HK1210141A1 - Hcv protease inhibitors and uses thereof - Google Patents
Hcv protease inhibitors and uses thereof Download PDFInfo
- Publication number
- HK1210141A1 HK1210141A1 HK15110728.1A HK15110728A HK1210141A1 HK 1210141 A1 HK1210141 A1 HK 1210141A1 HK 15110728 A HK15110728 A HK 15110728A HK 1210141 A1 HK1210141 A1 HK 1210141A1
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- nitrogen
- oxygen
- membered
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
-
- 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
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06165—Dipeptides with the first amino acid being heterocyclic and Pro-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
-
- 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
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- 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
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- 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
- C07K5/081—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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
- C07K5/0815—Tripeptides with the first amino acid being basic
-
- 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
- C07K5/0819—Tripeptides with the first amino acid being acidic
-
- 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
- C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1021—Tetrapeptides with the first amino acid being acidic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1024—Tetrapeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1611007P | 2007-12-21 | 2007-12-21 | |
| US61/016,110 | 2007-12-21 | ||
| US1647307P | 2007-12-23 | 2007-12-23 | |
| US61/016,473 | 2007-12-23 | ||
| US6037108P | 2008-06-10 | 2008-06-10 | |
| US61/060,371 | 2008-06-10 | ||
| US9866808P | 2008-09-19 | 2008-09-19 | |
| US61/098,668 | 2008-09-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK1210141A1 true HK1210141A1 (en) | 2016-04-15 |
Family
ID=40801568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK15110728.1A HK1210141A1 (en) | 2007-12-21 | 2015-10-29 | Hcv protease inhibitors and uses thereof |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US9163061B2 (fr) |
| EP (1) | EP2237667A4 (fr) |
| JP (2) | JP5755449B2 (fr) |
| KR (2) | KR20150117305A (fr) |
| CN (2) | CN104557861A (fr) |
| AU (1) | AU2008340257B2 (fr) |
| BR (1) | BRPI0821559A2 (fr) |
| CA (1) | CA2709535A1 (fr) |
| HK (1) | HK1210141A1 (fr) |
| MX (1) | MX2010006736A (fr) |
| NZ (1) | NZ586231A (fr) |
| RU (1) | RU2515318C2 (fr) |
| TW (2) | TW201518507A (fr) |
| WO (1) | WO2009082697A1 (fr) |
| ZA (1) | ZA201004302B (fr) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104557861A (zh) | 2007-12-21 | 2015-04-29 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| EP2237666A4 (fr) | 2007-12-21 | 2012-05-16 | Avila Therapeutics Inc | Inhibiteurs de hcv protéase et leurs utilisations |
| US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| PL2300013T5 (pl) | 2008-05-21 | 2025-04-28 | Takeda Pharmaceutical Company Limited | Pochodne fosforu jako inhibitor kinazy |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| US8188137B2 (en) | 2008-08-15 | 2012-05-29 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| CN102405284B (zh) * | 2008-09-05 | 2016-01-20 | 新基阿维罗米克斯研究公司 | 设计不可逆抑制剂的算法 |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US8603737B2 (en) * | 2008-09-19 | 2013-12-10 | Celgene Avilomics Research, Inc. | Methods for identifying HCV protease inhibitors |
