LU92667I2 - Paritaprevir, ou un sel ou ester pharmaceutiquement acceptable qui en dérive (viekirax) - Google Patents

Paritaprevir, ou un sel ou ester pharmaceutiquement acceptable qui en dérive (viekirax) Download PDF

Info

Publication number
LU92667I2
LU92667I2 LU92667C LU92667C LU92667I2 LU 92667 I2 LU92667 I2 LU 92667I2 LU 92667 C LU92667 C LU 92667C LU 92667 C LU92667 C LU 92667C LU 92667 I2 LU92667 I2 LU 92667I2
Authority
LU
Luxembourg
Prior art keywords
viekirax
paritaprevir
ester
drives
pharmaceutically acceptable
Prior art date
Application number
LU92667C
Other languages
English (en)
Original Assignee
Enanta Pharm Inc
Abb Vie Bahamas Ltd
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42005677&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU92667(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Enanta Pharm Inc, Abb Vie Bahamas Ltd filed Critical Enanta Pharm Inc
Publication of LU92667I2 publication Critical patent/LU92667I2/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/113General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides without change of the primary structure
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Virology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Biochemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Analytical Chemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
LU92667C 2008-09-11 2015-02-25 Paritaprevir, ou un sel ou ester pharmaceutiquement acceptable qui en dérive (viekirax) LU92667I2 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US19172508P 2008-09-11 2008-09-11
US20968909P 2009-03-10 2009-03-10
PCT/US2009/005082 WO2010030359A2 (fr) 2008-09-11 2009-09-10 Inhibiteurs macrocycliques de la sérine protéase de l'hépatite c

Publications (1)

Publication Number Publication Date
LU92667I2 true LU92667I2 (fr) 2015-11-24

Family

ID=42005677

Family Applications (1)

Application Number Title Priority Date Filing Date
LU92667C LU92667I2 (fr) 2008-09-11 2015-02-25 Paritaprevir, ou un sel ou ester pharmaceutiquement acceptable qui en dérive (viekirax)

Country Status (41)

Country Link
US (3) US8420596B2 (fr)
EP (5) EP2340029B1 (fr)
JP (4) JP5259537B2 (fr)
KR (3) KR101379365B1 (fr)
CN (3) CN103896950A (fr)
AR (3) AR073568A1 (fr)
AU (1) AU2009292182B2 (fr)
BR (2) BR122012005261A8 (fr)
CA (1) CA2736895C (fr)
CL (2) CL2011000512A1 (fr)
CO (1) CO6341565A2 (fr)
CR (1) CR20140180A (fr)
CY (6) CY1115137T1 (fr)
DK (5) DK2468287T3 (fr)
DO (1) DOP2011000077A (fr)
EA (2) EA020580B1 (fr)
EC (2) ECSP11010879A (fr)
ES (5) ES2475163T3 (fr)
GT (2) GT201100056AA (fr)
HK (4) HK1170936A1 (fr)
HR (5) HRP20140493T1 (fr)
HU (2) HUE039478T2 (fr)
IL (2) IL218441A (fr)
LT (2) LT2805726T (fr)
LU (1) LU92667I2 (fr)
MX (1) MX2011002486A (fr)
MY (1) MY159820A (fr)
NL (1) NL300730I2 (fr)
NO (1) NO2015014I1 (fr)
NZ (2) NZ605550A (fr)
PA (1) PA8842201A1 (fr)
PE (3) PE20140961A1 (fr)
PL (5) PL2468286T3 (fr)
PT (5) PT2468285E (fr)
SG (1) SG179414A1 (fr)
SI (5) SI2340029T1 (fr)
TR (1) TR201809771T4 (fr)
TW (3) TWI450723B (fr)
UY (3) UY32099A (fr)
WO (1) WO2010030359A2 (fr)
ZA (2) ZA201101558B (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UY32099A (es) 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
US8937150B2 (en) * 2009-06-11 2015-01-20 Abbvie Inc. Anti-viral compounds
AU2010298028A1 (en) * 2009-09-28 2012-04-19 Intermune, Inc. Cyclic peptide inhibitors of hepatitis C virus replication
US8933110B2 (en) 2010-01-25 2015-01-13 Enanta Pharmaceuticals, Inc. Hepatitis C virus inhibitors
WO2011091417A1 (fr) 2010-01-25 2011-07-28 Enanta Pharmaceuticals, Inc. Inhibiteurs du virus de l'hépatite c
AU2011224558B2 (en) * 2010-03-10 2014-02-27 Abbvie Ireland Unlimited Company Solid compositions
WO2012092411A2 (fr) * 2010-12-30 2012-07-05 Enanta Pharmaceuticals, Inc. Inhibiteurs macrocycliques de phénanthridine de sérine protéase d'hépatite c
MX2013007677A (es) * 2010-12-30 2013-07-30 Abbvie Inc Inhibidores macrociclicos de serina proteasa de hepatitis.
US9044480B1 (en) * 2011-03-03 2015-06-02 Abbvie Inc. Compositions and methods for treating HCV
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
US20130072528A1 (en) * 2011-09-16 2013-03-21 Abbvie Inc. Methods for Treating HCV
US8466159B2 (en) 2011-10-21 2013-06-18 Abbvie Inc. Methods for treating HCV
CN104383541A (zh) 2011-10-21 2015-03-04 艾伯维公司 用于治疗hcv的包含至少两种直接抗病毒剂和利巴韦林但无干扰素的方法
