JP5394063B2 - セリンプロテアーゼの阻害剤 - Google Patents
セリンプロテアーゼの阻害剤 Download PDFInfo
- Publication number
- JP5394063B2 JP5394063B2 JP2008528258A JP2008528258A JP5394063B2 JP 5394063 B2 JP5394063 B2 JP 5394063B2 JP 2008528258 A JP2008528258 A JP 2008528258A JP 2008528258 A JP2008528258 A JP 2008528258A JP 5394063 B2 JP5394063 B2 JP 5394063B2
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- aliphatic
- heterocycloaliphatic
- cycloaliphatic
- heteroaryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 C[S@]1(=[*+])=*C1(*)N(*)C* Chemical compound C[S@]1(=[*+])=*C1(*)N(*)C* 0.000 description 37
- MMSKTMKTGVHMAV-PRHODGIISA-N CC(C)(C)OC(N[C@](C1)([C@@H]1C=C)C(OC)=O)=O Chemical compound CC(C)(C)OC(N[C@](C1)([C@@H]1C=C)C(OC)=O)=O MMSKTMKTGVHMAV-PRHODGIISA-N 0.000 description 1
- IYTDBJIERXQERM-FYMLJLRASA-N CC(C)(C)[C@@H](C(N(C[C@@H](C/C(/c(c(OC)c1)cc(Cl)c1OC)=N\O)C1)[C@@H]1C(OC)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C/C(/c(c(OC)c1)cc(Cl)c1OC)=N\O)C1)[C@@H]1C(OC)=O)=O)NC(OC(C)(C)C)=O IYTDBJIERXQERM-FYMLJLRASA-N 0.000 description 1
- GANNGXNLFHYDNW-QXATTWAWSA-N CC(C)(C)[C@@H](C(N(C[C@](C1)(C2)ON=C2c(c(OC)c2)cc(Cl)c2OC)[C@@H]1C(OC)=O)=O)N Chemical compound CC(C)(C)[C@@H](C(N(C[C@](C1)(C2)ON=C2c(c(OC)c2)cc(Cl)c2OC)[C@@H]1C(OC)=O)=O)N GANNGXNLFHYDNW-QXATTWAWSA-N 0.000 description 1
- JMVJYPLTASZKHQ-KUHORTOSSA-N CC(C)Oc(c(C)c1)c(C)cc1/C(/CC(C[C@H]1C(OC)=O)CN1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=N/[O]=C Chemical compound CC(C)Oc(c(C)c1)c(C)cc1/C(/CC(C[C@H]1C(OC)=O)CN1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=N/[O]=C JMVJYPLTASZKHQ-KUHORTOSSA-N 0.000 description 1
- NPOMKHQWAVPNRY-UHFFFAOYSA-N CC(CC1CCCCC1)=C Chemical compound CC(CC1CCCCC1)=C NPOMKHQWAVPNRY-UHFFFAOYSA-N 0.000 description 1
- ICSNIELWKFNNIV-UHFFFAOYSA-N CC1(CC(O)O)CCOCC1 Chemical compound CC1(CC(O)O)CCOCC1 ICSNIELWKFNNIV-UHFFFAOYSA-N 0.000 description 1
- UAEPNZWRGJTJPN-UHFFFAOYSA-N CC1CCCCC1 Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
- UJQZTMFRMLEYQN-UHFFFAOYSA-N CC1COCCC1 Chemical compound CC1COCCC1 UJQZTMFRMLEYQN-UHFFFAOYSA-N 0.000 description 1
- HNGLTGSDTLFSOQ-ZJRZNQDASA-N CCC[C@@H](C(C(NC1CC1)=O)=O)NC([C@H](C[C@H](C/C(/c(cc1C)cc(C)c1OC(C)C)=N\[O]=C)C1)N1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=O Chemical compound CCC[C@@H](C(C(NC1CC1)=O)=O)NC([C@H](C[C@H](C/C(/c(cc1C)cc(C)c1OC(C)C)=N\[O]=C)C1)N1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=O HNGLTGSDTLFSOQ-ZJRZNQDASA-N 0.000 description 1
- NBKDCIGNMLGUJX-OLKXDRRNSA-N CCC[C@@H](C(C(NC1CC1)=O)O)NC([C@H]([C@H](C/C(/c(cc1C)cc(C)c1OC(C)C)=N\O)CC1)N1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=O Chemical compound CCC[C@@H](C(C(NC1CC1)=O)O)NC([C@H]([C@H](C/C(/c(cc1C)cc(C)c1OC(C)C)=N\O)CC1)N1C([C@H](C(C)(C)C)NC(CC1CCCCC1)=O)=O)=O NBKDCIGNMLGUJX-OLKXDRRNSA-N 0.000 description 1
- ASGYDUBZFVJESG-VIFPVBQESA-N CCC[C@H](C)C(C(CC(C)C)=[ClH])=N Chemical compound CCC[C@H](C)C(C(CC(C)C)=[ClH])=N ASGYDUBZFVJESG-VIFPVBQESA-N 0.000 description 1
