EA022891B1 - Применение макроциклических ингибиторов сериновых протеаз гепатита с - Google Patents
Применение макроциклических ингибиторов сериновых протеаз гепатита с Download PDFInfo
- Publication number
- EA022891B1 EA022891B1 EA201200390A EA201200390A EA022891B1 EA 022891 B1 EA022891 B1 EA 022891B1 EA 201200390 A EA201200390 A EA 201200390A EA 201200390 A EA201200390 A EA 201200390A EA 022891 B1 EA022891 B1 EA 022891B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- patient
- hexadecahydrocycloprop
- diazacyclopentadecin
- pyrrolo
- dioxo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General 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
- C07K1/113—General 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
-
- 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
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
- A61K31/407—Heterocyclic 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
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Abstract
Изобретение относится к макроциклам с активностью против вируса гепатита С (HCV) и пригодным для лечения инфекций HCV. Более конкретно изобретение относится к макроциклическим соединениям для лечения инфекции HCV у пациента.
Description
(57) Изобретение относится к макроциклам с активностью против вируса гепатита С (НСУ) и пригодным для лечения инфекций НСУ Более конкретно изобретение относится к макроциклическим соединениям для лечения инфекции НСУ у пациента.
Claims (7)
1. Применение соединения, представляющего собой (2К,6δ,13аδ,14аК,16аδ,Ζ)-N(циклопропилсульфонил)-5,16-диоксо-2-(фенантридин-6-илокси)-6-(пиразин-2-карбоксамидо)1,2,3,5,6,7,8,9,10,11,13а,14,14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-14а-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
2. Применение соединения, представляющего собой ^((УК/^тм^иаКУж^ХБиа(циклопропилсульфонилкарбамоил)-5,16-диоксо-2-(фенантридин-6-илокси)-1,2,3,5,6,7,8,9,10,11,13а,14, 14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-6-ил)-5-метилизоксазол-3-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
3. Применение соединения, представляющего собой (2К,6δ,13аδ,14аК,16аδ,Ζ)-N(циклопропилсульфонил)-6-(5-метилпиразин-2-карбоксамидо)-5,16-диоксо-2-(фенантридин-6-илокси)1,2,3,5,6,7,8,9,10,11,13а,14,14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-14а-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
4. Применение соединения, представляющего собой N-((2К,6δ,13аδ,14аК,16аδ,Ζ)-14а(циклопропилсульфонилкарбамоил)-5,16-диоксо-2-(фенантридин-6-илокси)-1,2,3,5,6,7,8,9,10,11,13а,14, 14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-6-ил)тиазол-5карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
5. Применение соединения, представляющего собой (2К,6δ,13аδ,14аК,16аδ,Ζ)-N(циклопропилсульфонил)-5,16-диоксо-2-(фенантридин-6-илокси)-6-(пиридазин-4-карбоксамидо)-1,2,3,5, 6,7,8,9,10,11,13а,14,14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-14а-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
6. Применение соединения, представляющего собой (2К,6δ,13аδ,14аК,16аδ,Ζ)-N(циклопропилсульфонил)-6-(1,5-диметил-1Н-пиразол-3-карбоксамидо)-5,16-диоксо-2-(фенантридин-6илокси)-1,2,3,5,6,7,8,9,10,11,13а,14,14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-14а-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
7. Применение соединения, представляющего собой (2К,6δ,13аδ,14аК,16аδ,Ζ)-N(циклопропилсульфонил)-6-(5-метил-1Н-пиразол-3-карбоксамидо)-5,16-диоксо-2-(фенантридин-6-илокси)-1,2,3,5,6,7,8,9,10,11,13а,14,14а,15,16,16а-гексадекагидроциклопропа[е]пирроло[1,2-а][1,4]диазациклопентадецин-14а-карбоксамид или его фармацевтически приемлемую соль, для лечения инфекции НСУ у пациента.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19172508P | 2008-09-11 | 2008-09-11 | |
US20968909P | 2009-03-10 | 2009-03-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201200390A1 EA201200390A1 (ru) | 2012-12-28 |
EA022891B1 true EA022891B1 (ru) | 2016-03-31 |
Family
ID=42005677
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201200390A EA022891B1 (ru) | 2008-09-11 | 2009-09-10 | Применение макроциклических ингибиторов сериновых протеаз гепатита с |
EA201170434A EA020580B1 (ru) | 2008-09-11 | 2009-09-10 | Макроциклические ингибиторы сериновых протеаз гепатита с |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201170434A EA020580B1 (ru) | 2008-09-11 | 2009-09-10 | Макроциклические ингибиторы сериновых протеаз гепатита с |
Country Status (41)
Families Citing this family (54)
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 |
KR20130026410A (en) * | 2009-09-28 | 2013-03-13 | 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 |
PE20130244A1 (es) | 2010-01-25 | 2013-03-10 | Enanta Pharm Inc | Inhibidores del virus de la hepatitis c |
NZ602288A (en) * | 2010-03-10 | 2014-02-28 | Abbvie Bahamas Ltd | Solid compositions comprising amorphous (2r,6s,13as,14ar,16as,z)-n-(cyclopropylsulfonyl)-6-(5-methylpyrazine-2-carboxamido)-5,16-dioxo-2-(phenanthridin-6-yloxy)-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a-carboxamide |
