JP2009513564A - Rna依存性rnaウイルス感染の治療用のリボヌクレオシド環状アセタール誘導体 - Google Patents
Rna依存性rnaウイルス感染の治療用のリボヌクレオシド環状アセタール誘導体 Download PDFInfo
- Publication number
- JP2009513564A JP2009513564A JP2008526091A JP2008526091A JP2009513564A JP 2009513564 A JP2009513564 A JP 2009513564A JP 2008526091 A JP2008526091 A JP 2008526091A JP 2008526091 A JP2008526091 A JP 2008526091A JP 2009513564 A JP2009513564 A JP 2009513564A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- amino
- hydrogen
- compound
- rna
- 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- Withdrawn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 C[C@@]12OC(*)O[C@@]1[C@@](C*)O[C@]2[n]1c(ncnc2N)c2nc1 Chemical compound C[C@@]12OC(*)O[C@@]1[C@@](C*)O[C@]2[n]1c(ncnc2N)c2nc1 0.000 description 5
- PGKAMJFHYIUFPI-ZFTUDXBASA-N CC12OC(c3ccc(C)cc3)O[C@@H]1[C@@H](CO)OC2[n]1c(ncnc2N)c2nc1 Chemical compound CC12OC(c3ccc(C)cc3)O[C@@H]1[C@@H](CO)OC2[n]1c(ncnc2N)c2nc1 PGKAMJFHYIUFPI-ZFTUDXBASA-N 0.000 description 1
- YTZVSLMSUIIZMF-AXFSXXMOSA-N CCC(CC)C1O[C@@]2(C)[C@H](N(C=CC(N)=N3)C3=O)O[C@H](CO)[C@H]2O1 Chemical compound CCC(CC)C1O[C@@]2(C)[C@H](N(C=CC(N)=N3)C3=O)O[C@H](CO)[C@H]2O1 YTZVSLMSUIIZMF-AXFSXXMOSA-N 0.000 description 1
- GTXVFMVPEMDEEI-DIVMBQBZSA-N CCC1O[C@@]2(C)[C@H]([n]3c(ncnc4N)c4nc3)O[C@H](CO)[C@H]2O1 Chemical compound CCC1O[C@@]2(C)[C@H]([n]3c(ncnc4N)c4nc3)O[C@H](CO)[C@H]2O1 GTXVFMVPEMDEEI-DIVMBQBZSA-N 0.000 description 1
- SSWDTBSGRXKTNH-VSUUEYMASA-N C[C@@]12OC(c(cc3)ccc3Cl)O[C@@H]1[C@@H](CO)OC2N(C=CC(N)=N1)C1=O Chemical compound C[C@@]12OC(c(cc3)ccc3Cl)O[C@@H]1[C@@H](CO)OC2N(C=CC(N)=N1)C1=O SSWDTBSGRXKTNH-VSUUEYMASA-N 0.000 description 1
- JGHRPNDTDBOYJQ-OQTGWLNSSA-N C[C@@]12OC(c(cc3)ccc3Cl)O[C@@H]1[C@@H](COC(C)=O)O[C@H]2[n]1c(ncnc2N)c2nc1 Chemical compound C[C@@]12OC(c(cc3)ccc3Cl)O[C@@H]1[C@@H](COC(C)=O)O[C@H]2[n]1c(ncnc2N)c2nc1 JGHRPNDTDBOYJQ-OQTGWLNSSA-N 0.000 description 1
- FHICBTYVACGZHO-OGCGGBLFSA-N C[C@@]12OC(c(cc3)ccc3OC)O[C@@H]1[C@@H](CO)O[C@H]2[n]1c(ncnc2N)c2nc1 Chemical compound C[C@@]12OC(c(cc3)ccc3OC)O[C@@H]1[C@@H](CO)O[C@H]2[n]1c(ncnc2N)c2nc1 FHICBTYVACGZHO-OGCGGBLFSA-N 0.000 description 1
- BTHVNTVDNRFPNF-JHJCAENVSA-N C[C@@]12OC(c3ccccc3)O[C@@H]1[C@@H](CO)O[C@H]2[n]1c(ncnc2N)c2nc1 Chemical compound C[C@@]12OC(c3ccccc3)O[C@@H]1[C@@H](CO)O[C@H]2[n]1c(ncnc2N)c2nc1 BTHVNTVDNRFPNF-JHJCAENVSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70670805P | 2005-08-09 | 2005-08-09 | |
| PCT/US2006/030549 WO2007021610A2 (en) | 2005-08-09 | 2006-08-04 | Ribonucleoside cyclic acetal derivatives for the treatment of rna-dependent rna viral infection |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009513564A true JP2009513564A (ja) | 2009-04-02 |
| JP2009513564A5 JP2009513564A5 (https=) | 2009-09-24 |
Family
ID=37758066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008526091A Withdrawn JP2009513564A (ja) | 2005-08-09 | 2006-08-04 | Rna依存性rnaウイルス感染の治療用のリボヌクレオシド環状アセタール誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7632821B2 (https=) |
| EP (1) | EP1915054A4 (https=) |
