MA32502B1 - Composes de quinoxaline macrocycliques en tant qu'inhibiteurs de protease ns3 du virus de l'hepatite c (hcv) - Google Patents
Composes de quinoxaline macrocycliques en tant qu'inhibiteurs de protease ns3 du virus de l'hepatite c (hcv)Info
- Publication number
- MA32502B1 MA32502B1 MA33556A MA33556A MA32502B1 MA 32502 B1 MA32502 B1 MA 32502B1 MA 33556 A MA33556 A MA 33556A MA 33556 A MA33556 A MA 33556A MA 32502 B1 MA32502 B1 MA 32502B1
- Authority
- MA
- Morocco
- Prior art keywords
- hcv
- hepatitis
- virus
- protease inhibitors
- quinoxaline compounds
- Prior art date
Links
- 241000711549 Hepacivirus C Species 0.000 title abstract 5
- 239000000137 peptide hydrolase inhibitor Substances 0.000 title abstract 2
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 title 1
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical class N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 title 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 150000002678 macrocyclic compounds Chemical class 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
-
- 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
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Biotechnology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
L'invention concerne un composé macrocyclique de la formule (i), et son utilisation en tant qu'inhibiteurs de la protéase ns3 du virus de l'hépatite c (hcv), et dans le traitement ou la prévention d'infections par hcv.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13555908P | 2008-07-22 | 2008-07-22 | |
| PCT/US2009/050915 WO2010011566A1 (fr) | 2008-07-22 | 2009-07-17 | Composés de quinoxaline macrocycliques en tant qu'inhibiteurs de protéase ns3 du virus de l'hépatite c (hcv) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32502B1 true MA32502B1 (fr) | 2011-07-03 |
Family
ID=41130248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33556A MA32502B1 (fr) | 2008-07-22 | 2011-01-25 | Composes de quinoxaline macrocycliques en tant qu'inhibiteurs de protease ns3 du virus de l'hepatite c (hcv) |
Country Status (43)
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| MY164469A (en) * | 2006-10-27 | 2017-12-15 | Msd Italia Srl | Hcv ns3 protease inhibitors |
| CA2720850A1 (fr) * | 2008-04-28 | 2009-11-05 | Merck Sharp & Dohme Corp. | Inhibiteurs de la protease hcv ns3 |
| SI2540350T1 (sl) | 2008-07-22 | 2015-01-30 | Merck Sharp & Dohme Corp. | Kombinacije makrocikliäśnih kinoksalinske spojine, ki je hcv ns3 proteazni inhibitor z drugimi hcv uäśinkovinami |
| US20190127365A1 (en) | 2017-11-01 | 2019-05-02 | Merck Sharp & Dohme Corp. | Inhibitors of hepatitis c virus replication |
| NZ595410A (en) | 2009-03-27 | 2013-12-20 | Merck Sharp & Dohme | Inhibitors of hepatitis c virus replication |
| MX2011012155A (es) * | 2009-05-13 | 2012-02-28 | Enanta Pharm Inc | Compuestos macrociclicos como inhibidores del virus de hepatitis c. |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| UA118080C2 (uk) * | 2009-06-11 | 2018-11-26 | Еббві Айрленд Анлімітед Компані | Противірусні сполуки |
| EP2459582B1 (fr) | 2009-07-30 | 2015-05-27 | Merck Sharp & Dohme Corp. | Inhibiteurs de protéase ns3 du virus de l'hépatite c |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| BR112013006693B1 (pt) * | 2010-09-21 | 2022-07-12 | Enanta Pharmaceuticals, Inc | Compostos inibidores da serino protease hcv derivada de prolina macrocíclica |
