JP2007532479A - C型肝炎ウイルスns3プロテアーゼの脱ペプチド化インヒビター - Google Patents
C型肝炎ウイルスns3プロテアーゼの脱ペプチド化インヒビター Download PDFInfo
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- JP2007532479A JP2007532479A JP2006541606A JP2006541606A JP2007532479A JP 2007532479 A JP2007532479 A JP 2007532479A JP 2006541606 A JP2006541606 A JP 2006541606A JP 2006541606 A JP2006541606 A JP 2006541606A JP 2007532479 A JP2007532479 A JP 2007532479A
- Authority
- JP
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- Prior art keywords
- pharmaceutical composition
- alkyl
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- compound according
- 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 CC1*CCC1 Chemical compound CC1*CCC1 0.000 description 23
- BYDLPLSQNDYWMI-UHFFFAOYSA-N CC(C)Nc1nc(-c2nc(cc(cc3)OC)c3c(O)c2)c[s]1 Chemical compound CC(C)Nc1nc(-c2nc(cc(cc3)OC)c3c(O)c2)c[s]1 BYDLPLSQNDYWMI-UHFFFAOYSA-N 0.000 description 3
- GHAZCVNUKKZTLG-UHFFFAOYSA-N CCN(C(CC1)=O)C1=O Chemical compound CCN(C(CC1)=O)C1=O GHAZCVNUKKZTLG-UHFFFAOYSA-N 0.000 description 2
- TXOGMHURCRTFPH-OBMXYNEQSA-N CC(C)(C)S(CC1(CCCCC1)NC(N[C@@H](CCCCCCCC(C1)[C@]1(C(O)=O)NC([C@H]1N2CCC1)=O)C2=O)=O)(=O)=O Chemical compound CC(C)(C)S(CC1(CCCCC1)NC(N[C@@H](CCCCCCCC(C1)[C@]1(C(O)=O)NC([C@H]1N2CCC1)=O)C2=O)=O)(=O)=O TXOGMHURCRTFPH-OBMXYNEQSA-N 0.000 description 1
- PDBIEZSRDYOPKV-UHFFFAOYSA-N CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1C=CCCCCCC(C(N(CCC1)C1(C1)C1O)=O)NC(NC(CN(C(c1ccccc11)=O)C1=O)C1CCC1)=O)N)O Chemical compound CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1C=CCCCCCC(C(N(CCC1)C1(C1)C1O)=O)NC(NC(CN(C(c1ccccc11)=O)C1=O)C1CCC1)=O)N)O PDBIEZSRDYOPKV-UHFFFAOYSA-N 0.000 description 1
- MLZTYLLZMCIKFQ-UHFFFAOYSA-N CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1C=CCCCCCC(C(N1C2CCC1)=O)NC(NC(CN(C(c1ccccc11)=O)C1=O)C1CCC1)=O)NC2=O)O Chemical compound CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1C=CCCCCCC(C(N1C2CCC1)=O)NC(NC(CN(C(c1ccccc11)=O)C1=O)C1CCC1)=O)NC2=O)O MLZTYLLZMCIKFQ-UHFFFAOYSA-N 0.000 description 1
- JNIDRAWAVODKNI-UHFFFAOYSA-N CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1CCCCCCCC(C(N1C2CCC1)=O)NC(NC(CN(CCC1)C1=O)C(C)(C)C)=O)NC2O)O Chemical compound CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C1)(C1CCCCCCCC(C(N1C2CCC1)=O)NC(NC(CN(CCC1)C1=O)C(C)(C)C)=O)NC2O)O JNIDRAWAVODKNI-UHFFFAOYSA-N 0.000 description 1
- NQRRDWDXLFTCKB-UHFFFAOYSA-N CC(CC(F)F)=C Chemical compound CC(CC(F)F)=C NQRRDWDXLFTCKB-UHFFFAOYSA-N 0.000 description 1
- LDRPULCXZDDSGE-UHFFFAOYSA-N CCCC(F)(F)F Chemical compound CCCC(F)(F)F LDRPULCXZDDSGE-UHFFFAOYSA-N 0.000 description 1
- DLVLVXHUDHSXAY-UHFFFAOYSA-N CCCCSCC1(CCCCC1)C(OC)=O Chemical compound CCCCSCC1(CCCCC1)C(OC)=O DLVLVXHUDHSXAY-UHFFFAOYSA-N 0.000 description 1
- WGKZVNMNKCVSLU-SUNYJGFJSA-N CC[C@@](CCCCCCC[C@@H](C(N1[C@H]2CCC1)=O)N)(C(O)=O)NC2=O Chemical compound CC[C@@](CCCCCCC[C@@H](C(N1[C@H]2CCC1)=O)N)(C(O)=O)NC2=O WGKZVNMNKCVSLU-SUNYJGFJSA-N 0.000 description 1
- HWYPASUNLYOJOJ-UHFFFAOYSA-N CN(CC(C1CCCCC1)N)S(c1ccc[s]1)(=O)=O Chemical compound CN(CC(C1CCCCC1)N)S(c1ccc[s]1)(=O)=O HWYPASUNLYOJOJ-UHFFFAOYSA-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
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
-
- 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
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0205—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Gastroenterology & Hepatology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52371503P | 2003-11-20 | 2003-11-20 | |
| PCT/US2004/039131 WO2005051980A1 (en) | 2003-11-20 | 2004-11-19 | Depeptidized inhibitors of hepatitis c virus ns3 protease |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007532479A true JP2007532479A (ja) | 2007-11-15 |
| JP2007532479A5 JP2007532479A5 (enExample) | 2007-12-27 |
