NO20081086L - Makrosykliske peptider som HCV NS3-proteaseinhibitorer - Google Patents

Makrosykliske peptider som HCV NS3-proteaseinhibitorer

Info

Publication number
NO20081086L
NO20081086L NO20081086A NO20081086A NO20081086L NO 20081086 L NO20081086 L NO 20081086L NO 20081086 A NO20081086 A NO 20081086A NO 20081086 A NO20081086 A NO 20081086A NO 20081086 L NO20081086 L NO 20081086L
Authority
NO
Norway
Prior art keywords
hcv
protease inhibitors
macrocyclic peptides
protease
macrocyclic
Prior art date
Application number
NO20081086A
Other languages
English (en)
Norwegian (no)
Inventor
M Katharine Holloway
Nigel J Liverton
Steven W Ludmerer
John A Mccauley
David B Olsen
Michael T Rudd
Joseph P Vacca
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of NO20081086L publication Critical patent/NO20081086L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/06—Tripeptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
NO20081086A 2005-08-01 2008-02-29 Makrosykliske peptider som HCV NS3-proteaseinhibitorer NO20081086L (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US70425605P 2005-08-01 2005-08-01
US72450905P 2005-10-07 2005-10-07
PCT/US2006/029635 WO2007016441A1 (fr) 2005-08-01 2006-07-28 Peptides macrocycliques en tant qu’inhibiteurs de la protéase ns3 du vhc

Publications (1)

Publication Number Publication Date
NO20081086L true NO20081086L (no) 2008-04-30

Family

ID=37404447

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20081086A NO20081086L (no) 2005-08-01 2008-02-29 Makrosykliske peptider som HCV NS3-proteaseinhibitorer

Country Status (16)

Country Link
US (1) US8278322B2 (fr)
EP (1) EP1913016B1 (fr)
JP (1) JP4705984B2 (fr)
KR (1) KR20080036598A (fr)
AU (1) AU2006275605B2 (fr)
BR (1) BRPI0614205A2 (fr)
CA (1) CA2615896C (fr)
CR (1) CR9731A (fr)
EC (1) ECSP088157A (fr)
IL (1) IL189166A0 (fr)
MA (1) MA29757B1 (fr)
MX (1) MX2008001588A (fr)
NO (1) NO20081086L (fr)
NZ (1) NZ565269A (fr)
RU (1) RU2008107972A (fr)
WO (1) WO2007016441A1 (fr)

