CN1902216A - 丙肝病毒ns3蛋白酶的去肽化抑制剂 - Google Patents
丙肝病毒ns3蛋白酶的去肽化抑制剂 Download PDFInfo
- Publication number
- CN1902216A CN1902216A CNA2004800399478A CN200480039947A CN1902216A CN 1902216 A CN1902216 A CN 1902216A CN A2004800399478 A CNA2004800399478 A CN A2004800399478A CN 200480039947 A CN200480039947 A CN 200480039947A CN 1902216 A CN1902216 A CN 1902216A
- Authority
- CN
- China
- Prior art keywords
- compound
- alkyl
- pharmaceutical composition
- cycloalkyl
- aryl
- 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*c1ccc2c(O)cc(-c3c[s]c(NC(C)C)n3)nc2c1 Chemical compound C*c1ccc2c(O)cc(-c3c[s]c(NC(C)C)n3)nc2c1 0.000 description 2
- BYDLPLSQNDYWMI-UHFFFAOYSA-N CC(C)Nc1nc(-c2nc3cc(OC)ccc3c(O)c2)c[s]1 Chemical compound CC(C)Nc1nc(-c2nc3cc(OC)ccc3c(O)c2)c[s]1 BYDLPLSQNDYWMI-UHFFFAOYSA-N 0.000 description 2
- UIAHQNZXTRIWNO-UHFFFAOYSA-N CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C(C1)C=CCCCCCC(C(N2C3CCC2)=O)NC(NC(CN(CCCN2C)S2(=O)=O)C2CCCCC2)=O)[N]1(C)C3=O)O Chemical compound CC(C)NC1=NC(c2nc3cc(OC)ccc3c(O)c2)=CS1[O]=C(C(C(C1)C=CCCCCCC(C(N2C3CCC2)=O)NC(NC(CN(CCCN2C)S2(=O)=O)C2CCCCC2)=O)[N]1(C)C3=O)O UIAHQNZXTRIWNO-UHFFFAOYSA-N 0.000 description 1
- YHZPORNFCJBZFP-MVGYMQKFSA-N CC(C)[C@@H](C(C1CC1)=O)NC(N[C@@H](C(C)(C)C)C(N(CCC1)[C@@H]1C([N](C)(CC1C=C)[C@H]1C(O)=O)=O)=O)=O Chemical compound CC(C)[C@@H](C(C1CC1)=O)NC(N[C@@H](C(C)(C)C)C(N(CCC1)[C@@H]1C([N](C)(CC1C=C)[C@H]1C(O)=O)=O)=O)=O YHZPORNFCJBZFP-MVGYMQKFSA-N 0.000 description 1
- OXPFXYUMLFSRLT-IRHUBVEQSA-N CN(CCCN1CC(C2CCC2)NC(N[C@@H](CCCCC/C=C\C(CN(C2)C([C@H]3N4CCC3)=O)[C@H]2C(O)=O)C4=O)=O)S1(=O)=O Chemical compound CN(CCCN1CC(C2CCC2)NC(N[C@@H](CCCCC/C=C\C(CN(C2)C([C@H]3N4CCC3)=O)[C@H]2C(O)=O)C4=O)=O)S1(=O)=O OXPFXYUMLFSRLT-IRHUBVEQSA-N 0.000 description 1
- CAVIQRVBJRNQQK-CSCRXJAFSA-N C[C@@H]([C@H](C(O)=O)NC([C@H](CCC1)N1C1=O)=O)/C=C\CCCCC[C@@H]1NC(N[C@@H](C1CCCCC1)C(c(cc1)ccc1N(C)C)=O)=O Chemical compound C[C@@H]([C@H](C(O)=O)NC([C@H](CCC1)N1C1=O)=O)/C=C\CCCCC[C@@H]1NC(N[C@@H](C1CCCCC1)C(c(cc1)ccc1N(C)C)=O)=O CAVIQRVBJRNQQK-CSCRXJAFSA-N 0.000 description 1
- OUXSTTGYHRVQFF-FWEHEUNISA-N OC([C@H](CC1CCC1)NC([C@H](CCC1)N1C([C@H](C1CCCCC1)NC(N[C@@H](C1CCCCC1)C(C1CC1)=O)=O)=O)=O)=O Chemical compound OC([C@H](CC1CCC1)NC([C@H](CCC1)N1C([C@H](C1CCCCC1)NC(N[C@@H](C1CCCCC1)C(C1CC1)=O)=O)=O)=O)=O OUXSTTGYHRVQFF-FWEHEUNISA-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)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (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 | |
| US60/523,715 | 2003-11-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1902216A true CN1902216A (zh) | 2007-01-24 |
Family
ID=34632818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2004800399478A Pending CN1902216A (zh) | 2003-11-20 | 2004-11-19 | 丙肝病毒ns3蛋白酶的去肽化抑制剂 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US7253160B2 (https=) |
| EP (1) | EP1689770A1 (https=) |
| JP (1) | JP2007532479A (https=) |
| CN (1) | CN1902216A (https=) |
| CA (1) | CA2546290A1 (https=) |
| MX (1) | MXPA06005683A (https=) |
| WO (1) | WO2005051980A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101951769A (zh) * | 2007-12-21 | 2011-01-19 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
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| 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 |
| NZ563361A (en) | 2005-06-02 | 2011-02-25 | Schering Corp | HCV protease inhibitors in combination with food |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| NZ563365A (en) * | 2005-06-02 | 2011-02-25 | Schering Corp | Combination of HCV protease inhibitors with a surfactant |
| US20060276404A1 (en) * | 2005-06-02 | 2006-12-07 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| AU2006276246B2 (en) * | 2005-07-25 | 2012-09-27 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis C virus replication |