Family
ID=34632818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006541606A Pending JP2007532479A (ja) | 2003-11-20 | 2004-11-19 | C型肝炎ウイルスns3プロテアーゼの脱ペプチド化インヒビター |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US7253160B2 (enExample) |
| EP (1) | EP1689770A1 (enExample) |
| JP (1) | JP2007532479A (enExample) |
| CN (1) | CN1902216A (enExample) |
| CA (1) | CA2546290A1 (enExample) |
| MX (1) | MXPA06005683A (enExample) |
| WO (1) | WO2005051980A1 (enExample) |
Families Citing this family (95)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1133649C (zh) | 1996-10-18 | 2004-01-07 | 沃泰克斯药物股份有限公司 | 丝氨酸蛋白酶、特别是丙型肝炎病毒ns3蛋白酶的抑制剂 |
| 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 |
| 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 |
| WO2006130666A2 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Medicaments and methods combining a hcv protease inhibitor and an akr competitor |
| ES2572980T3 (es) * | 2005-06-02 | 2016-06-03 | Merck Sharp & Dohme Corp. | Combinación de inhibidores de la proteasa del VHC con un tensioactivo |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| US8119602B2 (en) | 2005-06-02 | 2012-02-21 | Schering Corporation | Administration of HCV protease inhibitors in combination with food to improve bioavailability |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GEP20105124B (en) | 2005-07-25 | 2010-11-25 | Array Biopharma Inc | Novel macrocyclic inhibitors of hepatitis c virus replication |
| CA2618682C (en) | 2005-08-12 | 2011-06-21 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| 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 |
| 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 |
| US7705138B2 (en) | 2005-11-11 | 2010-04-27 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
| KR20140098867A (ko) | 2005-11-11 | 2014-08-08 | 버텍스 파마슈티칼스 인코포레이티드 | C형 간염 바이러스 변이체 |
| US7816348B2 (en) | 2006-02-03 | 2010-10-19 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US9526769B2 (en) * | 2006-06-06 | 2016-12-27 | Enanta Pharmaceuticals, Inc. | Macrocylic oximyl hepatitis C protease inhibitors |
| AR061629A1 (es) * | 2006-06-26 | 2008-09-10 | Enanta Pharm Inc | Quinoxalinil macrociclicos inhibidores de serina proteasa del virus de la hepatitis c. proceso de obtencion y composiciones farmaceuticas |
| WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| CA2656816A1 (en) * | 2006-08-04 | 2008-02-14 | Enanta Pharmaceuticals, Inc. | Tetrazolyl macrocyclic hepatitis c serine protease inhibitors |
| US7662779B2 (en) * | 2006-08-11 | 2010-02-16 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis C serine protease inhibitors |
| CN101506167A (zh) | 2006-08-17 | 2009-08-12 | 贝林格尔.英格海姆国际有限公司 | 病毒聚合酶抑制剂 |
| 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 |
| US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8003604B2 (en) * | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
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| US20100120716A1 (en) * | 2006-12-06 | 2010-05-13 | Phenomix Corporation | Macrocyclic hepatitis c serine protease inhibitors and uses therefor |
| CA2673111A1 (en) | 2006-12-07 | 2008-06-19 | Schering Corporation | Ph sensitive matrix formulation |
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| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000009558A1 (en) * | 1998-08-10 | 2000-02-24 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor peptides |
| WO2000009543A2 (en) * | 1998-08-10 | 2000-02-24 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| WO2000059929A1 (en) * | 1999-04-06 | 2000-10-12 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