JP2014502620A (ja) * | 2010-12-30 | 2014-02-03 | 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c型肝炎セリンプロテアーゼ阻害剤 |
CN103380132B (zh) * | 2010-12-30 | 2016-08-31 | 益安药业 | 菲啶大环丙型肝炎丝氨酸蛋白酶抑制剂 |
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 |
EP2755689A1 (en) * | 2011-09-16 | 2014-07-23 | AbbVie Inc. | Methods for treating hcv |
DE112012003457T5 (de) * | 2011-10-21 | 2015-03-12 | Abbvie Inc. | Kombinationsbehandlung (z.B. mit ABT-072 oder ABT-333 von DAAs zur Verwendung in der Behandlung von HCV) |
US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
EA201490837A1 (ru) * | 2011-10-21 | 2014-11-28 | Эббви Инк. | Способы лечения hcv, включающие по меньшей мере два противовирусных агента прямого действия, рибавирин, но не интерферон |
AU2015200715A1 (en) * | 2011-10-21 | 2015-03-05 | Abbvie Ireland Unlimited Company | Methods for treating HCV |
US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
US9034832B2 (en) | 2011-12-29 | 2015-05-19 | Abbvie Inc. | Solid compositions |
ES2563479T3 (es) * | 2012-01-11 | 2016-03-15 | Abbvie Inc. | Procedimientos para elaborar inhibidores de proteasa de VHC |
US20140024613A1 (en) | 2012-06-27 | 2014-01-23 | Abbvie Inc. | Methods for Treating HCV |
UA119315C2 (uk) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Інгібітори вірусу гепатиту с |
EP2872513A1 (en) * | 2012-07-12 | 2015-05-20 | AbbVie Inc. | Crystalline forms of an hcv inhibitor |
TW201408669A (zh) | 2012-08-08 | 2014-03-01 | Merck Sharp & Dohme | Hcv ns3蛋白酶抑制劑 |
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 |
WO2014070964A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
WO2014071007A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US9409943B2 (en) | 2012-11-05 | 2016-08-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US9434738B2 (en) * | 2013-01-10 | 2016-09-06 | Bristol-Myers Squibb Company | Macrocyclic benzofuran and azabenzofuran compounds for the treatment of hepatitis C |
JP6342922B2 (ja) | 2013-03-07 | 2018-06-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
SG11201507223TA (en) | 2013-03-15 | 2015-10-29 | Gilead Sciences Inc | Macrocyclic and bicyclic inhibitors of hepatitis c virus |
EP3016651A1 (en) | 2013-07-02 | 2016-05-11 | AbbVie Inc. | Methods for treating hcv |
LT3043803T (lt) | 2013-09-11 | 2022-08-10 | Emory University | Nukleotidų ir nukleozidų kompozicijos ir jų panaudojimas |
WO2015084953A1 (en) * | 2013-12-04 | 2015-06-11 | Abbvie Inc. | Crystal forms |
WO2015103490A1 (en) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Solid antiviral dosage forms |
WO2015116594A1 (en) | 2014-01-28 | 2015-08-06 | Abbvie Inc. | Dose adjustment in combination therapy of hepatitis c |
US20160074462A1 (en) | 2014-09-11 | 2016-03-17 | Abbvie Inc. | Method of Treating HCV |
US10059969B1 (en) | 2014-10-03 | 2018-08-28 | Abbvie Inc. | Process for the preparation of (S)-2-amino-non-8-enoic acid |
US10113152B1 (en) | 2014-10-03 | 2018-10-30 | Abbvie Inc. | Variant polypeptides capable of aminating aliphatic alpha keto acids |
MX2017006139A (es) * | 2014-11-10 | 2017-11-16 | Glaxosmithkline Intelectual Property (No 2) Ltd | Composiciones farmaceuticas de accion prolongada para hepatitis c. |
WO2016134058A1 (en) | 2015-02-18 | 2016-08-25 | Abbvie Inc. | Combinations useful to treat hepatitis c virus |
US20160375017A1 (en) | 2015-06-26 | 2016-12-29 | Abbvie Inc. | Solid Pharmaceutical Compositions for Treating HCV |
HUE060259T2 (hu) | 2015-07-22 | 2023-02-28 | Enanta Pharm Inc | Benzodiazepin származékok mint RSV-gátlók |
EA201892448A1 (ru) | 2016-04-28 | 2019-06-28 | Эмори Юниверсити | Алкинсодержащие нуклеотидные и нуклеозидные терапевтические композиции и связанные с ними способы применения |
EP3577100A4 (en) | 2017-02-01 | 2021-03-10 | Abbvie Inc. | ENZYMATIC PROCESS FOR THE PRODUCTION OF (±) -2- (DIFLUOROMETHYL) -1- (ALCOXYCARBONYL) -CYCLOPROPANECARBONIC ACID AND (±) -2- (VINYL) -1- (ALCOXYCARBONYLURE) -CYCLOPROPANEC |
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 |
CN113710276B (zh) | 2019-03-18 | 2024-03-29 | 英安塔制药有限公司 | 苯二氮䓬衍生物作为rsv抑制剂 |
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 (en) | 2020-07-07 | 2022-01-13 | Enanta Pharmaceuticals, Inc, | Dihydroquinoxaline and dihydropyridopyrazine derivatives as rsv inhibitors |
US11922331B2 (en) | 2020-08-26 | 2024-03-05 | Northrop Grumman Systems Corporation | Machine-learning-based predictive ice detection |
US11945824B2 (en) | 2020-10-19 | 2024-04-02 | Enanta Pharmaceuticals, Inc. | Heterocyclic compounds as anti-viral agents |
IL305189A (en) | 2021-02-26 | 2023-10-01 | Enanta Pharm Inc | Heterocyclic antiviral compounds |
Family Cites Families (252)
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 |
DE69829381T2 (de) | 1997-08-11 | 2006-04-13 | Boehringer Ingelheim (Canada) Ltd., Laval | Hepatitis c inhibitor peptide |
US20040058982A1 (en) | 1999-02-17 | 2004-03-25 | Bioavailability System, Llc | Pharmaceutical compositions |
WO1999050230A1 (en) | 1998-03-31 | 1999-10-07 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly 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 |
