|
US6458772B1
(en)
|
1909-10-07 |
2002-10-01 |
Medivir Ab |
Prodrugs
|
|
US3074929A
(en)
*
|
1955-08-11 |
1963-01-22 |
Burroughs Wellcome Co |
Glycosides of 6-mercaptopurine
|
|
GB924246A
(en)
|
1958-12-23 |
1963-04-24 |
Wellcome Found |
Purine derivatives and their preparation
|
|
US3116282A
(en)
|
1960-04-27 |
1963-12-31 |
Upjohn Co |
Pyrimidine nucleosides and process
|
|
GB984877A
(en)
|
1962-08-16 |
1965-03-03 |
Waldhof Zellstoff Fab |
Improvements in and relating to 6-halonucleosides
|
|
GB1163103A
(en)
|
1965-11-15 |
1969-09-04 |
Merck & Co Inc |
Ribofuranosyl Purine Derivatives
|
|
FR1498856A
(es)
|
1965-11-15 |
1968-01-10 |
|
|
|
DE1695411A1
(de)
|
1966-05-02 |
1971-04-15 |
Merck & Co Inc |
Substituierte Purin-Nucleoside und Verfahren zu deren Herstellung
|
|
FR1521076A
(fr)
|
1966-05-02 |
1968-04-12 |
Merck & Co Inc |
Nucléosides de purines substituées
|
|
US3480613A
(en)
|
1967-07-03 |
1969-11-25 |
Merck & Co Inc |
2-c or 3-c-alkylribofuranosyl - 1-substituted compounds and the nucleosides thereof
|
|
DE2122991C2
(de)
|
1971-05-04 |
1982-06-09 |
Schering Ag, 1000 Berlin Und 4619 Bergkamen |
Verfahren zur Herstellung von Cytosin- und 6-Azacytosinnucleosiden
|
|
USRE29835E
(en)
|
1971-06-01 |
1978-11-14 |
Icn Pharmaceuticals |
1,2,4-Triazole nucleosides
|
|
US3798209A
(en)
*
|
1971-06-01 |
1974-03-19 |
Icn Pharmaceuticals |
1,2,4-triazole nucleosides
|
|
US4022889A
(en)
*
|
1974-05-20 |
1977-05-10 |
The Upjohn Company |
Therapeutic compositions of antibiotic U-44,590 and methods for using the same
|
|
DE2508312A1
(de)
|
1975-02-24 |
1976-09-02 |
Schering Ag |
Neues verfahren zur herstellung von nucleosiden
|
|
US4058602A
(en)
|
1976-08-09 |
1977-11-15 |
The United States Of America As Represented By The Department Of Health, Education And Welfare |
Synthesis, structure, and antitumor activity of 5,6-dihydro-5-azacytidine
|
|
DE2757365A1
(de)
*
|
1977-12-20 |
1979-06-21 |
Schering Ag |
Neues verfahren zur herstellung von nucleosiden
|
|
DE2852721A1
(de)
|
1978-12-06 |
1980-06-26 |
Basf Ag |
Verfahren zur reindarstellung von kaliumribonat und ribonolacton
|
|
US4239753A
(en)
|
1978-12-12 |
1980-12-16 |
The Upjohn Company |
Composition of matter and process
|
|
US4522811A
(en)
*
|
1982-07-08 |
1985-06-11 |
Syntex (U.S.A.) Inc. |
Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
|
|
FR2562543B1
(fr)
|
1984-04-10 |
1987-09-25 |
Elf Aquitaine |
Nouveaux phosphonites cycliques, leur preparation et applications
|
|
NL8403224A
(nl)
|
1984-10-24 |
1986-05-16 |
Oce Andeno Bv |
Dioxafosforinanen, de bereiding ervan en de toepassing voor het splitsen van optisch actieve verbindingen.