Families Citing this family (88)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY140680A (en) 2002-05-20 2010-01-15 Bristol Myers Squibb Co Hepatitis c virus inhibitors
WO2006119061A2 (fr) 2005-05-02 2006-11-09 Merck & Co., Inc. Inhibiteurs de la protease ns3 du vhc
KR101269568B1 (ko) * 2005-07-04 2013-06-04 자난 사이텍 컴퍼니 리미티드 루테늄 착물 리간드, 루테늄 착물, 고정 루테늄 착물 촉매및 그의 제조방법과 용도
RU2008107972A (ru) 2005-08-01 2009-09-10 Мерк энд Ко., Инк. (US) Макроциклические пептиды в качестве ингибиторов ns3-протеазы hcv
US7741281B2 (en) 2005-11-03 2010-06-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
GB0609492D0 (en) * 2006-05-15 2006-06-21 Angeletti P Ist Richerche Bio Therapeutic agents
GB0612423D0 (en) * 2006-06-23 2006-08-02 Angeletti P Ist Richerche Bio Therapeutic agents
US7935670B2 (en) 2006-07-11 2011-05-03 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8138164B2 (en) 2006-10-24 2012-03-20 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
AU2007309546A1 (en) 2006-10-24 2008-05-02 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. HCV NS3 protease inhibitors
US8309540B2 (en) 2006-10-24 2012-11-13 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
WO2008057209A1 (fr) * 2006-10-27 2008-05-15 Merck & Co., Inc. Inhibiteurs de protéase ns3 du vhc
WO2008057208A2 (fr) * 2006-10-27 2008-05-15 Merck & Co., Inc. Inhibiteurs de protéase ns3 du vhc
US8343477B2 (en) 2006-11-01 2013-01-01 Bristol-Myers Squibb Company Inhibitors of hepatitis C virus
US7772180B2 (en) 2006-11-09 2010-08-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7763584B2 (en) 2006-11-16 2010-07-27 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8003604B2 (en) 2006-11-16 2011-08-23 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7888464B2 (en) 2006-11-16 2011-02-15 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
GB0625349D0 (en) 2006-12-20 2007-01-31 Angeletti P Ist Richerche Bio Therapeutic compounds
AU2007335962B2 (en) 2006-12-20 2012-09-06 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Antiviral indoles
GB0625345D0 (en) 2006-12-20 2007-01-31 Angeletti P Ist Richerche Bio Therapeutic compounds
US20100143886A1 (en) 2007-03-09 2010-06-10 Ludmerer Steven W In vivo hcv resistance to anti-viral inhibitors
CA2693537C (fr) 2007-07-17 2013-06-25 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Derives macrocycliques d'indole pour le traitement des infections d'hepatite c
CA2699891C (fr) * 2007-07-19 2013-10-22 Nigel Liverton Composes macrocycliques servant d'agents antiviraux
US8383583B2 (en) 2007-10-26 2013-02-26 Enanta Pharmaceuticals, Inc. Macrocyclic, pyridazinone-containing hepatitis C serine protease inhibitors
CL2008003384A1 (es) * 2007-11-14 2009-12-11 Enanta Pharm Inc Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c.
US8304385B2 (en) 2007-11-14 2012-11-06 Enanta Pharmaceuticals, Inc. Macrocyclic tetrazolyl hepatitis C serine protease inhibitors
EP2224801A4 (fr) 2007-12-14 2011-09-28 Enanta Pharm Inc Inhibiteurs macrocycliques, de type oximyle, des protéases à sérine du virus de l'hépatite c
US8273709B2 (en) 2007-12-14 2012-09-25 Enanta Pharmaceuticals, Inc. Triazole-containing macrocyclic HCV serine protease inhibitors
US8476257B2 (en) 2007-12-19 2013-07-02 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
WO2009085978A1 (fr) 2007-12-20 2009-07-09 Enanta Pharceuticals, Inc. Inhibiteurs de protéase de sérine de virus de l'hépatite c d'oxime carbocyclique couronnés
US8309685B2 (en) 2007-12-21 2012-11-13 Celgene Avilomics Research, Inc. HCV protease inhibitors and uses thereof
US8202996B2 (en) 2007-12-21 2012-06-19 Bristol-Myers Squibb Company Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide
US8293705B2 (en) 2007-12-21 2012-10-23 Avila Therapeutics, Inc. HCV protease inhibitors and uses thereof
KR20100131970A (ko) 2007-12-21 2010-12-16 아빌라 테라퓨틱스, 인크. Ｈｃｖ 프로테아제 억제제 및 이의 용도
KR20150117305A (ko) * 2007-12-21 2015-10-19 셀진 아빌로믹스 리서치, 인코포레이티드 Ｈｃｖ 프로테아제 억제제 및 이의 용도
EP2268285B1 (fr) * 2008-02-25 2018-06-27 Merck Sharp & Dohme Corp. Composés thérapeutiques
JP5490778B2 (ja) 2008-03-20 2014-05-14 エナンタ ファーマシューティカルズ インコーポレイテッド Ｃ型肝炎ウイルス阻害剤としてのフッ素化大環状化合物
US8163921B2 (en) 2008-04-16 2012-04-24 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8461107B2 (en) 2008-04-28 2013-06-11 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
EP2300491B1 (fr) 2008-05-29 2016-01-06 Bristol-Myers Squibb Company Inhibiteurs du virus de l hépatite c
US7964560B2 (en) 2008-05-29 2011-06-21 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
DK2540350T3 (da) 2008-07-22 2014-08-04 Merck Sharp & Dohme Kombinationer af en makrocyklisk quinoxalinforbindelse, hvilken er enhcv-ns3-protease-inhibitor med andre hcv-midler