| JP2012523419A (ja) | 2009-04-08 | 2012-10-04 | イデニク プハルマセウティカルス,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 |
| US8232246B2 (en) | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| 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 |
| EP2478361A4 (fr) | 2009-09-16 | 2014-05-21 | Celgene Avilomics Res Inc | Conjugués et inhibiteurs de protéine kinase |
| WO2011049908A2 (fr) * | 2009-10-19 | 2011-04-28 | Enanta Pharmaceuticals, Inc. | Composés bismacrocycliques à titre d'inhibiteurs du virus de l'hépatite c |
| US8362068B2 (en) | 2009-12-18 | 2013-01-29 | Idenix Pharmaceuticals, Inc. | 5,5-fused arylene or heteroarylene hepatitis C virus inhibitors |
| CN102812167A (zh) | 2009-12-30 | 2012-12-05 | 阿维拉制药公司 | 蛋白的配体-介导的共价修饰 |
| WO2012037259A1 (fr) * | 2010-09-15 | 2012-03-22 | Intermune, Inc. | Nouveaux inhibiteurs de la réplication du virus de l'hépatite c |
| US8951964B2 (en) | 2010-12-30 | 2015-02-10 | Abbvie Inc. | Phenanthridine macrocyclic hepatitis C serine protease inhibitors |
| MX2013007677A (es) | 2010-12-30 | 2013-07-30 | Abbvie Inc | Inhibidores macrociclicos de serina proteasa de hepatitis. |
| TW201309690A (zh) | 2011-02-10 | 2013-03-01 | Idenix Pharmaceuticals Inc | 巨環絲胺酸蛋白酶抑制劑,其醫藥組合物及其於治療hcv感染之用途 |
| US20120252721A1 (en) | 2011-03-31 | 2012-10-04 | Idenix Pharmaceuticals, Inc. | Methods for treating drug-resistant hepatitis c virus infection with a 5,5-fused arylene or heteroarylene hepatitis c virus inhibitor |
| EP2704572B1 (fr) | 2011-05-04 | 2015-12-30 | Ariad Pharmaceuticals, Inc. | Composés permettant d'inhiber la prolifération cellulaire dans les cancers induits par l'egfr |
| 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 |
| WO2012166459A1 (fr) * | 2011-05-27 | 2012-12-06 | Bristol-Myers Squibb Company | Tripeptides incorporant du deutérium en tant qu'inhibiteurs du virus de l'hépatite c |
| JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
| UA119315C2 (uk) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Інгібітори вірусу гепатиту с |
| JP2015533124A (ja) | 2012-10-08 | 2015-11-19 | アッヴィ・インコーポレイテッド | Hcvプロテアーゼ阻害剤を作製するのに有用な化合物 |
| 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 |
| WO2014071007A1 (fr) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
| US9598433B2 (en) | 2012-11-02 | 2017-03-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2014070974A1 (fr) | 2012-11-05 | 2014-05-08 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
| US9580463B2 (en) | 2013-03-07 | 2017-02-28 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US9617310B2 (en) | 2013-03-15 | 2017-04-11 | Gilead Sciences, Inc. | Inhibitors of hepatitis C virus |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| WO2015042375A1 (fr) | 2013-09-20 | 2015-03-26 | Idenix Pharmaceuticals, Inc. | Inhibiteurs du virus de l'hépatite c |
| WO2015103490A1 (fr) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Formes galéniques antivirales solides |
| WO2015134561A1 (fr) | 2014-03-05 | 2015-09-11 | Idenix Pharmaceuticals, Inc. | Compositions pharmaceutiques comprenant un inhibiteur de flaviviridae hétéroarylène fusionné en 5,5 et son utilisation pour le traitement ou la prévention d'une infection par les flaviviridae |
| EP3114122A1 (fr) | 2014-03-05 | 2017-01-11 | Idenix Pharmaceuticals LLC | Formes solides d'un composé inhibiteur des virus de la famille des flaviviridae et sels de celui-ci |
| JP6768270B2 (ja) * | 2015-08-03 | 2020-10-14 | 学校法人神戸学院 | ビオチン直接結合型タンパク質活性調節物質 |
| WO2020247736A1 (fr) * | 2019-06-07 | 2020-12-10 | University Of Massachusetts | Inhibiteurs de protéase ns3/4a du virus de l'hépatite c |