| JP5015154B2 (ja) | 2005-08-12 | 2012-08-29 | 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 | ウイルスポリメラーゼインヒビター |
| 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 |
| EP2392589A3 (en) | 2005-11-11 | 2012-06-20 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
| 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 |
| US7935670B2 (en) | 2006-07-11 | 2011-05-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN101674844A (zh) * | 2006-08-04 | 2010-03-17 | 英安塔制药有限公司 | 四唑基大环类c型肝炎丝氨酸蛋白酶抑制剂 |
| US7662779B2 (en) * | 2006-08-11 | 2010-02-16 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis C serine protease inhibitors |
| RU2009109355A (ru) | 2006-08-17 | 2010-09-27 | БЕРИНГЕР ИНГЕЛЬХАЙМ ИНТЕРНАЦИОНАЛЬ ГмбХ (DE) | Ингибиторы вырусной полимеразы |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
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| US20100120716A1 (en) * | 2006-12-06 | 2010-05-13 | Phenomix Corporation | Macrocyclic hepatitis c serine protease inhibitors and uses therefor |
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| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| EP1012180B1 (en) | 1997-08-11 | 2004-12-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor peptide analogues |
| AR022061A1 (es) * | 1998-08-10 | 2002-09-04 | Boehringer Ingelheim Ca Ltd | Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos. |
| US6323180B1 (en) * | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| 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 |
| AU2001251165A1 (en) | 2000-04-03 | 2001-10-15 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| ES2317900T3 (es) | 2000-04-05 | 2009-05-01 | Schering Corporation | Inhibidores de serina proteasa ns3 macrociclicos del virus de la hepatitis c que comprenden fragmentos n-ciclicas p2. |
| AU2001253621A1 (en) | 2000-04-19 | 2001-11-07 | Schering Corporation | Macrocyclic NS3-serine protease inhibitors of hepatitis C virus comprising alkyl and aryl alanine P2 moieties |
| 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 |
| WO2002008251A2 (en) | 2000-07-21 | 2002-01-31 | Corvas International, Inc. | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
| AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
| CN1498224A (zh) | 2000-07-21 | 2004-05-19 | ���鹫˾ | 用作丙型肝炎病毒ns3-丝氨酸蛋白酶抑制剂的新型肽 |
| AU3659102A (en) | 2000-12-12 | 2002-06-24 | Schering Corp | Diaryl peptides as ns3-serine protease inhibitors of hepatits c virus |
-
2004
- 2004-11-19 JP JP2006541606A patent/JP2007532479A/ja active Pending
- 2004-11-19 US US10/993,394 patent/US7253160B2/en not_active Expired - Fee Related
- 2004-11-19 WO PCT/US2004/039131 patent/WO2005051980A1/en not_active Ceased
- 2004-11-19 CA CA002546290A patent/CA2546290A1/en not_active Abandoned
- 2004-11-19 EP EP04811791A patent/EP1689770A1/en not_active Withdrawn
- 2004-11-19 MX MXPA06005683A patent/MXPA06005683A/es active IP Right Grant
- 2004-11-19 CN CNA2004800399478A patent/CN1902216A/zh active Pending
-
2007
- 2007-06-27 US US11/769,455 patent/US7442695B2/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101951769A (zh) * | 2007-12-21 | 2011-01-19 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| CN101951769B (zh) * | 2007-12-21 | 2014-12-31 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| US9676785B2 (en) | 2007-12-21 | 2017-06-13 | Celgene Car Llc | HCV protease inhibitors and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| US20070258947A1 (en) | 2007-11-08 |
| JP2007532479A (ja) | 2007-11-15 |
| US20050164921A1 (en) | 2005-07-28 |
| MXPA06005683A (es) | 2006-12-14 |
| US7253160B2 (en) | 2007-08-07 |
| US7442695B2 (en) | 2008-10-28 |
| WO2005051980A8 (en) | 2006-09-08 |
| EP1689770A1 (en) | 2006-08-16 |
| WO2005051980A1 (en) | 2005-06-09 |
| CA2546290A1 (en) | 2005-06-09 |
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