JP2004515464A - C型肝炎ウイルスのns3−セリンプロテアーゼ阻害剤としての新規イミダゾリジノン - Google Patents
C型肝炎ウイルスのns3−セリンプロテアーゼ阻害剤としての新規イミダゾリジノン Download PDFInfo
- Publication number
- JP2004515464A JP2004515464A JP2002514104A JP2002514104A JP2004515464A JP 2004515464 A JP2004515464 A JP 2004515464A JP 2002514104 A JP2002514104 A JP 2002514104A JP 2002514104 A JP2002514104 A JP 2002514104A JP 2004515464 A JP2004515464 A JP 2004515464A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- conhch
- compound
- group
- 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
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- 0 CCC(C(NC(*)*)=O)N(*C(*)*(*)*)C(**)=O Chemical compound CCC(C(NC(*)*)=O)N(*C(*)*(*)*)C(**)=O 0.000 description 8
- QTUNVERJNPLQGR-UHFFFAOYSA-N CC(C(C)=O)N(C)C Chemical compound CC(C(C)=O)N(C)C QTUNVERJNPLQGR-UHFFFAOYSA-N 0.000 description 1
- RPIFNVNQWSPEMY-UHFFFAOYSA-N CCCC(C(C(O)=O)O)NC(OC(C)(C)C)=O Chemical compound CCCC(C(C(O)=O)O)NC(OC(C)(C)C)=O RPIFNVNQWSPEMY-UHFFFAOYSA-N 0.000 description 1
- FARCWYMPKOYHFC-UHFFFAOYSA-N CCCC(C(C)C)(F)F Chemical compound CCCC(C(C)C)(F)F FARCWYMPKOYHFC-UHFFFAOYSA-N 0.000 description 1
- UOIWOHLIGKIYFE-UHFFFAOYSA-N CCCCCNC Chemical compound CCCCCNC UOIWOHLIGKIYFE-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/02—Linear peptides containing at least one abnormal peptide link
-
- 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
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
- C07D233/38—One oxygen atom with acyl radicals or hetero atoms directly attached to ring nitrogen atoms
-
- 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
- C07K5/0202—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-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
-
- 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)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Crystallography & Structural Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22011000P | 2000-07-21 | 2000-07-21 | |
| PCT/US2001/022828 WO2002008198A2 (en) | 2000-07-21 | 2001-07-19 | Novel imidazolidinones as ns3-serine protease inhibitors of hepatitis c virus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004515464A true JP2004515464A (ja) | 2004-05-27 |
| JP2004515464A5 JP2004515464A5 (https=) | 2008-04-10 |
Family
ID=22822106
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002514104A Pending JP2004515464A (ja) | 2000-07-21 | 2001-07-19 | C型肝炎ウイルスのns3−セリンプロテアーゼ阻害剤としての新規イミダゾリジノン |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6838475B2 (https=) |
| EP (1) | EP1301486B1 (https=) |
| JP (1) | JP2004515464A (https=) |
| AR (1) | AR034127A1 (https=) |
| AT (1) | ATE435211T1 (https=) |
| AU (1) | AU2001282922A1 (https=) |
| CA (1) | CA2410766A1 (https=) |
| DE (1) | DE60139127D1 (https=) |
| ES (1) | ES2327819T3 (https=) |
| WO (1) | WO2002008198A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008518919A (ja) * | 2004-10-29 | 2008-06-05 | シェーリング コーポレイション | 抗ウイルス物質としての置換5−カルボキシアミドピラゾールおよび置換[1,2,4]トリアゾール |
| KR101517640B1 (ko) | 2007-07-12 | 2015-05-07 | 에보니크 룀 게엠베하 | 활성화제를 포함한 에멀젼 중합체, 그의 제조 방법 및 2-성분 또는 다성분 시스템에서의 그의 용도 |
Families Citing this family (148)
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|---|---|---|---|---|
