AR047902A1 - Compuestos como inhibidores de ns3 serina proteasa del virus de hepatitis c - Google Patents
Compuestos como inhibidores de ns3 serina proteasa del virus de hepatitis cInfo
- Publication number
- AR047902A1 AR047902A1 ARP050100720A ARP050100720A AR047902A1 AR 047902 A1 AR047902 A1 AR 047902A1 AR P050100720 A ARP050100720 A AR P050100720A AR P050100720 A ARP050100720 A AR P050100720A AR 047902 A1 AR047902 A1 AR 047902A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heterocyclyl
- heteroaryl
- aryl
- cycloalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 8
- 241000700605 Viruses Species 0.000 title 1
- 208000006454 hepatitis Diseases 0.000 title 1
- 231100000283 hepatitis Toxicity 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- -1 heteroalkenyl Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 3
- 108091005804 Peptidases Proteins 0.000 abstract 2
- 239000004365 Protease Substances 0.000 abstract 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000001475 halogen functional group Chemical group 0.000 abstract 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 229930194542 Keto Natural products 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000005422 alkyl sulfonamido group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005281 alkyl ureido group Chemical group 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 125000001769 aryl amino group Chemical group 0.000 abstract 1
- 125000005421 aryl sulfonamido group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000005518 carboxamido group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000000468 ketone group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon 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
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Public Health (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- General Chemical & Material Sciences (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (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)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
Abstract
Compuestos los cuales tienen actividad inhibitoria de la proteasa del VHC así como también métodos para preparar ese tipo de compuestos. Entre otros, composiciones farmacéuticas que comprende ese tipo de compuestos así como también métodos para su utilizacion para tratar trastornos asociados con la proteasa de VHC. Reivindicacion 1: Un compuesto o enantiomeros, estereoisomeros, rotámeros, tautomeros, diastereomeros y racematos de dicho compuesto, o una sal, solvato o éster de dicho compuesto farmacéuticamente aceptable, teniendo dicho compuesto la estructura general mostrada en la formula (1), en la cual: R1 es H, OR8, NR9R10, o CHR9R10, en la cual R8, R9 y R10 pueden ser iguales o diferentes, siendo cada uno seleccionado independientemente del grupo formado por H, alquil-, alquenil-, alquinil-, aril-, heteroalquil-, heteroaril-, cicloalquil-, heterociclil-, arilalquil-, y heteroarilalquilo; A y M pueden ser iguales o diferentes, siendo cada uno seleccionado independientemente entre R, NR9R10, SR, SO2R, y halo; o A y M están conectados entre sí (en otras palabras A-E-L-M tomados en forma conjunta) de modo que la porcion de formula (2), que se muestra anteriormente en la formula (1) forma ya sea un cicloalquilo de tres, cuatro, seis u ocho miembros, un heterociclilo de cuatro a ocho miembros, un arilo de seis a diez miembros, o un heteroarilo de cinco a diez miembros; E es C(H) o C(R); L es C(H), C(R), CH2C(R), o C(R)CH2; R, R', R2, y R3 pueden ser iguales o diferentes, siendo cada uno seleccionado independientemente del grupo formado por H, alquil-, alquenil-, alquinil-, cicloalquil-, heteroalquil-, heterociclil-, aril-, heteroaril-, (cicloalquil)alquil-, (heterociclil)alquil-, aril-alquil- y heteroaril-alquil-; o alternativamente R y R' en NRR' están conectados entre sí de modo que NR9R10 forma un heterociclilo de cuatro a ocho miembros; Y se selecciona de las porciones de grupo formulas (3), donde Y30 e Y31 se seleccionan entre el grupo de formulas (3); X se selecciona entre O, NR15, N(C)R16, S, S(O) y