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HRP20110458T1 - Inhibitori rna-ovisne rna-polimeraze iz virusa hepatitisa c, te pripravci i liječenje u kojem se koriste - Google Patents

Inhibitori rna-ovisne rna-polimeraze iz virusa hepatitisa c, te pripravci i liječenje u kojem se koriste Download PDF

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Publication number
HRP20110458T1
HRP20110458T1 HR20110458T HRP20110458T HRP20110458T1 HR P20110458 T1 HRP20110458 T1 HR P20110458T1 HR 20110458 T HR20110458 T HR 20110458T HR P20110458 T HRP20110458 T HR P20110458T HR P20110458 T1 HRP20110458 T1 HR P20110458T1
Authority
HR
Croatia
Prior art keywords
ethyl
methyl
triazolo
cyclopentyl
pyran
Prior art date
Application number
HR20110458T
Other languages
English (en)
Croatian (hr)
Inventor
Gonzalez Javier
Michelle Jewell Tanya
Li Hui
Linton Angelica
Howard Tatlock John
Original Assignee
Pfizer 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 Pfizer Inc. filed Critical Pfizer Inc.
Publication of HRP20110458T1 publication Critical patent/HRP20110458T1/hr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Pyrane Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
HR20110458T 2004-08-18 2005-08-05 Inhibitori rna-ovisne rna-polimeraze iz virusa hepatitisa c, te pripravci i liječenje u kojem se koriste HRP20110458T1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US60261804P 2004-08-18 2004-08-18
PCT/IB2005/002697 WO2006018725A1 (fr) 2004-08-18 2005-08-05 Inhibiteurs de polymerase d'arn dependant d'arn du virus de l'hepatite c et compositions et traitement utilisant ces inhibiteurs

Publications (1)

Publication Number Publication Date
HRP20110458T1 true HRP20110458T1 (hr) 2011-07-31

Family

ID=35429645

Family Applications (1)

Application Number Title Priority Date Filing Date
HR20110458T HRP20110458T1 (hr) 2004-08-18 2005-08-05 Inhibitori rna-ovisne rna-polimeraze iz virusa hepatitisa c, te pripravci i liječenje u kojem se koriste

Country Status (42)