- HMRYLZJIPRVVCW-UHFFFAOYSA-N CCOC(C=C1CCOCC1)=O Chemical compound CCOC(C=C1CCOCC1)=O HMRYLZJIPRVVCW-UHFFFAOYSA-N 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N CCc1ccccc1 Chemical compound CCc1ccccc1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- ABXLKZNGMWTCCM-UHFFFAOYSA-N CNC(CC1CCC1)C(C(O)=O)O Chemical compound CNC(CC1CCC1)C(C(O)=O)O ABXLKZNGMWTCCM-UHFFFAOYSA-N 0.000 description 1
- YOIONBBMZSLNLR-YRNVUSSQSA-N COC(C/N=C/c1ccccc1)=O Chemical compound COC(C/N=C/c1ccccc1)=O YOIONBBMZSLNLR-YRNVUSSQSA-N 0.000 description 1
- PCTRUDFMZSFKSY-UHFFFAOYSA-N CS(C)CC1CCCCC1 Chemical compound CS(C)CC1CCCCC1 PCTRUDFMZSFKSY-UHFFFAOYSA-N 0.000 description 1
- PKUGPLMFLMBCEW-SSDOTTSWSA-N C[C@@H](C(C)(C)C=C)C(C)=[ClH] Chemical compound C[C@@H](C(C)(C)C=C)C(C)=[ClH] PKUGPLMFLMBCEW-SSDOTTSWSA-N 0.000 description 1
- CUKRIDTZJKXGKH-UHFFFAOYSA-N Cc1cc(CBr)cc(Cl)c1 Chemical compound Cc1cc(CBr)cc(Cl)c1 CUKRIDTZJKXGKH-UHFFFAOYSA-N 0.000 description 1
- GBAFWKTWLYVMIQ-UHFFFAOYSA-N ISCC(CC1)CCC11OCCO1 Chemical compound ISCC(CC1)CCC11OCCO1 GBAFWKTWLYVMIQ-UHFFFAOYSA-N 0.000 description 1
- RGQGOCQDINEUIZ-UEWDXFNNSA-N N#CC([C@H](CC1CC1)NOC(c1ccccc1)=O)O Chemical compound N#CC([C@H](CC1CC1)NOC(c1ccccc1)=O)O RGQGOCQDINEUIZ-UEWDXFNNSA-N 0.000 description 1
- JMJRYTGVHCAYCT-UHFFFAOYSA-N O=C1CCOCC1 Chemical compound O=C1CCOCC1 JMJRYTGVHCAYCT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or 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
- C07K5/06—Dipeptides
- C07K5/06191—Dipeptides 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
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
-
- 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
-
- 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
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
-
- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71153005P | 2005-08-26 | 2005-08-26 | |
| US60/711,530 | 2005-08-26 | ||
| PCT/US2006/033770 WO2007025307A2 (en) | 2005-08-26 | 2006-08-28 | Inhibitors of serine proteases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009506078A JP2009506078A (ja) | 2009-02-12 |
| JP2009506078A5 JP2009506078A5 (https=) | 2009-10-15 |
| JP5394063B2 true JP5394063B2 (ja) | 2014-01-22 |
Family
ID=37684363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008528258A Expired - Fee Related JP5394063B2 (ja) | 2005-08-26 | 2006-08-28 | セリンプロテアーゼの阻害剤 |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US7985762B2 (https=) |
| EP (3) | EP2366704B1 (https=) |
| JP (1) | JP5394063B2 (https=) |
| KR (1) | KR20080041715A (https=) |
| CN (1) | CN101316852A (https=) |
| AR (1) | AR055395A1 (https=) |
| AT (1) | ATE530554T1 (https=) |
| AU (1) | AU2006282771B2 (https=) |
| BR (1) | BRPI0615223A2 (https=) |
| CA (1) | CA2620621A1 (https=) |
| EA (1) | EA200800670A1 (https=) |
| EC (1) | ECSP088258A (https=) |
| ES (1) | ES2374943T3 (https=) |
| GE (1) | GEP20115280B (https=) |
| IL (1) | IL189668A0 (https=) |
| MX (1) | MX2008002606A (https=) |
| NO (1) | NO20081467L (https=) |
| NZ (1) | NZ566197A (https=) |