US8492386B2 (en) * 2011-10-21 2013-07-23 Abbvie Inc. Methods for treating HCV
AU2015200715A1 (en) * 2011-10-21 2015-03-05 Abbvie Ireland Unlimited Company Methods for treating HCV
PT107924A (pt) 2011-10-21 2014-12-03 Abbvie Inc Tratamento de combinação de daa (eg. com abt-072 ou abt-333) para utilização no tratamento de hcv
US9034832B2 (en) 2011-12-29 2015-05-19 Abbvie Inc. Solid compositions
JP6038179B2 (ja) * 2012-01-11 2016-12-07 アッヴィ・インコーポレイテッド Hcvプロテアーゼ阻害剤の製造方法
JP2015522022A (ja) 2012-06-27 2015-08-03 アッヴィ・インコーポレイテッド Hcvの処置に使用するためのabt−450およびリトナビルおよび例えばabt−072および/またはabt−333の併用処置
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
CN104603138A (zh) * 2012-07-12 2015-05-06 艾伯维公司 Hcv抑制剂的晶形
TW201408669A (zh) 2012-08-08 2014-03-01 Merck Sharp & Dohme Hcv ns3蛋白酶抑制劑
AU2012392557B2 (en) 2012-10-19 2017-06-01 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2914613B1 (fr) 2012-11-02 2017-11-22 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
US9334279B2 (en) 2012-11-02 2016-05-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US9643999B2 (en) 2012-11-02 2017-05-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2914614B1 (fr) 2012-11-05 2017-08-16 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
US9434738B2 (en) * 2013-01-10 2016-09-06 Bristol-Myers Squibb Company Macrocyclic benzofuran and azabenzofuran compounds for the treatment of hepatitis C
WO2014137869A1 (fr) 2013-03-07 2014-09-12 Bristol-Myers Squibb Company Inhibiteurs du virus de l'hépatite c
CA2902569A1 (fr) 2013-03-15 2014-09-18 Gilead Sciences, Inc. Inhibiteurs macrocycliques et bicycliques du virus de l'hepatite c
EP3016651A1 (fr) 2013-07-02 2016-05-11 AbbVie Inc. Méthodes de traitement du vhc
WO2015038596A1 (fr) 2013-09-11 2015-03-19 Emory University Compositions à base de nucléotide et de nucléoside et utilisations correspondantes
WO2015084953A1 (fr) 2013-12-04 2015-06-11 Abbvie Inc. Formes cristallines
EP3089757A1 (fr) 2014-01-03 2016-11-09 AbbVie Inc. Formes galéniques antivirales solides
EP3099295A1 (fr) 2014-01-28 2016-12-07 Abbvie Inc. Ajustement de dose en polythérapie de l'hépatite c
WO2016040588A1 (fr) 2014-09-11 2016-03-17 Abbvie Inc. Traitement du virus de l'hépatite c par l'administration de quatre composés différents anti-vhc avec des aliments
US10113152B1 (en) 2014-10-03 2018-10-30 Abbvie Inc. Variant polypeptides capable of aminating aliphatic alpha keto acids
US10059969B1 (en) 2014-10-03 2018-08-28 Abbvie Inc. Process for the preparation of (S)-2-amino-non-8-enoic acid
MA40844A (fr) * 2014-11-10 2017-09-20 Glaxosmithkline Ip No 2 Ltd Compositions pharmaceutiques à action prolongée pour l'hépatite c
WO2016134058A1 (fr) 2015-02-18 2016-08-25 Abbvie Inc. Combinaisons utiles pour traiter le virus de l'hépatite c
US20160375017A1 (en) 2015-06-26 2016-12-29 Abbvie Inc. Solid Pharmaceutical Compositions for Treating HCV
US9957281B2 (en) 2015-07-22 2018-05-01 Enanta Pharmaceuticals, Inc. Benzodiazepine derivatives as RSV inhibitors
US11192914B2 (en) 2016-04-28 2021-12-07 Emory University Alkyne containing nucleotide and nucleoside therapeutic compositions and uses related thereto
BR112019015886A2 (pt) 2017-02-01 2020-03-17 Abbvie Inc. Processos enzimáticos para a preparação de ácido (±)-2-(difluorometil)-1-(alcoxicarbonil)-ciclopropanocarboxílico e (±)-ácido 2-(vinil)-1-(alcoxicarbonil)-ciclopropanocarboxílico
CN107383021A (zh) * 2017-08-01 2017-11-24 安徽拜善晟制药有限公司 一种原料药帕利普韦的制备方法
BR112021018335A2 (pt) 2019-03-18 2021-11-23 Enanta Pharm Inc Derivados de benzodiazepina como inibidores de rsv
US11505558B1 (en) 2019-10-04 2022-11-22 Enanta Pharmaceuticals, Inc. Antiviral heterocyclic compounds
UY39032A (es) * 2020-01-24 2021-07-30 Enanta Pharm Inc Compuestos heterocíclicos como agentes antivirales
CN111378007B (zh) * 2020-05-08 2022-04-12 杭州濡湜生物科技有限公司 一种采用第二代Hoveyda-Grubbs催化剂制备帕利普韦的方法
WO2022010882A1 (fr) 2020-07-07 2022-01-13 Enanta Pharmaceuticals, Inc, Dérivés de dihydroquinoxaline et de dihydropyridopyrazine utilisés comme inhibiteurs de rsv
US11922331B2 (en) 2020-08-26 2024-03-05 Northrop Grumman Systems Corporation Machine-learning-based predictive ice detection
WO2022086840A1 (fr) 2020-10-19 2022-04-28 Enanta Pharmaceuticals, Inc. Composés hétérocycliques en tant qu'agents antiviraux
BR112023016970A2 (pt) 2021-02-26 2023-10-10 Enanta Pharm Inc Compostos heterocíclicos antivirais