Country Link
US (3) US7151105B2 (fr)
EP (1) EP1781662B1 (fr)
JP (1) JP4372195B2 (fr)
KR (1) KR100851178B1 (fr)
CN (2) CN101006092B (fr)
AP (1) AP2313A (fr)
AR (1) AR050699A1 (fr)
AT (1) ATE506364T1 (fr)
AU (1) AU2005273619B2 (fr)
BR (1) BRPI0514425A (fr)
CA (1) CA2577525C (fr)
CR (2) CR8935A (fr)
CY (1) CY1111480T1 (fr)
DE (1) DE602005027580D1 (fr)
DK (1) DK1781662T3 (fr)
EA (1) EA012605B1 (fr)
EC (1) ECSP077264A (fr)
ES (1) ES2361845T3 (fr)
GE (2) GEP20115305B (fr)
GT (1) GT200500221A (fr)
HN (1) HN2005000449A (fr)
HR (1) HRP20110458T1 (fr)
IL (2) IL180933A (fr)
MA (1) MA28803B1 (fr)
MX (1) MX2007001527A (fr)
MY (1) MY146123A (fr)
NI (1) NI200700043A (fr)
NL (1) NL1029755C2 (fr)
NO (1) NO20071274L (fr)
NZ (1) NZ552874A (fr)
PE (1) PE20060677A1 (fr)
PL (1) PL1781662T3 (fr)
PT (1) PT1781662E (fr)
RS (1) RS51794B (fr)
SI (1) SI1781662T1 (fr)
SV (1) SV2007002202A (fr)
TN (1) TNSN07066A1 (fr)
TW (1) TWI376379B (fr)
UA (1) UA88909C2 (fr)
UY (1) UY29068A1 (fr)
WO (1) WO2006018725A1 (fr)
ZA (1) ZA200700779B (fr)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101006092B (zh) * 2004-08-18 2013-04-17 辉瑞有限公司 C型肝炎病毒rna依赖型rna聚合酶的抑制剂、以及使用该抑制剂的组合物和治疗剂
CN102336758A (zh) 2005-08-24 2012-02-01 辉瑞有限公司 作为hcv聚合酶抑制剂的化合物及组合物
CA2686051A1 (fr) 2007-05-04 2008-11-13 Vertex Pharmaceuticals Incorporated Therapie combinee pour le traitement d'une infection par le vhc
EP2008996A1 (fr) * 2007-06-27 2008-12-31 Syngeta Participations AG Procédé de production de pyrazoles
EP2280989B1 (fr) 2008-06-06 2016-02-10 Scynexis, Inc. Analogues de la cyclosporine et leur utilisation dans le traitement d'infections par le vhc
EP2320905B1 (fr) 2008-08-11 2017-06-28 Glaxosmithkline LLC Nouveaux dérivés d'adénine
UA103195C2 (uk) 2008-08-11 2013-09-25 Глаксосмитклайн Ллк Похідні пурину для застосування у лікуванні алергій, запальних та інфекційних захворювань
CN102203095A (zh) 2008-08-11 2011-09-28 葛兰素史密丝克莱恩有限责任公司 用于治疗变应性疾病、炎性疾病和感染性疾病的嘌呤衍生物
UY32940A (es) 2009-10-27 2011-05-31 Bayer Cropscience Ag Amidas sustituidas con halogenoalquilo como insecticidas y acaricidas
EA201200650A1 (ru) 2009-10-30 2012-12-28 Бёрингер Ингельхайм Интернациональ Гмбх Курсы комбинированного лечения вируса гепатита с, включающие bi201335, интерферон-альфа и рибавирин
EP2325173A1 (fr) 2009-11-19 2011-05-25 Bayer CropScience AG Procédé de fabrication de chlorures d'acide 5-fluoro-1-alkyl-3-fluoralkyl-1H-pyrazole-4-carboxylique
NZ599963A (en) * 2009-12-18 2014-02-28 Boehringer Ingelheim Int Hcv combination therapy
JP5922587B2 (ja) 2010-02-10 2016-05-24 グラクソスミスクライン エルエルシー ６−アミノ−２−｛［（１ｓ）−１−メチルブチル］オキシ｝−９−［５−（１−ピペリジニル）ペンチル］−７，９−ジヒドロ−８ｈ−プリン−８−オンマレイン酸塩
JP2013519644A (ja) 2010-02-10 2013-05-30 グラクソスミスクライン エルエルシー プリン誘導体およびそれらの薬学的使用
MX2012013388A (es) * 2010-05-20 2012-12-10 Bayer Ip Gmbh Metodo para fabricar 1-alquil-3-difluorometil-5-hidroxipirazoles.
US8987307B2 (en) 2011-03-03 2015-03-24 Hoffmann-La Roche Inc. 3-amino-pyridines as GPBAR1 agonists
FR2972452B1 (fr) 2011-03-09 2013-03-15 Rhodia Operations Procede de preparation du difluoroacetonitrile et de ses derives
US9145369B2 (en) 2012-05-14 2015-09-29 Bayer Cropscience Ag Process for preparing 1-alkyl-3-fluoroalkyl-1H-pyrazole-4-carboxylic acid chlorides
US9163027B2 (en) 2012-11-21 2015-10-20 Stategics, Inc. Substituted triazolo-pyrimidine compounds for modulating cell proliferation differentiation and survival
JP6349329B2 (ja) 2013-01-17 2018-06-27 バイエル・クロップサイエンス・アクチェンゲゼルシャフト ５−フルオロ−１−メチル−３−ジフルオロメチル−１ｈ−ピラゾール−４−カルバルデヒドを調製する方法
US9487489B2 (en) 2013-02-06 2016-11-08 Bayer Cropscience Aktiengesellschaft Halogen-substituted pyrazole derivatives as pest-control agents
JP2017502964A (ja) 2014-01-03 2017-01-26 バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング 殺有害生物剤としての新規ピラゾリル−ヘテロアリールアミド類
WO2015110493A1 (fr) 2014-01-24 2015-07-30 Bayer Cropscience Ag Procédé de préparation de 1-alkyl-3-difluorométhyl-5-fluor-1h-pyrazole-4-carbaldéhydes et de 1-alkyl-3-difluorométhyl-5-fluor-1h-pyrazole-4-carboxylates
RU2676684C2 (ru) 2014-02-20 2019-01-10 ГлаксоСмитКлайн Интеллекчуал Проперти (No.2) Лимитед ПРОИЗВОДНЫЕ ПИРРОЛО[3,2-d]ПИРИМИДИНА В КАЧЕСТВЕ ИНДУКТОРОВ ЧЕЛОВЕЧЕСКОГО ИНТЕРФЕРОНА
SI3152199T1 (sl) 2014-06-03 2018-12-31 Idorsia Pharmaceuticals Ltd Pirazolne spojine in njihova uporaba kot blokatorji kalcijevega kanala tipa T
BR112017009648A2 (pt) 2014-11-13 2017-12-19 Glaxosmithkline Biologicals Sa composto, métodos para tratamento de doenças alérgicas ou outras condições inflamatórias ou prevenção de doença, de rinite alérgica ou asma, composição, e, uso de um composto.
WO2017093180A1 (fr) 2015-12-01 2017-06-08 Bayer Cropscience Aktiengesellschaft Dérivés hétérocycles bicycliques condensés utilisés en tant que produits de lutte antiparasitaire
RU2020113165A (ru) 2015-12-03 2020-06-09 Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед Циклические пуриновые динуклеотиды в качестве модуляторов sting
MX387353B (es) 2016-04-07 2025-03-18 Glaxosmithkline Ip Dev Ltd Amidas heterocíclicas útiles como moduladores de proteínas.
MX2018012266A (es) 2016-04-07 2019-05-30 Glaxosmithkline Ip Dev Ltd Amidas heterociclicas como moduladores de proteinas.
WO2018033455A1 (fr) 2016-08-15 2018-02-22 Bayer Cropscience Aktiengesellschaft Dérivés hétérocycliques bicycliques condensés utilisés comme pesticides
EP3301094A1 (fr) * 2016-09-30 2018-04-04 Mutabilis Nouveaux composés hétérocycliques et leur utilisation dans la prévention ou le traitement d'infections bactériennes
DK3554490T3 (da) 2016-12-16 2022-02-28 Idorsia Pharmaceuticals Ltd Farmaceutisk kombination omfattende en calciumkanalblokker type T
EP3577099B1 (fr) 2017-02-06 2024-01-24 Idorsia Pharmaceuticals Ltd Un procédé nouveau pour la préparation des 1-aryl-1-trifluorométhylcyclopropanes
AU2018344370C1 (en) 2017-10-04 2023-04-27 Bayer Aktiengesellschaft Derivatives of heterocyclic compounds as pest control agents
EP3692033A1 (fr) 2017-10-05 2020-08-12 GlaxoSmithKline Intellectual Property Development Limited Modulateurs de stimulateur des gènes (sting) d'interféron utiles dans le traitement du vih
JP7291130B2 (ja) 2017-10-05 2023-06-14 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッド インターフェロン遺伝子の刺激物質（ｓｔｉｎｇ）の調節物質
EP3765466B1 (fr) 2018-03-12 2022-05-25 Bayer Aktiengesellschaft Dérivés d'hétérocyclène bicycliques condensés en tant que pesticides
BR112020020081A2 (pt) 2018-04-20 2021-01-05 Bayer Aktiengesellschaft Derivados de heterocicleno como agentes de controle de pragas
GB201807924D0 (en) 2018-05-16 2018-06-27 Ctxt Pty Ltd Compounds
WO2020232378A1 (fr) 2019-05-16 2020-11-19 Silicon Swat, Inc. Dérivés d'acide acétique benzo[b][1,8]naphtyridine et leur procédés d'utilisation
EP3969438A1 (fr) 2019-05-16 2022-03-23 Stingthera, Inc. Dérivés d'acide oxoacridinyle acétique et procédés d'utilisation
GB201910305D0 (en) 2019-07-18 2019-09-04 Ctxt Pty Ltd Compounds
GB201910304D0 (en) 2019-07-18 2019-09-04 Ctxt Pty Ltd Compounds
WO2021119753A1 (fr) 2019-12-18 2021-06-24 Ctxt Pty Limited Composés
US12274700B1 (en) 2020-10-30 2025-04-15 Accencio LLC Methods of treating symptoms of coronavirus infection with RNA polymerase inhibitors
CN112194620B (zh) * 2020-12-04 2021-02-26 苏州开元民生科技股份有限公司 一种2-乙基-4-氰基吡啶的制备方法
CN113563167B (zh) * 2021-07-16 2023-09-08 南通华祥医药科技有限公司 一种2-甲基-1-四氢萘酮的制备方法