| CA2812779A1 (fr) | 2010-09-29 | 2012-04-19 | Merck Sharp & Dohme Corp. | Derives tetracycliques condenses et procedes d'utilisation de ceux-ci dans le traitement de maladies virales |
| MX2013003634A (es) * | 2010-09-29 | 2013-05-20 | Merck Sharp & Dohme | Derivados policiclicos heterociclicos y metodos de uso de los mismos para el tratamiento de enfermedades virales. |
| WO2012082672A2 (fr) | 2010-12-14 | 2012-06-21 | Merck Sharp & Dohme Corp. | Procédé et intermédiaires pour la préparation de macrolactames |
| WO2012122716A1 (fr) | 2011-03-17 | 2012-09-20 | Merck Sharp & Dohme Corp. | Dérivés tétracycliques de xanthène et leurs procédés d'utilisation pour le traitement de maladies virales |
| 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 |
| US9249204B2 (en) * | 2011-06-01 | 2016-02-02 | Jyant Technologies, Inc. | Chemokine-immunoglobulin fusion polypeptides, compositions, method of making and use thereof |
| AU2012299218A1 (en) | 2011-08-19 | 2014-02-20 | Merck Sharp & Dohme Corp. | Crystal forms of a HCV protease inhibitor |
| US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
| US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| SE1450130A1 (sv) | 2011-10-21 | 2014-05-07 | Abbvie Inc | Förfaranden för att behandla hcv innefattande minst två direktverkande antivirala agenser, ribavirin men inte interferon |
| EP2583680A3 (fr) | 2011-10-21 | 2013-06-12 | Abbvie Inc. | Traitement seul (PSI-7977) ou combinatoire dans l'utilisation pour le traitement du VHC |
| RU2014122154A (ru) * | 2011-10-31 | 2015-12-10 | Мерк Шарп И Доум Корп. | Композиции, пригодные для лечения вирусных заболеваний |
| US9328138B2 (en) | 2011-11-15 | 2016-05-03 | Msd Italia S.R.L. | HCV NS3 protease inhibitors |
| US9034832B2 (en) | 2011-12-29 | 2015-05-19 | Abbvie Inc. | Solid compositions |
| UA119315C2 (uk) * | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Інгібітори вірусу гепатиту с |
| BR112015007879A2 (pt) | 2012-10-19 | 2017-07-04 | Bristol Myers Squibb Co | inibidores do vírus da hepatite c |
| 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 |
| US9409943B2 (en) | 2012-11-05 | 2016-08-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2014110687A1 (fr) | 2013-01-16 | 2014-07-24 | Merck Sharp & Dohme Corp. | Composés tétracycliques substitués par thiazolyle et leurs procédés d'utilisation pour le traitement de maladies virales |
| EP2964664B1 (fr) | 2013-03-07 | 2017-01-11 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
| US11484534B2 (en) | 2013-03-14 | 2022-11-01 | Abbvie Inc. | Methods for treating HCV |
| CN105073758B (zh) * | 2013-03-15 | 2017-08-11 | 吉利德科学公司 | 丙型肝炎病毒抑制剂 |
| US9873707B2 (en) | 2013-10-18 | 2018-01-23 | Merck Sharp & Dohme Corp. | Methods and intermediates for preparing macrolactams |
| WO2015095430A1 (fr) * | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Procédés et intermédiaires pour la préparation de macrolactames |
| WO2015100144A1 (fr) * | 2013-12-23 | 2015-07-02 | Gilead Sciences, Inc. | Formes cristallines d'un composé antiviral |
| TR201906413T4 (tr) | 2013-12-23 | 2019-05-21 | Gilead Sciences Inc | Bir makrosiklik hcv ns3 inhibe edici tripeptidin sentezi. |
| WO2015103490A1 (fr) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Formes galéniques antivirales solides |
| WO2015119924A2 (fr) * | 2014-02-05 | 2015-08-13 | Merck Sharp & Dohme Corp. | Combinaisons à dose fixe de composés antiviraux |
