JP3889708B2 - C型肝炎トリペプチド阻害剤 - Google Patents
C型肝炎トリペプチド阻害剤 Download PDFInfo
- Publication number
- JP3889708B2 JP3889708B2 JP2002561494A JP2002561494A JP3889708B2 JP 3889708 B2 JP3889708 B2 JP 3889708B2 JP 2002561494 A JP2002561494 A JP 2002561494A JP 2002561494 A JP2002561494 A JP 2002561494A JP 3889708 B2 JP3889708 B2 JP 3889708B2
- Authority
- JP
- Japan
- Prior art keywords
- compound
- mmol
- alkyl
- phenyl
- nmr
- 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@@](*)[N+](*1ICC2(CC2)C1)[O-])N Chemical compound **([C@@](*)[N+](*1ICC2(CC2)C1)[O-])N 0.000 description 2
- JZVUAOCDNFNSGQ-UHFFFAOYSA-N COc1ccc2c(O)cc(-c3ccccc3)nc2c1 Chemical compound COc1ccc2c(O)cc(-c3ccccc3)nc2c1 JZVUAOCDNFNSGQ-UHFFFAOYSA-N 0.000 description 2
- BNDQLOJNPMUCLB-WDGNGZAQSA-N CC(C)(C)C(C(N(CC(C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C(N[O](C=C)C(N/S(/C1CC1)=C/C)=O)=O)=O)NC(Oc1ccccc1)=O Chemical compound CC(C)(C)C(C(N(CC(C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C(N[O](C=C)C(N/S(/C1CC1)=C/C)=O)=O)=O)NC(Oc1ccccc1)=O BNDQLOJNPMUCLB-WDGNGZAQSA-N 0.000 description 1
- ATUAHVYILYZCRT-UHFFFAOYSA-N CC(C)(C)OC(N(CC1(CC1)C1)C1=C)=O Chemical compound CC(C)(C)OC(N(CC1(CC1)C1)C1=C)=O ATUAHVYILYZCRT-UHFFFAOYSA-N 0.000 description 1
- GFVADPFCJYFOQI-JPQCJXECSA-N CC(C)(C)OC(NC(C1)(C1C=C)C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)C1C(N[C@](C1)([C@@H]1C=C)C(N/S(/C1CC1)=C/C)=O)=O)=O)=O Chemical compound CC(C)(C)OC(NC(C1)(C1C=C)C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)C1C(N[C@](C1)([C@@H]1C=C)C(N/S(/C1CC1)=C/C)=O)=O)=O)=O GFVADPFCJYFOQI-JPQCJXECSA-N 0.000 description 1
- WCYLIGGIKNKWQX-RXMQYKEDSA-N CC(C)(C)[C@@H](C(OC)=O)N Chemical compound CC(C)(C)[C@@H](C(OC)=O)N WCYLIGGIKNKWQX-RXMQYKEDSA-N 0.000 description 1
- YLEGTXRUUIUTPE-LLVKDONJSA-O CC(C)(C)[C@@H](C(OC)=O)NS(c(cccc1)c1[NH+]=O)(=O)=O Chemical compound CC(C)(C)[C@@H](C(OC)=O)NS(c(cccc1)c1[NH+]=O)(=O)=O YLEGTXRUUIUTPE-LLVKDONJSA-O 0.000 description 1
- CUIIIITYFSTBBL-ASHOXZOSSA-N CC(C)[C@@H](C(N(C[C@@H](C1)Oc2cc(-c3ccccc3)nc3c2ccc(OC)c3)[C@@H]1C(N[C@](C1)(C1C=C)C(NS(C1CCC1)(=O)=O)=O)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)[C@@H](C(N(C[C@@H](C1)Oc2cc(-c3ccccc3)nc3c2ccc(OC)c3)[C@@H]1C(N[C@](C1)(C1C=C)C(NS(C1CCC1)(=O)=O)=O)=O)=O)NC(OC(C)(C)C)=O CUIIIITYFSTBBL-ASHOXZOSSA-N 0.000 description 1
- OIVDUDDLYCSSCG-UHFFFAOYSA-N CCC(C1)C1(N)O Chemical compound CCC(C1)C1(N)O OIVDUDDLYCSSCG-UHFFFAOYSA-N 0.000 description 1
- YANWFZGPYVFZJD-UHFFFAOYSA-N CO[N+](c1ccccc1S(Cl)(=O)=O)=O Chemical compound CO[N+](c1ccccc1S(Cl)(=O)=O)=O YANWFZGPYVFZJD-UHFFFAOYSA-N 0.000 description 1
- PCAHUWITUFWEIF-UEYQJSFASA-N C[C@H]([C@@](C)(C(NS(c1cccc2c1cccc2)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2cc(-c3ccccc3)nc3c2ccc(OC)c3)N1C(C(C(C)(C)C)NC(OC(C)(C)C)=O)=O)=O)C=C Chemical compound C[C@H]([C@@](C)(C(NS(c1cccc2c1cccc2)(=O)=O)=O)NC([C@H](C[C@H](C1)Oc2cc(-c3ccccc3)nc3c2ccc(OC)c3)N1C(C(C(C)(C)C)NC(OC(C)(C)C)=O)=O)=O)C=C PCAHUWITUFWEIF-UEYQJSFASA-N 0.000 description 1
- GUQHLYHTAZNLQX-UHFFFAOYSA-N NS(CC1CCC1)(=O)=O Chemical compound NS(CC1CCC1)(=O)=O GUQHLYHTAZNLQX-UHFFFAOYSA-N 0.000 description 1
- ZFQCRLNKHHXELH-UHFFFAOYSA-N O=C(OC1CCCC1)Cl Chemical compound O=C(OC1CCCC1)Cl ZFQCRLNKHHXELH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N OC1CCCC1 Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-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