US8207341B2 (en) 2008-09-04 2012-06-26 Bristol-Myers Squibb Company Process or synthesizing substituted isoquinolines
UY32099A (es) 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
US8563505B2 (en) 2008-09-29 2013-10-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8044087B2 (en) 2008-09-29 2011-10-25 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8283310B2 (en) 2008-12-15 2012-10-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
JP2012512878A (ja) 2008-12-19 2012-06-07 ギリアード サイエンシーズ， インコーポレイテッド Ｈｃｖｎｓ３プロテアーゼインヒビター
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).
CA2758072A1 (fr) 2009-04-08 2010-10-14 Idenix Pharmaceuticals, Inc. Inhibiteurs macrocycliques de la serine protease
CA2761650C (fr) 2009-05-13 2015-05-26 Enanta Pharmaceuticals, Inc. Composes macrocycliques comme inhibiteurs du virus de l'hepatite c
US8232246B2 (en) 2009-06-30 2012-07-31 Abbott Laboratories Anti-viral compounds
EP2459582B1 (fr) 2009-07-30 2015-05-27 Merck Sharp & Dohme Corp. Inhibiteurs de protéase ns3 du virus de l'hépatite c
WO2011017389A1 (fr) 2009-08-05 2011-02-10 Idenix Pharmaceuticals, Inc. Inhibiteurs macrocycliques de la sérine protéase macrocyclique utiles contre les infections virales, en particulier le virus de l’hépatite c
WO2011049908A2 (fr) 2009-10-19 2011-04-28 Enanta Pharmaceuticals, Inc. Composés bismacrocycliques à titre d'inhibiteurs du virus de l'hépatite c
CN103096891A (zh) 2010-06-24 2013-05-08 判米德有限公司 利用羟氯喹或羟氯喹和抗病毒剂的组合治疗丙型肝炎病毒相关疾病
WO2012016186A1 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de kinases macrocycliques et leurs utilisations
CA2812261C (fr) 2010-09-21 2017-02-21 Enanta Pharmaceuticals, Inc. Inhibiteurs de la serine protease du vhc derivee de la proline macrocyclique
US8729014B2 (en) 2010-11-01 2014-05-20 Rfs Pharma, Llc Specific HCV NS3 protease inhibitors
JP6034802B2 (ja) 2010-12-14 2016-11-30 メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． 大環状ラクタムの調製のための方法および中間体
US8937041B2 (en) 2010-12-30 2015-01-20 Abbvie, Inc. Macrocyclic hepatitis C serine protease inhibitors
EP2658858A4 (fr) 2010-12-30 2014-06-25 Enanta Pharm Inc Inhibiteurs macrocycliques de phénanthridine de sérine protéase d'hépatite c
US9353100B2 (en) 2011-02-10 2016-05-31 Idenix Pharmaceuticals Llc Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections
US8957203B2 (en) 2011-05-05 2015-02-17 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US10201584B1 (en) 2011-05-17 2019-02-12 Abbvie Inc. Compositions and methods for treating HCV
US8691757B2 (en) 2011-06-15 2014-04-08 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US8912141B2 (en) 2011-06-23 2014-12-16 Panmed Ltd. Treatment of hepatitis C virus
US9243038B2 (en) 2011-07-01 2016-01-26 President And Fellows Of Harvard College Macrocyclic insulin-degrading enzyme (IDE) inhibitors and uses thereof
CN103889439A (zh) 2011-08-19 2014-06-25 默沙东公司 Hcv蛋白酶抑制剂的晶体形式
UA119315C2 (uk) * 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
WO2014064534A2 (fr) 2012-10-05 2014-05-01 Chrontech Pharma Ab Aiguille d'injection, dispositif, compositions immunogènes et procédé d'utilisation
SI2909205T1 (sl) 2012-10-19 2017-02-28 Bristol-Myers Squibb Company 9-metil substituiran heksadekahidrociklopropa(e)pirolo(1,2-A)(1,4)diazaciklopentadecinil karbamat derivati kot nestrukturalni 3 (NS3) proteazni inhibitorji za zdravljenje hepatitis C virusnih infekcij
US9643999B2 (en) 2012-11-02 2017-05-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
WO2014071007A1 (fr) 2012-11-02 2014-05-08 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
WO2014070964A1 (fr) 2012-11-02 2014-05-08 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
EP2914614B1 (fr) 2012-11-05 2017-08-16 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
WO2014137869A1 (fr) 2013-03-07 2014-09-12 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
US11484534B2 (en) 2013-03-14 2022-11-01 Abbvie Inc. Methods for treating HCV
EA029088B1 (ru) * 2013-03-15 2018-02-28 Джилид Сайэнс, Инк. Макроциклические и бициклические ингибиторы вируса гепатита c
CN105636923A (zh) 2013-10-18 2016-06-01 默沙东公司 用于制备大环内酯酰胺的方法和中间体
EP3089757A1 (fr) 2014-01-03 2016-11-09 AbbVie Inc. Formes galéniques antivirales solides
WO2016172631A2 (fr) 2015-04-24 2016-10-27 President And Fellows Of Harvard College Inhibiteurs sélectifs de substrats d'enzyme dégradant l'insuline (ide) et utilisations associées
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
WO2017197055A1 (fr) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Dégronimères hétérocycliques pour la dégradation de protéines cibles
TWI658568B (zh) * 2017-01-03 2019-05-01 Leadtrend Technology Corporation 高壓半導體元件以及同步整流控制器
WO2019168654A2 (fr) * 2018-02-09 2019-09-06 President And Fellows Of Harvard College Bibliothèque de macrocycles à matrice d'adn