| US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
Family Cites Families (99)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5371017A (en) * | 1990-04-04 | 1994-12-06 | Chiron Corporation | Hepatitis C virus protease |
| GB9623908D0 (en) * | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| AU1416099A (en) * | 1997-11-28 | 1999-06-16 | Schering Corporation | Single-chain recombinant complexes of hepatitis c virus ns3 protease and ns4a cofactor peptide |
| US7122627B2 (en) * | 1999-07-26 | 2006-10-17 | Bristol-Myers Squibb Company | Lactam inhibitors of Hepatitis C virus NS3 protease |
| AU2001253206A1 (en) * | 2000-04-05 | 2001-10-23 | Tularik, Inc. | Ns5b hcv polymerase inhibitors |
| SK14952002A3 (sk) * | 2000-04-19 | 2003-03-04 | Schering Corporation | Makrocyklické zlúčeniny, farmaceutický prostriedok s ich obsahom a ich použitie |
| AR029851A1 (es) * | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
| AU2002248147B2 (en) * | 2000-11-20 | 2006-04-06 | Bristol-Myers Squibb Company | Hepatitis C tripeptide inhibitors |
| US6825347B2 (en) * | 2001-05-21 | 2004-11-30 | Research Corporation Technologies, Inc. | Uronium and immonium salts for peptide coupling |
| US6867185B2 (en) * | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| KR20040077767A (ko) * | 2002-01-23 | 2004-09-06 | 쉐링 코포레이션 | C형 간염 바이러스 감염 치료용 ns3-세린 프로테아제억제제로서의 프롤린 화합물 |
| US6642204B2 (en) | 2002-02-01 | 2003-11-04 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor tri-peptides |
| US7091184B2 (en) * | 2002-02-01 | 2006-08-15 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor tri-peptides |
| MXPA04009938A (es) | 2002-04-11 | 2004-12-13 | Vertex Pharma | Inhibidores de serina proteasas, en particular la proteasa ns3-ns4a del hcv. |
| CA2483494A1 (fr) | 2002-04-25 | 2003-11-06 | Emory University | Sondes proteiques dirigees semi-synthetiques destinees a l'identification et l'inhibition de sites actifs et procedes associes |
| ES2361011T3 (es) | 2002-05-20 | 2011-06-13 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c. |
| JP4312711B2 (ja) * | 2002-05-20 | 2009-08-12 | ブリストル−マイヤーズ スクイブ カンパニー | ヘテロ環式スルホンアミドc型肝炎ウイルス阻害剤 |
| MY140680A (en) * | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| ES2315568T3 (es) * | 2002-05-20 | 2009-04-01 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c basados en cicloalquilo p1' sustituido. |
| 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 |
| CA2505849C (fr) * | 2002-07-30 | 2013-11-05 | Morphosys Ip Gmbh | Nouveaux vecteurs tricistroniques et utilisations de ceux-ci |
| EP1408031A1 (fr) * | 2002-10-09 | 2004-04-14 | 3 D Gene Pharma | Derivés de pyrolidine comme médicaments contre Hepatitis C |
| AU2003290584B2 (en) * | 2002-11-01 | 2009-07-16 | Viropharma Incorporated | Benzofuran compounds, compositions and methods for treatment and prophylaxis of hepatitis C viral infections and associated diseases |
| US20040180815A1 (en) * | 2003-03-07 | 2004-09-16 | Suanne Nakajima | Pyridazinonyl macrocyclic hepatitis C serine protease inhibitors |
| EP1601685A1 (fr) * | 2003-03-05 | 2005-12-07 | Boehringer Ingelheim International GmbH | Composes d'inhibition de l'hepatite c |
| WO2004101602A2 (fr) * | 2003-03-05 | 2004-11-25 | Boehringer Ingelheim International Gmbh | Analogues de peptides inhibiteurs de l'hepatite c |
| US20040265917A1 (en) | 2003-04-07 | 2004-12-30 | Dennis Benjamin | Methods of measuring the ability of a test compound to inactivate a biological target in cells of a subject |
