JP2010508360A - C型肝炎ウイルスの阻害剤 - Google Patents
C型肝炎ウイルスの阻害剤 Download PDFInfo
- Publication number
- JP2010508360A JP2010508360A JP2009535434A JP2009535434A JP2010508360A JP 2010508360 A JP2010508360 A JP 2010508360A JP 2009535434 A JP2009535434 A JP 2009535434A JP 2009535434 A JP2009535434 A JP 2009535434A JP 2010508360 A JP2010508360 A JP 2010508360A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- mmol
- hcv
- compound
- 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.)
- Withdrawn
Links
- 0 CCC([C@]1C[C@](CCCC(**CC[C@@](CNC)*C)=O)C1)=* Chemical compound CCC([C@]1C[C@](CCCC(**CC[C@@](CNC)*C)=O)C1)=* 0.000 description 12
- NHZWCYNEHQXFQE-UHFFFAOYSA-N C=[O]c1nc(-c2ccccc2)ccn1 Chemical compound C=[O]c1nc(-c2ccccc2)ccn1 NHZWCYNEHQXFQE-UHFFFAOYSA-N 0.000 description 1
- VNMCEYCCKZZGHQ-LWKPJOBUSA-N CC(C)(C)OC(N(CC(C1)Oc2c3[o]nc(C)c3nc(-c(cc3)ccc3F)c2)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CC(C1)Oc2c3[o]nc(C)c3nc(-c(cc3)ccc3F)c2)[C@@H]1C(O)=O)=O VNMCEYCCKZZGHQ-LWKPJOBUSA-N 0.000 description 1
- ZQEBQGAAWMOMAI-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)C1C(O)=O)=O ZQEBQGAAWMOMAI-UHFFFAOYSA-N 0.000 description 1
- LFKDJXLFVYVEFG-UHFFFAOYSA-N CC(C)(C)OC(N)=O Chemical compound CC(C)(C)OC(N)=O LFKDJXLFVYVEFG-UHFFFAOYSA-N 0.000 description 1
- ZITSMHNTPLVPSI-YIDMKWSQSA-N CC(C)(C)OC(N[C@@H](CCCCC/C=C\[C@H](C1)[C@]1(C(O)=O)NC([C@H]1N2CCC1)=O)C2=O)=O Chemical compound CC(C)(C)OC(N[C@@H](CCCCC/C=C\[C@H](C1)[C@]1(C(O)=O)NC([C@H]1N2CCC1)=O)C2=O)=O ZITSMHNTPLVPSI-YIDMKWSQSA-N 0.000 description 1
- VRODMOMYNFZSFC-MRLMVZBDSA-N CC(C)(C)OC(N[C@@H](CCCOC/C=C\C(C1)[C@H]1C(NS(C1CC1)(=O)=O)=O)C(N(C[C@@H](C1)OCc2ccccc2)[C@@H]1C(N)=O)=O)=O Chemical compound CC(C)(C)OC(N[C@@H](CCCOC/C=C\C(C1)[C@H]1C(NS(C1CC1)(=O)=O)=O)C(N(C[C@@H](C1)OCc2ccccc2)[C@@H]1C(N)=O)=O)=O VRODMOMYNFZSFC-MRLMVZBDSA-N 0.000 description 1
- RLXAOJXQUJXJQV-ZDUSSCGKSA-N CC(C)(C)OC(N[C@@H](CN(CCCC=C)C1CC1)C(O)=O)=O Chemical compound CC(C)(C)OC(N[C@@H](CN(CCCC=C)C1CC1)C(O)=O)=O RLXAOJXQUJXJQV-ZDUSSCGKSA-N 0.000 description 1
- UDSUJFMZPGOEQG-VIFPVBQESA-N CC(C)(OC(N[C@](C1)(C(O)=O)C1=C)=O)S Chemical compound CC(C)(OC(N[C@](C1)(C(O)=O)C1=C)=O)S UDSUJFMZPGOEQG-VIFPVBQESA-N 0.000 description 1
- WXUCBUGUUVYAAN-YNODCEANSA-N COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O Chemical compound COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O WXUCBUGUUVYAAN-YNODCEANSA-N 0.000 description 1
- FXINDYXFGNANSA-UHFFFAOYSA-N COCC1(CC1)S(N)(=O)=O Chemical compound COCC1(CC1)S(N)(=O)=O FXINDYXFGNANSA-UHFFFAOYSA-N 0.000 description 1
- MTBCEAHKLOSWCG-UHFFFAOYSA-L C[Sn+](CCCCS)(N)(O)O Chemical compound C[Sn+](CCCCS)(N)(O)O MTBCEAHKLOSWCG-UHFFFAOYSA-L 0.000 description 1
- VFPFMOXMHVQFNR-UHFFFAOYSA-N Clc1c(cc[s]2)c2ccn1 Chemical compound Clc1c(cc[s]2)c2ccn1 VFPFMOXMHVQFNR-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
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86383706P | 2006-11-01 | 2006-11-01 | |
| PCT/US2007/083120 WO2008057871A2 (en) | 2006-11-01 | 2007-10-31 | Inhibitors of hepatitis c virus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010508360A true JP2010508360A (ja) | 2010-03-18 |
| JP2010508360A5 JP2010508360A5 (Direct) | 2010-10-28 |
Family
ID=39218835
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009535434A Withdrawn JP2010508360A (ja) | 2006-11-01 | 2007-10-31 | C型肝炎ウイルスの阻害剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8343477B2 (Direct) |