| WO2015119919A1 (fr) * | 2014-02-05 | 2015-08-13 | Merck Sharp & Dohme Corp. | Composition pharmaceutique d'inhibiteurs sélectifs de la ns3/4a du hcv |
| CN106413736A (zh) * | 2014-06-06 | 2017-02-15 | 艾伯维公司 | 晶型 |
| WO2017023714A1 (fr) * | 2015-08-04 | 2017-02-09 | Merck Sharp & Dohme Corp. | Combinaisons à dose fixée de composés antiviraux |
| US20180228828A1 (en) * | 2015-08-04 | 2018-08-16 | Merck Sharp & Dohme Corp. | Fixed-dose combinations of antiviral compounds |
| CN105753806B (zh) * | 2016-02-02 | 2018-06-05 | 厦门市蔚嘉化学科技有限公司 | 一种利托那韦中间体的非均相合成方法及其应用 |
| EA201892448A1 (ru) | 2016-04-28 | 2019-06-28 | Эмори Юниверсити | Алкинсодержащие нуклеотидные и нуклеозидные терапевтические композиции и связанные с ними способы применения |
| CN109562113A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的螺环降解决定子体 |
| WO2017197051A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères de c3-glutarimide liés à une amine pour la dégradation de protéines cibles |
| ES2989988T3 (es) | 2016-05-10 | 2024-11-28 | C4 Therapeutics Inc | Degronímeros heterorocíclicos para la degradación de proteínas diana |
| WO2017197046A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères de type glutarimide liés au carbone c3 pour la dégradation de protéines cibles |
| CN112661775A (zh) * | 2016-05-16 | 2021-04-16 | 深圳市塔吉瑞生物医药有限公司 | 一种取代的大环喹喔啉化合物及其药物组合物及应用 |
| RU2650610C1 (ru) | 2017-02-28 | 2018-04-16 | Васильевич Иващенко Александр | Противовирусная композиция и способ ее применения |
| CN110769822A (zh) | 2017-06-20 | 2020-02-07 | C4医药公司 | 用于蛋白降解的n/o-连接的降解决定子和降解决定子体 |
| WO2020247736A1 (fr) * | 2019-06-07 | 2020-12-10 | University Of Massachusetts | Inhibiteurs de protéase ns3/4a du virus de l'hépatite c |
| CN111057045A (zh) * | 2019-12-18 | 2020-04-24 | 安徽红杉生物医药科技有限公司 | Hcv ns3/4a蛋白酶抑制剂中间体及其合成方法、应用 |
| US20230218644A1 (en) | 2020-04-16 | 2023-07-13 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
| US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
Family Cites Families (107)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3480613A (en) | 1967-07-03 | 1969-11-25 | Merck & Co Inc | 2-c or 3-c-alkylribofuranosyl - 1-substituted compounds and the nucleosides thereof |
| US6128582A (en) | 1996-04-30 | 2000-10-03 | Vertex Pharmaceuticals Incorporated | Molecules comprising an IMPDH-like binding pocket and encoded data storage medium capable of graphically displaying them |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| GB9707659D0 (en) | 1997-04-16 | 1997-06-04 | Peptide Therapeutics Ltd | Hepatitis C NS3 Protease inhibitors |
| WO1999007734A2 (fr) | 1997-08-11 | 1999-02-18 | Boehringer Ingelheim (Canada) Ltd. | Analogues de peptides inhibiteurs de l'hepatite c |
| DK1003775T3 (da) | 1997-08-11 | 2005-05-30 | Boehringer Ingelheim Ca Ltd | Hepatitis C-inhibitorpeptider |
| IT1299134B1 (it) | 1998-02-02 | 2000-02-29 | Angeletti P Ist Richerche Bio | Procedimento per la produzione di peptidi con proprieta' inibitrici della proteasi ns3 del virus hcv, peptidi cosi' ottenibili e peptidi |
| AU2787199A (en) | 1998-02-25 | 1999-09-15 | Emory University | 2'-fluoronucleosides |
| GB9806815D0 (en) | 1998-03-30 | 1998-05-27 | Hoffmann La Roche | Amino acid derivatives |
| EP1066247B1 (fr) | 1998-03-31 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de serine protease, particulierement de la protease ns3 du virus de l'hepatite c |