| TW (1) | TW200730533A (https=) |
| WO (1) | WO2007025307A2 (https=) |
| ZA (1) | ZA200801793B (https=) |
Families Citing this family (87)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AP1019A (en) * | 1996-10-18 | 2001-10-16 | Vertex Pharma | Inhibitors of serinre proteases, particularly hepatitis C virus NS3 protease. |
| AU2001251165A1 (en) * | 2000-04-03 | 2001-10-15 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| WO2004092161A1 (en) * | 2003-04-11 | 2004-10-28 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| EP1646642A2 (en) * | 2003-07-18 | 2006-04-19 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| UY28500A1 (es) * | 2003-09-05 | 2005-04-29 | Vertex Pharma | Inhibidores de proteasas de serina, en particular proteasa ns3-ns4a del vhc. |
| WO2005028502A1 (en) * | 2003-09-18 | 2005-03-31 | Vertex Pharmaceuticals, Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| WO2005037860A2 (en) * | 2003-10-10 | 2005-04-28 | Vertex Pharmaceuticals Incoporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| CA2543696A1 (en) * | 2003-10-27 | 2005-05-12 | Vertex Pharmaceuticals Incorporated | Combinations for hcv treatment |
| WO2005077969A2 (en) * | 2004-02-04 | 2005-08-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| AU2006276246B2 (en) | 2005-07-25 | 2012-09-27 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis C virus replication |
| US8399615B2 (en) | 2005-08-19 | 2013-03-19 | Vertex Pharmaceuticals Incorporated | Processes and intermediates |
| US7964624B1 (en) * | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| 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 |
| AU2007217355B2 (en) | 2006-02-27 | 2012-06-21 | Vertex Pharmaceuticals Incorporated | Co-crystals comprising VX-950 and pharmaceutical compositions comprising the same |
| WO2007109080A2 (en) | 2006-03-16 | 2007-09-27 | Vertex Pharmaceuticals Incorporated | Deuterated hepatitis c protease inhibitors |
| AU2007249668B2 (en) | 2006-04-11 | 2011-04-07 | Novartis Ag | HCV/HIV inhibitors and their uses |
| US7935670B2 (en) | 2006-07-11 | 2011-05-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| NZ575186A (en) * | 2006-08-28 | 2012-03-30 | Vertex Pharma | Method for identifying protease inhibitors |
| EA200900472A1 (ru) * | 2006-09-22 | 2009-10-30 | Ранбакси Лабораторис Лимитед | Ингибиторы фосфодиэстеразы iv типа |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| 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 |
| 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 |
| HRP20120330T1 (hr) | 2007-02-27 | 2012-05-31 | Vertex Pharmaceuticals Incorporated | Sukristali i farmaceutski pripravci koji ih sadrže |
| WO2008106058A2 (en) * | 2007-02-27 | 2008-09-04 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| FR2914920B1 (fr) * | 2007-04-11 | 2011-09-09 | Clariant Specialty Fine Chem F | Procede de deacetalisation d'alpha-aminoacetals. |
| ES2381410T3 (es) | 2007-05-04 | 2012-05-28 | Vertex Pharmceuticals Incorporated | Terapia de combinación paa el tratamiento de infecciones por VHC |