| JP (1) | JP2009513564A (https=) |
| AU (1) | AU2006280175B2 (https=) |
| CA (1) | CA2618560A1 (https=) |
| WO (1) | WO2007021610A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150002844A (ko) * | 2012-04-18 | 2015-01-07 | 바이오크리스트파마슈티컬즈,인코포레이티드 | 바이러스 폴리머라아제를 억제하기 위한 조성물 및 방법 |
| JP2023553243A (ja) * | 2021-12-16 | 2023-12-21 | アスカレシス バイオサイエンス カンパニー リミテッド | ヌクレオシド誘導体及びその使用方法 |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| HUE033832T2 (en) | 2002-11-15 | 2018-01-29 | Idenix Pharmaceuticals Llc | 2'-methyl nucleosides in combination with interferon and Flaviviridae mutation |
| US8058260B2 (en) * | 2006-05-22 | 2011-11-15 | Xenoport, Inc. | 2′-C-methyl-ribofuranosyl cytidine prodrugs, pharmaceutical compositions and uses thereof |
| CA2685520A1 (en) | 2007-05-10 | 2008-11-20 | Biocryst Pharmaceuticals, Inc. | Tetrahydrofuro [3 4-d] dioxolane compounds for use in the treatment of viral infections and cancer |
| GB0709791D0 (en) * | 2007-05-22 | 2007-06-27 | Angeletti P Ist Richerche Bio | Antiviral agents |
| WO2010036407A2 (en) | 2008-05-15 | 2010-04-01 | Biocryst Pharmaceuticals, Inc. | Antiviral nucleoside analogs |
| EP2691409B1 (en) | 2011-03-31 | 2018-02-21 | Idenix Pharmaceuticals LLC. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| TW201329096A (zh) | 2011-09-12 | 2013-07-16 | Idenix Pharmaceuticals Inc | 經取代羰氧基甲基磷酸醯胺化合物及用於治療病毒感染之藥學組成物 |
| US8507460B2 (en) | 2011-10-14 | 2013-08-13 | Idenix Pharmaceuticals, Inc. | Substituted 3′,5′-cyclic phosphates of purine nucleotide compounds and pharmaceutical compositions for the treatment of viral infections |
| US9296778B2 (en) | 2012-05-22 | 2016-03-29 | Idenix Pharmaceuticals, Inc. | 3′,5′-cyclic phosphate prodrugs for HCV infection |
| CA2873315A1 (en) | 2012-05-22 | 2013-11-28 | Idenix Pharamaceuticals, Inc. | D-amino acid compounds for liver disease |
| WO2013177188A1 (en) | 2012-05-22 | 2013-11-28 | Idenix Pharmaceuticals, Inc. | 3',5'-cyclic phosphoramidate prodrugs for hcv infection |
| SG11201407336PA (en) | 2012-05-25 | 2015-03-30 | Janssen Sciences Ireland Uc | Uracyl spirooxetane nucleosides |
| WO2014052638A1 (en) | 2012-09-27 | 2014-04-03 | Idenix Pharmaceuticals, Inc. | Esters and malonates of sate prodrugs |
| KR102001280B1 (ko) | 2012-10-08 | 2019-07-17 | 아이데닉스 파마슈티칼스 엘엘씨 | Hcv 감염에 대한 2'-클로로 뉴클레오시드 유사체 |
| WO2014066239A1 (en) | 2012-10-22 | 2014-05-01 | Idenix Pharmaceuticals, Inc. | 2',4'-bridged nucleosides for hcv infection |
| EP2935304A1 (en) | 2012-12-19 | 2015-10-28 | IDENIX Pharmaceuticals, Inc. | 4'-fluoro nucleosides for the treatment of hcv |
| US9339541B2 (en) | 2013-03-04 | 2016-05-17 | Merck Sharp & Dohme Corp. | Thiophosphate nucleosides for the treatment of HCV |
| US9309275B2 (en) | 2013-03-04 | 2016-04-12 | Idenix Pharmaceuticals Llc | 3′-deoxy nucleosides for the treatment of HCV |
| WO2014160484A1 (en) | 2013-03-13 | 2014-10-02 | Idenix Pharmaceuticals, Inc. | Amino acid phosphoramidate pronucleotides of 2'-cyano, azido and amino nucleosides for the treatment of hcv |