|
|
JPS61204193A
(ja)
|
1985-03-05 |
1986-09-10 |
Takeda Chem Ind Ltd |
シトシンヌクレオシド類の製造法
|
|
US5223263A
(en)
*
|
1988-07-07 |
1993-06-29 |
Vical, Inc. |
Liponucleotide-containing liposomes
|
|
US6448392B1
(en)
|
1985-03-06 |
2002-09-10 |
Chimerix, Inc. |
Lipid derivatives of antiviral nucleosides: liposomal incorporation and method of use
|
|
US4605659A
(en)
|
1985-04-30 |
1986-08-12 |
Syntex (U.S.A.) Inc. |
Purinyl or pyrimidinyl substituted hydroxycyclopentane compounds useful as antivirals
|
|
US4754026A
(en)
*
|
1985-06-04 |
1988-06-28 |
Takeda Chemical Industries, Ltd. |
Conversion of uracil derivatives to cytosine derivatives
|
|
DE3714473A1
(de)
|
1987-04-30 |
1988-11-10 |
Basf Ag |
Kontinuierliches verfahren zur epimerisierung von zuckern, insbesondere von d-arabinose zu d-ribose
|
|
GB8719367D0
(en)
|
1987-08-15 |
1987-09-23 |
Wellcome Found |
Therapeutic compounds
|
|
US5246924A
(en)
|
1987-09-03 |
1993-09-21 |
Sloan-Kettering Institute For Cancer Research |
Method for treating hepatitis B virus infections using 1-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-5-ethyluracil
|
|
US4880784A
(en)
|
1987-12-21 |
1989-11-14 |
Brigham Young University |
Antiviral methods utilizing ribofuranosylthiazolo[4,5-d]pyrimdine derivatives
|
|
US5122517A
(en)
*
|
1988-06-10 |
1992-06-16 |
Regents Of The University Of Minnesota |
Antiviral combination comprising nucleoside analogs
|
|
GB8815265D0
(en)
*
|
1988-06-27 |
1988-08-03 |
Wellcome Found |
Therapeutic nucleosides
|
|
US6252060B1
(en)
*
|
1988-07-07 |
2001-06-26 |
Nexstar Pharmaceuticals, Inc. |
Antiviral liponucleosides: treatment of hepatitis B
|
|
US6599887B2
(en)
|
1988-07-07 |
2003-07-29 |
Chimerix, Inc. |
Methods of treating viral infections using antiviral liponucleotides
|
|
SE8802687D0
(sv)
|
1988-07-20 |
1988-07-20 |
Astra Ab |
Nucleoside derivatives
|
|
US5744600A
(en)
*
|
1988-11-14 |
1998-04-28 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Phosphonomethoxy carbocyclic nucleosides and nucleotides
|
|
US5616702A
(en)
|
1988-11-15 |
1997-04-01 |
Merrell Pharmaceuticals Inc. |
2-'-ethenylidene cytidine, uridine and guanosine derivatives
|
|
US5705363A
(en)
*
|
1989-03-02 |
1998-01-06 |
The Women's Research Institute |
Recombinant production of human interferon τ polypeptides and nucleic acids
|
|
US5021562A
(en)
*
|
1989-05-15 |
1991-06-04 |
Monsanto Company |
Method for azide displacement of α-triflates of 1,5-lactones
|
|
US5411947A
(en)
*
|
1989-06-28 |
1995-05-02 |
Vestar, Inc. |
Method of converting a drug to an orally available form by covalently bonding a lipid to the drug
|
|
US5194654A
(en)
*
|
1989-11-22 |
1993-03-16 |
Vical, Inc. |
Lipid derivatives of phosphonoacids for liposomal incorporation and method of use
|
|
US5463092A
(en)
|
1989-11-22 |
1995-10-31 |
Vestar, Inc. |
Lipid derivatives of phosphonacids for liposomal incorporation and method of use
|
|
US6060592A
(en)
*
|
1990-01-11 |
2000-05-09 |
Isis Pharmaceuticals, Inc. |
Pyrimidine nucleoside compounds and oligonucleoside compounds containing same
|
|
US5200514A
(en)
*
|
1990-01-19 |
1993-04-06 |
University Of Georgia Research Foundation, Inc. |
Synthesis of 2'-deoxypyrimidine nucleosides
|
|
US5204466A
(en)
*
|
1990-02-01 |
1993-04-20 |
Emory University |
Method and compositions for the synthesis of bch-189 and related compounds
|
|
FR2662165B1
(fr)
|
1990-05-18 |
1992-09-11 |
Univ Paris Curie |
Derives nucleosidiques branches, leur procede de preparation et leur utilisation a titre de medicament.