SO2; G es NH o O; y R15, R16, R17, R18, R19, T1, T2, T3 y T4 pueden ser iguales o diferentes, siendo cada uno seleccionado independientemente del grupo formado por H, alquilo, heteroalquilo, alquenilo, heteroalquenilo, alquinilo, heteroalquinilo, cicloalquilo, heterociclilo, arilo, arilalquilo, heteroarilo y heteroarilalquilo, o alternativamente, R17 y R18 están conectados entre sí para formar un cicloalquilo o heterociclilo de tres a ocho miembros; donde cada uno de dicho alquilo, arilo, heteroarilo, cicloalquilo o heterociclilo puede estar no sustituido u opcionalmente independientemente sustituidos con una o más porciones seleccionados del grupo formado por: hidroxi, alcoxi, ariloxi, tio, alquiltio, ariltio, amino, amido, alquilamino, arilamino, alquilsulfonilo, arilsulfonilo, sulfonamido, alquilo, arilo, heteroarilo, alquilsulfonamido, arilsulfonamido, ceto, carboxi, carbalcoxi, carboxamido, alcoxicarbonilamino, alcoxicarboniloxi, alquilureido, arilureido, halo, ciano y nitro.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54850704P | 2004-02-27 | 2004-02-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR047902A1 true AR047902A1 (es) | 2006-03-01 |
Family
ID=34962171
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050100720A AR047902A1 (es) | 2004-02-27 | 2005-02-25 | Compuestos como inhibidores de ns3 serina proteasa del virus de hepatitis c |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US7192957B2 (es) |
| EP (1) | EP1748983A2 (es) |
| JP (1) | JP2007525510A (es) |
| KR (1) | KR20060127162A (es) |
| CN (1) | CN1946691A (es) |
| AR (1) | AR047902A1 (es) |
| AU (1) | AU2005222055A1 (es) |
| BR (1) | BRPI0508095A (es) |
| CA (1) | CA2557247A1 (es) |
| EC (1) | ECSP066795A (es) |
| IL (1) | IL177545A0 (es) |
| NO (1) | NO20064356L (es) |
| RU (1) | RU2006134005A (es) |
| TW (1) | TW200602037A (es) |
| WO (1) | WO2005087721A2 (es) |
| ZA (1) | ZA200607104B (es) |
Families Citing this family (58)
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| US7635694B2 (en) * | 2004-02-27 | 2009-12-22 | Schering Corporation | Cyclobutenedione-containing compounds as inhibitors of hepatitis C virus NS3 serine protease |
| US20060275366A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation |
| WO2006130666A2 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Medicaments and methods combining a hcv protease inhibitor and an akr competitor |
| AR055198A1 (es) * | 2005-06-02 | 2007-08-08 | Schering Corp | Formulaciones farmaceuticas y metodos de tratamiento que las utilizan |
| US20060276407A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| US20060276406A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| US20070021351A1 (en) * | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| CA2611145A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation useful for treating disorders associated with 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 |
| EP1891089B1 (en) | 2005-06-02 | 2014-11-05 | Merck Sharp & Dohme Corp. | HCV protease inhibitors in combination with food |
| 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 |
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| WO2023133174A1 (en) * | 2022-01-07 | 2023-07-13 | Merck Sharp & Dohme Llc | Protease inhibitors for treating or preventing coronavirus infection |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1341629C (en) | 1987-11-18 | 2012-05-08 | Chiron Corporation | Hepatitis c diagnostics and vaccines |
| EP0381216B1 (en) | 1989-02-01 | 1995-12-27 | Asahi Glass Company Ltd. | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
| EP1304335B1 (en) | 1990-04-04 | 2009-06-10 | Novartis Vaccines and Diagnostics, Inc. | 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 |
| DE69709671T2 (de) | 1996-10-18 | 2002-08-22 | Vertex Pharmaceuticals Inc., Cambridge | Inhibitoren von serinproteasen, insbesondere von ns3-protease des hepatitis-c-virus |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| JP4452401B2 (ja) | 1997-08-11 | 2010-04-21 | ベーリンガー インゲルハイム (カナダ) リミテッド | C型肝炎ウイルス阻害ペプチドアナログ |