| JP4231524B2 (ja) * | 2003-04-10 | 2009-03-04 | 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 | 大環状化合物の製造方法 |
| ATE422895T1 (de) | 2003-04-16 | 2009-03-15 | Bristol Myers Squibb Co | Makrocyclische isochinolinpeptidinhibitoren des hepatitis-c-virus |
| CL2004001161A1 (es) * | 2003-05-21 | 2005-04-08 | Boehringer Ingelheim Int | Compuestos describe compuestos derivados de quinolina; composicion farmaceutica; y su uso para tratar una enfermedad causada por el virus de la hepatitis c. |
| US20050014136A1 (en) * | 2003-05-28 | 2005-01-20 | Innogenetics N.V. | Modified HCV NS5 |
| US20050053617A1 (en) * | 2003-05-28 | 2005-03-10 | Erik Depla | Modified HCV NS3 |
| US7273851B2 (en) | 2003-06-05 | 2007-09-25 | Enanta Pharmaceuticals, Inc. | Tri-peptide hepatitis C serine protease inhibitors |
| EP1692157B1 (fr) | 2003-10-10 | 2013-04-17 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de serine proteases, en particulier la ns3-ns4a protease du hcv |
| US7491794B2 (en) * | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| EP1680137B1 (fr) | 2003-10-14 | 2012-11-21 | F. Hoffmann-La Roche Ltd. | Composé macrocyclique à groupe acide carboxylique et acylsulfonamide comme inhibiteur de la réplication du virus de l'hépatite C |
| US7132504B2 (en) * | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7135462B2 (en) * | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2005051980A1 (fr) | 2003-11-20 | 2005-06-09 | Schering Corporation | Inhibiteurs depourvus de liaisons peptidiques de la protease ns3 du virus de l'hepatite c |
| GEP20104926B (en) | 2004-03-30 | 2010-03-25 | Intermune Inc | Macrocyclic compounds as inhibitors of viral replication |
| US7399749B2 (en) | 2004-05-20 | 2008-07-15 | Schering Corporation | Substituted prolines as inhibitors of hepatitis C virus NS3 serine protease |
| US7514557B2 (en) | 2004-05-25 | 2009-04-07 | Boehringer Ingelheim International Gmbh | Process for preparing acyclic HCV protease inhibitors |
| CA2556669C (fr) | 2004-06-28 | 2012-05-01 | Boehringer Ingelheim International Gmbh | Analogues peptidiques d'inhibiteurs de l'hepatite c |
| AR050174A1 (es) | 2004-07-16 | 2006-10-04 | Gilead Sciences Inc | Derivados de fosfonatos con actividad antiviral. composiciones farmaceuticas |
| UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
| WO2006007708A1 (fr) | 2004-07-20 | 2006-01-26 | Boehringer Engelheim International Gmbh | Analogues peptidiques inhibiteurs de l'hepatite c |
| ATE513844T1 (de) | 2004-08-27 | 2011-07-15 | Schering Corp | Acylsulfonamidverbindungen als inhibitoren der ns3-serinprotease des hepatitis-c-virus |
| CA2578428A1 (fr) | 2004-09-17 | 2006-03-30 | Boehringer Ingelheim International Gmbh | Reaction de metathese cyclisante en milieu fluide supercritique |
| US7402568B2 (en) * | 2004-09-29 | 2008-07-22 | Enanta Pharmaceuticals, Inc. | Bicyclic 9a-azalide derivatives |
| US7323447B2 (en) * | 2005-02-08 | 2008-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PL1863833T3 (pl) | 2005-03-08 | 2014-03-31 | Boehringer Ingelheim Int | Sposób otrzymywania związków makrocyklicznych |
| US20080207760A1 (en) | 2005-04-11 | 2008-08-28 | Achillion Pharmaceuticals, Inc. | Pharmaceutical Compositions For and Methods of Inhibiting Hcv |
| AU2006242475B2 (en) * | 2005-05-02 | 2011-07-07 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20060276405A1 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods for treating hepatitis C |