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3786063A (en) 1971-05-24 1974-01-15 Universal Oil Prod Co Thiazolethiosulfonates
DE2155360C3 (de) * 1971-11-08 1980-04-03 Cassella Ag, 6000 Frankfurt Verfahren zur Herstellung von Acylbernsteinsäuredialkylestern
CA1144937A (fr) 1977-12-22 1983-04-19 Dke J.E. Helgstrand Derives aromatiques, composes pharmaceutiques et methode pour combattre les infections a virus
US4326058A (en) 1979-02-05 1982-04-20 Sumitomo Chemical Company, Limited Organo-phosphoric esters and their production and use
US4489077A (en) 1983-03-23 1984-12-18 Warner-Lambert Company 3-Isoxa-zolyl-2H-1,2-benzothiazine-3-carboxamide, 1,1-dioxides
US6174868B1 (en) 1992-09-10 2001-01-16 Isis Pharmaceuticals, Inc. Compositions and methods for treatment of hepatitis C virus-associated diseases
CA2167537A1 (fr) 1993-07-19 1995-02-02 Tsuneo Ozeki Inhibiteur de la proliferation du virus de l¨hepatite c
HUT75225A (en) 1993-11-19 1997-04-28 Parke Davis & Co 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents
CA2176043A1 (fr) 1993-11-19 1995-05-26 Warner-Lambert Company Derives de la 5,6-dihydropyrone en tant qu'inhibiteurs de la protease et agents antiviraux
US5840751A (en) 1993-11-19 1998-11-24 Warner-Lambert Company 5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents
US5808062A (en) 1993-11-19 1998-09-15 Warner-Lambert Company Pyrone derivatives as protease inhibitors and antiviral agents
US5504104A (en) 1993-11-19 1996-04-02 Warner-Lambert Company Tricyclic pyrone derivatives as protease inhibitors and antiviral agents
US5834506A (en) 1996-11-01 1998-11-10 Warner-Lambert Company Dihydropyrones with improved antiviral activity
NZ510013A (en) 1998-09-11 2003-11-28 Warner Lambert Co Dihydropyrones with selected heterocycles replacing the phenyls bearing polar substituents used as HIV protease inhibitors
US6512006B1 (en) 1999-12-09 2003-01-28 Warner-Lambert Company HIV protease inhibitors
EP1256628A3 (fr) 2001-05-10 2003-03-19 Agouron Pharmaceuticals, Inc. ARN polymerase NS5B du virus de la hepatite C et mutants derivés de la polymerase
DOP2003000641A (es) * 2002-05-10 2003-11-15 Pfizer Inhibidores de las arn polimerasa dependiente de arn del virus de las hepatitis c y composiciones y tratamiento que los usan
US7148226B2 (en) * 2003-02-21 2006-12-12 Agouron Pharmaceuticals, Inc. Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same
CN101006092B (zh) * 2004-08-18 2013-04-17 辉瑞有限公司 C型肝炎病毒rna依赖型rna聚合酶的抑制剂、以及使用该抑制剂的组合物和治疗剂