| EP2981542B1 (en) | 2013-04-01 | 2021-09-15 | Idenix Pharmaceuticals LLC | 2',4'-fluoro nucleosides for the treatment of hcv |
| US10005779B2 (en) | 2013-06-05 | 2018-06-26 | Idenix Pharmaceuticals Llc | 1′,4′-thio nucleosides for the treatment of HCV |
| WO2015017713A1 (en) | 2013-08-01 | 2015-02-05 | Idenix Pharmaceuticals, Inc. | D-amino acid phosphoramidate pronucleotides of halogeno pyrimidine compounds for liver disease |
| WO2015161137A1 (en) | 2014-04-16 | 2015-10-22 | Idenix Pharmaceuticals, Inc. | 3'-substituted methyl or alkynyl nucleosides for the treatment of hcv |
| CA3182565A1 (en) | 2015-03-06 | 2016-09-15 | Atea Pharmaceuticals, Inc. | .beta.-d-2'-deoxy-2'-.alpha.-fluoro-2'-.beta.-c-substituted-2-modified-n6-substituted purine nucleotides for hcv treatment |
| EP4491236A3 (en) | 2016-05-10 | 2025-04-02 | C4 Therapeutics, Inc. | Heterocyclic degronimers for target protein degradation |
| EP3454862B1 (en) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
| CN109790143A (zh) | 2016-05-10 | 2019-05-21 | C4医药公司 | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 |
| CN109641874A (zh) | 2016-05-10 | 2019-04-16 | C4医药公司 | 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体 |
| US10711029B2 (en) | 2016-07-14 | 2020-07-14 | Atea Pharmaceuticals, Inc. | Beta-d-2′-deoxy-2′-alpha-fluoro-2′-beta-c-substituted-4′fluoro-n6-substituted-6-amino-2-substituted purine nucleotides for the treatment of hepatitis c virus infection |
| DK3512863T3 (da) | 2016-09-07 | 2022-03-07 | Atea Pharmaceuticals Inc | 2¿-substituerede-N6-substituerede purinnukleotider til behandling af RNA-virus |
| CN115477679A (zh) | 2017-02-01 | 2022-12-16 | 阿堤亚制药公司 | 用于治疗丙型肝炎病毒的核苷酸半硫酸盐 |
| EP4717317A2 (en) | 2017-06-20 | 2026-04-01 | C4 Therapeutics, Inc. | N/o-linked degrons and degronimers for protein degradation |
| EP3773753A4 (en) | 2018-04-10 | 2021-12-22 | ATEA Pharmaceuticals, Inc. | TREATMENT OF PATIENTS INFECTED WITH THE HEPATITIS C VIRUS WITH CIRRHOSIS |
| US10874687B1 (en) | 2020-02-27 | 2020-12-29 | Atea Pharmaceuticals, Inc. | Highly active compounds against COVID-19 |
| KR20240022574A (ko) | 2021-06-17 | 2024-02-20 | 아테아 파마슈티컬즈, 인크. | 유리한 항-hcv 조합 요법 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5134154A (en) | 1989-10-20 | 1992-07-28 | Merrell Dow Pharmaceuticals Inc. | Phenoxy-heterocyclic compounds |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| GB9707659D0 (en) | 1997-04-16 | 1997-06-04 | Peptide Therapeutics Ltd | Hepatitis C NS3 Protease inhibitors |
| ES2241157T3 (es) | 1997-08-11 | 2005-10-16 | Boehringer Ingelheim (Canada) Ltd. | Peptidos inhibidores de la hepatitis c. |
| EP1012180B1 (en) | 1997-08-11 | 2004-12-01 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis c inhibitor peptide analogues |
| IT1299134B1 (it) | 1998-02-02 | 2000-02-29 | Angeletti P Ist Richerche Bio | Procedimento per la produzione di peptidi con proprieta' inibitrici della proteasi ns3 del virus hcv, peptidi cosi' ottenibili e peptidi |