| GB9812523D0 (en) | 1998-06-10 | 1998-08-05 | Angeletti P Ist Richerche Bio | Peptide inhibitors of hepatitis c virus ns3 protease |
| DE69908376T2 (de) | 1998-08-10 | 2004-04-01 | The Hokkaido Electric Power Co., Inc., Sapporo | Verfahren zur herstellung normaler glykopeptide |
| US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| AU764479B2 (en) | 1998-10-29 | 2003-08-21 | Bristol-Myers Squibb Company | Compounds derived from an amine nucleus that are inhibitors of IMPDH enzyme |
| US6608027B1 (en) | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
| UA74546C2 (en) | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
| DK1196414T3 (da) | 1999-06-25 | 2003-11-24 | Vertex Pharma | Prolægemiddel af carbamathæmmer for IMPDH |
| CA2363274A1 (fr) | 1999-12-27 | 2001-07-05 | Japan Tobacco Inc. | Composes a noyaux fusionnes et leurs utilisations comme medicaments contre l'hepatite c |
| US6495677B1 (en) | 2000-02-15 | 2002-12-17 | Kanda S. Ramasamy | Nucleoside compounds |
| US6455508B1 (en) | 2000-02-15 | 2002-09-24 | Kanda S. Ramasamy | Methods for treating diseases with tirazole and pyrrolo-pyrimidine ribofuranosyl nucleosides |
| JP2003523978A (ja) | 2000-02-18 | 2003-08-12 | シャイアー・バイオケム・インコーポレイテッド | ヌクレオシドアナログを用いるflavivirus感染の処置もしくは予防するための方法 |
| JP4748911B2 (ja) | 2000-04-05 | 2011-08-17 | シェーリング コーポレイション | N−環状p2部分を含むc型肝炎ウイルスの大環状ns3‐セリンプロテアーゼ阻害剤 |
| WO2001077091A2 (fr) | 2000-04-05 | 2001-10-18 | Tularik Inc. | Inhibiteurs de polymerases ns5b vhc |
| ES2319732T3 (es) | 2000-04-13 | 2009-05-12 | Pharmasset, Inc. | Derivados de nucleosido 3'- o 2'-hidroximetilo sustituido para el tratamiento de infecciones virales. |
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| JP5230052B2 (ja) | 2000-05-26 | 2013-07-10 | イデニクス(ケイマン)リミテツド | フラビウイルスおよびペスチウイルス治療のための方法および組成物 |
| US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
| GB0017676D0 (en) | 2000-07-19 | 2000-09-06 | Angeletti P Ist Richerche Bio | Inhibitors of viral polymerase |
| ATE448019T1 (de) | 2000-08-10 | 2009-11-15 | Trustees Boston College | Wiederverwendbare methathese-katalysatoren |
| US6955174B2 (en) | 2000-08-18 | 2005-10-18 | Uryovascular Systems, Inc. | Cryotherapy method for detecting and treating vulnerable plaque |
| US20030008841A1 (en) | 2000-08-30 | 2003-01-09 | Rene Devos | Anti-HCV nucleoside derivatives |
| US6809101B2 (en) | 2000-09-01 | 2004-10-26 | Shionogi & Co., Ltd. | Compounds having anti-hepatitis C virus effect |
| ATE491459T1 (de) | 2000-10-18 | 2011-01-15 | Pharmasset Inc | Modifizierte nukleoside zur behandlung von virusinfektionen und abnormaler zellulärer proliferation |
| CN1301994C (zh) | 2000-12-12 | 2007-02-28 | 先灵公司 | 作为c型肝炎病毒ns3-丝氨酸蛋白酶抑制剂的二芳基肽 |
| AU2002230763A1 (en) | 2000-12-13 | 2008-01-03 | Bristol-Myers Squibb Pharma Company | Inhibitors of hepatitis c virus ns3 protease |
| WO2002048165A2 (fr) | 2000-12-15 | 2002-06-20 | Pharmasset Ltd. | Agents antiviraux utilises dans le traitement des infections par les flaviviridae |
| EP1346724A4 (fr) | 2000-12-26 | 2004-11-17 | Mitsubishi Pharma Corp | Remedes pour l'hepatite c |
| DZ3487A1 (fr) | 2001-01-22 | 2002-07-25 | Merck Sharp & Dohme | Derives de nucleoside comme inhibiteurs de l'arn polymerase virale d'arn-dependant |
| GB0114286D0 (en) | 2001-06-12 | 2001-08-01 | Hoffmann La Roche | Nucleoside Derivatives |