Family Cites Families (252)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5831002A (en) 1992-05-20 1998-11-03 Basf Aktiengesellschaft Antitumor peptides
US5861297A (en) 1996-09-27 1999-01-19 Merck & Co., Inc. Detergent-free hepatitis C protease
US6767991B1 (en) 1997-08-11 2004-07-27 Boehringer Ingelheim (Canada) Ltd. Hepatitis C inhibitor peptides
IL134232A0 (en) 1997-08-11 2001-04-30 Boehringer Ingelheim Ca Ltd Hepatitis c inhibitor peptides
US20040058982A1 (en) 1999-02-17 2004-03-25 Bioavailability System, Llc Pharmaceutical compositions
DK1066247T3 (da) 1998-03-31 2007-04-02 Vertex Pharma Inhibitorer af serinproteaser, især hepatitis C virus NS3 protease
US6323180B1 (en) 1998-08-10 2001-11-27 Boehringer Ingelheim (Canada) Ltd Hepatitis C inhibitor tri-peptides
AR022061A1 (es) 1998-08-10 2002-09-04 Boehringer Ingelheim Ca Ltd Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos.
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
US6608027B1 (en) 1999-04-06 2003-08-19 Boehringer Ingelheim (Canada) Ltd Macrocyclic peptides active against the hepatitis C virus
US7122627B2 (en) 1999-07-26 2006-10-17 Bristol-Myers Squibb Company Lactam inhibitors of Hepatitis C virus NS3 protease
US6774212B2 (en) 1999-12-03 2004-08-10 Bristol-Myers Squibb Pharma Company Alpha-ketoamide inhibitors of hepatitis C virus NS3 protease
JP2003525294A (ja) 2000-02-29 2003-08-26 ブリストル−マイヤーズ スクイブ ファーマ カンパニー C型肝炎ウイルスns3プロテアーゼの阻害剤
US6921753B2 (en) 2000-06-27 2005-07-26 Pfizer Inc Purine derivatives
US6846806B2 (en) 2000-10-23 2005-01-25 Bristol-Myers Squibb Company Peptide inhibitors of Hepatitis C virus NS3 protein
ES2263687T3 (es) 2000-11-20 2006-12-16 Bristol-Myers Squibb Company Inhibidores tripeptidicos de la hepatitis c.
US6727366B2 (en) 2000-12-13 2004-04-27 Bristol-Myers Squibb Pharma Company Imidazolidinones and their related derivatives as hepatitis C virus NS3 protease inhibitors
US6653295B2 (en) 2000-12-13 2003-11-25 Bristol-Myers Squibb Company Inhibitors of hepatitis C virus NS3 protease
FR2821272B1 (fr) 2001-02-23 2004-12-17 Synt Em Composes constitues d'une molecule analgesique liee a un vecteur capable de vectoriser ladite molecule a travers la barriere hematoencephalique et compositions pharmaceutiques les contenant
WO2003025563A1 (fr) 2001-09-16 2003-03-27 Chemometec A/S Procede et systeme de detection et eventuellement d'isolement de particules peu abondantes
AU2002337765A1 (en) 2001-09-26 2003-04-07 Bristol-Myers Squibb Company Compounds useful for treating hepatitus c virus
US6867185B2 (en) 2001-12-20 2005-03-15 Bristol-Myers Squibb Company Inhibitors of hepatitis C virus
CA2369711A1 (fr) 2002-01-30 2003-07-30 Boehringer Ingelheim (Canada) Ltd. Peptides macrocycliques qui agissent contre le virus de l'hepatite c
US7119072B2 (en) 2002-01-30 2006-10-10 Boehringer Ingelheim (Canada) Ltd. Macrocyclic peptides active against the hepatitis C virus
CA2370396A1 (fr) 2002-02-01 2003-08-01 Boehringer Ingelheim (Canada) Ltd. Tri-peptides inhibiteur de l'hepatite c
US6642204B2 (en) 2002-02-01 2003-11-04 Boehringer Ingelheim International Gmbh Hepatitis C inhibitor tri-peptides
US7091184B2 (en) 2002-02-01 2006-08-15 Boehringer Ingelheim International Gmbh Hepatitis C inhibitor tri-peptides
CA2369970A1 (fr) 2002-02-01 2003-08-01 Boehringer Ingelheim (Canada) Ltd. Tri-peptides inhibiteur de l'hepatite c
US6828301B2 (en) 2002-02-07 2004-12-07 Boehringer Ingelheim International Gmbh Pharmaceutical compositions for hepatitis C viral protease inhibitors
AU2003301959A1 (en) 2002-05-20 2004-06-03 Bristol-Myers Squibb Company Substituted cycloalkyl p1' hepatitis c virus inhibitors
US20060199773A1 (en) 2002-05-20 2006-09-07 Sausker Justin B Crystalline forms of (1R,2S)-N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(6-methoxy-1-isoquinolinyl)oxy]-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethenyl-cyclopropanecarboxamide, monopotassium salt
MY140680A (en) 2002-05-20 2010-01-15 Bristol Myers Squibb Co Hepatitis c virus inhibitors
JP4312718B2 (ja) 2002-05-20 2009-08-12 ブリストル−マイヤーズ スクイブ カンパニー C型肝炎ウイルス阻害剤
WO2003099316A1 (fr) 2002-05-20 2003-12-04 Bristol-Myers Squibb Company Sulfamides heterocycliques en tant qu'inhibiteurs du virus de l'hepatite c
US20030232386A1 (en) 2002-06-17 2003-12-18 Shah Dinesh O. Assay conjugate and uses thereof
EP1523483A4 (fr) 2002-06-26 2006-03-08 Bristol Myers Squibb Co Pyrazinones amino-bicycliques et pyridinones utilisees comme inhibiteurs de coagulation de la serine protease
WO2004014852A2 (fr) 2002-08-12 2004-02-19 Bristol-Myers Squibb Company Iminothiazolidinones s'utilisant comme inhibiteurs de replication du vhc
US20040138109A1 (en) 2002-09-30 2004-07-15 Boehringer Ingelheim Pharmaceuticals, Inc. Potent inhibitor of HCV serine protease
US20050075279A1 (en) 2002-10-25 2005-04-07 Boehringer Ingelheim International Gmbh Macrocyclic peptides active against the hepatitis C virus
US20050159345A1 (en) 2002-10-29 2005-07-21 Boehringer Ingelheim International Gmbh Composition for the treatment of infection by Flaviviridae viruses
US7601709B2 (en) 2003-02-07 2009-10-13 Enanta Pharmaceuticals, Inc. Macrocyclic hepatitis C serine protease inhibitors
JP2007524576A (ja) * 2003-02-07 2007-08-30 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 大環状のc型肝炎セリンプロテアーゼ阻害剤
US20040180815A1 (en) 2003-03-07 2004-09-16 Suanne Nakajima Pyridazinonyl macrocyclic hepatitis C serine protease inhibitors
WO2004101605A1 (fr) 2003-03-05 2004-11-25 Boehringer Ingelheim International Gmbh Composes d'inhibition de l'hepatite c
UY28240A1 (es) 2003-03-27 2004-11-08 Boehringer Ingelheim Pharma Fases cristalinas de un potente inhibidor de la hcv
MXPA05010338A (es) 2003-04-02 2005-11-17 Boehringer Ingelheim Int Composiciones farmaceuticas para inhibidores de la proteasa del virus de la hepatitis c.