| JP2010526834A (ja) * | 2007-05-10 | 2010-08-05 | 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ペプチド阻害剤 |
| EP2100881A1 (en) * | 2008-03-13 | 2009-09-16 | Laboratorios Almirall, S.A. | Pyrimidyl- or pyridinylaminobenzoic acid derivatives |
| UY31272A1 (es) * | 2007-08-10 | 2009-01-30 | Almirall Lab | Nuevos derivados de ácido azabifenilaminobenzoico |
| NZ583699A (en) | 2007-08-30 | 2012-04-27 | Vertex Pharma | Co-crystals of vx-950 (telaprevir) other components and pharmaceutical compositions comprising the same |
| CN101868452B (zh) | 2007-10-10 | 2014-08-06 | 诺华股份有限公司 | 螺环吡咯烷类与其对抗hcv和hiv感染的应用 |
| WO2009053828A2 (en) * | 2007-10-22 | 2009-04-30 | Enanta Pharmaceuticals, Inc. | P3 hydroxyamino macrocyclic hepatitis c serine protease inhibitors |
| US8383583B2 (en) | 2007-10-26 | 2013-02-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic, pyridazinone-containing hepatitis C serine protease inhibitors |
| 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 |
| ES2437147T3 (es) | 2008-02-04 | 2014-01-09 | Idenix Pharmaceuticals, Inc. | Inhibidores de serina proteasa macrocíclicos |
| CN102015652A (zh) | 2008-03-20 | 2011-04-13 | 益安药业 | 作为丙型肝炎病毒抑制剂的氟化大环化合物 |
| US8163921B2 (en) | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2300491B1 (en) | 2008-05-29 | 2016-01-06 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8044087B2 (en) | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| KR20110075019A (ko) * | 2008-10-15 | 2011-07-05 | 인터뮨, 인크. | 치료용 항바이러스성 펩티드 |
| US8283310B2 (en) | 2008-12-15 | 2012-10-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2210615A1 (en) * | 2009-01-21 | 2010-07-28 | Almirall, S.A. | Combinations comprising methotrexate and DHODH inhibitors |
| TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
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| CN101316852A (zh) | 2008-12-03 |
| EP2366704A1 (en) | 2011-09-21 |
| AU2006282771B2 (en) | 2012-08-09 |
| ECSP088258A (es) | 2008-06-30 |
| CA2620621A1 (en) | 2007-03-01 |
| WO2007025307A3 (en) | 2007-04-26 |
| AU2006282771A1 (en) | 2007-03-01 |
| WO2007025307A2 (en) | 2007-03-01 |
| BRPI0615223A2 (pt) | 2009-07-14 |
| EP2364984A1 (en) | 2011-09-14 |
| AR055395A1 (es) | 2007-08-22 |
| MX2008002606A (es) | 2008-03-14 |
| EP1917269B1 (en) | 2011-10-26 |
| KR20080041715A (ko) | 2008-05-13 |
| US20110165120A1 (en) | 2011-07-07 |
| US20070179167A1 (en) | 2007-08-02 |
| GEP20115280B (en) | 2011-09-12 |
| EA200800670A1 (ru) | 2009-12-30 |
| ES2374943T3 (es) | 2012-02-23 |
| TW200730533A (en) | 2007-08-16 |
| NZ566197A (en) | 2011-07-29 |
| EP1917269A2 (en) | 2008-05-07 |
| IL189668A0 (en) | 2008-06-05 |
| ZA200801793B (en) | 2008-12-31 |
| JP2009506078A (ja) | 2009-02-12 |
| EP2366704B1 (en) | 2013-10-23 |
| US7985762B2 (en) | 2011-07-26 |
| US8440706B2 (en) | 2013-05-14 |
| NO20081467L (no) | 2008-05-15 |
| ATE530554T1 (de) | 2011-11-15 |
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