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| HU216017B (hu) | 1987-11-18 | 1999-04-28 | Chiron Corp. | Eljárás HCV-1 polipeptidek, HCV-1 polinukleotidok, rekombináns vektorok és gazdasejtek, valamint immunesszé kit, hepatitis C vírusfertőzés elleni vakcinák, a fertőzés kimutatására szolgáló diagnosztikumok előállítására, és immunvizsgálati és vírustenyészt |
| ATE132182T1 (de) | 1989-02-01 | 1996-01-15 | Asahi Glass Co Ltd | Azeotrope oder azeotropähnliche zusammensetzung auf der basis von chlorfluorkohlenwasserstoffen |
| DK0527788T3 (da) | 1990-04-04 | 2004-09-06 | Chiron Corp | Hepatitis C virus protease |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| CN1133649C (zh) | 1996-10-18 | 2004-01-07 | 沃泰克斯药物股份有限公司 | 丝氨酸蛋白酶、特别是丙型肝炎病毒ns3蛋白酶的抑制剂 |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| US6143715A (en) | 1997-08-11 | 2000-11-07 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis C inhibitor peptide analogues |
| US6608027B1 (en) | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
| ATE297946T1 (de) | 2000-04-03 | 2005-07-15 | Vertex Pharma | Inhibitoren von serin proteasen, speziell der hepatitis-c-virus ns3-protease |
| HK1047947A1 (zh) | 2000-04-05 | 2003-03-14 | Schering Corporation | 包含n-环状p2部分的丙型肝炎病毒的大环ns3-丝氨酸蛋白酶抑制剂 |
| PE20011288A1 (es) | 2000-04-19 | 2001-12-12 | Schering Corp | Compuestos macrociclicos como inhibidores de la serina proteasa ns3/ns4 del virus de la hepatitis c (vhc) |
| EP1301527A2 (en) | 2000-07-21 | 2003-04-16 | Corvas International, Inc. | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
| AR034127A1 (es) | 2000-07-21 | 2004-02-04 | Schering Corp | Imidazolidinonas como inhibidores de ns3-serina proteasa del virus de hepatitis c, composicion farmaceutica, un metodo para su preparacion, y el uso de las mismas para la manufactura de un medicamento |
| AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
| SI1385870T1 (sl) | 2000-07-21 | 2010-08-31 | Schering Corp | Peptidi kot NS3-serin proteazni inhibitorji virusa hepatitisa C |
| IL155842A0 (en) | 2000-12-12 | 2003-12-23 | Schering Corp | Diaryl peptides as ns3-serine protease inhibitors of hepatitis c virus |
-
2004
- 2004-11-19 EP EP04811791A patent/EP1689770A1/en not_active Withdrawn
- 2004-11-19 JP JP2006541606A patent/JP2007532479A/ja active Pending
- 2004-11-19 WO PCT/US2004/039131 patent/WO2005051980A1/en not_active Ceased
- 2004-11-19 CN CNA2004800399478A patent/CN1902216A/zh active Pending
- 2004-11-19 US US10/993,394 patent/US7253160B2/en not_active Expired - Fee Related
- 2004-11-19 MX MXPA06005683A patent/MXPA06005683A/es active IP Right Grant
- 2004-11-19 CA CA002546290A patent/CA2546290A1/en not_active Abandoned
-
2007
- 2007-06-27 US US11/769,455 patent/US7442695B2/en not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000009558A1 (en) * | 1998-08-10 | 2000-02-24 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor peptides |
| WO2000009543A2 (en) * | 1998-08-10 | 2000-02-24 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| JP2002522557A (ja) * | 1998-08-10 | 2002-07-23 | ベーリンガー インゲルハイム (カナダ) リミテッド | C型肝炎インヒビターペプチド |
| JP2002522554A (ja) * | 1998-08-10 | 2002-07-23 | ベーリンガー インゲルハイム (カナダ) リミテッド | C型肝炎インヒビタートリペプチド |
| WO2000059929A1 (en) * | 1999-04-06 | 2000-10-12 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
| JP2002542160A (ja) * | 1999-04-06 | 2002-12-10 | ベーリンガー インゲルハイム (カナダ) リミテッド | C型肝炎に対して活性な大環状ぺプチド |
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA06005683A (es) | 2006-12-14 |
| CA2546290A1 (en) | 2005-06-09 |
| CN1902216A (zh) | 2007-01-24 |
| WO2005051980A8 (en) | 2006-09-08 |
| WO2005051980A1 (en) | 2005-06-09 |
| EP1689770A1 (en) | 2006-08-16 |
| US7442695B2 (en) | 2008-10-28 |
| US20070258947A1 (en) | 2007-11-08 |
| US20050164921A1 (en) | 2005-07-28 |
| US7253160B2 (en) | 2007-08-07 |
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