| EP (1) | EP2089385B1 (Direct) |
| JP (1) | JP2010508360A (Direct) |
| CN (1) | CN101646667A (Direct) |
| NO (1) | NO20091704L (Direct) |
| WO (1) | WO2008057871A2 (Direct) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| RU2008152171A (ru) * | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
| BRPI0811020A2 (pt) * | 2007-05-03 | 2015-07-21 | Intermune Inc | Composto, composição farmacêutica e métodos de inibição da atividade da protease ns3/ns4, de tratamento da fibrose hepática, de intensificação da função hepática em indivíduo com infecção do vírus da hepatite c e métodos de síntese de compostos, de administração de inibidor da infecção do vírus da hepatite c (hcv) e de distribuição de forma de dosagem oral. |
| AR066528A1 (es) * | 2007-05-10 | 2009-08-26 | Array Biopharma Inc | Peptidos inhibidores de la replicacion del virus de la hepatitis c |
| AR067180A1 (es) * | 2007-06-29 | 2009-09-30 | Gilead Sciences Inc | Compuestos antivirales |
| AU2009210789B2 (en) * | 2008-02-04 | 2014-01-30 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| AP2010005416A0 (en) * | 2008-04-15 | 2010-10-31 | Intermune Inc | Novel macrocyclic inhibitors of hepatitis c virus replication. |
| US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| AR075584A1 (es) * | 2009-02-27 | 2011-04-20 | Intermune Inc | COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO. |
| WO2010118078A1 (en) | 2009-04-08 | 2010-10-14 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| CA2761650C (en) | 2009-05-13 | 2015-05-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic compounds as hepatitis c virus inhibitors |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| JP2013501068A (ja) | 2009-08-05 | 2013-01-10 | アイディニックス ファーマシューティカルズ インコーポレイテッド | 大環状セリンプロテアーゼ阻害剤 |
| CN102741270B (zh) * | 2009-09-28 | 2015-07-22 | 英特穆恩公司 | C型肝炎病毒复制的环肽抑制剂 |
| US9193740B2 (en) * | 2009-10-19 | 2015-11-24 | Enanta Pharmaceuticals, Inc. | Bismacrocyclic compounds as hepatitis C virus inhibitors |
| EP2655362A1 (en) | 2010-12-22 | 2013-10-30 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
| CN103534256B (zh) | 2010-12-30 | 2016-08-10 | 益安药业 | 大环丙型肝炎丝氨酸蛋白酶抑制剂 |
| KR20140003521A (ko) | 2010-12-30 | 2014-01-09 | 이난타 파마슈티칼스, 인코포레이티드 | 페난트리딘 매크로사이클릭 c형 간염 세린 프로테아제 억제제 |
| AR085352A1 (es) | 2011-02-10 | 2013-09-25 | Idenix Pharmaceuticals Inc | Inhibidores macrociclicos de serina proteasa, sus composiciones farmaceuticas y su uso para tratar infecciones por hcv |
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| BR112015007879A2 (pt) | 2012-10-19 | 2017-07-04 | Bristol Myers Squibb Co | inibidores do vírus da hepatite c |
| US9334279B2 (en) | 2012-11-02 | 2016-05-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2014070964A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2014070974A1 (en) | 2012-11-05 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US9580463B2 (en) | 2013-03-07 | 2017-02-28 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
| CN103965286B (zh) * | 2014-04-22 | 2017-11-03 | 南京安赛莱医药科技有限公司 | 丙型肝炎病毒(hcv)ns3蛋白酶抑制剂 |
| DK3328827T3 (da) | 2015-07-31 | 2023-10-02 | Univ Johns Hopkins | Prodrugs af glutaminanaloger |
| WO2017023787A1 (en) | 2015-07-31 | 2017-02-09 | The Johns Hopkins University | Methods and compositions for treating metabolic reprogramming disorders |
| US10842763B2 (en) | 2015-07-31 | 2020-11-24 | The Johns Hopkins University | Methods for cancer and immunotherapy using prodrugs of glutamine analogs |