Family Cites Families (101)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3480613A (en) 1967-07-03 1969-11-25 Merck & Co Inc 2-c or 3-c-alkylribofuranosyl - 1-substituted compounds and the nucleosides thereof
US6128582A (en) 1996-04-30 2000-10-03 Vertex Pharmaceuticals Incorporated Molecules comprising an IMPDH-like binding pocket and encoded data storage medium capable of graphically displaying them
GB9623908D0 (en) 1996-11-18 1997-01-08 Hoffmann La Roche Amino acid derivatives
GB9707659D0 (en) 1997-04-16 1997-06-04 Peptide Therapeutics Ltd Hepatitis C NS3 Protease inhibitors
WO1999007734A2 (fr) 1997-08-11 1999-02-18 Boehringer Ingelheim (Canada) Ltd. Analogues de peptides inhibiteurs de l'hepatite c
EP1003775B1 (fr) 1997-08-11 2005-03-16 Boehringer Ingelheim (Canada) Ltd. Peptides inhibiteurs de l'hepatite c
IT1299134B1 (it) 1998-02-02 2000-02-29 Angeletti P Ist Richerche Bio Procedimento per la produzione di peptidi con proprieta' inibitrici della proteasi ns3 del virus hcv, peptidi cosi' ottenibili e peptidi
DK1058686T3 (da) 1998-02-25 2007-03-05 Univ Emory 2'-fluornukleosider
GB9806815D0 (en) 1998-03-30 1998-05-27 Hoffmann La Roche Amino acid derivatives
EP1066247B1 (fr) 1998-03-31 2006-11-22 Vertex Pharmaceuticals Incorporated Inhibiteurs de serine protease, particulierement de la protease ns3 du virus de l'hepatite c
GB9812523D0 (en) 1998-06-10 1998-08-05 Angeletti P Ist Richerche Bio Peptide inhibitors of hepatitis c virus ns3 protease
US6323180B1 (en) 1998-08-10 2001-11-27 Boehringer Ingelheim (Canada) Ltd Hepatitis C inhibitor tri-peptides
EP1106626B1 (fr) 1998-08-10 2003-05-28 Hokkaido Electric Power Company, Incorporated Preparation de glycopeptides ordinaires
AU764479B2 (en) 1998-10-29 2003-08-21 Bristol-Myers Squibb Company Compounds derived from an amine nucleus that are inhibitors of IMPDH enzyme
US6608027B1 (en) 1999-04-06 2003-08-19 Boehringer Ingelheim (Canada) Ltd Macrocyclic peptides active against the hepatitis C virus
UA74546C2 (en) 1999-04-06 2006-01-16 Boehringer Ingelheim Ca Ltd Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition
PT1196414E (pt) 1999-06-25 2003-12-31 Vertex Pharma Pro-farmacos de inibidores carbamato de impdh
CA2363274A1 (fr) 1999-12-27 2001-07-05 Japan Tobacco Inc. Composes a noyaux fusionnes et leurs utilisations comme medicaments contre l'hepatite c
US6455508B1 (en) 2000-02-15 2002-09-24 Kanda S. Ramasamy Methods for treating diseases with tirazole and pyrrolo-pyrimidine ribofuranosyl nucleosides
US6495677B1 (en) 2000-02-15 2002-12-17 Kanda S. Ramasamy Nucleoside compounds
SK11922002A3 (sk) 2000-02-18 2003-06-03 Shire Biochem Inc. Použitie analógov nukleozidov na liečenie alebo prevenciu infekcií spôsobených flavivírusom
IL151934A0 (en) * 2000-04-05 2003-04-10 Schering Corp Macrocyclic ns3-serine protease inhibitors of hepatitis c virus comprising n-cyclic p2 moieties
WO2001077091A2 (fr) 2000-04-05 2001-10-18 Tularik Inc. Inhibiteurs de polymerases ns5b vhc
DE60136620D1 (de) 2000-04-13 2009-01-02 Pharmasset Inc 3 oder 2 hydroxymethyl substituierte nucleoside derivate und ihre verwendung zur behandlung von virusinfektionen