ATE327246T1 (de) | 2000-11-20 | 2006-06-15 | Bristol Myers Squibb Co | Hepatitis c tripeptid inhibitoren |
WO2002048157A2 (en) | 2000-12-13 | 2002-06-20 | 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 |
EP1438582A1 (en) | 2001-09-16 | 2004-07-21 | ChemoMetec A/S | Method and a system for detecting and optionally isolating a rare event particle |
US20030134853A1 (en) | 2001-09-26 | 2003-07-17 | Priestley Eldon Scott | Compounds useful for treating hepatitis C virus |
US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
CA2369711A1 (en) | 2002-01-30 | 2003-07-30 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
US7119072B2 (en) | 2002-01-30 | 2006-10-10 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis C virus |
US7091184B2 (en) | 2002-02-01 | 2006-08-15 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor tri-peptides |
US6642204B2 (en) | 2002-02-01 | 2003-11-04 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor tri-peptides |
CA2369970A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
CA2370396A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
US6828301B2 (en) | 2002-02-07 | 2004-12-07 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for hepatitis C viral protease inhibitors |
JP4271148B2 (ja) | 2002-05-20 | 2009-06-03 | ブリストル−マイヤーズ スクイブ カンパニー | 置換シクロアルキルp1’c型肝炎ウイルスインヒビター |
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 |
ES2361011T3 (es) | 2002-05-20 | 2011-06-13 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c. |
MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
WO2003099316A1 (en) | 2002-05-20 | 2003-12-04 | Bristol-Myers Squibb Company | Heterocyclicsulfonamide hepatitis c virus inhibitors |
US20030232386A1 (en) | 2002-06-17 | 2003-12-18 | Shah Dinesh O. | Assay conjugate and uses thereof |
WO2004002405A2 (en) | 2002-06-26 | 2004-01-08 | Bristol-Myers Squibb Company | Amino-bicyclic pyrazinones and pyridinones |
US7183302B2 (en) | 2002-08-12 | 2007-02-27 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of HCV replication |
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 |
EP1601685A1 (en) | 2003-03-05 | 2005-12-07 | Boehringer Ingelheim International GmbH | Hepatitis c inhibiting compounds |
UY28240A1 (es) | 2003-03-27 | 2004-11-08 | Boehringer Ingelheim Pharma | Fases cristalinas de un potente inhibidor de la hcv |
CA2520886A1 (en) | 2003-04-02 | 2004-11-04 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for hepatitis c viral protease inhibitors |
EP1615949A1 (en) | 2003-04-10 | 2006-01-18 | Boehringer Ingelheim International GmbH | Process for the preparation of macrocyclic compounds by ruthenium complex catalysed metathesis reaction |
EP1615947A2 (en) | 2003-04-10 | 2006-01-18 | Boehringer Ingelheim International GmbH | Process for preparing macrocyclic compounds |
ATE422895T1 (de) | 2003-04-16 | 2009-03-15 | Bristol Myers Squibb Co | Makrocyclische isochinolinpeptidinhibitoren des hepatitis-c-virus |
DK1615613T3 (da) * | 2003-04-18 | 2010-03-22 | Enanta Pharm Inc | Quinoxalinyl-makrocykliske hepatitis C serin protease-inhibitorer |
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 |
KR20060094083A (ko) | 2003-09-22 | 2006-08-28 | 베링거 인겔하임 인터내셔날 게엠베하 | C형 간염 바이러스에 대해 활성인 마크로사이클릭펩타이드 |
RU2006113880A (ru) | 2003-09-26 | 2007-11-20 | Шеринг Корпорейшн (US) | Макроциклические ингибиторы сериновой протеиназы ns3 вируса гепатита с |
CA2540858C (en) | 2003-10-14 | 2009-12-08 | Intermune, Inc. | Macrocyclic carboxylic acids and acylsulfonamides as inhibitors of hcv replication |
US7491794B2 (en) | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
US7132504B2 (en) | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
CN1902216A (zh) | 2003-11-20 | 2007-01-24 | 先灵公司 | 丙肝病毒ns3蛋白酶的去肽化抑制剂 |
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 |
FR2863268B1 (fr) | 2003-12-09 | 2006-02-24 | Sod Conseils Rech Applic | Nouveaux derives du 2-hydroxytetrahydrofuranne et leur application a titre de medicaments |
EP1742913A1 (en) | 2003-12-11 | 2007-01-17 | Schering Corporation | Inhibitors of hepatitis c virus ns3/ns4a serine protease |
DE602005025855D1 (de) | 2004-01-21 | 2011-02-24 | Boehringer Ingelheim Pharma | Makrocyclische peptide mit wirkung gegen das hepatitis-c-virus |
DE602005011402D1 (de) | 2004-01-28 | 2009-01-15 | Boehringer Ingelheim Pharma | Übergangsmetallnebenprodukte enthaltenden reaktionslösungen |
PT1713823E (pt) | 2004-01-30 | 2010-02-02 | Medivir Ab | Inibidores da protease ns-3 da serina do hcv |
CA2556917C (en) | 2004-03-15 | 2013-07-09 | Boehringer Ingelheim International, Gmbh | Process for preparing macrocyclic compounds |
AP2006003763A0 (en) | 2004-03-30 | 2006-10-31 | Intermune Inc | Macrocyclic compounds as inhibitors of viral replication |
EP1753775B1 (en) | 2004-05-25 | 2012-12-26 | Boehringer Ingelheim International GmbH | Process for preparing acyclic hcv protease inhibitors |
EP1763531A4 (en) | 2004-06-28 | 2009-07-01 | Boehringer Ingelheim Int | ANALOGUE OF HEPATITIS-C INHIBITING PEPTIDES |