|
|
CA2083961A1
(en)
*
|
1990-05-29 |
1991-11-30 |
Henk Van Den Bosch |
Synthesis of glycerol di- and triphosphate derivatives
|
|
US5627165A
(en)
|
1990-06-13 |
1997-05-06 |
Drug Innovation & Design, Inc. |
Phosphorous prodrugs and therapeutic delivery systems using same
|
|
US5372808A
(en)
|
1990-10-17 |
1994-12-13 |
Amgen Inc. |
Methods and compositions for the treatment of diseases with consensus interferon while reducing side effect
|
|
US5543390A
(en)
|
1990-11-01 |
1996-08-06 |
State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University |
Covalent microparticle-drug conjugates for biological targeting
|
|
US5149794A
(en)
|
1990-11-01 |
1992-09-22 |
State Of Oregon |
Covalent lipid-drug conjugates for drug targeting
|
|
US5256641A
(en)
|
1990-11-01 |
1993-10-26 |
State Of Oregon |
Covalent polar lipid-peptide conjugates for immunological targeting
|
|
US5543389A
(en)
|
1990-11-01 |
1996-08-06 |
State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education On Behalf Of The Oregon Health Sciences University, A Non Profit Organization |
Covalent polar lipid-peptide conjugates for use in salves
|
|
US5827819A
(en)
|
1990-11-01 |
1998-10-27 |
Oregon Health Sciences University |
Covalent polar lipid conjugates with neurologically active compounds for targeting
|
|
IL100502A
(en)
|
1991-01-03 |
1995-12-08 |
Iaf Biochem Int |
PHARMACEUTICAL PREPARATIONS CONTAINING CIS-4-AMINO-1-) 2-HYDROXIMETHIL-1,3-OXETYOLEN-5-IL (-
|
|
JPH04266880A
(ja)
|
1991-02-22 |
1992-09-22 |
Japan Tobacco Inc |
3 −dpa− ラクトンの製造方法
|
|
US5157027A
(en)
|
1991-05-13 |
1992-10-20 |
E. R. Squibb & Sons, Inc. |
Bisphosphonate squalene synthetase inhibitors and method
|
|
JPH0525152A
(ja)
|
1991-07-22 |
1993-02-02 |
Japan Tobacco Inc |
3−dpa−ラクトンの製造法
|
|
US5554728A
(en)
|
1991-07-23 |
1996-09-10 |
Nexstar Pharmaceuticals, Inc. |
Lipid conjugates of therapeutic peptides and protease inhibitors
|
|
TW224053B
(es)
|
1991-09-13 |
1994-05-21 |
Paul B Chretien |
|
|
US5676942A
(en)
|
1992-02-10 |
1997-10-14 |
Interferon Sciences, Inc. |
Composition containing human alpha interferon species proteins and method for use thereof
|
|
US5256797A
(en)
|
1992-06-22 |
1993-10-26 |
Eli Lilly And Company |
Process for separating 2-deoxy-2,2-difluoro-D-ribofuranosyl alkylsulfonate anomers
|
|
US5371210A
(en)
|
1992-06-22 |
1994-12-06 |
Eli Lilly And Company |
Stereoselective fusion glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
|
US5401861A
(en)
*
|
1992-06-22 |
1995-03-28 |
Eli Lilly And Company |
Low temperature process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates
|
|
US5821357A
(en)
|
1992-06-22 |
1998-10-13 |
Eli Lilly And Company |
Stereoselective glycosylation process for preparing 2'-deoxy-2',2'-difluoropurine and triazole nucleosides
|
|
US5606048A
(en)
*
|
1992-06-22 |
1997-02-25 |
Eli Lilly And Company |
Stereoselective glycosylation process for preparing 2'-Deoxy-2', 2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
|
DE4224737A1
(de)
|
1992-07-27 |
1994-02-03 |
Herbert Prof Dr Schott |
Neue Cytosinnucleosidanaloga, Verfahren zu ihrer Herstellung und ihre Verwendung