| AP1019A (en) | 1996-10-18 | 2001-10-16 | Vertex Pharma | Inhibitors of serinre 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 |
| WO2002048157A2 (en) * | 2000-12-13 | 2002-06-20 | Bristol-Myers Squibb Pharma Company | Imidazolidinones and their related derivatives as hepatitis c virus ns3 protease inhibitors |
| CN100352819C (zh) | 2002-01-23 | 2007-12-05 | 先灵公司 | 作为ns3-丝氨酸蛋白酶抑制剂的脯氨酸化合物用于制备治疗丙型肝炎病毒感染的药物 |
| US7119072B2 (en) | 2002-01-30 | 2006-10-10 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis C virus |
| 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 |
| ATE337309T1 (de) | 2002-04-01 | 2006-09-15 | Pfizer | Pyranon- und pyrandioninhibitoren der rna- abhängigen rna-polymerase des hepatitis-c-virus |
| AU2003223602B8 (en) | 2002-04-11 | 2010-05-27 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis C virus NS3-NS4 protease |
| BR0312271A (pt) | 2002-06-28 | 2007-11-06 | Idenix Cayman Ltd | compostos, composições e seus usos para o tratamento de infecções por flaviviridae |
| EP1408031A1 (en) * | 2002-10-09 | 2004-04-14 | 3 D Gene Pharma | Pyrolidine derivatives useful in treatment of hepatitis C virus infection |
| US20050075279A1 (en) | 2002-10-25 | 2005-04-07 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| AU2004240704B9 (en) | 2003-05-21 | 2009-10-22 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor compounds |
| EP2345657A1 (en) | 2003-05-30 | 2011-07-20 | Pharmasset, Inc. | Modified fluorinated nucleoside analogues |
| EP1658302B1 (en) | 2003-07-25 | 2010-08-25 | IDENIX Pharmaceuticals, Inc. | Purine nucleoside analogues for treating diseases caused by flaviviridae including hepatitis c |
| WO2005021584A2 (en) | 2003-08-26 | 2005-03-10 | Schering Corporation | Novel peptidomimetic ns3-serine protease inhibitors of hepatitis c virus |
| UY28500A1 (es) | 2003-09-05 | 2005-04-29 | Vertex Pharma | Inhibidores de proteasas de serina, en particular proteasa ns3-ns4a del vhc. |
| RS20060197A (sr) | 2003-09-22 | 2008-09-29 | Boehringer Ingelheim International Gmbh., | Makrociklični peptidi koji su aktivni protiv hepatitisa c virusa |
| JP4525982B2 (ja) | 2003-09-26 | 2010-08-18 | シェーリング コーポレイション | C型肝炎ウイルスのns3セリンプロテアーゼの大環状インヒビター |
| WO2005037860A2 (en) | 2003-10-10 | 2005-04-28 | Vertex Pharmaceuticals Incoporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| US8187874B2 (en) | 2003-10-27 | 2012-05-29 | Vertex Pharmaceuticals Incorporated | Drug discovery method |
| EP1944042A1 (en) | 2003-10-27 | 2008-07-16 | Vertex Pharmceuticals Incorporated | Combinations for HCV treatment |
| JP2007532479A (ja) | 2003-11-20 | 2007-11-15 | シェーリング コーポレイション | 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 |
| EP1730167B1 (en) | 2004-01-21 | 2011-01-12 | Boehringer Ingelheim International GmbH | Macrocyclic peptides active against the hepatitis c virus |
| PL1713822T3 (pl) | 2004-01-30 | 2010-08-31 | Medivir Ab | Inhibitory proteazy serynowej HCV NS-3 |
| WO2005077969A2 (en) | 2004-02-04 | 2005-08-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease |
| US20070049593A1 (en) | 2004-02-24 | 2007-03-01 | Japan Tobacco Inc. | Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor |
| HRP20090250T1 (hr) | 2004-02-24 | 2009-06-30 | Japan Tobacco | Kondenzirani heterociklički spojevi i njihova upotreba kao inhibitora hcv polimeraze |
