JP2008511633A - C型肝炎ウィルスns3セリンプロテアーゼの阻害因子としてのアシルスルホンアミド化合物 - Google Patents
C型肝炎ウィルスns3セリンプロテアーゼの阻害因子としてのアシルスルホンアミド化合物 Download PDFInfo
- Publication number
- JP2008511633A JP2008511633A JP2007530123A JP2007530123A JP2008511633A JP 2008511633 A JP2008511633 A JP 2008511633A JP 2007530123 A JP2007530123 A JP 2007530123A JP 2007530123 A JP2007530123 A JP 2007530123A JP 2008511633 A JP2008511633 A JP 2008511633A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- alkyl
- group
- heterocyclyl
- cycloalkyl
- 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.)
- Pending
Links
- 0 *C(C(N(*)S*)=O)NC(C(*(*)I(C1)N)N1C(C(*)NC(*)=O)=O)=O Chemical compound *C(C(N(*)S*)=O)NC(C(*(*)I(C1)N)N1C(C(*)NC(*)=O)=O)=O 0.000 description 18
- UBQKCCHYAOITMY-UHFFFAOYSA-N O=C1NC=CC=C1 Chemical compound O=C1NC=CC=C1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 2
- TXCSXQIXCYFAGS-SECBINFHSA-N CC(C)(C)[C@@H](CN(C(CC(C)(C)C1)=O)C1=O)NN Chemical compound CC(C)(C)[C@@H](CN(C(CC(C)(C)C1)=O)C1=O)NN TXCSXQIXCYFAGS-SECBINFHSA-N 0.000 description 1
- STGZHADBOYHFOQ-SECBINFHSA-N CC(C)(C)[C@@H](CN(CCC1)C1=O)NNC Chemical compound CC(C)(C)[C@@H](CN(CCC1)C1=O)NNC STGZHADBOYHFOQ-SECBINFHSA-N 0.000 description 1
- OEOFZFABMYEBLO-SNVBAGLBSA-N CC(C)(C)[C@@H](CN(CCCC1)C1=O)NNC Chemical compound CC(C)(C)[C@@H](CN(CCCC1)C1=O)NNC OEOFZFABMYEBLO-SNVBAGLBSA-N 0.000 description 1
- AOBPSMAIMHXPMO-SECBINFHSA-N CC(C)(C)[C@@H](CN(CCCN1)C1=O)NN=C Chemical compound CC(C)(C)[C@@H](CN(CCCN1)C1=O)NN=C AOBPSMAIMHXPMO-SECBINFHSA-N 0.000 description 1
- VSLKVZOTEBFANB-MRVPVSSYSA-N CC(C)(C)[C@@H](CN(CCN1)C1=O)NC Chemical compound CC(C)(C)[C@@H](CN(CCN1)C1=O)NC VSLKVZOTEBFANB-MRVPVSSYSA-N 0.000 description 1
- CKGAKFYHKSMMCK-NOCYLUDSSA-N CC(C)C(CC1)[C@@H](C(N[C@](C2)([C@@H]2C=C)C(NS(C2CC2)(=O)=O)=O)=O)N1C(C(C(C)(C)C)NC(NC(CN(C)S(C)(=O)=O)C(C)(C)C)=O)=O Chemical compound CC(C)C(CC1)[C@@H](C(N[C@](C2)([C@@H]2C=C)C(NS(C2CC2)(=O)=O)=O)=O)N1C(C(C(C)(C)C)NC(NC(CN(C)S(C)(=O)=O)C(C)(C)C)=O)=O CKGAKFYHKSMMCK-NOCYLUDSSA-N 0.000 description 1
- XMXXNGJLGGOBSS-GHMZBOCLSA-N CC(C)[C@@H](CC1)[C@@H](C(C)=O)N1C(C)=O Chemical compound CC(C)[C@@H](CC1)[C@@H](C(C)=O)N1C(C)=O XMXXNGJLGGOBSS-GHMZBOCLSA-N 0.000 description 1
- SXDWBLMANYMYSB-CBMCFHRWSA-N CC([C@H]([C@@H](C(Br)Br)C(C1)C=C)N1C(C)=O)=O Chemical compound CC([C@H]([C@@H](C(Br)Br)C(C1)C=C)N1C(C)=O)=O SXDWBLMANYMYSB-CBMCFHRWSA-N 0.000 description 1
- QPKBHUZATPKWNT-ZIAGYGMSSA-N CC([C@H]([C@@H](CC1CCCC1)CC1)N1C(C)=O)=O Chemical compound CC([C@H]([C@@H](CC1CCCC1)CC1)N1C(C)=O)=O QPKBHUZATPKWNT-ZIAGYGMSSA-N 0.000 description 1
- HPRITURHSXTUDO-JGVFFNPUSA-N CC([C@H]([C@H](CC1)C(Cl)Cl)N1C(C)=O)=O Chemical compound CC([C@H]([C@H](CC1)C(Cl)Cl)N1C(C)=O)=O HPRITURHSXTUDO-JGVFFNPUSA-N 0.000 description 1
- ZOLOOMHRCHIDJK-BIIVOSGPSA-N CC([C@H]([C@H]([C@@H]1C2)C1(F)F)N2C(C)=O)=O Chemical compound CC([C@H]([C@H]([C@@H]1C2)C1(F)F)N2C(C)=O)=O ZOLOOMHRCHIDJK-BIIVOSGPSA-N 0.000 description 1