DE102004033312A1 (de) | 2004-07-08 | 2006-01-26 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Kontinuierliches Metatheseverfahren mit Ruthenium-Katalysatoren |
PL1778702T3 (pl) | 2004-07-16 | 2011-12-30 | Gilead Sciences Inc | Związki przeciwwirusowe |
UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
ATE512971T1 (de) | 2004-07-20 | 2011-07-15 | Boehringer Ingelheim Int | Peptidanaloga als hepatitis c-hemmer |
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 |
JP2008513454A (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 | 大環状hcvプロテアーゼインヒビターの調製方法 |
EP1794179A1 (en) | 2004-09-17 | 2007-06-13 | Boehringer Ingelheim International Gmbh | Ring-closing metathesis process in supercritical fluid |
EP1799194B1 (en) | 2004-09-24 | 2011-11-16 | Boehringer Ingelheim Pharmaceuticals Inc. | A new class of surfactant-like materials comprising vitamin e tpgs and a water soluble polymer |
WO2007001406A2 (en) * | 2004-10-05 | 2007-01-04 | Chiron Corporation | Aryl-containing macrocyclic compounds |
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 |
CN103172697A (zh) | 2005-03-08 | 2013-06-26 | 贝林格尔.英格海姆国际有限公司 | 制备大环化合物的方法 |
EP1876899A2 (de) | 2005-04-25 | 2008-01-16 | Basf Aktiengesellschaft | Verwendung von 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidinen, neue azolopyrimidine, verfahren zu ihrer herstellung und sie enthaltende mittel |
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 |
EP1888619B1 (en) | 2005-05-25 | 2013-04-17 | 2cureX ApS | Compounds modifying apoptosis |
WO2006130687A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis c virus protease inhibitor |
US20070004635A1 (en) | 2005-06-02 | 2007-01-04 | Schering Corporation | Method of treating interferon non-responders using HCV protease inhibitor |
US20060275366A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation |
EP1919478B1 (en) | 2005-06-02 | 2016-03-23 | Merck Sharp & Dohme Corp. | Combination of hcv protease inhibitors with a surfactant |
WO2006130666A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Medicaments and methods combining a hcv protease inhibitor and an akr competitor |
WO2006130688A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Compounds for inhibiting cathepsin activity |
NZ563369A (en) | 2005-06-02 | 2011-03-31 | Schering Corp | Controlled-release formulation useful for treating disorders associated with hepatitus C virus |
WO2006130626A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Method for modulating activity of hcv protease through use of a novel hcv protease inhibitor to reduce duration of treatment period |
WO2006130552A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis c virus |
WO2006130627A2 (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 |
US20070237818A1 (en) | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
NZ563361A (en) | 2005-06-02 | 2011-02-25 | Schering Corp | HCV protease inhibitors in combination with food |
US7608592B2 (en) | 2005-06-30 | 2009-10-27 | Virobay, Inc. | HCV inhibitors |
EP2886549A1 (en) | 2005-07-04 | 2015-06-24 | Zannan Scitech Co., Ltd. | Ruthenium complex ligand, ruthenium complex and the use of the complex as a catalyst in olefin metathesis reactions |
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 |
WO2007009227A1 (en) | 2005-07-20 | 2007-01-25 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor peptide analogs |
NZ594105A (en) | 2005-07-25 | 2013-02-22 | Intermune Inc | Novel macrocyclic inhibitors of hepatitis c virus replication |
CN101273052B (zh) | 2005-07-29 | 2016-01-13 | 爱尔兰詹森科学公司 | 丙型肝炎病毒的大环抑制剂 |
DE602006019741D1 (de) | 2005-07-29 | 2011-03-03 | Medivir Ab | Makrocyclische inhibitoren des hepatitis-c-virus |
JO2768B1 (en) | 2005-07-29 | 2014-03-15 | تيبوتيك فارماسيوتيكالز ليمتد | Large cyclic inhibitors of hepatitis C virus |
CN101282978B (zh) | 2005-07-29 | 2012-07-11 | 泰博特克药品有限公司 | 丙型肝炎病毒的大环抑制剂 |
ES2456617T3 (es) | 2005-07-29 | 2014-04-23 | Janssen R&D Ireland | Inhibidores macrocíclicos del virus de la hepatitis C |
PE20070211A1 (es) * | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
PE20070343A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Inhibidores macrociclicos del virus de la hepatitis c |
KR20080036598A (ko) | 2005-08-01 | 2008-04-28 | 머크 앤드 캄파니 인코포레이티드 | Hcv ns3 프로테아제 억제제로서의 마크로사이클릭펩티드 |
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 |
WO2007044893A2 (en) | 2005-10-11 | 2007-04-19 | Intermune, Inc. | Compounds and methods for inhibiting hepatitis c viral replication |
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. |
US20100018355A1 (en) | 2006-05-04 | 2010-01-28 | Crawford Ted C | Head cap for a wrench head, wrench and method utilizing the same |
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 |
WO2007140200A2 (en) | 2006-05-25 | 2007-12-06 | 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 |
US8268776B2 (en) | 2006-06-06 | 2012-09-18 | 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 |
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 |