| GB9806815D0 (en) | 1998-03-30 | 1998-05-27 | Hoffmann La Roche | Amino acid derivatives |
| DK1066247T3 (da) | 1998-03-31 | 2007-04-02 | Vertex Pharma | Inhibitorer af serinproteaser, især hepatitis C virus NS3 protease |
| GB9812523D0 (en) | 1998-06-10 | 1998-08-05 | Angeletti P Ist Richerche Bio | Peptide inhibitors of hepatitis c virus ns3 protease |
| 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 |
| AU3659102A (en) | 2000-12-12 | 2002-06-24 | Schering Corp | Diaryl peptides as ns3-serine protease inhibitors of hepatits c virus |
| WO2002048116A2 (en) | 2000-12-13 | 2002-06-20 | Bristol-Myers Squibb Pharma Company | Inhibitors of hepatitis c virus ns3 protease |
| AU2003221188A1 (en) * | 2002-04-22 | 2003-11-03 | Matsushita Electric Industrial Co., Ltd. | Magnetoresistance effect element, magnetic head comprising it, magnetic memory, and magnetic recorder |
| AU2003232071A1 (en) * | 2002-05-06 | 2003-11-17 | Genelabs Technologies, Inc. | Nucleoside derivatives for treating hepatitis c virus infection |
| EP1773355B1 (en) * | 2004-06-24 | 2014-06-25 | Merck Sharp & Dohme Corp. | Nucleoside aryl phosphoramidates for the treatment of rna-dependent rna viral infection |
-
2006
- 2006-08-04 CA CA002618560A patent/CA2618560A1/en not_active Abandoned
- 2006-08-04 AU AU2006280175A patent/AU2006280175B2/en not_active Ceased
- 2006-08-04 JP JP2008526091A patent/JP2009513564A/ja not_active Withdrawn
- 2006-08-04 WO PCT/US2006/030549 patent/WO2007021610A2/en not_active Ceased
- 2006-08-04 US US11/990,051 patent/US7632821B2/en not_active Expired - Fee Related
- 2006-08-04 EP EP06789454A patent/EP1915054A4/en not_active Withdrawn
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150002844A (ko) * | 2012-04-18 | 2015-01-07 | 바이오크리스트파마슈티컬즈,인코포레이티드 | 바이러스 폴리머라아제를 억제하기 위한 조성물 및 방법 |
| JP2015514772A (ja) * | 2012-04-18 | 2015-05-21 | バイオクリスト ファーマスーティカルズ,インコーポレイテッドBiocryst Pharmaceuticals,Inc. | ウイルスポリメラーゼを阻害するための組成物および方法 |
| JP2018111692A (ja) * | 2012-04-18 | 2018-07-19 | バイオクリスト ファーマスーティカルズ,インコーポレイテッドBiocryst Pharmaceuticals,Inc. | ウイルスポリメラーゼを阻害するための組成物および方法 |
| KR102156819B1 (ko) | 2012-04-18 | 2020-09-16 | 바이오크리스트파마슈티컬즈,인코포레이티드 | 바이러스 폴리머라아제를 억제하기 위한 조성물 및 방법 |
| JP2023553243A (ja) * | 2021-12-16 | 2023-12-21 | アスカレシス バイオサイエンス カンパニー リミテッド | ヌクレオシド誘導体及びその使用方法 |
| JP7504517B2 (ja) | 2021-12-16 | 2024-06-24 | アスカレシス バイオサイエンス カンパニー リミテッド | ヌクレオシド誘導体及びその使用方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2618560A1 (en) | 2007-02-22 |
| EP1915054A2 (en) | 2008-04-30 |
| US7632821B2 (en) | 2009-12-15 |
| US20090099126A1 (en) | 2009-04-16 |
| WO2007021610A2 (en) | 2007-02-22 |
| AU2006280175A1 (en) | 2007-02-22 |
| EP1915054A4 (en) | 2010-09-01 |
| WO2007021610A3 (en) | 2007-10-04 |
| AU2006280175B2 (en) | 2011-09-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090724 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090724 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20120426 |