- HKFVAHBQOAVFOQ-UMBWVZCYSA-N CCOc(cc1)cc2c1c(O[C@H](C[C@@H]1C(/C=C/C(C3)([C@H]3C=C)C(NS(C3CC3)(=O)=O)=O)=O)CN1C([C@@H](Cc1ccccc1)N(C)C)=O)cc(-c1ccccc1)n2 Chemical compound CCOc(cc1)cc2c1c(O[C@H](C[C@@H]1C(/C=C/C(C3)([C@H]3C=C)C(NS(C3CC3)(=O)=O)=O)=O)CN1C([C@@H](Cc1ccccc1)N(C)C)=O)cc(-c1ccccc1)n2 HKFVAHBQOAVFOQ-UMBWVZCYSA-N 0.000 description 1
- YDVYHEXBRNKDJG-MUWHJKNJSA-N C[C@H](C[C@H]1C(C)=O)CN1C(C)=O Chemical compound C[C@H](C[C@H]1C(C)=O)CN1C(C)=O YDVYHEXBRNKDJG-MUWHJKNJSA-N 0.000 description 1
Classifications
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0217—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -C(=O)-C-N-C(=O)-N-C-C(=O)-
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Virology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60523404P | 2004-08-27 | 2004-08-27 | |
| PCT/US2005/030249 WO2006026352A1 (en) | 2004-08-27 | 2005-08-25 | Acylsulfonamide compounds as inhibitors of hepatitis c virus ns3 serine protease |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008511633A true JP2008511633A (ja) | 2008-04-17 |
| JP2008511633A5 JP2008511633A5 (enExample) | 2008-09-25 |
Family
ID=35561671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007530123A Pending JP2008511633A (ja) | 2004-08-27 | 2005-08-25 | C型肝炎ウィルスns3セリンプロテアーゼの阻害因子としてのアシルスルホンアミド化合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7550559B2 (enExample) |
| EP (1) | EP1797111B1 (enExample) |
| JP (1) | JP2008511633A (enExample) |
| CN (1) | CN101068828A (enExample) |
| AT (1) | ATE513844T1 (enExample) |
| CA (1) | CA2577812A1 (enExample) |
| MX (1) | MX2007002371A (enExample) |
| WO (1) | WO2006026352A1 (enExample) |
Families Citing this family (116)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ335276A (en) | 1996-10-18 | 2000-09-29 | Vertex Pharma | Inhibitors of serine proteases, particularly hepatitis C virus (HCV) NS3 (Non Structural Protein 3) 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 |
| US7176208B2 (en) * | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| MY148123A (en) | 2003-09-05 | 2013-02-28 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| US7491794B2 (en) * | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| US7323447B2 (en) | 2005-02-08 | 2008-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20070021351A1 (en) * | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| WO2006130552A2 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis c virus |
| JP2008545748A (ja) * | 2005-06-02 | 2008-12-18 | シェーリング コーポレイション | C型肝炎ウイルスに関連する障害を処置するために有用な徐放処方物 |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| US20060275366A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation |
| US8119602B2 (en) | 2005-06-02 | 2012-02-21 | Schering Corporation | Administration of HCV protease inhibitors in combination with food to improve bioavailability |
| US7772178B2 (en) * | 2005-06-02 | 2010-08-10 | Schering Corporation | Pharmaceutical formulations and methods of treatment using the same |