AR061629A1 (es) | 2006-06-26 | 2008-09-10 | Enanta Pharm Inc | Quinoxalinil macrociclicos inhibidores de serina proteasa del virus de la hepatitis c. proceso de obtencion y composiciones farmaceuticas |
WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
MX2009000486A (es) | 2006-07-13 | 2009-01-27 | Achillion Pharmaceuticals Inc | Peptidos de 4-amino-4-oxobutanoilo como inhibidores de replicacion viral. |
WO2008019303A2 (en) | 2006-08-04 | 2008-02-14 | Enanta Pharmaceuticals, Inc. | Pyridazinonyl macrocyclic hepatitis c serine protease inhibitors |
CN101674844A (zh) | 2006-08-04 | 2010-03-17 | 英安塔制药有限公司 | 四唑基大环类c型肝炎丝氨酸蛋白酶抑制剂 |
US7635683B2 (en) | 2006-08-04 | 2009-12-22 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl tripeptide hepatitis C virus inhibitors |
US20090035271A1 (en) | 2007-08-01 | 2009-02-05 | Ying Sun | Tetrazolyl macrocyclic hepatitis c serine protease inhibitors |
US7605126B2 (en) | 2006-08-11 | 2009-10-20 | Enanta Pharmaceuticals, Inc. | Acylaminoheteroaryl hepatitis C virus protease inhibitors |
WO2008022006A2 (en) | 2006-08-11 | 2008-02-21 | 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 |
US7582605B2 (en) | 2006-08-11 | 2009-09-01 | Enanta Pharmaceuticals, Inc. | Phosphorus-containing hepatitis C serine protease inhibitors |
WO2008021960A2 (en) | 2006-08-11 | 2008-02-21 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis c serine protease inhibitors |
US7687459B2 (en) | 2006-08-11 | 2010-03-30 | Enanta Pharmaceuticals, Inc. | Arylalkoxyl hepatitis C virus protease inhibitors |
MX2009003403A (es) | 2006-09-27 | 2009-04-09 | Coley Pharm Group Inc | Composiciones de ligandos de tlr y antivirales. |
US8841413B2 (en) | 2006-10-03 | 2014-09-23 | Cadila Healthcare Limited | Antidiabetic compounds |
US20120220520A1 (en) | 2006-10-17 | 2012-08-30 | Van T Klooster Gerben Albert Eleutherius | Bioavailable combinations for hcv treatment |
WO2008051475A2 (en) | 2006-10-24 | 2008-05-02 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
JP5345941B2 (ja) | 2006-10-24 | 2013-11-20 | メルク・シャープ・アンド・ドーム・コーポレーション | Hcvns3プロテアーゼ阻害剤 |
BRPI0718161A2 (pt) | 2006-10-27 | 2013-11-26 | Merck & Co Inc | Composto, composição farmacêutica, e, uso do composto. |
US8377874B2 (en) * | 2006-10-27 | 2013-02-19 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
US20080107623A1 (en) | 2006-11-01 | 2008-05-08 | Bristol-Myers Squibb Company | Inhibitors of Hepatitis C Virus |
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 |
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 |
US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
BRPI0718798A2 (pt) | 2006-11-17 | 2013-12-03 | Tibotec Pharm Ltd | Inibidores macrocíclicos de vírus da hepatite c |
WO2008070733A2 (en) | 2006-12-06 | 2008-06-12 | Phenomix Corporation | Macrocyclic hepatitis c serine protease inhibitors and uses therefor |
EP2111227A1 (en) | 2007-01-08 | 2009-10-28 | Phenomix Corporation | Macrocyclic hepatitis c protease inhibitors |
US7541351B2 (en) | 2007-01-11 | 2009-06-02 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
CN105037347B (zh) | 2007-02-01 | 2018-06-01 | 泰博特克药品有限公司 | Hcv巨环抑制剂的多晶形 |
US20080207528A1 (en) | 2007-02-01 | 2008-08-28 | Syaulan Yang | Hcv protease inhibitors |
CN101641349A (zh) | 2007-02-08 | 2010-02-03 | 泰博特克药品有限公司 | 嘧啶取代的大环抑制剂 |
CA2677015C (en) | 2007-02-08 | 2015-05-26 | Tibotec Pharmaceuticals Ltd. | Hcv inhibiting macrocyclic phenylcarbamates |
US20100087382A1 (en) | 2007-02-16 | 2010-04-08 | Boehringer Ingelheim International Gmbh | Inhibitors of Hepatitis C NS3 Protease |
JP2010519266A (ja) | 2007-02-20 | 2010-06-03 | ノバルティス アーゲー | Hcvns3プロテアーゼ阻害剤としての大員環化合物 |
JP2010519339A (ja) | 2007-02-26 | 2010-06-03 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Hcv複製阻害剤として有用な三級アミン置換ペプチド |
US8063051B2 (en) | 2007-03-19 | 2011-11-22 | Astrazeneca Ab | 9-substituted-8-oxo-adenine compounds as toll-like receptor (TLR7) modulators |
WO2008124384A2 (en) | 2007-04-03 | 2008-10-16 | Aegerion Pharmaceuticals, Inc. | Combinations of mtp inhibitors with cholesterol absorption inhibitors or interferon for treating hepatitis c |
BRPI0810665A2 (pt) | 2007-04-24 | 2014-11-04 | Hoffmann La Roche | Processo para a preparação de intermediário de inibidor da protease de hcv |
US20080279821A1 (en) | 2007-04-26 | 2008-11-13 | Deqiang Niu | Arylpiperidinyl and arylpyrrolidinyl macrocyclic 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 |
US7906513B2 (en) | 2007-04-26 | 2011-03-15 | Enanta Pharmaceuticals, Inc. | Hydrazide-containing hepatitis C serine protease inhibitors |
JP2010528987A (ja) | 2007-05-03 | 2010-08-26 | インターミューン・インコーポレーテッド | C型肝炎ウイルス複製の新規大環状阻害剤 |
BRPI0811447A2 (pt) | 2007-05-10 | 2014-10-29 | Intermune Inc | Compostos, composição farmacêutica e métodos de inibição da atividade da protease ns3/ns4, de tratamento da fibrose hepática e de intensificação da função hepática num indivíduo tendo infecção de vírus da hepatite c. |
US20090005387A1 (en) | 2007-06-26 | 2009-01-01 | Deqiang Niu | Quinoxalinyl macrocyclic hepatitis c virus serine protease inhibitors |