| US20070237818A1 (en) | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| EP1891089B1 (fr) | 2005-06-02 | 2014-11-05 | Merck Sharp & Dohme Corp. | Inhibiteurs de protease du VHC en combinaison avec des aliments |
| US20060276404A1 (en) | 2005-06-02 | 2006-12-07 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| WO2006130553A2 (fr) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methode destinee au traitement de troubles et de maladies ne repondant pas aux interferons, dans laquelle est utilise un inhibiteur de la protease du vhc |
| EP1898941A2 (fr) | 2005-06-02 | 2008-03-19 | Schering Corporation | Formulation a liberation controlee pour le traitement de maladies liees au virus de la hepatite c |
| US20060281689A1 (en) | 2005-06-02 | 2006-12-14 | Schering Corporation | Method for modulating activity of HCV protease through use of a novel HCV protease inhibitor to reduce duration of treatment period |
| JP5160415B2 (ja) | 2005-06-02 | 2013-03-13 | メルク・シャープ・アンド・ドーム・コーポレーション | 医薬処方物およびそれを用いる治療方法 |
| WO2006130688A2 (fr) | 2005-06-02 | 2006-12-07 | Schering Corporation | Procedes de dosage asymetrique |
| US20070021351A1 (en) | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| WO2006130554A2 (fr) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methodes de traitement du virus de l'hepatite c |
| WO2006130552A2 (fr) | 2005-06-02 | 2006-12-07 | Schering Corporation | Methodes de traitement du virus de l'hepatite c |
| US7608592B2 (en) * | 2005-06-30 | 2009-10-27 | Virobay, Inc. | HCV inhibitors |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI389908B (zh) | 2005-07-14 | 2013-03-21 | Gilead Sciences Inc | 抗病毒化合物類 |
| WO2007009227A1 (fr) | 2005-07-20 | 2007-01-25 | Boehringer Ingelheim International Gmbh | Analogues de peptides inhibiteurs de l'hepatite c |
| AR057456A1 (es) | 2005-07-20 | 2007-12-05 | Merck & Co Inc | Inhibidores de la proteasa ns3 del vhc |
| CN101263156A (zh) * | 2005-07-25 | 2008-09-10 | 因特蒙公司 | C型肝炎病毒复制的新颖大环抑制剂 |
| RU2008107972A (ru) * | 2005-08-01 | 2009-09-10 | Мерк энд Ко., Инк. (US) | Макроциклические пептиды в качестве ингибиторов ns3-протеазы hcv |
| CN101415705B (zh) | 2005-10-11 | 2011-10-26 | 因特蒙公司 | 抑制丙型肝炎病毒复制的化合物和方法 |
| 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 |
| WO2007089618A2 (fr) | 2006-01-27 | 2007-08-09 | Phenomix Corporation | Inhibiteurs de la sérine protéase de l'hépatite c et leurs utilisations |
| US20070224167A1 (en) | 2006-02-09 | 2007-09-27 | Schering Corporation | Novel HCV inhibitor combinations and methods |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| KR20090024834A (ko) | 2006-07-05 | 2009-03-09 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 억제제 |
| US7635683B2 (en) * | 2006-08-04 | 2009-12-22 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl tripeptide hepatitis C virus inhibitors |
| US7605126B2 (en) * | 2006-08-11 | 2009-10-20 | Enanta Pharmaceuticals, Inc. | Acylaminoheteroaryl hepatitis C virus protease inhibitors |
| US7662779B2 (en) * | 2006-08-11 | 2010-02-16 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis C serine protease inhibitors |
| US7582605B2 (en) * | 2006-08-11 | 2009-09-01 | Enanta Pharmaceuticals, Inc. | Phosphorus-containing hepatitis C serine protease inhibitors |
| US7687459B2 (en) * | 2006-08-11 | 2010-03-30 | Enanta Pharmaceuticals, Inc. | Arylalkoxyl hepatitis C virus protease inhibitors |
| AU2007309546A1 (en) | 2006-10-24 | 2008-05-02 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | HCV NS3 protease inhibitors |
| EP2083844B1 (fr) | 2006-10-27 | 2013-11-27 | Merck Sharp & Dohme Corp. | Inhibiteurs de protéase ns3 du vhc |