MY164523A (en) 2000-05-23 2017-12-29 Univ Degli Studi Cagliari Methods and compositions for treating hepatitis c virus
CZ301182B6 (cs) 2000-05-26 2009-12-02 Idenix (Cayman) Limited Použití nukleosidových derivátu pro výrobu farmaceutických prostredku pro lécení infekcí vyvolaných flaviviry a pestiviry
US6448281B1 (en) 2000-07-06 2002-09-10 Boehringer Ingelheim (Canada) Ltd. Viral polymerase inhibitors
GB0017676D0 (en) 2000-07-19 2000-09-06 Angeletti P Ist Richerche Bio Inhibitors of viral polymerase
WO2002014376A2 (fr) 2000-08-10 2002-02-21 Trustees Of Boston College Catalyseurs de metathese recyclables
US6955174B2 (en) 2000-08-18 2005-10-18 Uryovascular Systems, Inc. Cryotherapy method for detecting and treating vulnerable plaque
US20030008841A1 (en) 2000-08-30 2003-01-09 Rene Devos Anti-HCV nucleoside derivatives
AU2001282528A1 (en) 2000-09-01 2002-03-22 Shionogi And Co., Ltd. Compounds having anti-hepatitis c virus effect
PT1411954E (pt) 2000-10-18 2011-03-16 Pharmasset Inc Nucleosídeos modificados para o tratamento de infecções virais e proliferação celular anormal
MXPA03005219A (es) 2000-12-12 2003-09-25 Schering Corp Peptidos diarilicos como inhibidores de ns3-serina proteasa en hepatitis de virus c.
AU2002230763A1 (en) 2000-12-13 2008-01-03 Bristol-Myers Squibb Pharma Company Inhibitors of hepatitis c virus ns3 protease
KR20030081343A (ko) 2000-12-15 2003-10-17 파마셋, 리미티드 플라비비리다에 감염 치료용 항바이러스제
WO2002051425A1 (fr) 2000-12-26 2002-07-04 Mitsubishi Pharma Corporation Remedes pour l'hepatite c
ES2532836T3 (es) 2001-01-22 2015-04-01 Merck Sharp & Dohme Corp. Derivados de nucleósidos como inhibidores de la ARN polimerasa viral dependiente de ARN
GB0114286D0 (en) 2001-06-12 2001-08-01 Hoffmann La Roche Nucleoside Derivatives
EP1423095B1 (fr) 2001-08-14 2016-09-28 Tel Aviv University Future Technology Development L.P. Particules de glycosaminoglycane lipidees et utilisation de celles-ci dans l'apport de medicament et de gene a des fins de diagnostic et de therapie
AU2002330154A1 (en) 2001-09-28 2003-04-07 Centre National De La Recherche Scientifique Methods and compositions for treating hepatitis c virus using 4'-modified nucleosides
WO2003026675A1 (fr) 2001-09-28 2003-04-03 Idenix (Cayman) Limited Procedes et compositions pour traiter des flavivirus et des pestivirus au moyen d'un nucleoside modifie en position 4'
EP1465862A1 (fr) 2002-01-17 2004-10-13 SmithKline Beecham Corporation Derives de cetoamides a substitution cycloalkyle, utiles comme inhibiteurs de cathepsine k
GB0201179D0 (en) 2002-01-18 2002-03-06 Angeletti P Ist Richerche Bio Therapeutic agents
CA2369711A1 (fr) * 2002-01-30 2003-07-30 Boehringer Ingelheim (Canada) Ltd. Peptides macrocycliques qui agissent contre le virus de l'hepatite c
US7323453B2 (en) 2002-02-13 2008-01-29 Merck & Co., Inc. Methods of inhibiting orthopoxvirus replication with nucleoside compounds
WO2003093290A2 (fr) 2002-05-06 2003-11-13 Genelabs Technologies, Inc. Derives nucleosidiques destines au traitement de l'infection par le virus de l'hepatite c