|
|
CA2105112C
(en)
|
1992-09-01 |
2005-08-02 |
Thomas C. Britton |
A process for anomerizing nucleosides
|
|
GB9226729D0
(en)
|
1992-12-22 |
1993-02-17 |
Wellcome Found |
Therapeutic combination
|
|
GB9307043D0
(en)
|
1993-04-05 |
1993-05-26 |
Norsk Hydro As |
Chemical compounds
|
|
US6156501A
(en)
|
1993-10-26 |
2000-12-05 |
Affymetrix, Inc. |
Arrays of modified nucleic acid probes and methods of use
|
|
US5587362A
(en)
|
1994-01-28 |
1996-12-24 |
Univ. Of Ga Research Foundation |
L-nucleosides
|
|
US5696277A
(en)
|
1994-11-15 |
1997-12-09 |
Karl Y. Hostetler |
Antiviral prodrugs
|
|
AU674639B2
(en)
|
1994-12-13 |
1997-01-02 |
Akira Matsuda |
3'-substituted nucleoside derivatives
|
|
DE19513330A1
(de)
*
|
1995-04-03 |
1996-10-10 |
Schering Ag |
Neues Verfahren zur Herstellung von Nucleosiden
|
|
US5977061A
(en)
|
1995-04-21 |
1999-11-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
N6 - substituted nucleotide analagues and their use
|
|
ATE459361T1
(de)
|
1995-09-07 |
2010-03-15 |
Univ Georgia |
Therapeutische azidverbindungen
|
|
US5908621A
(en)
*
|
1995-11-02 |
1999-06-01 |
Schering Corporation |
Polyethylene glycol modified interferon therapy
|
|
US5980884A
(en)
|
1996-02-05 |
1999-11-09 |
Amgen, Inc. |
Methods for retreatment of patients afflicted with Hepatitis C using consensus interferon
|
|
GB9609932D0
(en)
*
|
1996-05-13 |
1996-07-17 |
Hoffmann La Roche |
Use of IL-12 and IFN alpha for the treatment of infectious diseases
|
|
ES2195970T3
(es)
|
1996-10-16 |
2003-12-16 |
Ribapharm Inc |
L-ribavirina y usos de la misma.
|
|
AU740916B2
(en)
*
|
1996-10-28 |
2001-11-15 |
University Of Washington |
Induction of viral mutation by incorporation of miscoding ribonucleoside analogs into viral RNA
|
|
US6248878B1
(en)
*
|
1996-12-24 |
2001-06-19 |
Ribozyme Pharmaceuticals, Inc. |
Nucleoside analogs
|
|
US6472373B1
(en)
|
1997-09-21 |
2002-10-29 |
Schering Corporation |
Combination therapy for eradicating detectable HCV-RNA in antiviral treatment naive patients having chronic hepatitis C infection
|
|
US6172046B1
(en)
*
|
1997-09-21 |
2001-01-09 |
Schering Corporation |
Combination therapy for eradicating detectable HCV-RNA in patients having chronic Hepatitis C infection
|
|
PT1058686E
(pt)
*
|
1998-02-25 |
2007-01-31 |
Raymond F Schinazi |
2'-fluoronucleósidos
|
|
KR100389853B1
(ko)
*
|
1998-03-06 |
2003-08-19 |
삼성전자주식회사 |
카타로그정보의기록및재생방법
|
|
US6312662B1
(en)
|
1998-03-06 |
2001-11-06 |
Metabasis Therapeutics, Inc. |
Prodrugs phosphorus-containing compounds
|
|
US6833361B2
(en)
*
|
1998-05-26 |
2004-12-21 |
Ribapharm, Inc. |
Nucleosides having bicyclic sugar moiety
|
|
NZ508249A
(en)
*
|
1998-06-08 |
2003-02-28 |
F |
Use of PEG-IFN-alpha conjugates in association with ribavirin for the treatment of chronic hepatitis C
|
|
US6444652B1
(en)
*
|
1998-08-10 |
2002-09-03 |
Novirio Pharmaceuticals Limited |
β-L-2'-deoxy-nucleosides for the treatment of hepatitis B
|
|
MXPA01001507A
(es)
|
1998-08-10 |
2003-09-10 |
Novirio Pharmaceuticals Ltd |
°l-2'desoxi-nucleosidos para el tratamiento de hepatitis b.