| EP2086982B1 (fr) | 2006-10-27 | 2018-08-29 | Merck Sharp & Dohme Corp. | Inhibiteurs de protéase ns3 du vhc |
| US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2481807A3 (fr) | 2007-03-09 | 2013-04-03 | Merck Sharp & Dohme Corp. | Résistance HCV in vivo à des inhibiteurs anti-viraux |
| AU2008309589B2 (en) | 2007-10-10 | 2012-07-05 | Novartis Ag | Spiropyrrolidines and their use against HCV and HIV infection |
| EP2222161A4 (fr) * | 2007-12-05 | 2011-09-28 | Enanta Pharm Inc | Dérivés de quinoxalinyle |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| CN104557861A (zh) | 2007-12-21 | 2015-04-29 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| EP2237666A4 (fr) | 2007-12-21 | 2012-05-16 | Avila Therapeutics Inc | Inhibiteurs de hcv protéase et leurs utilisations |
| US8188137B2 (en) | 2008-08-15 | 2012-05-29 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| US8603737B2 (en) | 2008-09-19 | 2013-12-10 | Celgene Avilomics Research, Inc. | Methods for identifying HCV protease inhibitors |
-
2008
- 2008-12-19 CN CN201410718124.3A patent/CN104557861A/zh active Pending
- 2008-12-19 WO PCT/US2008/087725 patent/WO2009082697A1/fr not_active Ceased
- 2008-12-19 KR KR1020157027032A patent/KR20150117305A/ko not_active Ceased
- 2008-12-19 MX MX2010006736A patent/MX2010006736A/es active IP Right Grant
- 2008-12-19 EP EP08865122A patent/EP2237667A4/fr not_active Withdrawn
- 2008-12-19 TW TW103133572A patent/TW201518507A/zh unknown
- 2008-12-19 US US12/339,680 patent/US9163061B2/en not_active Expired - Fee Related
- 2008-12-19 JP JP2010539883A patent/JP5755449B2/ja not_active Expired - Fee Related
- 2008-12-19 CA CA2709535A patent/CA2709535A1/fr not_active Abandoned
- 2008-12-19 KR KR1020107015717A patent/KR101683559B1/ko not_active Expired - Fee Related
- 2008-12-19 NZ NZ586231A patent/NZ586231A/xx not_active IP Right Cessation
- 2008-12-19 BR BRPI0821559-6A patent/BRPI0821559A2/pt active Search and Examination
- 2008-12-19 RU RU2010125106/04A patent/RU2515318C2/ru not_active IP Right Cessation
- 2008-12-19 CN CN200880127244.9A patent/CN101951770B/zh not_active Expired - Fee Related
- 2008-12-19 TW TW97149689A patent/TW200932255A/zh unknown
- 2008-12-19 AU AU2008340257A patent/AU2008340257B2/en not_active Ceased
-
2010
- 2010-06-17 ZA ZA2010/04302A patent/ZA201004302B/en unknown
-
2015
- 2015-02-02 JP JP2015018286A patent/JP2015113346A/ja not_active Ceased
- 2015-10-19 US US14/887,092 patent/US20160235805A1/en not_active Abandoned
- 2015-10-29 HK HK15110728.1A patent/HK1210141A1/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2015113346A (ja) | 2015-06-22 |
| KR20100131971A (ko) | 2010-12-16 |
| WO2009082697A1 (fr) | 2009-07-02 |
| EP2237667A4 (fr) | 2012-05-16 |
| RU2515318C2 (ru) | 2014-05-10 |
| TW200932255A (en) | 2009-08-01 |
| TW201518507A (zh) | 2015-05-16 |
| MX2010006736A (es) | 2010-10-15 |
| KR20150117305A (ko) | 2015-10-19 |
| JP5755449B2 (ja) | 2015-07-29 |
| NZ586231A (en) | 2012-12-21 |
| BRPI0821559A2 (pt) | 2015-06-16 |
| AU2008340257A1 (en) | 2009-07-02 |
| RU2010125106A (ru) | 2012-01-27 |
| KR101683559B1 (ko) | 2016-12-08 |
| US20090306085A1 (en) | 2009-12-10 |
| CN104557861A (zh) | 2015-04-29 |
| CN101951770A (zh) | 2011-01-19 |
| US9163061B2 (en) | 2015-10-20 |
| CN101951770B (zh) | 2014-12-31 |
| ZA201004302B (en) | 2011-10-26 |
| EP2237667A1 (fr) | 2010-10-13 |
| AU2008340257B2 (en) | 2015-06-11 |
| CA2709535A1 (fr) | 2009-07-02 |
| US20160235805A1 (en) | 2016-08-18 |
| JP2011509242A (ja) | 2011-03-24 |
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