| US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| 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. |
| 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 |
| JP2001049593A (ja) | 1999-07-22 | 2001-02-20 | E I Du Pont De Nemours & Co | 全芳香族合成繊維からなる繊維紙及びその製造方法及び積層板 |
| ATE297946T1 (de) | 2000-04-03 | 2005-07-15 | Vertex Pharma | Inhibitoren von serin proteasen, speziell der hepatitis-c-virus ns3-protease |
| CA2405521C (en) | 2000-04-05 | 2010-06-29 | Schering Corporation | Macrocyclic ns3-serine protease inhibitors of hepatitis c virus comprising n-cyclic p2 moieties |
| NZ521456A (en) | 2000-04-19 | 2004-07-30 | Schering Corp | Macrocyclic NS3-Serine protease inhibitors of hepatitis C virus comprising alkyl and aryl alanine P2 moieties |
| CA2418199A1 (en) | 2000-07-21 | 2002-01-31 | 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 |
| US7169760B2 (en) | 2000-07-21 | 2007-01-30 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| ATE461207T1 (de) * | 2000-07-21 | 2010-04-15 | Schering Corp | Peptide als inhibitoren der ns3-serinprotease des hepatitis c virus |
| US7244721B2 (en) * | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| HUP0303436A2 (hu) * | 2000-12-12 | 2004-01-28 | Schering Corp. | Diaril-peptidek mint a hepatitis C vírus NS3-szerin proteáz inhibitorai, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk |
| JP4460294B2 (ja) * | 2001-10-24 | 2010-05-12 | 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 | 縮合環系を組み込んだ、セリンプロテアーゼ、特にc型肝炎ウイルスns3−ns4aプロテアーゼの阻害剤 |
| DE60329367D1 (de) | 2002-01-23 | 2009-11-05 | Schering Corp | Verwendung bei der bekämpfung von hepatitis c virusinfektion |
| CA2557307A1 (en) * | 2004-02-27 | 2005-09-22 | Schering Corporation | 3,4-(cyclopentyl)-fused proline compounds as inhibitors of hepatitis c virus ns3 serine protease |
| JP4874227B2 (ja) * | 2004-02-27 | 2012-02-15 | 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インヒビターとしての環状p4’sを有する新規ケトアミド |
-
2005
- 2005-02-24 WO PCT/US2005/005772 patent/WO2005087721A2/en not_active Ceased
- 2005-02-24 EP EP05723589A patent/EP1748983A2/en not_active Withdrawn
- 2005-02-24 AU AU2005222055A patent/AU2005222055A1/en not_active Abandoned
- 2005-02-24 RU RU2006134005/04A patent/RU2006134005A/ru not_active Application Discontinuation
- 2005-02-24 CN CNA2005800127105A patent/CN1946691A/zh active Pending
- 2005-02-24 KR KR1020067017295A patent/KR20060127162A/ko not_active Withdrawn
- 2005-02-24 JP JP2007500946A patent/JP2007525510A/ja not_active Ceased
- 2005-02-24 CA CA002557247A patent/CA2557247A1/en not_active Abandoned
- 2005-02-24 BR BRPI0508095-9A patent/BRPI0508095A/pt not_active IP Right Cessation
- 2005-02-24 TW TW094105621A patent/TW200602037A/zh unknown
- 2005-02-24 US US11/065,509 patent/US7192957B2/en not_active Expired - Fee Related
- 2005-02-25 AR ARP050100720A patent/AR047902A1/es unknown
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2006
- 2006-08-17 IL IL177545A patent/IL177545A0/en unknown
- 2006-08-24 ZA ZA200607104A patent/ZA200607104B/xx unknown
- 2006-08-25 EC EC2006006795A patent/ECSP066795A/es unknown
- 2006-09-26 NO NO20064356A patent/NO20064356L/no not_active Application Discontinuation
- 2006-10-03 US US11/542,228 patent/US7718691B2/en not_active Expired - Fee Related
- 2006-10-03 US US11/542,156 patent/US7759499B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US7718691B2 (en) | 2010-05-18 |
| BRPI0508095A (pt) | 2007-07-17 |
| NO20064356L (no) | 2006-11-24 |
| AU2005222055A1 (en) | 2005-09-22 |
| US7192957B2 (en) | 2007-03-20 |
| ECSP066795A (es) | 2006-11-16 |
| RU2006134005A (ru) | 2008-04-10 |
| US20050288233A1 (en) | 2005-12-29 |
| US7759499B2 (en) | 2010-07-20 |
| ZA200607104B (en) | 2008-09-25 |
| CN1946691A (zh) | 2007-04-11 |
| WO2005087721A2 (en) | 2005-09-22 |
| JP2007525510A (ja) | 2007-09-06 |
| KR20060127162A (ko) | 2006-12-11 |
| TW200602037A (en) | 2006-01-16 |
| CA2557247A1 (en) | 2005-09-22 |
| US20070032434A1 (en) | 2007-02-08 |
| IL177545A0 (en) | 2006-12-10 |
| EP1748983A2 (en) | 2007-02-07 |
| US20070049536A1 (en) | 2007-03-01 |
| WO2005087721A3 (en) | 2005-11-10 |
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