JP2007505114A5 - - Google Patents

Download PDF

Info

Publication number
JP2007505114A5
JP2007505114A5 JP2006526121A JP2006526121A JP2007505114A5 JP 2007505114 A5 JP2007505114 A5 JP 2007505114A5 JP 2006526121 A JP2006526121 A JP 2006526121A JP 2006526121 A JP2006526121 A JP 2006526121A JP 2007505114 A5 JP2007505114 A5 JP 2007505114A5
Authority
JP
Japan
Prior art keywords
alkyl
hydrogen
trifluoromethyl
alkoxy
halogen
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
JP2006526121A
Other languages
English (en)
Japanese (ja)
Other versions
JP4897484B2 (ja
JP2007505114A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/027533 external-priority patent/WO2005034850A2/en
Publication of JP2007505114A publication Critical patent/JP2007505114A/ja
Publication of JP2007505114A5 publication Critical patent/JP2007505114A5/ja
Application granted granted Critical
Publication of JP4897484B2 publication Critical patent/JP4897484B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2006526121A 2003-09-11 2004-08-24 C型肝炎ウイルスを治療するためのシクロアルキル複素環化合物 Expired - Fee Related JP4897484B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US50206703P 2003-09-11 2003-09-11
US60/502,067 2003-09-11
PCT/US2004/027533 WO2005034850A2 (en) 2003-09-11 2004-08-24 Cycloalkyl heterocycles for treating hepatitis c virus

Publications (3)

Publication Number Publication Date
JP2007505114A JP2007505114A (ja) 2007-03-08
JP2007505114A5 true JP2007505114A5 (enExample) 2007-10-11
JP4897484B2 JP4897484B2 (ja) 2012-03-14

Family

ID=34434839

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006526121A Expired - Fee Related JP4897484B2 (ja) 2003-09-11 2004-08-24 C型肝炎ウイルスを治療するためのシクロアルキル複素環化合物

Country Status (7)

Country Link
US (1) US7112601B2 (enExample)
EP (1) EP1663105B1 (enExample)
JP (1) JP4897484B2 (enExample)
AT (1) ATE498398T1 (enExample)
DE (1) DE602004031435D1 (enExample)
ES (1) ES2358904T3 (enExample)
WO (1) WO2005034850A2 (enExample)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT502258B1 (de) * 2005-07-22 2007-09-15 Univ Wien Cox-i-inhibitorverbindungen
WO2007019397A2 (en) * 2005-08-05 2007-02-15 Genelabs Technologies, Inc. 6-membered aryl and heteroaryl derivatives for the treatment of hepatitis c virus
BRPI0716060A2 (pt) * 2006-08-17 2013-09-17 Boehringer Ingelheim Int inibidores de polimerase viral.
AU2008219622A1 (en) 2007-02-28 2008-09-04 Conatus Pharmaceuticals, Inc. Methods for the treatment of liver diseases using specified matrix metalloproteinase (MMP) inhibitors
WO2008106167A1 (en) * 2007-02-28 2008-09-04 Conatus Pharmaceuticals, Inc. Combination therapy comprising matrix metalloproteinase inhibitors and caspase inhibitors for the treatment of liver diseases
EP2494991A1 (en) 2007-05-04 2012-09-05 Vertex Pharmaceuticals Incorporated Combination therapy for the treatment of HCV infection
WO2009028418A1 (ja) 2007-08-24 2009-03-05 Sapporo Medical University シクロスポリンa結合タンパク質
EA201000948A1 (ru) 2007-12-19 2011-02-28 Бёрингер Ингельхайм Интернациональ Гмбх Ингибиторы вирусной полимеразы
UY32099A (es) 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
MX2011007195A (es) 2009-01-07 2013-07-12 Scynexis Inc Derivado de ciclosporina para el uso en el tratamiento de infección de virus de hepatitis c (vhc) y virus de inmunodeficiencia humana (vih).
MX2013007677A (es) 2010-12-30 2013-07-30 Abbvie Inc Inhibidores macrociclicos de serina proteasa de hepatitis.
EP2658858A4 (en) 2010-12-30 2014-06-25 Enanta Pharm Inc MACROCYCLIC INHIBITORS OF HEPATITIS C SERINE PROTEASE PHENANTHRIDINE
US10201584B1 (en) 2011-05-17 2019-02-12 Abbvie Inc. Compositions and methods for treating HCV
WO2015103490A1 (en) 2014-01-03 2015-07-09 Abbvie, Inc. Solid antiviral dosage forms
US11724997B2 (en) 2018-03-01 2023-08-15 Annapurna Bio, Inc. Compounds and compositions for treating conditions associated with APJ receptor activity