| EP1737881B1 (en) | 2004-02-27 | 2009-06-24 | Schering Corporation | Novel compounds as inhibitors of hepatitis c virus ns3 serine protease |
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| DE602005015834D1 (de) | 2004-02-27 | 2009-09-17 | Schering Corp | 3,4-(cyclopentyl)kondensierte prolinverbindungen als inhibitoren der ns3-serinprotease des hepatitis-c-virus |
| WO2005087721A2 (en) | 2004-02-27 | 2005-09-22 | Schering Corporation | Compounds as inhibitors of hepatitis c virus ns3 serine protease |
| DE602005015452D1 (de) | 2004-05-20 | 2009-08-27 | Schering Corp | Substituierte proline als hemmer der ns3-serinprotease des hepatits-c-virus |
| JP4914355B2 (ja) | 2004-07-20 | 2012-04-11 | 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 | C型肝炎インヒビターペプチド類似体 |
| UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
| CN101023094B (zh) | 2004-07-21 | 2011-05-18 | 法莫赛特股份有限公司 | 烷基取代的2-脱氧-2-氟代-d-呋喃核糖基嘧啶和嘌呤及其衍生物的制备 |
| CA2577812A1 (en) | 2004-08-27 | 2006-03-09 | Schering Corporation | Acylsulfonamide compounds as inhibitors of hepatitis c virus ns3 serine protease |
| AU2005285045B2 (en) | 2004-09-14 | 2011-10-13 | Gilead Sciences, Inc. | Preparation of 2'fluoro-2'- alkyl- substituted or other optionally substituted ribofuranosyl pyrimidines and purines and their derivatives |
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| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
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- 2001-07-19 JP JP2002514104A patent/JP2004515464A/ja active Pending
- 2001-07-19 EP EP01961676A patent/EP1301486B1/en not_active Expired - Lifetime
- 2001-07-19 DE DE60139127T patent/DE60139127D1/de not_active Expired - Lifetime
- 2001-07-19 CA CA002410766A patent/CA2410766A1/en not_active Abandoned
- 2001-07-19 US US09/909,077 patent/US6838475B2/en not_active Expired - Fee Related
- 2001-07-19 AT AT01961676T patent/ATE435211T1/de not_active IP Right Cessation
- 2001-07-19 AU AU2001282922A patent/AU2001282922A1/en not_active Abandoned
- 2001-07-19 ES ES01961676T patent/ES2327819T3/es not_active Expired - Lifetime
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| WO1998017679A1 (en) * | 1996-10-18 | 1998-04-30 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| WO1999050230A1 (en) * | 1998-03-31 | 1999-10-07 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008518919A (ja) * | 2004-10-29 | 2008-06-05 | シェーリング コーポレイション | 抗ウイルス物質としての置換5−カルボキシアミドピラゾールおよび置換[1,2,4]トリアゾール |
| JP4762995B2 (ja) * | 2004-10-29 | 2011-08-31 | シェーリング コーポレイション | 抗ウイルス物質としての置換5−カルボキシアミドピラゾールおよび置換[1,2,4]トリアゾール |
| KR101517640B1 (ko) | 2007-07-12 | 2015-05-07 | 에보니크 룀 게엠베하 | 활성화제를 포함한 에멀젼 중합체, 그의 제조 방법 및 2-성분 또는 다성분 시스템에서의 그의 용도 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20020102235A1 (en) | 2002-08-01 |
| WO2002008198A2 (en) | 2002-01-31 |
| CA2410766A1 (en) | 2002-01-31 |
| AR034127A1 (es) | 2004-02-04 |
| DE60139127D1 (de) | 2009-08-13 |
| ATE435211T1 (de) | 2009-07-15 |
| EP1301486A2 (en) | 2003-04-16 |
| ES2327819T3 (es) | 2009-11-04 |
| EP1301486B1 (en) | 2009-07-01 |
| US6838475B2 (en) | 2005-01-04 |
| WO2002008198A3 (en) | 2002-07-18 |
| AU2001282922A1 (en) | 2002-02-05 |
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