US7148347B2 (en) 2003-04-10 2006-12-12 Boehringer Ingelheim International Gmbh Process for preparing macrocyclic compounds
CA2521835A1 (fr) 2003-04-10 2004-10-21 Boehringer Ingelheim International Gmbh Procede pour preparer des composes macrocycliques par reaction de metathese catalysee par complexe de ruthenium
ES2386161T3 (es) 2003-04-16 2012-08-10 Bristol-Myers Squibb Company Proceso para separar una mezcla de enantiómeros de éster alquílico usando una enzima
DE602004023924D1 (en) * 2003-04-18 2009-12-17 Enanta Pharm Inc Ease-hemmer
US7176208B2 (en) 2003-04-18 2007-02-13 Enanta Pharmaceuticals, Inc. Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors
AU2004240704B9 (en) 2003-05-21 2009-10-22 Boehringer Ingelheim International Gmbh Hepatitis C inhibitor compounds
US7273851B2 (en) 2003-06-05 2007-09-25 Enanta Pharmaceuticals, Inc. Tri-peptide hepatitis C serine protease inhibitors
US7112601B2 (en) 2003-09-11 2006-09-26 Bristol-Myers Squibb Company Cycloalkyl heterocycles for treating hepatitis C virus
MXPA06003141A (es) 2003-09-22 2006-06-05 Boehringer Ingelheim Int Peptidos macrociclicos activos contra el virus de la hepatitis c.
CA2540031A1 (fr) 2003-09-26 2005-04-07 Schering Corporation Inhibiteurs macrocycliques de la serine protease ns3 du virus de l'hepatite c
US7491794B2 (en) 2003-10-14 2009-02-17 Intermune, Inc. Macrocyclic compounds as inhibitors of viral replication
KR100853579B1 (ko) 2003-10-14 2008-08-21 인터뮨, 인크. Hcv 복제 억제제로서 거대고리 카르복실산 및아실술폰아미드
US7132504B2 (en) 2003-11-12 2006-11-07 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7309708B2 (en) 2003-11-20 2007-12-18 Birstol-Myers Squibb Company Hepatitis C virus inhibitors
US7135462B2 (en) 2003-11-20 2006-11-14 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
JP2007532479A (ja) 2003-11-20 2007-11-15 シェーリング コーポレイション C型肝炎ウイルスns3プロテアーゼの脱ペプチド化インヒビター
FR2863268B1 (fr) 2003-12-09 2006-02-24 Sod Conseils Rech Applic Nouveaux derives du 2-hydroxytetrahydrofuranne et leur application a titre de medicaments
CN100509784C (zh) 2003-12-11 2009-07-08 先灵公司 丙型肝炎病毒ns3/ns4a丝氨酸蛋白酶的抑制剂
ATE495185T1 (de) 2004-01-21 2011-01-15 Boehringer Ingelheim Int Makrocyclische peptide mit wirkung gegen das hepatitis-c-virus
WO2005075502A1 (fr) 2004-01-28 2005-08-18 Boehringer Ingelheim International Gmbh Procede d'elimination de metaux de transition a partir de solutions reactionnelles comportant des sous-produits de metaux de transition
JP4902361B2 (ja) 2004-01-30 2012-03-21 メディヴィル・アクチエボラーグ Hcvns−3セリンプロテアーゼインヒビター
BRPI0508867A (pt) 2004-03-15 2007-09-04 Boehringer Ingelheim Int processo para a preparação de compostos macrocìclicos
CA2560897C (fr) 2004-03-30 2012-06-12 Intermune, Inc. Composes macrocycliques inhibiteurs de replication virale
CA2568008C (fr) 2004-05-25 2014-01-28 Boehringer Ingelheim International Gmbh Processus de preparation d'inhibiteurs de protease hcv acyclique
WO2006000085A1 (fr) 2004-06-28 2006-01-05 Boehringer Ingelheim International Gmbh Analogues peptidiques d'inhibiteurs de l'hepatite c
DE102004033312A1 (de) 2004-07-08 2006-01-26 Boehringer Ingelheim Pharma Gmbh & Co. Kg Kontinuierliches Metatheseverfahren mit Ruthenium-Katalysatoren
EP1778702B1 (fr) 2004-07-16 2011-07-13 Gilead Sciences, Inc. Composes antiviraux
JP4914355B2 (ja) 2004-07-20 2012-04-11 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング C型肝炎インヒビターペプチド類似体
UY29016A1 (es) 2004-07-20 2006-02-24 Boehringer Ingelheim Int Analogos de dipeptidos inhibidores de la hepatitis c
US7153848B2 (en) 2004-08-09 2006-12-26 Bristol-Myers Squibb Company Inhibitors of HCV replication
US7348425B2 (en) 2004-08-09 2008-03-25 Bristol-Myers Squibb Company Inhibitors of HCV replication
US7375218B2 (en) 2004-09-17 2008-05-20 Boehringer Ingelheim International Gmbh Process for preparing macrocyclic HCV protease inhibitors
JP2008513452A (ja) 2004-09-17 2008-05-01 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 超臨界流体中の閉環複分解方法
ATE533473T1 (de) 2004-09-24 2011-12-15 Boehringer Ingelheim Pharma Neue klasse von surfuctantähnlichen materialien mit vitamin-e-tpgs und wasserlöslichem polymer
WO2007001406A2 (fr) * 2004-10-05 2007-01-04 Chiron Corporation Composes macrocycliques contenant un aryle
US20090036708A1 (en) 2004-10-14 2009-02-05 Lanqi Jia Novel Process for the Preparation of Nonracemic Long Chain alpha-Amino Acid Derivatives
BRPI0517463A (pt) 2004-10-21 2008-10-07 Pfizer inibidores da protease do vìrus da hepatite c, composições e tratamentos usando os mesmos
US7323447B2 (en) 2005-02-08 2008-01-29 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
BRPI0607817B8 (pt) 2005-03-08 2021-05-25 Boehringer Ingelheim Int compostos macrocíclicos e seu processo de preparação
US20080188494A1 (en) 2005-04-25 2008-08-07 Basf Aktiengesellschaft Use Of 5-Alkyl-6-Phenylalkyl-7-Aminoazolopyrimidines, Novel Azolopyrimidines, Processes For Their Preparation And Compositions Comprising Them
US7879797B2 (en) 2005-05-02 2011-02-01 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
US7592336B2 (en) 2005-05-10 2009-09-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
WO2006128455A2 (fr) 2005-05-25 2006-12-07 2Curex Aps Composes modifiant l'apoptose
NZ563361A (en) 2005-06-02 2011-02-25 Schering Corp HCV protease inhibitors in combination with food
US20060276406A1 (en) 2005-06-02 2006-12-07 Schering Corporation Methods of treating hepatitis C virus
US20070004635A1 (en) 2005-06-02 2007-01-04 Schering Corporation Method of treating interferon non-responders using HCV protease inhibitor
US20060276405A1 (en) 2005-06-02 2006-12-07 Schering Corporation Methods for treating hepatitis C
US20060276407A1 (en) 2005-06-02 2006-12-07 Schering Corporation Methods of treating hepatitis C virus
EP1898941A2 (fr) 2005-06-02 2008-03-19 Schering Corporation Formulation a liberation controlee pour le traitement de maladies liees au virus de la hepatite c