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ322674A (en) * 1995-10-17 1999-08-30 Searle & Co Method of detecting cyclooxygenase-2
AU756627B2 (en) 1998-07-27 2003-01-16 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Diketoacid-derivatives as inhibitors of polymerases
IL141456A0 (en) 1998-08-21 2002-03-10 Viropharma Inc Rhodanine derivatives and pharmaceutical compositions containing the same
CN1324250A (zh) 1998-09-04 2001-11-28 维洛药品公司 治疗或预防病毒感染及其所致疾病的方法
WO2000018231A1 (en) 1998-09-25 2000-04-06 Viropharma Incorporated Methods for treating or preventing viral infections and associated diseases
WO2000024725A1 (en) * 1998-10-26 2000-05-04 Vertex Pharmaceuticals Incorporated Pentacyclic compounds useful as inhibitors of hepatitis c virus ns3 helicase
AU1262001A (en) 1999-11-04 2001-05-14 Biochem Pharma Inc. Method for the treatment or prevention of flaviviridae viral infection using nucleoside analogues
US6770666B2 (en) 1999-12-27 2004-08-03 Japan Tobacco Inc. Fused-ring compounds and use thereof as drugs
SK13752001A3 (sk) 1999-12-27 2002-07-02 Japan Tobacco, Inc. Zlúčeniny s fúzovanými kruhmi a ich použitie ako liečiv
US6448281B1 (en) 2000-07-06 2002-09-10 Boehringer Ingelheim (Canada) Ltd. Viral polymerase inhibitors
EP1256628A3 (en) 2001-05-10 2003-03-19 Agouron Pharmaceuticals, Inc. Hepatitis c virus (hcv) ns5b rna polymerase and mutants thereof
PL395097A1 (pl) 2001-06-11 2011-10-10 Vertex Pharmaceuticals (Canada) Incorporated Sposób wytwarzania związku o wzorze A stanowiącego pochodną tiofenu
AR035543A1 (es) * 2001-06-26 2004-06-16 Japan Tobacco Inc Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
CA2448737C (en) 2001-07-20 2010-06-01 Boehringer Ingelheim (Canada) Ltd. Viral polymerase inhibitors
EP2335700A1 (en) 2001-07-25 2011-06-22 Boehringer Ingelheim (Canada) Ltd. Hepatitis C virus polymerase inhibitors with a heterobicylic structure
WO2003026587A2 (en) * 2001-09-26 2003-04-03 Bristol-Myers Squibb Company Compounds useful for treating hepatitus c virus

Similar Documents

Publication Publication Date Title
JP2007505114A5 (enExample)
JP2007508359A5 (enExample)
JP2013517281A5 (enExample)
RU2386622C2 (ru) Гетероароматические производные мочевины и их применение в качестве активаторов глюкокиназы
JP2005523310A5 (enExample)
JP2006508935A5 (enExample)
CA2522024A1 (en) Cgrp receptor antagonists
JP2010539152A5 (enExample)
WO2009010660A3 (fr) Indazoles substitues, leur preparation et leur utilisation en therapeutique
MEP22008A (en) Derivatives of n-[heteroaryl(piperidine-2-yl)methyl]benzamide, preparation method thereof and application of same in therapeutics
JP2007519618A5 (enExample)
JP2006500348A5 (enExample)
JP2006521359A5 (enExample)
RU2011129383A (ru) Производное амина, обладающее антагостической активностью в отношении рецептора npy y5
JP2010504286A5 (enExample)
JP2008513500A5 (enExample)
JP2009534471A5 (enExample)
HRP20070430T3 (en) (3-oxo-3,4-dihydro-quinoxalin-2-yl-amino)-benzamide derivatives and related compounds as glycogen phosphorylase inhibitors for the treatment of diabetes and obesity
NO20074763L (no) (1,5-difenyl-1H-pyrazol-3-yl)oksadiazolderivater, fremgangsmate ved fremstilling derav og anvendelse av samme i terapi
RU2007134383A (ru) Производные 1,5-диарилпиррола, их получение и применение в терапии
JP2006528646A5 (enExample)
DE602005016775D1 (de) Heterocyclische, ein azol enthaltende sulfonamidinhibitoren der beta-amyloid-produktion
JP2012514020A5 (enExample)
JP2011512412A5 (enExample)
JP2008520637A5 (enExample)