|
|
US6277830B1
(en)
|
1998-10-16 |
2001-08-21 |
Schering Corporation |
5′-amino acid esters of ribavirin and the use of same to treat hepatitis C with interferon
|
|
CA2252144A1
(en)
|
1998-10-16 |
2000-04-16 |
University Of Alberta |
Dual action anticancer prodrugs
|
|
WO2000026225A2
(en)
|
1998-11-05 |
2000-05-11 |
Centre National De La Recherche Scientifique |
Nucleosides with anti-hepatitis b virus activity
|
|
WO2000050424A1
(en)
|
1999-02-22 |
2000-08-31 |
Biochem Pharma Inc. |
[1,8] naphthyridine derivatives having antiviral activity
|
|
US6831069B2
(en)
|
1999-08-27 |
2004-12-14 |
Ribapharm Inc. |
Pyrrolo[2,3-d]pyrimidine nucleoside analogs
|
|
US6752981B1
(en)
*
|
1999-09-08 |
2004-06-22 |
Metabasis Therapeutics, Inc. |
Prodrugs for liver specific drug delivery
|
|
US6566365B1
(en)
*
|
1999-11-04 |
2003-05-20 |
Biochem Pharma Inc. |
Method for the treatment of Flaviviridea viral infection using nucleoside analogues
|
|
HK1049841A1
(zh)
|
1999-12-22 |
2003-05-30 |
Metabasis Therapeutics, Inc. |
新瞵酸二酰胺药物前体
|
|
US7056895B2
(en)
*
|
2000-02-15 |
2006-06-06 |
Valeant Pharmaceuticals International |
Tirazole nucleoside analogs and methods for using same
|
|
US6455508B1
(en)
|
2000-02-15 |
2002-09-24 |
Kanda S. Ramasamy |
Methods for treating diseases with tirazole and pyrrolo-pyrimidine ribofuranosyl nucleosides
|
|
US6495677B1
(en)
|
2000-02-15 |
2002-12-17 |
Kanda S. Ramasamy |
Nucleoside compounds
|
|
KR20030005197A
(ko)
|
2000-02-18 |
2003-01-17 |
샤이어 바이오켐 인코포레이티드 |
뉴클레오시드유도체를 이용한 플라비바이러스 감염의 치료또는 예방 방법
|
|
US7094770B2
(en)
*
|
2000-04-13 |
2006-08-22 |
Pharmasset, Ltd. |
3′-or 2′-hydroxymethyl substituted nucleoside derivatives for treatment of hepatitis virus infections
|
|
WO2001081359A1
(en)
*
|
2000-04-20 |
2001-11-01 |
Schering Corporation |
Ribavirin-interferon alfa combination therapy for eradicating detectable hcv-rna in patients having chronic hepatitis c infection
|
|
MY164523A
(en)
*
|
2000-05-23 |
2017-12-29 |
Univ Degli Studi Cagliari |
Methods and compositions for treating hepatitis c virus
|
|
CA2410579C
(en)
*
|
2000-05-26 |
2010-04-20 |
Jean-Pierre Sommadossi |
Methods and compositions for treating flaviviruses and pestiviruses
|
|
US6787526B1
(en)
|
2000-05-26 |
2004-09-07 |
Idenix Pharmaceuticals, Inc. |
Methods of treating hepatitis delta virus infection with β-L-2′-deoxy-nucleosides
|
|
CN100490818C
(zh)
*
|
2000-05-26 |
2009-05-27 |
诺瓦蒂斯有限公司 |
β-L-2′-脱氧核苷在制备用于治疗丁型肝炎病毒感染的药物中的用途
|
|
US6875751B2
(en)
*
|
2000-06-15 |
2005-04-05 |