WO2006130626A2 (fr) 2005-06-02 2006-12-07 Schering Corporation Procede de modulation de l'activite de la protease du vhc au moyen d'un nouvel inhibiteur de la protease du vhc aux fins de la reduction de la duree du traitement
US20060275366A1 (en) 2005-06-02 2006-12-07 Schering Corporation Controlled-release formulation
US20070021351A1 (en) 2005-06-02 2007-01-25 Schering Corporation Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor
US20070237818A1 (en) 2005-06-02 2007-10-11 Malcolm Bruce A Controlled-release formulation of HCV protease inhibitor and methods using the same
US20060276404A1 (en) 2005-06-02 2006-12-07 Anima Ghosal Medicaments and methods combining a HCV protease inhibitor and an AKR competitor
AU2006252553B2 (en) 2005-06-02 2012-03-29 Merck Sharp & Dohme Corp. Combination of HCV protease inhibitors with a surfactant
US20060287248A1 (en) 2005-06-02 2006-12-21 Schering Corporation Asymmetric dosing methods
US7608592B2 (en) 2005-06-30 2009-10-27 Virobay, Inc. HCV inhibitors
JP5406525B2 (ja) 2005-07-04 2014-02-05 ツァナン・サイテック・カンパニー・リミテッド ルテニウム錯体配位子、ルテニウム錯体、固定化ルテニウム錯体触媒及びその調製方法と用途
US7601686B2 (en) 2005-07-11 2009-10-13 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
TW200738742A (en) 2005-07-14 2007-10-16 Gilead Sciences Inc Antiviral compounds
TWI389908B (zh) 2005-07-14 2013-03-21 Gilead Sciences Inc 抗病毒化合物類
EP1910378B1 (fr) 2005-07-20 2012-06-20 Boehringer Ingelheim International GmbH Analogues de peptides inhibiteurs de l'hepatite c
EP1924594A2 (fr) 2005-07-25 2008-05-28 Intermune, Inc. Nouveaux inhibiteurs macrocycliques de la multiplication du virus de l' hépatite c
RU2436787C2 (ru) 2005-07-29 2011-12-20 Тиботек Фармасьютикалз Лтд. Макроциклические ингибиторы вируса гепатита с
PE20070343A1 (es) 2005-07-29 2007-05-12 Medivir Ab Inhibidores macrociclicos del virus de la hepatitis c
AU2006274862B2 (en) 2005-07-29 2012-03-22 Medivir Ab Macrocyclic inhibitors of hepatitis C virus
PE20070211A1 (es) 2005-07-29 2007-05-12 Medivir Ab Compuestos macrociclicos como inhibidores del virus de hepatitis c
EP1912997B1 (fr) 2005-07-29 2011-09-14 Tibotec Pharmaceuticals Inhibiteurs macrocycliques du virus de l'hépatite c
PL1919904T3 (pl) 2005-07-29 2014-06-30 Janssen R&D Ireland Makrocykliczne inhibitory wirusa zapalenia wątroby typu C
JO2768B1 (en) 2005-07-29 2014-03-15 تيبوتيك فارماسيوتيكالز ليمتد Large cyclic inhibitors of hepatitis C virus
WO2007016441A1 (fr) 2005-08-01 2007-02-08 Merck & Co., Inc. Peptides macrocycliques en tant qu’inhibiteurs de la protéase ns3 du vhc
AR055395A1 (es) 2005-08-26 2007-08-22 Vertex Pharma Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c
DK1934243T3 (da) * 2005-09-09 2011-09-05 Boehringer Ingelheim Int Cykliserende metathesefremgangsmåde til fremstilling af makrocykliske peptider
US7399758B2 (en) 2005-09-12 2008-07-15 Meanwell Nicholas A Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
US7473688B2 (en) 2005-09-13 2009-01-06 Bristol-Myers Squibb Company Indolobenzazepine HCV NS5B inhibitors
US7723336B2 (en) 2005-09-22 2010-05-25 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
EP1999129B1 (fr) 2005-10-11 2010-12-29 Intermune, Inc. Composés et méthodes pour l'inhibition de la réplication du virus de l'hépatite c
US7772183B2 (en) 2005-10-12 2010-08-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7741281B2 (en) 2005-11-03 2010-06-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7456165B2 (en) 2006-02-08 2008-11-25 Bristol-Myers Squibb Company HCV NS5B inhibitors
MX2008012225A (es) 2006-03-23 2008-12-03 Schering Corp Combinaciones de inhibidores de proteasa de virus de hepatitis c e inhibidores de isoenzima 3a4 del citocromo p450, y metodos de tratamiento relacionados con las mismas.
WO2007130592A2 (fr) 2006-05-04 2007-11-15 Crawford Ted C Coiffe pour tête de clé, clé et procédé d'utilisation correspondant
GB0609492D0 (en) 2006-05-15 2006-06-21 Angeletti P Ist Richerche Bio Therapeutic agents
US7456166B2 (en) 2006-05-17 2008-11-25 Bristol-Myers Squibb Company Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
US7521443B2 (en) 2006-05-17 2009-04-21 Bristol-Myers Squibb Company Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
US7521441B2 (en) 2006-05-22 2009-04-21 Bristol-Myers Squibb Company Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
US7521442B2 (en) 2006-05-25 2009-04-21 Bristol-Myers Squibb Company Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
US9526769B2 (en) 2006-06-06 2016-12-27 Enanta Pharmaceuticals, Inc. Macrocylic oximyl hepatitis C protease inhibitors
US20070281884A1 (en) 2006-06-06 2007-12-06 Ying Sun Macrocyclic oximyl hepatitis C protease inhibitors
US8268776B2 (en) 2006-06-06 2012-09-18 Enanta Pharmaceuticals, Inc. Macrocylic oximyl hepatitis C protease inhibitors
US7452876B2 (en) 2006-06-08 2008-11-18 Bristol-Myers Squibb Company Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors
GB0612423D0 (en) 2006-06-23 2006-08-02 Angeletti P Ist Richerche Bio Therapeutic agents
PE20080992A1 (es) 2006-06-26 2008-08-06 Enanta Pharm Inc Quinoxalinil macrociclicos inhibidores de serina proteasa del virus de la hepatitis c
US7935670B2 (en) 2006-07-11 2011-05-03 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
PT2041156E (pt) 2006-07-13 2014-02-21 Achillion Pharmaceuticals Inc Péptidos 4-amino-4-oxobutanoil como inibidores da replicação viral
WO2008019303A2 (fr) 2006-08-04 2008-02-14 Enanta Pharmaceuticals, Inc. Inhibiteurs de sérine protéases de l'hépatite c macrocycliques de type pyridazinonyle
US20090035271A1 (en) 2007-08-01 2009-02-05 Ying Sun Tetrazolyl macrocyclic hepatitis c serine protease inhibitors
US7635683B2 (en) 2006-08-04 2009-12-22 Enanta Pharmaceuticals, Inc. Quinoxalinyl tripeptide hepatitis C virus inhibitors
CA2656816A1 (fr) 2006-08-04 2008-02-14 Enanta Pharmaceuticals, Inc. Inhibiteurs de serine proteases de l'hepatite c macrocycliques de type tetrazolyle