| US20060276407A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| 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 |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2305696A3 (en) * | 2005-07-25 | 2011-10-12 | Intermune, Inc. | Macrocyclic inhibitors of Hepatitis C virus replication |
| ES2401661T3 (es) * | 2005-08-02 | 2013-04-23 | Vertex Pharmaceuticals Incorporated | Inhibidores de serina proteasas |
| 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 |
| US7964624B1 (en) | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| EA200801050A1 (ru) | 2005-10-11 | 2008-12-30 | Интермьюн, Инк. | Соединения и способы ингибирования репликации вирусного гепатита с |
| 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 |
| EP1991229A2 (en) | 2006-02-27 | 2008-11-19 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| JP2009531315A (ja) | 2006-03-16 | 2009-09-03 | バーテックス ファーマシューティカルズ インコーポレイテッド | 重水素化c型肝炎プロテアーゼインヒビター |
| JP2009536158A (ja) * | 2006-04-11 | 2009-10-08 | ノバルティス アクチエンゲゼルシャフト | Hcv阻害剤 |
| US20080045530A1 (en) * | 2006-04-11 | 2008-02-21 | Trixi Brandl | Organic Compounds and Their Uses |
| EP2518079A3 (en) | 2006-04-11 | 2012-12-12 | Novartis AG | HCV/HIV inhibitors and their uses |
| RU2008152171A (ru) * | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
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| 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 |
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| KR101396696B1 (ko) * | 2007-10-10 | 2014-05-16 | 노파르티스 아게 | 스피로피롤리딘, 및 hcv 및 hiv 감염에 대한 그의 용도 |
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| RU2490272C2 (ru) * | 2008-02-04 | 2013-08-20 | Айденикс Фармасьютикалз, Инк. | Макроциклические ингибиторы серинпротеазы |
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- 2005-08-25 MX MX2007002371A patent/MX2007002371A/es active IP Right Grant
- 2005-08-25 AT AT05790914T patent/ATE513844T1/de not_active IP Right Cessation
- 2005-08-25 CA CA002577812A patent/CA2577812A1/en not_active Abandoned
- 2005-08-25 CN CNA2005800362904A patent/CN101068828A/zh active Pending
- 2005-08-25 US US11/211,771 patent/US7550559B2/en not_active Expired - Lifetime
- 2005-08-25 JP JP2007530123A patent/JP2008511633A/ja active Pending
- 2005-08-25 EP EP05790914A patent/EP1797111B1/en not_active Expired - Lifetime
- 2005-08-25 WO PCT/US2005/030249 patent/WO2006026352A1/en not_active Ceased
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| WO2001074768A2 (en) * | 2000-04-03 | 2001-10-11 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| WO2002060926A2 (en) * | 2000-11-20 | 2002-08-08 | Bristol-Myers Squibb Company | Hepatitis c tripeptide inhibitors |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2006026352A1 (en) | 2006-03-09 |
| EP1797111A1 (en) | 2007-06-20 |
| CA2577812A1 (en) | 2006-03-09 |
| ATE513844T1 (de) | 2011-07-15 |
| US20060046956A1 (en) | 2006-03-02 |
| US7550559B2 (en) | 2009-06-23 |
| EP1797111B1 (en) | 2011-06-22 |
| MX2007002371A (es) | 2007-04-23 |
| CN101068828A (zh) | 2007-11-07 |
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