MY140680A (en) 2002-05-20 2010-01-15 Bristol Myers Squibb Co Hepatitis c virus inhibitors
AU2003269890A1 (en) 2002-06-21 2004-01-06 Isis Pharmaceuticals, Inc. Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
CA2488484A1 (fr) 2002-06-27 2004-01-08 Merck & Co., Inc. Derives nucleosidiques utilises comme inhibiteurs de l'arn polymerase arn-dependante virale
ES2469569T3 (es) 2002-06-28 2014-06-18 Idenix Pharmaceuticals, Inc. Prof�rmacos de nucle�sidos modificados en 2' y 3' para el tratamiento de infecciones de Flaviviridae
CA2490200C (fr) 2002-06-28 2012-01-03 Idenix (Cayman) Limited 2'- et 3'-promedicaments de nucleosides pour le traitement d'infections par flaviviridae
AU2003248748A1 (en) 2002-06-28 2004-01-19 Idenix (Cayman) Limited 2'-c-methyl-3'-o-l-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections
US20060264389A1 (en) 2002-07-16 2006-11-23 Balkrishen Bhat Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
CA2492607A1 (fr) 2002-07-25 2004-02-05 Micrologix Biotech Inc. Nucleosides d de 7-deaza antiviraux et leurs utilisations
AU2003257157C1 (en) 2002-08-01 2010-03-18 Pharmasset Inc. Compounds with the bicyclo[4.2.1] nonane system for the treatment of Flaviviridae infections
PL376043A1 (en) 2002-09-30 2005-12-12 Genelabs Technologies, Inc. Nucleoside derivatives for treating hepatitis c virus infection
AU2003290584B2 (en) 2002-11-01 2009-07-16 Viropharma Incorporated Benzofuran compounds, compositions and methods for treatment and prophylaxis of hepatitis C viral infections and associated diseases
US20040254159A1 (en) 2003-02-27 2004-12-16 Hasvold Lisa A. Heterocyclic kinase inhibitors
CA2516016C (fr) 2003-03-05 2012-05-29 Boehringer Ingelheim International Gmbh Composes d'inhibition de l'hepatite c
UA81028C2 (en) 2003-04-02 2007-11-26 Boehringer Ingelheim Int Pharmaceutical compositions for hepatitis c viral protease inhibitors
GB0307891D0 (en) 2003-04-04 2003-05-14 Angeletti P Ist Richerche Bio Chemical compounds,compositions and uses
EP1629000B1 (fr) 2003-04-16 2009-02-18 Bristol-Myers Squibb Company Peptide d'isoquinoleine macrocyclique inhibiteurs du virus de l'hepatite c
US7176208B2 (en) * 2003-04-18 2007-02-13 Enanta Pharmaceuticals, Inc. Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors
CN103204903A (zh) 2003-05-21 2013-07-17 贝林格尔.英格海姆国际有限公司 丙型肝炎抑制剂化合物
EP3521297B1 (fr) 2003-05-30 2021-12-22 Gilead Pharmasset LLC Analogues de nucléoside fluorés modifiés
GB0313250D0 (en) 2003-06-09 2003-07-16 Angeletti P Ist Richerche Bio Therapeutic agents
WO2005000864A1 (fr) 2003-06-19 2005-01-06 F. Hoffmann-La Roche Ag Methodes de preparation de derives de 4'azido nucleoside
TW200510425A (en) 2003-08-13 2005-03-16 Japan Tobacco Inc Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor
GB0321003D0 (en) 2003-09-09 2003-10-08 Angeletti P Ist Richerche Bio Compounds, compositions and uses
GB0323845D0 (en) 2003-10-10 2003-11-12 Angeletti P Ist Richerche Bio Chemical compounds,compositions and uses
US7132504B2 (en) 2003-11-12 2006-11-07 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP1730167B1 (fr) 2004-01-21 2011-01-12 Boehringer Ingelheim International GmbH Peptides macrocycliques actifs contre le virus de l'hepatite c
