-28 2011-12-29 Novartis Ag Substituted aminobutyric derivatives as neprilysin inhibitors
KR101442897B1 (ko) 2009-05-28 2014-09-23 노파르티스 아게 네프릴리신 억제제로서의 치환된 아미노프로피온산 유도체
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
RU2598708C2 (ru) 2010-01-14 2016-09-27 Новартис Аг Применение агента, обладающего модифицирующими свойствами в отношении гормонов надпочечников
US8877815B2 (en) 2010-11-16 2014-11-04 Novartis Ag Substituted carbamoylcycloalkyl acetic acid derivatives as NEP
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
AU2012282109B2 (en) 2011-07-08 2016-06-23 Novartis Ag Method of treating atherosclerosis in high triglyceride subjects
UY35144A (es) 2012-11-20 2014-06-30 Novartis Ag Miméticos lineales sintéticos de apelina para el tratamiento de insuficiencia cardiaca
NZ710574A (en) 2013-02-14 2017-11-24 Novartis Ag Substituted bisphenyl butanoic phosphonic acid derivatives as nep (neutral endopeptidase) inhibitors
US9340582B2 (en) 2013-07-25 2016-05-17 Novartis Ag Bioconjugates of synthetic apelin polypeptides
WO2015013168A1 (en) 2013-07-25 2015-01-29 Novartis Ag Cyclic polypeptides for the treatment of heart failure
CA2972871A1 (en) 2015-01-23 2016-07-28 Novartis Ag Synthetic apelin fatty acid conjugates with improved half-life
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
EP3887388A1 (en) 2018-11-27 2021-10-06 Novartis AG Cyclic peptides as proprotein convertase subtilisin/kexin type 9 (pcsk9) inhibitors for the treatment of metabolic disorders
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
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

Family Cites Families (21)

* 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
US5026712A (en) * 1985-06-05 1991-06-25 Schering Ag Novel imidazo[1,5-a]pyridines, useful as cardiovascular and CNS agents
JPH0670064B2 (ja) 1986-12-08 1994-09-07 三井石油化学工業株式会社 二環性イミダゾ−ル誘導体
US5057521A (en) * 1988-10-26 1991-10-15 Ciba-Geigy Corporation Use of bicyclic imidazole compounds for the treatment of hyperaldosteronism
AU6015796A (en) 1995-06-14 1997-01-15 Yamanouchi Pharmaceutical Co., Ltd. Fused imidazole derivatives and medicinal composition thereof
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
CN100572363C (zh) 2000-11-17 2009-12-23 武田药品工业株式会社 咪唑衍生物、其制备方法及其用途
CA2700690C (en) * 2002-01-10 2013-09-10 Takeda Pharmaceutical Company Limited Process for producing reformatsky reagent in stable form
WO2004075890A1 (ja) * 2003-02-26 2004-09-10 Takeda Pharmaceutical Company 安定化されたイミダゾール誘導体含有医薬組成物、イミダゾ-ル誘導体の安定化方法
EP1607092A4 (en) * 2003-03-17 2010-12-15 Takeda Pharmaceutical CONTROLLED RELEASE COMPOSITIONS
JP2008500999A (ja) * 2004-05-28 2008-01-17 シュペーデル・エクスペリメンタ・アーゲー 複素環式化合物およびアルドステロンシンターゼ阻害薬としてのそれらの使用
BRPI0510410A (pt) * 2004-05-28 2007-10-23 Speedel Experimenta Ag compostos orgánicos
TW200616623A (en) * 2004-05-28 2006-06-01 Speedel Experimenta Ag Organic compounds
EP1854463A4 (en) * 2005-03-03 2011-03-23 Takeda Pharmaceutical COMPOSITION WITH CONTROLLED RELEASE
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
AR056888A1 (es) * 2005-12-09 2007-10-31 Speedel Experimenta Ag Derivados de heterociclil imidazol
TW200813071A (en) * 2006-04-12 2008-03-16 Speedel Experimenta Ag Spiro-imidazo compounds
TW200808812A (en) * 2006-04-12 2008-02-16 Speedel Experimenta Ag Imidazo compounds
TW200808813A (en) * 2006-04-12 2008-02-16 Speedel Experimenta Ag Imidazo compounds

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