KR20150006905A (ko) | 2007-06-29 | 2015-01-19 | 길리애드 사이언시즈, 인코포레이티드 | 항바이러스 화합물 |
AR067180A1 (es) | 2007-06-29 | 2009-09-30 | Gilead Sciences Inc | Compuestos antivirales |
WO2009005677A2 (en) | 2007-06-29 | 2009-01-08 | Gilead Sciences, Inc. | Antiviral compounds |
CA2699891C (en) | 2007-07-19 | 2013-10-22 | Nigel Liverton | Macrocyclic compounds as antiviral agents |
WO2009014730A1 (en) | 2007-07-26 | 2009-01-29 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
WO2009053828A2 (en) | 2007-10-22 | 2009-04-30 | Enanta Pharmaceuticals, Inc. | P3 hydroxyamino macrocyclic hepatitis c serine protease inhibitors |
US20090111757A1 (en) | 2007-10-25 | 2009-04-30 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
US8426360B2 (en) | 2007-11-13 | 2013-04-23 | Enanta Pharmaceuticals, Inc. | Carbocyclic oxime hepatitis C virus serine protease inhibitors |
CN101918410B (zh) | 2007-11-20 | 2013-02-27 | 百时美施贵宝公司 | 与环丙基稠合的吲哚并苯并氮杂*hcv ns5b抑制剂 |
WO2009070689A1 (en) | 2007-11-29 | 2009-06-04 | Enanta Pharmaceuticals, Inc. | Bicyclic, c5-substituted proline derivatives as inhibitors of the hepatitis c virus ns3 protease |
WO2009070692A1 (en) | 2007-11-29 | 2009-06-04 | Enanta Pharmaceuticals, Inc. | C5-substituted, proline-derived, macrocyclic hepatitis c serine protease inhibitors |
US8268777B2 (en) | 2007-12-05 | 2012-09-18 | Enanta Pharmaceuticals, Inc. | Oximyl macrocyclic derivatives |
MX2010006209A (es) * | 2007-12-05 | 2010-08-10 | Enanta Pharm Inc | Derivados de quinoxalinilo. |
EP2224920A4 (en) | 2007-12-06 | 2012-05-09 | Enanta Pharm Inc | PROCESS FOR THE PREPARATION OF MACROCYCLIC OXIMYL HEPATITIS C PROTEASE INHIBITORS |
US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
JP5439384B2 (ja) | 2007-12-21 | 2014-03-12 | エフ.ホフマン−ラ ロシュ アーゲー | 大員環の製造方法 |
US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
RU2523790C2 (ru) | 2007-12-21 | 2014-07-27 | Авила Терапьютикс, Инк. | Ингибиторы протеазы вируса гепатита с и их применение |
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 |
JP5755449B2 (ja) | 2007-12-21 | 2015-07-29 | セルジーン アビロミクス リサーチ, インコーポレイテッド | Hcvプロテアーゼ阻害剤およびその使用 |
EP2250174B1 (en) | 2008-02-04 | 2013-08-28 | IDENIX Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
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 (en) | 2008-05-09 | 2009-11-12 | Boehringer Ingelheim International Gmbh | A method for preparing 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 |
WO2009148923A1 (en) | 2008-05-29 | 2009-12-10 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
RU2496514C2 (ru) | 2008-06-05 | 2013-10-27 | Займоджинетикс, Инк. | Применение пэгилированных интерферонов типа iii для лечения гепатита с |
UY31950A (es) | 2008-07-01 | 2010-01-29 | Medivir Ab | Inhibidores de ciclopropil-polimerasa |
WO2010015545A1 (en) | 2008-08-07 | 2010-02-11 | F. Hoffmann-La Roche Ag | Process for the preparation of a macrocycle |
US8765667B2 (en) | 2008-08-20 | 2014-07-01 | Michael Eissenstat | HCV protease inhibitors |
US20100185419A1 (en) | 2008-09-05 | 2010-07-22 | Avila Therapeutics, Inc. | Algorithm for designing irreversible inhibitors |
UY32099A (es) * | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
WO2010033466A1 (en) | 2008-09-16 | 2010-03-25 | Phenomix Corporation | Macrocyclic inhibitors of hepatitis c protease |
CN102159571B (zh) | 2008-09-16 | 2014-10-01 | 贝林格尔.英格海姆国际有限公司 | 强效hcv抑制剂2-噻唑基-4-喹啉基-氧基衍生物的结晶形式 |
AU2009293493B2 (en) | 2008-09-17 | 2014-09-18 | Boehringer Ingelheim International Gmbh | Combination of HCV NS3 protease inhibitor with interferon and ribavirin |
US8603737B2 (en) | 2008-09-19 | 2013-12-10 | Celgene Avilomics Research, Inc. | Methods for identifying HCV protease inhibitors |
EP2344487A4 (en) | 2008-09-23 | 2012-03-21 | Boehringer Ingelheim Int | HEPATITIS C INHIBITOR COMPOUNDS |
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 |
ES2435799T3 (es) | 2008-10-09 | 2013-12-23 | Anadys Pharmaceuticals, Inc. | Un método de inhibición del virus de la hepatitis C mediante combinación de una 5,6-dihidro-1H-piridin-2-ona y de uno o más compuestos antivirales adicionales |
WO2010048468A1 (en) | 2008-10-23 | 2010-04-29 | Concert Pharmaceuticals, Inc. | Deuterated macrocyclic inhibitors of viral ns3 protease |
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 |
NZ592110A (en) | 2008-11-20 | 2012-06-29 | Achillion Pharmaceuticals Inc | Cyclic carboxamide compounds and analogues thereof as of hepatitis c virus |
MX2011005151A (es) | 2008-11-21 | 2011-05-30 | Boehringer Ingelheim Int | Composicion farmaceutica de un potente inhibidor de hvc para su administracion oral. |
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 |
AU2009335904A1 (en) | 2008-12-19 | 2011-08-04 | Gilead Sciences, Inc. | HCV NS3 protease inhibitors |
US20100196321A1 (en) | 2009-01-30 | 2010-08-05 | Glaxosmithkline Llc | Compounds |
EP2413955A4 (en) | 2009-04-01 | 2012-12-26 | Amylin Pharmaceuticals Inc | AGONIST COMPOUNDS OF GLP-1 RECEPTORS HAVING CONFORMATIONAL CONSTRAINTS AT THEIR N-TERMINAL END |
TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