ES2322602T3 (es) 2004-02-24 2009-06-23 Japan Tobacco, Inc. Compuestos heterotetraciclicos condensados y su uso como inhibidor de polimerasa del vhc.
GB0413087D0 (en) 2004-06-11 2004-07-14 Angeletti P Ist Richerche Bio Therapeutic compounds
GB0416396D0 (en) 2004-07-22 2004-08-25 Angeletti P Ist Richerche Bio Therapeutic agents
US7153848B2 (en) 2004-08-09 2006-12-26 Bristol-Myers Squibb Company Inhibitors of HCV replication
WO2006021341A1 (fr) 2004-08-23 2006-03-02 F. Hoffmann-La Roche Ag 4’-azido-nucléosides antiviraux
GB0419850D0 (en) 2004-09-07 2004-10-13 Angeletti P Ist Richerche Bio Therapeutic agents
WO2006046030A2 (fr) 2004-10-26 2006-05-04 Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa Derives d'indole tetracyclique utilises en tant qu'agents antiviraux
WO2006119061A2 (fr) 2005-05-02 2006-11-09 Merck & Co., Inc. Inhibiteurs de la protease ns3 du vhc
GB0509326D0 (en) 2005-05-09 2005-06-15 Angeletti P Ist Richerche Bio Therapeutic compounds
TWI387603B (zh) 2005-07-20 2013-03-01 Merck Sharp & Dohme Ｈｃｖ ｎｓ３蛋白酶抑制劑
RU2008107972A (ru) 2005-08-01 2009-09-10 Мерк энд Ко., Инк. (US) Макроциклические пептиды в качестве ингибиторов ns3-протеазы hcv
WO2007028789A1 (fr) 2005-09-07 2007-03-15 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Dérivés de quinazoline en tant qu'agents antiviraux
GB0518390D0 (en) 2005-09-09 2005-10-19 Angeletti P Ist Richerche Bio Therapeutic compounds
GB0519797D0 (en) 2005-09-29 2005-11-09 Istituto Di Ricerche D Biolog Therapeutic agents
GB0609492D0 (en) 2006-05-15 2006-06-21 Angeletti P Ist Richerche Bio Therapeutic agents
EP2029741A4 (fr) 2006-06-08 2011-03-16 Merck Sharp & Dohme Procédé rapide pour déterminer la sensibilité aux inhibiteurs de séquences de protéase ns3/4a clonées à partir d'échantillons cliniques
GB0612423D0 (en) 2006-06-23 2006-08-02 Angeletti P Ist Richerche Bio Therapeutic agents
US8309540B2 (en) 2006-10-24 2012-11-13 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
US8138164B2 (en) 2006-10-24 2012-03-20 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
AU2007309546A1 (en) 2006-10-24 2008-05-02 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. HCV NS3 protease inhibitors
WO2008057208A2 (fr) 2006-10-27 2008-05-15 Merck & Co., Inc. Inhibiteurs de protéase ns3 du vhc
WO2008057209A1 (fr) 2006-10-27 2008-05-15 Merck & Co., Inc. Inhibiteurs de protéase ns3 du vhc
JP2010509080A (ja) 2006-11-09 2010-03-25 ツインブレード、テクノロジーズ、ホールディング、スウェーデン、アクチボラグ ハブ装置
US20100143886A1 (en) 2007-03-09 2010-06-10 Ludmerer Steven W In vivo hcv resistance to anti-viral inhibitors
EP2170888B1 (fr) 2007-06-29 2015-04-22 Gilead Sciences, Inc. Dérivés de purine et leur utilisation comme modulateurs du récepteur de type toll-7
CA2699891C (fr) 2007-07-19 2013-10-22 Nigel Liverton Composes macrocycliques servant d'agents antiviraux
CL2008003384A1 (es) 2007-11-14 2009-12-11 Enanta Pharm Inc Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c.
US8304385B2 (en) 2007-11-14 2012-11-06 Enanta Pharmaceuticals, Inc. Macrocyclic tetrazolyl hepatitis C serine protease inhibitors