| JP4537057B2 (ja) | 2001-08-14 | 2010-09-01 | テルアビブ・ユニバーシティ・フューチャー・テクノロジー・デベロップメント・エルピー | 脂質化グリコサミノグリカン粒子ならびに診断及び処置のための薬物及び遺伝子送達におけるその使用 |
| WO2003026589A2 (fr) | 2001-09-28 | 2003-04-03 | Idenix (Cayman) Limited | Procedes et compositions pour le traitement du virus de l'hepatite c au moyen de nucleosides modifies en 4' |
| US20040006002A1 (en) | 2001-09-28 | 2004-01-08 | Jean-Pierre Sommadossi | Methods and compositions for treating flaviviruses and pestiviruses using 4'-modified nucleoside |
| JP2005515254A (ja) | 2002-01-17 | 2005-05-26 | スミスクライン ビーチャム コーポレーション | カテプシンk阻害剤として有用なシクロアルキルケトアミド誘導体 |
| GB0201179D0 (en) | 2002-01-18 | 2002-03-06 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| CA2369711A1 (fr) | 2002-01-30 | 2003-07-30 | Boehringer Ingelheim (Canada) Ltd. | Peptides macrocycliques qui agissent contre le virus de l'hepatite c |
| US7323453B2 (en) | 2002-02-13 | 2008-01-29 | Merck & Co., Inc. | Methods of inhibiting orthopoxvirus replication with nucleoside compounds |
| EP1381619B1 (fr) | 2002-03-28 | 2005-01-12 | Council of Scientific and Industrial Research | 8-(c-beta-d-glucopyranosyl)-7,3',4'-trihydroxyflavone, technique d'isolation de cette substance du i pterocarpus marsupium /i et composition pharmaceutique destinee a traiter le diabete |
| US20040063658A1 (en) | 2002-05-06 | 2004-04-01 | Roberts Christopher Don | Nucleoside derivatives for treating hepatitis C virus infection |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| WO2004000858A2 (fr) | 2002-06-21 | 2003-12-31 | Merck & Co., Inc. | Derives nucleosidiques utilises comme inhibiteurs de l'arn polymerase virale arn-dependante |
| EP1572945A2 (fr) | 2002-06-27 | 2005-09-14 | Merck & Co., Inc. | Derives nucleosidiques utilises comme inhibiteurs de l'arn polymerase arn-dependante virale |
| WO2004003000A2 (fr) | 2002-06-28 | 2004-01-08 | Idenix (Cayman) Limited | Promedicaments 2' et 3' de nucleoside permettant de traiter des infections par les flaviviridae |
| TW200500375A (en) | 2002-06-28 | 2005-01-01 | Idenix Cayman Ltd | Modified 2' and 3'-nucleoside prodrugs for treating flaviviridae |
| AP2005003213A0 (en) | 2002-06-28 | 2005-03-31 | Univ Cagliari | 2'-C-methyl-3'-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections. |
| WO2004007512A2 (fr) | 2002-07-16 | 2004-01-22 | Merck & Co., Inc. | Derives de nucleosides utilises en tant qu'inhibiteurs de l'arn polymerase virale arn-dependante |
| KR20050037559A (ko) | 2002-07-25 | 2005-04-22 | 마이크로로직스 바이오테크, 인코포레이티드 | 항바이러스성 7-데아자 d-뉴클레오시드 및 그의 용도 |
| SG174624A1 (en) | 2002-08-01 | 2011-10-28 | Pharmasset Inc | Compounds with the bicyclo[4.2.1]nonane system for the treatment of flaviviridae infections |
| TW200418498A (en) | 2002-09-30 | 2004-10-01 | Genelabs Tech Inc | Nucleoside derivatives for treating hepatitis C virus infection |
| WO2004041201A2 (fr) | 2002-11-01 | 2004-05-21 | Viropharma Incorporated | Composes de benzofurane, compositions et methodes utilisees pour le traitement et la prophylaxie des infections virales induites par l'hepatite c et des maladies associees |
| US20040254159A1 (en) | 2003-02-27 | 2004-12-16 | Hasvold Lisa A. | Heterocyclic kinase inhibitors |
| EP1601685A1 (fr) | 2003-03-05 | 2005-12-07 | Boehringer Ingelheim International GmbH | Composes d'inhibition de l'hepatite c |
| WO2004093915A1 (fr) | 2003-04-02 | 2004-11-04 | Boehringer Ingelheim International, Gmbh | Compositions pharmaceutiques contenant des inhibiteurs de protease virale de l'hepatite c |