EA022212B1 (ru) | 2009-04-24 | 2015-11-30 | Кадила Хелзкэр Лимитед | Короткоцепочечные пептиды в качестве агониста рецептора паратиреоидного гормона (pth) |
WO2010135520A1 (en) | 2009-05-20 | 2010-11-25 | Chimerix, Inc. | Compounds, compositions and methods for treating viral infection |
US8703700B2 (en) | 2009-05-22 | 2014-04-22 | Sequoia Pharmaceuticals, Inc. | Bimacrocylic HCV NS3 protease inhibitors |
US8232246B2 (en) | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
WO2011009961A1 (en) | 2009-07-24 | 2011-01-27 | Virologik Gmbh | Combination of proteasome inhibitors and anti-hepatitis medication for treating hepatitis |
JP2013501068A (ja) | 2009-08-05 | 2013-01-10 | アイディニックス ファーマシューティカルズ インコーポレイテッド | 大環状セリンプロテアーゼ阻害剤 |
KR101670319B1 (ko) | 2009-09-15 | 2016-10-28 | 타이젠 바이오테크놀러지 컴퍼니 리미티드 | Hcv 프로테아제 저해제 |
WO2011063501A1 (en) | 2009-11-24 | 2011-06-03 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor compounds |
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 |
US20110178107A1 (en) | 2010-01-20 | 2011-07-21 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
-
2009
- 2009-09-09 UY UY0001032099A patent/UY32099A/es active IP Right Grant
- 2009-09-10 NZ NZ592170A patent/NZ592170A/xx unknown
- 2009-09-10 EP EP12160849.1A patent/EP2468286B1/en active Active
- 2009-09-10 EP EP09813360.6A patent/EP2340029B1/en active Active
- 2009-09-10 PL PL09813360T patent/PL2340029T3/pl unknown
- 2009-09-10 MY MYPI2011001033A patent/MY159820A/en unknown
- 2009-09-10 PL PL12161047T patent/PL2468287T3/pl unknown
- 2009-09-10 PE PE2012000653A patent/PE20121312A1/es not_active Application Discontinuation
- 2009-09-10 JP JP2009208935A patent/JP5259537B2/ja active Active
- 2009-09-10 SI SI200930970T patent/SI2468287T1/sl unknown
- 2009-09-10 DK DK09813360.6T patent/DK2340029T3/da active
- 2009-09-10 TW TW102140577A patent/TWI510245B/zh not_active IP Right Cessation
- 2009-09-10 DK DK12160849.1T patent/DK2468286T3/da active
- 2009-09-10 AU AU2009292182A patent/AU2009292182B2/en active Active
- 2009-09-10 NZ NZ605550A patent/NZ605550A/en not_active IP Right Cessation
- 2009-09-10 ES ES12160779.0T patent/ES2525922T3/es active Active
- 2009-09-10 DK DK14181565.4T patent/DK2805726T3/en active
- 2009-09-10 SG SG2012014080A patent/SG179414A1/en unknown
- 2009-09-10 DK DK12161047.1T patent/DK2468287T3/da active
- 2009-09-10 PL PL12160779T patent/PL2468285T3/pl unknown
- 2009-09-10 PE PE2011000597A patent/PE20110704A1/es active IP Right Grant
- 2009-09-10 SI SI200931090T patent/SI2468285T1/sl unknown
- 2009-09-10 BR BR122012005261A patent/BR122012005261A8/pt active Search and Examination
- 2009-09-10 TR TR2018/09771T patent/TR201809771T4/tr unknown
- 2009-09-10 SI SI200930952T patent/SI2468286T1/sl unknown
- 2009-09-10 CA CA2736895A patent/CA2736895C/en active Active
- 2009-09-10 EP EP12160779.0A patent/EP2468285B1/en active Active
- 2009-09-10 ES ES12160849.1T patent/ES2475815T3/es active Active
- 2009-09-10 ES ES12161047.1T patent/ES2475163T3/es active Active
- 2009-09-10 EP EP14181565.4A patent/EP2805726B1/en active Active
- 2009-09-10 HU HUE14181565A patent/HUE039478T2/hu unknown
- 2009-09-10 MX MX2011002486A patent/MX2011002486A/es active IP Right Grant
- 2009-09-10 PT PT121610471T patent/PT2468287E/pt unknown
- 2009-09-10 PA PA20098842201A patent/PA8842201A1/es unknown
- 2009-09-10 BR BRPI0918724A patent/BRPI0918724B8/pt active IP Right Grant
- 2009-09-10 AR ARP090103469A patent/AR073568A1/es active IP Right Grant
- 2009-09-10 TW TW101110209A patent/TWI450723B/zh not_active IP Right Cessation
- 2009-09-10 EP EP12161047.1A patent/EP2468287B1/en active Active
- 2009-09-10 PT PT98133606T patent/PT2340029E/pt unknown
- 2009-09-10 PT PT141815654T patent/PT2805726T/pt unknown
- 2009-09-10 WO PCT/US2009/005082 patent/WO2010030359A2/en active Application Filing
- 2009-09-10 SI SI200931860T patent/SI2805726T1/sl unknown
- 2009-09-10 TW TW098130581A patent/TWI429449B/zh active
- 2009-09-10 SI SI200930895T patent/SI2340029T1/sl unknown
- 2009-09-10 PT PT121608491T patent/PT2468286E/pt unknown
- 2009-09-10 PT PT121607790T patent/PT2468285E/pt unknown
- 2009-09-10 EA EA201200390A patent/EA022891B1/ru not_active IP Right Cessation
- 2009-09-10 ES ES09813360.6T patent/ES2459390T3/es active Active
- 2009-09-10 US US12/584,716 patent/US8420596B2/en active Active
- 2009-09-10 LT LTEP14181565.4T patent/LT2805726T/lt unknown
- 2009-09-10 EA EA201170434A patent/EA020580B1/ru active Protection Beyond IP Right Term
- 2009-09-10 PE PE2013002396A patent/PE20140961A1/es not_active Application Discontinuation
- 2009-09-10 PL PL14181565T patent/PL2805726T3/pl unknown
- 2009-09-10 DK DK12160779.0T patent/DK2468285T3/en active
- 2009-09-10 ES ES14181565.4T patent/ES2677644T3/es active Active
- 2009-09-10 PL PL12160849T patent/PL2468286T3/pl unknown
- 2009-09-11 CN CN200910175949.4A patent/CN101775017B/zh active Active
- 2009-09-11 KR KR1020090086079A patent/KR101379365B1/ko active Protection Beyond IP Right Term
- 2009-09-11 CN CN201410116146.2A patent/CN103896950A/zh active Pending