US7582605B2 (en) 2006-08-11 2009-09-01 Enanta Pharmaceuticals, Inc. Phosphorus-containing hepatitis C serine protease inhibitors
US7605126B2 (en) 2006-08-11 2009-10-20 Enanta Pharmaceuticals, Inc. Acylaminoheteroaryl hepatitis C virus protease inhibitors
WO2008021960A2 (fr) 2006-08-11 2008-02-21 Enanta Pharmaceuticals, Inc. Inhibiteurs triazolyle macrocycliques de la sérine protéase de l'hépatite c
WO2008022006A2 (fr) 2006-08-11 2008-02-21 Enanta Pharmaceuticals, Inc. Inhibiteurs de protéase du virus de l'hépatite c arylalcoxyle
US7687459B2 (en) 2006-08-11 2010-03-30 Enanta Pharmaceuticals, Inc. Arylalkoxyl hepatitis C virus protease inhibitors
US20080038225A1 (en) 2006-08-11 2008-02-14 Ying Sun Triazolyl acyclic hepatitis c serine protease inhibitors
JP2010504982A (ja) 2006-09-27 2010-02-18 コーリー ファーマシューティカル グループ,インコーポレイテッド Tlrのリガンドと抗ウイルス剤との組成物
NZ576023A (en) 2006-10-03 2012-06-29 Cadila Healthcare Ltd Antidiabetic compounds comprising a fragment of a glucagon peptide and derivatives thereof
US20120220520A1 (en) 2006-10-17 2012-08-30 Van T Klooster Gerben Albert Eleutherius Bioavailable combinations for hcv treatment
WO2008051475A2 (fr) 2006-10-24 2008-05-02 Merck & Co., Inc. Inhibiteurs de la protéase ns3 du vhc
CN101583372A (zh) 2006-10-24 2009-11-18 默克公司 Hcv ns3蛋白酶抑制剂
BRPI0718161A2 (pt) 2006-10-27 2013-11-26 Merck & Co Inc Composto, composição farmacêutica, e, uso do composto.
CN101568346B (zh) 2006-10-27 2015-11-25 默沙东公司 Hcv ns3蛋白酶抑制剂
US20080107625A1 (en) 2006-11-01 2008-05-08 Bristol-Myers Squibb Company Inhibitors of Hepatitis C Virus
US8343477B2 (en) 2006-11-01 2013-01-01 Bristol-Myers Squibb Company Inhibitors of hepatitis C virus
US20080107623A1 (en) 2006-11-01 2008-05-08 Bristol-Myers Squibb Company Inhibitors of Hepatitis C Virus
US20080108632A1 (en) 2006-11-02 2008-05-08 Taigen Biotechnology Co., Ltd. Hcv protease inhibitors
US7772180B2 (en) 2006-11-09 2010-08-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7888464B2 (en) 2006-11-16 2011-02-15 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
US8637663B2 (en) 2006-11-17 2014-01-28 Janssen R&D Ireland Macrocyclic inhibitors of hepatitis C virus
WO2008070733A2 (fr) 2006-12-06 2008-06-12 Phenomix Corporation Inhibiteurs de serine protéase d'hépatite macrocycliques et leurs utilisations
KR20090101372A (ko) 2007-01-08 2009-09-25 페노믹스 코포레이션 매크로시클릭 c형 간염 프로테아제 억제제
US7541351B2 (en) 2007-01-11 2009-06-02 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US8143402B2 (en) 2007-02-01 2012-03-27 Tibotec Pharmaceuticals Ltd. Polymorphic forms of a macrocyclic inhibitor of HCV
WO2008095058A1 (fr) 2007-02-01 2008-08-07 Taigen Biotechnology Co. Ltd. Inhibiteurs de la protéase du virus de l'hépatite c
BRPI0807482A2 (pt) 2007-02-08 2014-05-13 Tibotec Pharm Ltd Fenilcarbamatos macrocíclicos inibidores de hcv
AU2008212758B2 (en) 2007-02-08 2014-01-30 Medivir Ab Pyrimidine substituted macrocyclic HCV inhibitors
JP2010518128A (ja) 2007-02-16 2010-05-27 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング C型肝炎ns3プロテアーゼのインヒビター
BRPI0807887A2 (pt) 2007-02-20 2014-06-17 Novartis Ag Compostos macrocíclicos como inibidores de hcv ns3 protease.
EP2125113A2 (fr) 2007-02-26 2009-12-02 Achillion Pharmaceuticals, Inc. Peptides substitués par une amine tertiaire utiles comme inhibiteurs de la réplication du virus de l'hépatite c
JP5329444B2 (ja) 2007-03-19 2013-10-30 アストラゼネカ・アクチエボラーグ Toll様受容体(tlr7)モジュレーターとしての9−置換−8−オキソ−アデニン化合物
WO2008124384A2 (fr) 2007-04-03 2008-10-16 Aegerion Pharmaceuticals, Inc. Méthodes de traitement de l'hépatite c
MX2009011370A (es) 2007-04-24 2009-11-05 Hoffmann La Roche Proceso para el intermediario del inhibidor proteasa de hcv.
US7906513B2 (en) 2007-04-26 2011-03-15 Enanta Pharmaceuticals, Inc. Hydrazide-containing hepatitis C serine protease inhibitors
US8377872B2 (en) 2007-04-26 2013-02-19 Enanta Pharmaceuticals, Inc. Cyclic P3 tripeptide hepatitis C serine protease inhibitors
US20080267917A1 (en) 2007-04-26 2008-10-30 Deqiang Niu N-functionalized amides as hepatitis c serine protease inhibitors
US20080279821A1 (en) 2007-04-26 2008-11-13 Deqiang Niu Arylpiperidinyl and arylpyrrolidinyl macrocyclic hepatitis c serine protease inhibitors
CA2686138A1 (fr) 2007-05-03 2008-11-13 Intermune, Inc. Inhibiteurs macrocycliques innovants de la replication du virus de l'hepatite c
AP2009005057A0 (en) 2007-05-10 2009-12-31 Array Biopharma Inc Novel peptide inhibitors of hepatitis c virus replication
US20090005387A1 (en) 2007-06-26 2009-01-01 Deqiang Niu Quinoxalinyl macrocyclic hepatitis c virus serine protease inhibitors
US20090047252A1 (en) 2007-06-29 2009-02-19 Gilead Sciences, Inc. Antiviral compounds
NZ582096A (en) 2007-06-29 2012-05-25 Gilead Sciences Inc Antiviral compounds that inhibit hepatitis c virus (hcv)
AU2008271117B2 (en) 2007-06-29 2013-10-24 Gilead Sciences, Inc. Antiviral compounds
EP2178902B1 (fr) * 2007-07-19 2012-11-28 Istituto di Ricerche di Biologia Molecolare P. Angeletti S.R.L. Composes macrocycliques servant d'agents antiviraux
WO2009014730A1 (fr) 2007-07-26 2009-01-29 Idenix Pharmaceuticals, Inc. Inhibiteurs macrocycliques de la sérine protéase
WO2009053828A2 (fr) 2007-10-22 2009-04-30 Enanta Pharmaceuticals, Inc. Inhibiteurs p3-hydroxyamino macrocycliques des sérine protéases de l'hépatite c
WO2009055335A2 (fr) 2007-10-25 2009-04-30 Taigen Biotechnology Co., Ltd. Inhibiteurs des protéases du vhc
US8426360B2 (en) 2007-11-13 2013-04-23 Enanta Pharmaceuticals, Inc. Carbocyclic oxime hepatitis C virus serine protease inhibitors
MX2010005226A (es) 2007-11-20 2010-05-27 Bristol Myers Squibb Co Inhibidores de ns5b de hcv de indolobenzazepina fusionados a ciclopropilo.
US8263549B2 (en) 2007-11-29 2012-09-11 Enanta Pharmaceuticals, Inc. C5-substituted, proline-derived, macrocyclic hepatitis C serine protease inhibitors