Also Published As

Publication number Publication date
WO2007016441A1 (fr) 2007-02-08
CA2615896C (fr) 2012-11-13
US20110028494A1 (en) 2011-02-03
CR9731A (es) 2008-04-10
AU2006275605A1 (en) 2007-02-08
ECSP088157A (es) 2008-02-20
EP1913016B1 (fr) 2013-01-16
CA2615896A1 (fr) 2007-02-08
NZ565269A (en) 2010-03-26
EP1913016A1 (fr) 2008-04-23
BRPI0614205A2 (pt) 2016-11-22
JP2009503080A (ja) 2009-01-29
MX2008001588A (es) 2008-02-19
IL189166A0 (en) 2008-08-07
US8278322B2 (en) 2012-10-02
MA29757B1 (fr) 2008-09-01
RU2008107972A (ru) 2009-09-10
KR20080036598A (ko) 2008-04-28
JP4705984B2 (ja) 2011-06-22
AU2006275605B2 (en) 2011-01-06

Similar Documents

Publication Publication Date Title
NO20081086L (no) Makrosykliske peptider som HCV NS3-proteaseinhibitorer
NO20080879L (no) HCV-NS3-proteaseinhibitorer
NO20092053L (no) HCV NS3-proteaseinhibitorer
WO2006119061A3 (fr) Inhibiteurs de la protease ns3 du vhc
WO2008051477A3 (fr) Inhibiteurs de la protéase hcv ns3
WO2008057208A3 (fr) Inhibiteurs de protéase ns3 du vhc
WO2008051514A3 (fr) Inhibiteurs de la protéase ns3 du hcv
WO2008051475A3 (fr) Inhibiteurs de la protéase ns3 du vhc
MY152070A (en) Macrocyclic quinxaline compounds as hcv ns3 protease inhibitors
MX2011006631A (es) Inhibidores de proteasa ns3 del virus hcv.
EA200900297A1 (ru) Ингибиторы вируса гепатита с
EA200802346A1 (ru) Циклопропилконденсированные индолобензазепиновые ингибиторы белка ns5b вируса гепатита с
ATE483712T1 (de) Hcv-ns5b-inhibitoren
NO20090438L (no) Hepatit C virus inhibitorer
ATE474827T1 (de) Hcv-replikationshemmer
NO20090447L (no) Hepatittt C virusinhibitorer
WO2007008657A3 (fr) Inhibiteurs du virus de l'hepatite c
NO20044808L (no) Heterosykliske sulfonamider som er hepatitt C virus inhibitorer
EA200901101A1 (ru) Макроциклические соединения в качестве ингибиторов протеазы ns3 вгс
ATE512971T1 (de) Peptidanaloga als hepatitis c-hemmer
TW200745120A (en) Indolobenzazepine HCV NS5B inhibitors
NO20091704L (no) Inhibitorer av hepatitt C virus
NO20091707L (no) Inhibitorer av hepatitt C virus
NO20091845L (no) Macrocykliske peptider som hepatitt C virus-inhibitorer
WO2010034105A8 (fr) Composés inhibiteurs de l'hépatite c

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application