-
- 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
- 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
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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)
- 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)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Treating Waste Gases (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24996800P | 2000-11-20 | 2000-11-20 | |
| PCT/US2001/045145 WO2002060926A2 (en) | 2000-11-20 | 2001-11-20 | Hepatitis c tripeptide inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004538251A JP2004538251A (ja) | 2004-12-24 |
| JP2004538251A5 JP2004538251A5 (https=) | 2005-06-30 |
| JP3889708B2 true JP3889708B2 (ja) | 2007-03-07 |
Family
ID=22945765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002561494A Expired - Fee Related JP3889708B2 (ja) | 2000-11-20 | 2001-11-20 | C型肝炎トリペプチド阻害剤 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6872805B2 (https=) |
| EP (1) | EP1337550B1 (https=) |
| JP (1) | JP3889708B2 (https=) |
| CN (1) | CN100391967C (https=) |
| AT (1) | ATE327246T1 (https=) |
| AU (1) | AU2002248147B2 (https=) |
| BR (1) | BR0115447A (https=) |
| CA (1) | CA2429359A1 (https=) |
| DE (1) | DE60119968T2 (https=) |
| ES (1) | ES2263687T3 (https=) |
| HU (1) | HUP0500456A3 (https=) |
| MX (1) | MXPA03004299A (https=) |
| PE (1) | PE20020707A1 (https=) |
| WO (1) | WO2002060926A2 (https=) |
Families Citing this family (219)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100509388B1 (ko) | 1996-10-18 | 2005-08-23 | 버텍스 파마슈티칼스 인코포레이티드 | 세린 프로테아제, 특히 간염 c 바이러스 ns3 프로테아제의 저해제 |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| EP1423522A2 (en) * | 2001-01-23 | 2004-06-02 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hepatitis c virus replicons and replicon enhanced cells |
| US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| 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 |
| WO2003085375A2 (en) * | 2002-04-04 | 2003-10-16 | Achillion Pharmaceuticals, Inc. | Hcv antiviral and cytotoxicity drug screening assay |
| KR20040099425A (ko) | 2002-04-11 | 2004-11-26 | 버텍스 파마슈티칼스 인코포레이티드 | 세린 프로테아제, 특히 c형 간염 바이러스 ns3-ns4프로테아제의 억제제 |
| MXPA04009986A (es) * | 2002-04-12 | 2005-08-16 | Achillion Pharmaceuticals Inc | Metodo para sintetizar beta-l-5-fluoro-2¦,3¦-didesoxi-2¦,3¦-dideshidrocitidina (¦-l-fd4c). |
| JP4312711B2 (ja) * | 2002-05-20 | 2009-08-12 | ブリストル−マイヤーズ スクイブ カンパニー | ヘテロ環式スルホンアミドc型肝炎ウイルス阻害剤 |
| MY140680A (en) * | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| JP4271148B2 (ja) * | 2002-05-20 | 2009-06-03 | ブリストル−マイヤーズ スクイブ カンパニー | 置換シクロアルキルp1’c型肝炎ウイルスインヒビター |
| WO2004032827A2 (en) | 2002-05-20 | 2004-04-22 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| TW200500375A (en) | 2002-06-28 | 2005-01-01 | Idenix Cayman Ltd | Modified 2' and 3'-nucleoside prodrugs for treating flaviviridae |
| US20050075279A1 (en) * | 2002-10-25 | 2005-04-07 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| JP4733023B2 (ja) | 2003-04-16 | 2011-07-27 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルスの大環状イソキノリンペプチド阻害剤 |
| US7176208B2 (en) * | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| CL2004001161A1 (es) | 2003-05-21 | 2005-04-08 | Boehringer Ingelheim Int | Compuestos describe compuestos derivados de quinolina; composicion farmaceutica; y su uso para tratar una enfermedad causada por el virus de la hepatitis c. |