- 2009-09-11 CN CN2012100719006A patent/CN102641271B/zh not_active Expired - Fee Related
-
2011
- 2011-02-28 ZA ZA2011/01558A patent/ZA201101558B/en unknown
- 2011-03-08 CO CO11028271A patent/CO6341565A2/es active IP Right Grant
- 2011-03-09 EC EC2011010879A patent/ECSP11010879A/es unknown
- 2011-03-10 DO DO2011000077A patent/DOP2011000077A/es unknown
- 2011-03-10 CL CL2011000512A patent/CL2011000512A1/es unknown
- 2011-03-28 GT GT201100056AK patent/GT201100056AA/es unknown
-
2012
- 2012-01-06 HK HK12100145.0A patent/HK1159515A1/xx unknown
- 2012-01-06 HK HK12111721.9A patent/HK1170936A1/xx not_active IP Right Cessation
- 2012-01-06 HK HK12111723.7A patent/HK1170937A1/zh not_active IP Right Cessation
- 2012-01-06 HK HK12111722.8A patent/HK1171184A1/xx not_active IP Right Cessation
- 2012-02-08 ZA ZA2012/00950A patent/ZA201200950B/en unknown
- 2012-03-01 IL IL218441A patent/IL218441A/en active IP Right Grant
- 2012-03-02 JP JP2012046166A patent/JP5534533B2/ja not_active Expired - Fee Related
- 2012-03-13 KR KR20120025541A patent/KR101487726B1/ko active IP Right Grant
- 2012-03-28 UY UY0001033981A patent/UY33981A/es not_active Application Discontinuation
- 2012-04-04 US US13/439,551 patent/US8642538B2/en active Active
- 2012-04-19 AR ARP120101342A patent/AR086181A2/es unknown
- 2012-06-04 EC ECSP12011947 patent/ECSP12011947A/es unknown
- 2012-06-07 CL CL2012001495A patent/CL2012001495A1/es unknown
-
2013
- 2013-04-25 JP JP2013092319A patent/JP5902123B2/ja not_active Expired - Fee Related
- 2013-04-25 JP JP2013092318A patent/JP5801342B2/ja not_active Expired - Fee Related
- 2013-12-10 GT GT201100056BA patent/GT201100056BA/es unknown
- 2013-12-11 AR ARP130104634A patent/AR093924A2/es unknown
-
2014
- 2014-01-08 UY UY0001035259A patent/UY35259A/es not_active Application Discontinuation
- 2014-01-31 US US14/170,199 patent/US9309279B2/en active Active
- 2014-03-24 KR KR1020140034200A patent/KR20140056195A/ko not_active Application Discontinuation
- 2014-04-22 CR CR20140180A patent/CR20140180A/es unknown
- 2014-05-27 CY CY20141100378T patent/CY1115137T1/el unknown
- 2014-05-29 HR HRP20140492AT patent/HRP20140492T1/hr unknown
- 2014-05-29 HR HRP20140494AT patent/HRP20140494T1/hr unknown
- 2014-05-29 HR HRP20140493AT patent/HRP20140493T1/hr unknown
- 2014-06-27 CY CY20141100473T patent/CY1115202T1/el unknown
- 2014-07-11 CY CY20141100521T patent/CY1115379T1/el unknown
- 2014-10-02 IL IL234969A patent/IL234969A0/en unknown
- 2014-12-02 HR HRP20141169AT patent/HRP20141169T1/hr unknown
- 2014-12-31 CY CY20141101094T patent/CY1115844T1/el unknown
-
2015
- 2015-02-25 LU LU92667C patent/LU92667I2/xx unknown
- 2015-03-04 LT LTPA2015011C patent/LTC2340029I2/lt unknown
- 2015-03-26 CY CY2015014C patent/CY2015014I1/el unknown
- 2015-04-08 NL NL300730C patent/NL300730I1/nl unknown
- 2015-04-15 HU HUS1500020C patent/HUS1500020I1/hu unknown
- 2015-04-22 NO NO2015014C patent/NO2015014I1/no not_active IP Right Cessation
-
2018
- 2018-07-10 HR HRP20181075TT patent/HRP20181075T1/hr unknown
- 2018-07-16 CY CY181100737T patent/CY1120780T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA022891B1 (ru) | Применение макроциклических ингибиторов сериновых протеаз гепатита с | |
EA200900969A1 (ru) | Макроциклические ингибиторы протеазы гепатита с | |
ES2322602T3 (es) | Compuestos heterotetraciclicos condensados y su uso como inhibidor de polimerasa del vhc. | |
NZ581606A (en) | Novel macrocyclic inhibitors of hepatitis c virus replication | |
MX2009008872A (es) | Compuestos macrociclicos como inhibidores de proteasa ns3 del virus de hepatitis c. | |
NZ579296A (en) | Spirocyclic compounds as inhibitors of serine proteases for the treatment of HCV infections | |
ECSP056181A (es) | Compuestos Inhibidores de la Hepatitis C | |
EA200800371A1 (ru) | Ингибиторы ns3 протеазы вгс | |
MY152070A (en) | Macrocyclic quinxaline compounds as hcv ns3 protease inhibitors | |
RS20060197A (en) | Macrocyclic peptides active against the hepatitis c virus | |
EA200802346A1 (ru) | Циклопропилконденсированные индолобензазепиновые ингибиторы белка ns5b вируса гепатита с | |
WO2007016476A3 (en) | Hepatitis c serine protease inhibitors and uses therefor | |
TW200745035A (en) | Cyclopropyl fused indolobenzazepine HCV NS5B inhibitors | |
PE20140039A1 (es) | Inhibidores de serina proteasa de hepatitis c a base de macrociclicos de fenantridina | |
EA200901241A1 (ru) | Соединения для лечения гепатита с | |
DE602005010607D1 (de) | Zyklosporinanalog | |
TH104730B (th) | การยับยั้งโปรตีนเอส ns3-ns4a ของ hcv | |
TH127004B (th) | สารประกอบต้านไวรัสเฮเทอโรไซคลิก (Heterocyclic Anitvirus Compound) | |
TH124666B (th) | สไปโรไซคลิก โพรลีน และการใช้สารเหล่านั้นในการรักษาการติดเชื้อ hcv |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ND4A | Extension of term of a eurasian patent | ||
ND4A | Extension of term of a eurasian patent | ||
ND4A | Extension of term of a eurasian patent | ||
PC4A | Registration of transfer of a eurasian patent by assignment | ||
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM RU |