| GB0307891D0 (en) | 2003-04-04 | 2003-05-14 | Angeletti P Ist Richerche Bio | Chemical compounds,compositions and uses |
| EP1629000B1 (fr) | 2003-04-16 | 2009-02-18 | Bristol-Myers Squibb Company | Peptide d'isoquinoleine macrocyclique inhibiteurs du virus de l'hepatite c |
| US7176208B2 (en) | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| CA2522577C (fr) | 2003-05-21 | 2011-04-26 | Boehringer Ingelheim International Gmbh | Composes inhibiteurs de l'hepatite c |
| CN100503628C (zh) | 2003-05-30 | 2009-06-24 | 法莫赛特股份有限公司 | 修饰的氟化核苷类似物 |
| GB0313250D0 (en) | 2003-06-09 | 2003-07-16 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| MXPA05013452A (es) | 2003-06-19 | 2006-03-09 | Hoffmann La Roche | Proceso para preparar derivados de 4'-azidonucleosido. |
| TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
| GB0321003D0 (en) | 2003-09-09 | 2003-10-08 | Angeletti P Ist Richerche Bio | Compounds, compositions and uses |
| GB0323845D0 (en) | 2003-10-10 | 2003-11-12 | Angeletti P Ist Richerche Bio | Chemical compounds,compositions and uses |
| US7132504B2 (en) | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CA2549851C (fr) | 2004-01-21 | 2012-09-11 | Boehringer Ingelheim International Gmbh | Peptides macrocycliques actifs contre le virus de l'hepatite c |
| ATE428714T1 (de) | 2004-02-24 | 2009-05-15 | Japan Tobacco Inc | Kondensierte heterotetracyclische verbindungen und deren verwendung als hcv-polymerase-inhibitor |
| GB0413087D0 (en) | 2004-06-11 | 2004-07-14 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| GB0416396D0 (en) | 2004-07-22 | 2004-08-25 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US7153848B2 (en) | 2004-08-09 | 2006-12-26 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| CN101044151B (zh) | 2004-08-23 | 2011-01-19 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒的4'-叠氮基-核苷 |
| GB0419850D0 (en) | 2004-09-07 | 2004-10-13 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| EP1807397A2 (fr) | 2004-10-26 | 2007-07-18 | Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. | Derives d'indole tetracycliques utilises comme agents antiviraux |
| US7834145B2 (en) | 2005-03-22 | 2010-11-16 | Merck Sharp & Dohme Corp. | HCV protease substrates |
| AU2006242475B2 (en) * | 2005-05-02 | 2011-07-07 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| GB0509326D0 (en) | 2005-05-09 | 2005-06-15 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| TWI387603B (zh) * | 2005-07-20 | 2013-03-01 | Merck Sharp & Dohme | Hcv ns3蛋白酶抑制劑 |
| US7462035B2 (en) | 2005-07-27 | 2008-12-09 | Physical Optics Corporation | Electrical connector configured as a fastening element |
| EP1913016B1 (fr) * | 2005-08-01 | 2013-01-16 | Merck Sharp & Dohme Corp. | Peptides macrocycliques en tant qu inhibiteurs de la protéase ns3 du vhc |
| WO2007028789A1 (fr) | 2005-09-07 | 2007-03-15 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa | Dérivés de quinazoline en tant qu'agents antiviraux |
| GB0518390D0 (en) | 2005-09-09 | 2005-10-19 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| GB0519797D0 (en) | 2005-09-29 | 2005-11-09 | Istituto Di Ricerche D Biolog | Therapeutic agents |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US20090203008A1 (en) | 2006-06-08 | 2009-08-13 | Ludmerer Steven W | Rapid method to determine inhibitor sensitivity of NS3/4A protease sequences cloned from clinical samples |
| GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| UY30437A1 (es) * | 2006-06-26 | 2008-01-31 | Enanta Pharm Inc | Quinoxalinil macroceclicos inhibidores de serina proteasa del virus de la hepatitis c |
| AU2007309546A1 (en) | 2006-10-24 | 2008-05-02 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | HCV NS3 protease inhibitors |
| 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 |
| MY164469A (en) | 2006-10-27 | 2017-12-15 | Msd Italia Srl | Hcv ns3 protease inhibitors |
| US8377874B2 (en) * | 2006-10-27 | 2013-02-19 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| CA2705449C (fr) | 2006-11-09 | 2017-01-10 | Twinblade Technologies Holding Sweden Ab | Dispositif moyeu |
| WO2008112108A1 (fr) | 2007-03-09 | 2008-09-18 | Merck & Co., Inc. | Résistance in vivo du vhc à des inhibiteurs anti-viraux |
| JP5395068B2 (ja) | 2007-06-29 | 2014-01-22 | ギリアード サイエンシーズ, インコーポレイテッド | トール様受容体7の調節物質としてのプリン誘導体およびその使用 |
| WO2009010804A1 (fr) | 2007-07-19 | 2009-01-22 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Composes macrocycliques servant d'agents antiviraux |
| JP2011503201A (ja) | 2007-11-14 | 2011-01-27 | 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 | 大環状テトラゾリルc型肝炎セリンプロテアーゼ阻害剤 |
| CL2008003384A1 (es) | 2007-11-14 | 2009-12-11 | Enanta Pharm Inc | Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c. |
| CA2720850A1 (fr) * | 2008-04-28 | 2009-11-05 | Merck Sharp & Dohme Corp. | Inhibiteurs de la protease hcv ns3 |
| SI2540350T1 (sl) | 2008-07-22 | 2015-01-30 | Merck Sharp & Dohme Corp. | Kombinacije makrocikliäśnih kinoksalinske spojine, ki je hcv ns3 proteazni inhibitor z drugimi hcv uäśinkovinami |
-
2009
- 2009-07-17 SI SI200930956T patent/SI2540350T1/sl unknown
- 2009-07-17 EP EP09790553A patent/EP2310095B1/fr active Active
- 2009-07-17 UA UAA201102068A patent/UA100436C2/uk unknown
- 2009-07-17 DK DK12181546.8T patent/DK2540350T3/da active
- 2009-07-17 PE PE2011000067A patent/PE20110212A1/es active IP Right Grant
- 2009-07-17 JP JP2011520110A patent/JP4920797B2/ja active Active
- 2009-07-17 SI SI200930359T patent/SI2310095T1/sl unknown
- 2009-07-17 BR BRPI0916235A patent/BRPI0916235B8/pt active IP Right Grant
- 2009-07-17 PT PT121815468T patent/PT2540350E/pt unknown
- 2009-07-17 EP EP12181546.8A patent/EP2540350B1/fr active Active
- 2009-07-17 MX MX2011000826A patent/MX2011000826A/es active IP Right Grant
- 2009-07-17 PT PT09790553T patent/PT2310095E/pt unknown
- 2009-07-17 RS RS20140375A patent/RS53420B/sr unknown
- 2009-07-17 ES ES09790553T patent/ES2392611T3/es active Active
- 2009-07-17 ME MEP-2012-463A patent/ME02024B/me unknown
- 2009-07-17 MY MYPI20110310 patent/MY152070A/en unknown
- 2009-07-17 ME MEP-2014-375A patent/ME02132B/fr unknown
- 2009-07-17 NZ NZ590638A patent/NZ590638A/en not_active IP Right Cessation
- 2009-07-17 CA CA2731177A patent/CA2731177C/fr active Active
- 2009-07-17 EP EP12181533.6A patent/EP2540349B1/fr active Active
- 2009-07-17 PL PL09790553T patent/PL2310095T3/pl unknown
- 2009-07-17 WO PCT/US2009/050915 patent/WO2010011566A1/fr not_active Ceased
- 2009-07-17 EA EA201170241A patent/EA019327B1/ru active Protection Beyond IP Right Term
- 2009-07-17 DK DK09790553.3T patent/DK2310095T3/da active
- 2009-07-17 AU AU2009274190A patent/AU2009274190B2/en active Active
- 2009-07-17 HR HRP20120866AT patent/HRP20120866T1/hr unknown
- 2009-07-17 CN CN200980137118.6A patent/CN102159285B/zh active Active