US8030307B2 (en) 2007-11-29 2011-10-04 Enanta Pharmaceuticals, Inc. Bicyclic, C5-substituted proline derivatives as inhibitors of the hepatitis C virus NS3 protease
CA2708042A1 (fr) 2007-12-05 2009-06-11 Enanta Pharmaceuticals, Inc. Derives de quinoxalinyle
US8268777B2 (en) 2007-12-05 2012-09-18 Enanta Pharmaceuticals, Inc. Oximyl macrocyclic derivatives
CA2708047A1 (fr) 2007-12-06 2009-06-11 Enanta Pharmaceuticals, Inc. Procede de preparation d'inhibiteurs de protease de l'hepatite c oximyle macrocycliques
US8293705B2 (en) 2007-12-21 2012-10-23 Avila Therapeutics, 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
US8309685B2 (en) 2007-12-21 2012-11-13 Celgene Avilomics Research, Inc. HCV protease inhibitors and uses thereof
KR101629523B1 (ko) 2007-12-21 2016-06-10 에프. 호프만-라 로슈 아게 대환 화합물의 제조방법
CN104557861A (zh) 2007-12-21 2015-04-29 阿维拉制药公司 Hcv蛋白酶抑制剂和其用途
RU2523790C2 (ru) 2007-12-21 2014-07-27 Авила Терапьютикс, Инк. Ингибиторы протеазы вируса гепатита с и их применение
BRPI0908021A2 (pt) 2008-02-04 2015-07-21 Idenix Pharmaceuticals Inc Composto, composição farmacêutica, e, usos do composto ou da composição farmacêutica
US20100081713A1 (en) 2008-03-19 2010-04-01 CombinatoRx, (Singapore) Pte. Ltd. Compositions and methods for treating viral infections
MX2010011306A (es) 2008-04-15 2010-11-09 Intermune Inc Nuevos inhibidores macrociclicos de la replicacion del virus de la hepatitis c.
US8163921B2 (en) 2008-04-16 2012-04-24 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
WO2009137432A1 (fr) 2008-05-09 2009-11-12 Boehringer Ingelheim International Gmbh Procédé pour la fabrication de macrocycles
US20090285774A1 (en) 2008-05-15 2009-11-19 Bristol-Myers Squibb Company Hepatitis C Virus Inhibitors
US20090285773A1 (en) 2008-05-15 2009-11-19 Bristol-Myers Squibb Company Hepatitis C Virus Inhibitors
CN101580535B (zh) 2008-05-16 2012-10-03 太景生物科技股份有限公司 丙型肝炎病毒蛋白酶抑制剂
CN102046648A (zh) 2008-05-29 2011-05-04 百时美施贵宝公司 丙型肝炎病毒抑制剂
US7964560B2 (en) 2008-05-29 2011-06-21 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
CA2727026A1 (fr) 2008-06-05 2009-12-10 Zymogenetics, Llc Utilisation d'interferons de type iii pegyles dans le traitement de l'hepatite c
TW201012814A (en) 2008-07-01 2010-04-01 Centocor Ortho Biotech Products L P Cyclopropyl polymerase inhibitors
JP5728752B2 (ja) 2008-08-07 2015-06-03 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 大環状化合物の製造方法
US8765667B2 (en) 2008-08-20 2014-07-01 Michael Eissenstat HCV protease inhibitors
WO2010028236A1 (fr) 2008-09-05 2010-03-11 Avila Therapeutics, Inc. Algorithme pour concevoir des inhibiteurs irréversibles
UY32099A (es) * 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
ES2474992T3 (es) 2008-09-16 2014-07-10 Boehringer Ingelheim International Gmbh Formas cristalinas de un derivado de 2-tiazolil-4-quinolinil-oxi, un potente inhibidor de HCV
WO2010033466A1 (fr) 2008-09-16 2010-03-25 Phenomix Corporation Inhibiteurs macrocycliques de la protéase du virus de l'hépatite c
CN102159245B (zh) 2008-09-17 2013-07-24 贝林格尔.英格海姆国际有限公司 Hcv ns3蛋白酶抑制剂与干扰素和利巴韦林的组合
US8603737B2 (en) 2008-09-19 2013-12-10 Celgene Avilomics Research, Inc. Methods for identifying HCV protease inhibitors
EP2344487A4 (fr) 2008-09-23 2012-03-21 Boehringer Ingelheim Int Composés inhibiteurs de l'hépatite c
US8044087B2 (en) 2008-09-29 2011-10-25 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US20100080770A1 (en) 2008-09-29 2010-04-01 Bristol-Myers Squibb Company Hepatitis C Virus Inhibitors
US8563505B2 (en) 2008-09-29 2013-10-22 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
TWI480272B (zh) 2008-10-09 2015-04-11 Anadys Pharmaceuticals Inc 藉由5,6-二氫-1h-吡啶-2-酮與一或多種其他抗病毒化合物的組合物抑制c型肝炎病毒的方法
WO2010048468A1 (fr) 2008-10-23 2010-04-29 Concert Pharmaceuticals, Inc. Inhibiteurs macrocycliques deutériés de la protéase virale ns3
US8296141B2 (en) * 2008-11-19 2012-10-23 At&T Intellectual Property I, L.P. System and method for discriminative pronunciation modeling for voice search
EP2350114A1 (fr) 2008-11-20 2011-08-03 Achillion Pharmaceuticals, Inc. Composés cycliques de carboxamide et analogues de ceux-ci utilisés comme inhibiteurs du virus de l hépatite c
SG171771A1 (en) 2008-11-21 2011-07-28 Boehringer Ingelheim Int Pharmaceutical composition of a potent hcv inhibitor for oral administration
US20100272674A1 (en) 2008-12-04 2010-10-28 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
EP2393493A4 (fr) 2009-01-30 2013-07-17 Glaxosmithkline Llc Composés
EP2413955A4 (fr) 2009-04-01 2012-12-26 Amylin Pharmaceuticals Inc Composés agonistes des récepteurs au glp-1 présentant des contraintes conformationnelles au niveau de leur extrémité n-terminale
TW201040181A (en) 2009-04-08 2010-11-16 Idenix Pharmaceuticals Inc Macrocyclic serine protease inhibitors
CN102405229A (zh) 2009-04-24 2012-04-04 卡迪拉保健有限公司 作为甲状旁腺激素(pth)受体激动剂的短链肽
US20100297079A1 (en) 2009-05-20 2010-11-25 Chimerix, Inc. Compounds, compositions and methods for treating viral infection
CA2763122A1 (fr) 2009-05-22 2010-11-25 Sequoia Pharmaceuticals Inc. Inhibiteurs de la protease ns3 du virus de l'hepatite c bimacrocyclique
US8232246B2 (en) 2009-06-30 2012-07-31 Abbott Laboratories Anti-viral compounds
US20110020272A1 (en) 2009-07-24 2011-01-27 Ulrich Schubert Combination therapy for treating hepatitis viral infection
TW201117812A (en) 2009-08-05 2011-06-01 Idenix Pharmaceuticals Inc Macrocyclic serine protease inhibitors
US8389560B2 (en) 2009-09-15 2013-03-05 Taigen Biotechnology Co., Ltd. HCV protease inhibitors
JP2013511562A (ja) 2009-11-24 2013-04-04 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング C型肝炎阻害化合物
EP2504343A4 (fr) 2009-11-24 2013-04-17 Boehringer Ingelheim Int Composés inhibiteurs de l'hépatite c
US20110178107A1 (en) 2010-01-20 2011-07-21 Taigen Biotechnology Co., Ltd. Hcv protease inhibitors