| ES2930258T3 (es) | 2017-10-06 | 2022-12-09 | Univ Johns Hopkins | Nuevos antagonistas de glutamina y usos de los mismos |
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| EP0475255A3 (en) * | 1990-09-12 | 1993-04-14 | F. Hoffmann-La Roche Ag | Process for the preparation of optically pure (s)-alpha-((tert-butylsulfonyl)methyl)hydro cinnamic acid |
| CA2268391A1 (en) | 1996-10-18 | 1998-04-30 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| DK1003775T3 (da) | 1997-08-11 | 2005-05-30 | Boehringer Ingelheim Ca Ltd | Hepatitis C-inhibitorpeptider |
| IL134233A0 (en) | 1997-08-11 | 2001-04-30 | Boehringer Ingelheim Ca 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 |
| 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 |
| RU2355700C9 (ru) | 2000-07-21 | 2010-03-20 | Шеринг Корпорейшн | Новые пептиды как ингибиторы ns3-серинпротеазы вируса гепатита с |
| US7244721B2 (en) | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| CN100391967C (zh) | 2000-11-20 | 2008-06-04 | 布里斯托尔-迈尔斯斯奎布公司 | 丙型肝炎三肽抑制剂 |
| US6867185B2 (en) | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| CA2369711A1 (en) | 2002-01-30 | 2003-07-30 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis c virus |
| CA2370396A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| CA2369970A1 (en) | 2002-02-01 | 2003-08-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor tri-peptides |
| US6828301B2 (en) | 2002-02-07 | 2004-12-07 | Boehringer Ingelheim International Gmbh | Pharmaceutical compositions for hepatitis C viral protease inhibitors |
| AU2003248535A1 (en) | 2002-05-20 | 2003-12-12 | Bristol-Myers Squibb Company | Heterocyclicsulfonamide hepatitis c virus inhibitors |
| PL213029B1 (pl) | 2002-05-20 | 2012-12-31 | Bristol Myers Squibb Co | Podstawiona pochodna cykloalkilowa, zawierajaca ja kompozycja oraz ich zastosowanie |
| US20060199773A1 (en) | 2002-05-20 | 2006-09-07 | Sausker Justin B | Crystalline forms of (1R,2S)-N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(6-methoxy-1-isoquinolinyl)oxy]-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethenyl-cyclopropanecarboxamide, monopotassium salt |
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| AU2003299519A1 (en) | 2002-05-20 | 2004-05-04 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
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| JP2008511633A (ja) | 2004-08-27 | 2008-04-17 | シェーリング コーポレイション | C型肝炎ウィルスns3セリンプロテアーゼの阻害因子としてのアシルスルホンアミド化合物 |
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-
2007
- 2007-10-25 US US11/923,918 patent/US8343477B2/en active Active
- 2007-10-31 JP JP2009535434A patent/JP2010508360A/ja not_active Withdrawn
- 2007-10-31 CN CN200780049038A patent/CN101646667A/zh active Pending
- 2007-10-31 EP EP07863696.6A patent/EP2089385B1/en active Active
- 2007-10-31 WO PCT/US2007/083120 patent/WO2008057871A2/en not_active Ceased
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2009
- 2009-04-29 NO NO20091704A patent/NO20091704L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CN101646667A (zh) | 2010-02-10 |
| EP2089385B1 (en) | 2016-01-06 |
| EP2089385A2 (en) | 2009-08-19 |
| US20080107624A1 (en) | 2008-05-08 |
| NO20091704L (no) | 2009-07-27 |
| US8343477B2 (en) | 2013-01-01 |
| WO2008057871A3 (en) | 2008-10-09 |
| WO2008057871A2 (en) | 2008-05-15 |
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