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US20060122399A1 (en) 2006-06-08
CR20110153A (es) 2011-04-26
PT1781662E (pt) 2011-07-01
NO20071274L (no) 2007-05-14
KR100851178B1 (ko) 2008-08-08
PL1781662T3 (pl) 2011-08-31
UY29068A1 (es) 2006-03-31
KR20070044057A (ko) 2007-04-26
TW200612898A (en) 2006-05-01
GEP20094751B (en) 2009-08-10
ZA200700779B (en) 2008-11-26
CN101006092A (zh) 2007-07-25
PE20060677A1 (es) 2006-08-11
TNSN07066A1 (fr) 2008-06-02
US7622605B2 (en) 2009-11-24
DK1781662T3 (da) 2011-06-27
CR8935A (es) 2007-07-24
GT200500221A (es) 2006-06-21
EA012605B1 (ru) 2009-10-30
JP2008509984A (ja) 2008-04-03
EA200700338A1 (ru) 2007-08-31
NL1029755C2 (nl) 2006-10-18
CN101538268A (zh) 2009-09-23
AR050699A1 (es) 2006-11-15
MA28803B1 (fr) 2007-08-01
AU2005273619A1 (en) 2006-02-23
US20090281122A1 (en) 2009-11-12
BRPI0514425A (pt) 2008-06-10
HK1109617A1 (en) 2008-06-13
AP2007003918A0 (en) 2007-02-28
US20070015764A1 (en) 2007-01-18
CY1111480T1 (el) 2015-08-05
JP4372195B2 (ja) 2009-11-25
IL180933A (en) 2011-08-31
CA2577525A1 (fr) 2006-02-23
AU2005273619B2 (en) 2009-05-28
SI1781662T1 (sl) 2011-07-29
UA88909C2 (ru) 2009-12-10
ATE506364T1 (de) 2011-05-15
MY146123A (en) 2012-06-29
NI200700043A (es) 2008-01-02
CA2577525C (fr) 2010-03-30
CN101538268B (zh) 2011-07-27
IL192919A0 (en) 2009-02-11
ES2361845T3 (es) 2011-06-22
NZ552874A (en) 2010-04-30
MX2007001527A (es) 2007-03-27
NL1029755A1 (nl) 2006-02-21
US7151105B2 (en) 2006-12-19
IL180933A0 (en) 2007-07-04
GEP20115305B (en) 2011-10-10
US8268835B2 (en) 2012-09-18
RS51794B (en) 2011-12-31
AP2313A (en) 2011-10-31
EP1781662A1 (fr) 2007-05-09
EP1781662B1 (fr) 2011-04-20
SV2007002202A (es) 2007-03-20
DE602005027580D1 (de) 2011-06-01
ECSP077264A (es) 2007-04-26
HN2005000449A (es) 2009-10-30
WO2006018725A1 (fr) 2006-02-23
CN101006092B (zh) 2013-04-17
TWI376379B (en) 2012-11-11

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