Also Published As

Publication number Publication date
SI2468287T1 (sl) 2014-08-29
ES2459390T3 (es) 2014-05-09
LTC2340029I2 (lt) 2016-12-27
DK2468286T3 (da) 2014-07-28
EA022891B1 (ru) 2016-03-31
KR101487726B1 (ko) 2015-01-29
PE20140961A1 (es) 2014-08-24
JP2013163680A (ja) 2013-08-22
HUE039478T2 (hu) 2019-01-28
CO6341565A2 (es) 2011-11-21
HK1170937A1 (zh) 2013-03-15
CA2736895C (fr) 2016-02-09
NZ592170A (en) 2013-02-22
JP2010065035A (ja) 2010-03-25
US20120196792A1 (en) 2012-08-02
EP2340029A4 (fr) 2012-06-13
ECSP12011947A (es) 2012-07-31
US8642538B2 (en) 2014-02-04
HRP20140492T1 (hr) 2014-09-12
DK2468285T3 (en) 2015-01-19
EP2468287A1 (fr) 2012-06-27
ZA201200950B (en) 2013-09-25
AR093924A2 (es) 2015-06-24
JP5534533B2 (ja) 2014-07-02
TW201231064A (en) 2012-08-01
TR201809771T4 (tr) 2018-07-23
EA020580B1 (ru) 2014-12-30
TWI450723B (zh) 2014-09-01
BRPI0918724A8 (pt) 2017-10-03
ES2677644T3 (es) 2018-08-06
NL300730I1 (fr) 2016-01-07
KR20120044316A (ko) 2012-05-07
CY1115844T1 (el) 2017-01-25
WO2010030359A2 (fr) 2010-03-18
WO2010030359A3 (fr) 2010-05-27
EP2468285B1 (fr) 2014-10-15
ES2475815T3 (es) 2014-07-11
TWI510245B (zh) 2015-12-01
GT201100056AA (es) 2014-09-26
ES2525922T3 (es) 2015-01-02
US20140148573A1 (en) 2014-05-29
TW201417826A (zh) 2014-05-16
IL218441A (en) 2015-09-24
JP5259537B2 (ja) 2013-08-07
NL300730I2 (fr) 2016-01-07
IL234969A0 (en) 2014-11-30
US20100144608A1 (en) 2010-06-10
AR086181A2 (es) 2013-11-27
NO2015014I1 (no) 2015-05-04
TWI429449B (zh) 2014-03-11
EP2340029A2 (fr) 2011-07-06
HRP20141169T1 (hr) 2015-02-13
PL2805726T3 (pl) 2018-11-30
SI2340029T1 (sl) 2014-08-29
CY2015014I1 (el) 2016-08-31
EP2805726A1 (fr) 2014-11-26
EP2468285A1 (fr) 2012-06-27
MY159820A (en) 2017-02-15
PL2468286T3 (pl) 2014-09-30
AU2009292182B2 (en) 2013-06-06
CN102641271B (zh) 2013-12-25
CY1115137T1 (el) 2016-04-13
US9309279B2 (en) 2016-04-12
BRPI0918724A2 (pt) 2013-06-18
CY1115202T1 (el) 2017-04-26
PL2340029T3 (pl) 2014-12-31
KR20140056195A (ko) 2014-05-09
HRP20181075T1 (hr) 2018-09-07
SI2805726T1 (sl) 2018-09-28
DK2468287T3 (da) 2014-07-28
CN101775017B (zh) 2014-04-30
SG179414A1 (en) 2012-04-27
GT201100056BA (es) 2015-04-22
PA8842201A1 (es) 2010-04-21
SI2468286T1 (sl) 2014-08-29
CA2736895A1 (fr) 2010-03-18
EP2468286B1 (fr) 2014-04-23
MX2011002486A (es) 2011-04-26
PT2468286E (pt) 2014-07-15
KR20100031092A (ko) 2010-03-19
HRP20140493T1 (hr) 2014-07-18
JP5801342B2 (ja) 2015-10-28
CN101775017A (zh) 2010-07-14
EP2468287B1 (fr) 2014-04-23
KR101379365B1 (ko) 2014-03-31
DOP2011000077A (es) 2011-04-30
HK1159515A1 (en) 2012-08-03
PL2468285T3 (pl) 2015-03-31
DK2805726T3 (en) 2018-07-30
CY1120780T1 (el) 2019-12-11
JP2012136546A (ja) 2012-07-19
ZA201101558B (en) 2018-11-28
PE20121312A1 (es) 2012-10-28
CL2012001495A1 (es) 2013-07-12
PE20110704A1 (es) 2011-11-12
LT2805726T (lt) 2018-08-10
EA201170434A1 (ru) 2011-10-31
SI2468285T1 (sl) 2015-01-30
CY2015014I2 (el) 2016-08-31
CN102641271A (zh) 2012-08-22
EP2805726B1 (fr) 2018-05-02
BRPI0918724B1 (pt) 2019-12-03
EA201200390A1 (ru) 2012-12-28
PL2468287T3 (pl) 2014-09-30
JP5902123B2 (ja) 2016-04-13
CY1115379T1 (el) 2017-01-04
CN103896950A (zh) 2014-07-02
BR122012005261A2 (pt) 2015-07-14
HK1171184A1 (en) 2013-03-22
CR20140180A (es) 2014-06-03
AU2009292182A1 (en) 2010-03-18
PT2468285E (pt) 2015-02-04
UY33981A (es) 2013-10-31
BR122012005261A8 (pt) 2017-09-19
US8420596B2 (en) 2013-04-16
HRP20140494T1 (hr) 2014-07-04
IL218441A0 (en) 2012-04-30
NZ605550A (en) 2014-06-27
EP2468286A1 (fr) 2012-06-27
ECSP11010879A (es) 2011-04-29
TW201023875A (en) 2010-07-01
HK1170936A1 (en) 2013-03-15
JP2013227314A (ja) 2013-11-07
UY32099A (es) 2010-04-30
DK2340029T3 (da) 2014-06-10
AR073568A1 (es) 2010-11-17
PT2468287E (pt) 2014-07-15
PT2805726T (pt) 2018-07-23
WO2010030359A8 (fr) 2011-05-12
CL2011000512A1 (es) 2011-06-17
NO2015014I2 (no) 2015-04-22
HUS1500020I1 (hu) 2018-12-28
PT2340029E (pt) 2014-05-13
ES2475163T3 (es) 2014-07-10
UY35259A (es) 2015-08-31
BRPI0918724B8 (pt) 2021-05-25
EP2340029B1 (fr) 2014-03-05

Similar Documents

Publication Publication Date Title
LU92667I2 (fr) Paritaprevir, ou un sel ou ester pharmaceutiquement acceptable qui en dérive (viekirax)
LU92668I2 (fr) Ombitasvir, ou un sel pharmaceutiquement acceptable qui en dérive (viekirax)
NO2020037I1 (no) alpelisib eller et farmasøytisk akseptabelt salt derav
NO2023047I1 (no) Cedazuridine, or a pharmaceutically acceptable salt thereof
NO2024006I1 (no) Piflufolastat (18F) or a pharmaceutically acceptable salt thereof
NO2019024I1 (no) Brigatinib eller et farmasøytisk akseptabelt salt derav
NO2020006I1 (no) upadacitinib or a pharmaceutically acceptable salt thereof
NO2022033I1 (no) Rimegepant or a pharmaceutically acceptable salt thereof
NO2020038I1 (no) Ozanimod, or a pharmaceutically acceptable salt thereof, including the hydrochloride salt
NO2017059I2 (no) ribosiklib eller et farmasøytisk akseptabelt salt derav
NO2016016I1 (no) Lesinurad, eller et farmasøytisk akseptabelt salt derav
NO20091125L (no) Stigerorsklemme
ATE450271T1 (de) Impfstoff
IT1391473B1 (it) Dispositivo di monitoraggio per un apparecchio antincendio.
NO2023002I1 (no) Lasmiditan or a pharmaceutically acceptable salt thereof
FR2933381B1 (fr) Distributeur a tete amovible.
BRPI1008708A2 (pt) gastroscópio.
FR2942385B1 (fr) Grille-pain.
BRPI0815716A2 (pt) Decapagem secundária econômica.
FI20095741A (fi) Suihkutuspää
ITAL20080002A1 (it) Livellatrice a controllo laser
BRPI0912193A2 (pt) compostos terapêuticos.
NL2002599A1 (nl) Hoogwerker.
FR2899083B1 (fr) Grille-pain
FR2914669B1 (fr) Escalier escamotable.