| HUE029877T2 (en) | 2003-05-30 | 2017-04-28 | Gilead Pharmasset Llc | Modified fluorinated nucleoside analogues |
| US20050075309A1 (en) | 2003-07-25 | 2005-04-07 | Richard Storer | Purine nucleoside analogues for treating Flaviviridae including hepatitis C |
| TWI359147B (en) | 2003-09-05 | 2012-03-01 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv n |
| ES2361997T3 (es) | 2003-09-22 | 2011-06-27 | Boehringer Ingelheim International Gmbh | Péptidos macrocíclicos activos contra el virus de la hepatitis c. |
| WO2005037860A2 (en) | 2003-10-10 | 2005-04-28 | Vertex Pharmaceuticals Incoporated | 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 |
| EP1944042A1 (en) | 2003-10-27 | 2008-07-16 | Vertex Pharmceuticals Incorporated | Combinations for HCV treatment |
| US8187874B2 (en) | 2003-10-27 | 2012-05-29 | Vertex Pharmaceuticals Incorporated | Drug discovery method |
| US7132504B2 (en) * | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7135462B2 (en) * | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GB0500020D0 (en) | 2005-01-04 | 2005-02-09 | Novartis Ag | Organic compounds |
| ATE495185T1 (de) | 2004-01-21 | 2011-01-15 | Boehringer Ingelheim Int | Makrocyclische peptide mit wirkung gegen das hepatitis-c-virus |
| JP4902361B2 (ja) | 2004-01-30 | 2012-03-21 | メディヴィル・アクチエボラーグ | Hcvns−3セリンプロテアーゼインヒビター |
| CN1938332B (zh) | 2004-02-04 | 2011-10-19 | 沃泰克斯药物股份有限公司 | 丝氨酸蛋白酶、特别是hcv ns3-ns4a蛋白酶的抑制剂 |
| CN102911161A (zh) | 2004-02-20 | 2013-02-06 | 贝林格尔.英格海姆国际有限公司 | 病毒聚合酶抑制剂 |
| AP2006003763A0 (en) * | 2004-03-30 | 2006-10-31 | Intermune Inc | Macrocyclic compounds as inhibitors of viral replication |
| CA2556669C (en) | 2004-06-28 | 2012-05-01 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor peptide analogs |
| RS51974B (sr) * | 2004-07-16 | 2012-02-29 | Gilead Sciences Inc. | Antivirusna jedinjenja |
| UY29016A1 (es) | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
| 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 |
| 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 |
| US7597884B2 (en) | 2004-08-09 | 2009-10-06 | Alios Biopharma, Inc. | Hyperglycosylated polypeptide variants and methods of use |
| ATE513844T1 (de) | 2004-08-27 | 2011-07-15 | Schering Corp | Acylsulfonamidverbindungen als inhibitoren der ns3-serinprotease des hepatitis-c-virus |
| US8492539B2 (en) | 2004-09-14 | 2013-07-23 | Gilead Pharmasset Llc | Preparation of 2′-fluoro-2′-alkyl-substituted or other optionally substituted ribofuranosyl pyrimidines and purines and their derivatives |
| 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 |
| WO2006119646A1 (en) | 2005-05-13 | 2006-11-16 | Virochem Pharma Inc. | Compounds and methods for the treatment or prevention of flavivirus infections |
| AU2006259348B2 (en) | 2005-06-17 | 2010-07-22 | Novartis Ag | Use of sanglifehrin in HCV |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI389908B (zh) * | 2005-07-14 | 2013-03-21 | Gilead Sciences Inc | 抗病毒化合物類 |
| JP2009501732A (ja) * | 2005-07-20 | 2009-01-22 | 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 |
| MX2008001166A (es) | 2005-07-25 | 2008-03-18 | Intermune Inc | Nuevos inhibidores macrociclicos de la replicacion del virus de hepatitis c. |
| PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
| KR20080033481A (ko) * | 2005-08-02 | 2008-04-16 | 버텍스 파마슈티칼스 인코포레이티드 | 세린 프로테아제의 억제제 |
| US8076365B2 (en) | 2005-08-12 | 2011-12-13 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US8399615B2 (en) | 2005-08-19 | 2013-03-19 | Vertex Pharmaceuticals Incorporated | Processes and intermediates |
| PL385229A1 (pl) | 2005-08-19 | 2008-09-29 | Vertex Pharmaceuticals Incorporated | Sposoby i związki pośrednie |
| 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 |
| AU2006301966A1 (en) | 2005-10-11 | 2007-04-19 | Array Biopharma, Inc. | Compounds and methods for inhibiting hepatitis C viral replication |
| 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 |
| EP1991229A2 (en) | 2006-02-27 | 2008-11-19 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| EP1993994A2 (en) | 2006-03-16 | 2008-11-26 | Vertex Pharmceuticals Incorporated | Deuterated hepatitis c protease inhibitors |
| EP2007789B1 (en) | 2006-04-11 | 2015-05-20 | Novartis AG | Spirocyclic HCV/HIV inhibitors and their uses |
| KR20090024834A (ko) * | 2006-07-05 | 2009-03-09 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 억제제 |
| EP2049474B1 (en) | 2006-07-11 | 2015-11-04 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| NZ574605A (en) | 2006-07-13 | 2011-11-25 | Achillion Pharmaceuticals Inc | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| CA2656816A1 (en) * | 2006-08-04 | 2008-02-14 | Enanta Pharmaceuticals, Inc. | Tetrazolyl macrocyclic hepatitis c serine protease inhibitors |
| EP1886685A1 (en) | 2006-08-11 | 2008-02-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods, uses and compositions for modulating replication of hcv through the farnesoid x receptor (fxr) activation or inhibition |
| JP2010500978A (ja) | 2006-08-17 | 2010-01-14 | 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 |
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- 2001-11-20 CA CA002429359A patent/CA2429359A1/en not_active Abandoned
- 2001-11-20 MX MXPA03004299A patent/MXPA03004299A/es active IP Right Grant
- 2001-11-20 CN CNB018221106A patent/CN100391967C/zh not_active Expired - Fee Related
- 2001-11-20 US US10/001,850 patent/US6872805B2/en not_active Expired - Lifetime
- 2001-11-20 PE PE2001001155A patent/PE20020707A1/es not_active Application Discontinuation
- 2001-11-20 HU HU0500456A patent/HUP0500456A3/hu unknown
- 2001-11-20 AT AT01997024T patent/ATE327246T1/de not_active IP Right Cessation
- 2001-11-20 JP JP2002561494A patent/JP3889708B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1531547A (zh) | 2004-09-22 |
| WO2002060926A2 (en) | 2002-08-08 |
| PE20020707A1 (es) | 2002-08-11 |
| US20020111313A1 (en) | 2002-08-15 |
| ATE327246T1 (de) | 2006-06-15 |
| WO2002060926A3 (en) | 2003-03-13 |
| AU2002248147B2 (en) | 2006-04-06 |
| BR0115447A (pt) | 2005-10-18 |
| US6872805B2 (en) | 2005-03-29 |
| DE60119968T2 (de) | 2007-01-18 |
| DE60119968D1 (en) | 2006-06-29 |
| CA2429359A1 (en) | 2002-08-08 |
| ES2263687T3 (es) | 2006-12-16 |
| EP1337550B1 (en) | 2006-05-24 |
| EP1337550A2 (en) | 2003-08-27 |
| JP2004538251A (ja) | 2004-12-24 |
| HUP0500456A3 (en) | 2012-05-02 |
| HUP0500456A2 (hu) | 2005-08-29 |
| MXPA03004299A (es) | 2004-02-12 |
| CN100391967C (zh) | 2008-06-04 |
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