- 2009-07-17 ES ES12181546.8T patent/ES2491090T3/es active Active
- 2009-07-17 KR KR1020117003982A patent/KR101313675B1/ko active Active
- 2009-07-17 PL PL12181546T patent/PL2540350T3/pl unknown
- 2009-07-17 RS RS20120463A patent/RS52534B/sr unknown
- 2009-07-17 US US12/504,955 patent/US7973040B2/en active Active
- 2009-07-21 TW TW098124597A patent/TWI441638B/zh active
- 2009-07-21 AR ARP090102779A patent/AR072588A1/es active IP Right Grant
-
2011
- 2011-01-11 IL IL210580A patent/IL210580A/en active Protection Beyond IP Right Term
- 2011-01-13 TN TN2011000014A patent/TN2011000014A1/fr unknown
- 2011-01-19 NI NI201100023A patent/NI201100023A/es unknown
- 2011-01-19 CO CO11005448A patent/CO6351757A2/es active IP Right Grant
- 2011-01-20 DO DO2011000023A patent/DOP2011000023A/es unknown
- 2011-01-20 SV SV2011003813A patent/SV2011003813A/es unknown
- 2011-01-20 HN HN2011000209A patent/HN2011000209A/es unknown
- 2011-01-21 EC EC2011010777A patent/ECSP11010777A/es unknown
- 2011-01-21 CL CL2011000145A patent/CL2011000145A1/es unknown
- 2011-01-25 MA MA33556A patent/MA32502B1/fr unknown
- 2011-02-15 CR CR20110089A patent/CR20110089A/es unknown
- 2011-05-20 US US13/112,281 patent/US8080654B2/en active Active
-
2012
- 2012-11-28 CY CY20121101150T patent/CY1113752T1/el unknown
-
2014
- 2014-07-18 HR HRP20140693AT patent/HRP20140693T1/hr unknown
- 2014-08-01 CY CY20141100582T patent/CY1115503T1/el unknown
-
2016
- 2016-12-26 FR FR16C1027C patent/FR16C1027I2/fr active Active
- 2016-12-29 LT LTPA2016049C patent/LTC2310095I2/lt unknown
- 2016-12-30 NL NL300857C patent/NL300857I2/nl unknown
-
2017
- 2017-01-03 LU LU00002C patent/LUC00002I2/fr unknown
- 2017-01-10 HU HUS1700001C patent/HUS1700001I1/hu unknown
- 2017-01-20 CY CY2017005C patent/CY2017005I1/el unknown
- 2017-01-20 NO NO2017004C patent/NO2017004I2/no unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA32502B1 (fr) | Composes de quinoxaline macrocycliques en tant qu'inhibiteurs de protease ns3 du virus de l'hepatite c (hcv) | |
| WO2008051477A3 (fr) | Inhibiteurs de la protéase hcv ns3 | |
| MX2009004556A (es) | Inhibidores de la proteasa ns3 del hcv. | |
| WO2008057208A3 (fr) | Inhibiteurs de protéase ns3 du vhc | |
| WO2008051514A3 (fr) | Inhibiteurs de la protéase ns3 du hcv | |
| WO2008051475A3 (fr) | Inhibiteurs de la protéase ns3 du vhc | |
| GEP20125683B (en) | Serine proteases inhibitors for hcv infections treatment | |
| MX2011006631A (es) | Inhibidores de proteasa ns3 del virus hcv. | |
| EP1924593B8 (fr) | Inhibiteurs de la protease ns3 du vhc | |
| WO2008057995A3 (fr) | Inhibiteurs de protéase de vhc | |
| EA200901101A1 (ru) | Макроциклические соединения в качестве ингибиторов протеазы ns3 вгс | |
| WO2006119061A3 (fr) | Inhibiteurs de la protease ns3 du vhc | |
| EA201071315A1 (ru) | Ингибиторы протеазы вируса гепатита с | |
| WO2013074386A3 (fr) | Inhibiteurs de la protéase ns3 du vhc | |
| ATE469155T1 (de) | Cyclopropyl-fusionierte indolbenzazepin-hcv-ns5b- hemmer | |
| DK1987038T3 (da) | HCV NS5B-hæmmere | |
| EA201270423A1 (ru) | Ингибиторы протеазы hcv | |
| WO2008106058A3 (fr) | Inhibiteurs de sérine protéases | |
| WO2012019299A9 (fr) | Composés inhibiteurs de l'hépatite c | |
| WO2010034105A8 (fr) | Composés inhibiteurs de l'hépatite c | |
| UA90909C2 (en) | Hcv ns3 protease inhibitors | |
| UA95990C2 (en) | Hcv ns3 protease inhibitors |