Idenix Pharmaceuticals, Inc. |
3′-prodrugs of 2′-deoxy-β-L-nucleosides
|
|
US6815542B2
(en)
*
|
2000-06-16 |
2004-11-09 |
Ribapharm, Inc. |
Nucleoside compounds and uses thereof
|
|
KR100426030B1
(ko)
*
|
2000-07-22 |
2004-04-03 |
(주) 한켐 |
락톤계 당화합물에서의 키랄성 전환방법
|
|
US20030008841A1
(en)
*
|
2000-08-30 |
2003-01-09 |
Rene Devos |
Anti-HCV nucleoside derivatives
|
|
KR20090089922A
(ko)
*
|
2000-10-18 |
2009-08-24 |
파마셋 인코포레이티드 |
바이러스 감염 및 비정상적인 세포 증식의 치료를 위한 변형된 뉴클레오시드
|
|
JP2004533805A
(ja)
|
2000-10-18 |
2004-11-11 |
フアーマセツト・リミテツド |
疾患細胞中の核酸の多重定量
|
|
AU2002213343A1
(en)
|
2000-10-18 |
2002-04-29 |
Schering Corporation |
Ribavirin-pegylated interferon alfa HCV combination therapy
|
|
US20040266723A1
(en)
|
2000-12-15 |
2004-12-30 |
Otto Michael J. |
Antiviral agents for treatment of Flaviviridae infections
|
|
SI1355916T1
(sl)
*
|
2001-01-22 |
2007-04-30 |
Merck & Co Inc |
Nukleozidni derivati kot inhibitorji RNA-odvisne RNA virusne polimeraze
|
|
US7105499B2
(en)
*
|
2001-01-22 |
2006-09-12 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase
|
|
US6927291B2
(en)
|
2001-03-01 |
2005-08-09 |
Pharmasset, Ltd. |
Method for the synthesis of 2′,3′-dideoxy-2′,3′-didehydronucleosides
|
|
GB0112617D0
(en)
*
|
2001-05-23 |
2001-07-18 |
Hoffmann La Roche |
Antiviral nucleoside derivatives
|
|
GB0114286D0
(en)
|
2001-06-12 |
2001-08-01 |
Hoffmann La Roche |
Nucleoside Derivatives
|
|
JP2005503358A
(ja)
|
2001-06-22 |
2005-02-03 |
フアーマセツト・リミテツド |
β−2’−または3’−ハロヌクレオシド
|
|
WO2003024461A1
(en)
*
|
2001-09-20 |
2003-03-27 |
Schering Corporation |
Hcv combination therapy
|
|
JP2005536440A
(ja)
*
|
2001-09-28 |
2005-12-02 |
イデニクス(ケイマン)リミテツド |
4’位が修飾されたヌクレオシドを使用するフラビウイルスおよびペスチウイルスの治療のための方法および組成物
|
|
US7105527B2
(en)
*
|
2001-12-14 |
2006-09-12 |
Otto Michael J |
N4-acylcytosine nucleosides for treatment of viral infections
|
|
BR0307712A
(pt)
|
2002-02-14 |
2005-05-24 |
Pharmasset Ltd |
Composto, composição e uso dos mesmos no tratamento de infecções por flaviviridae e proliferação celular anormal
|
|
JP2005525358A
(ja)
*
|
2002-02-28 |
2005-08-25 |
ビオタ インコーポレーティッド |
ヌクレオチド模倣体およびそのプロドラッグ
|
|
US7247621B2
(en)
*
|
2002-04-30 |
2007-07-24 |
Valeant Research & Development |
Antiviral phosphonate compounds and methods therefor
|
|
AU2003232071A1
(en)
*
|
2002-05-06 |
2003-11-17 |
Genelabs Technologies, Inc. |
Nucleoside derivatives for treating hepatitis c virus infection
|
|
CN1678326A
(zh)
*
|
2002-06-28 |
2005-10-05 |
埃迪尼克斯(开曼)有限公司 |
用于治疗黄病毒感染的2'-c-甲基-3'-o-l-缬氨酸酯核糖呋喃基胞苷
|
|
US7094768B2
(en)
*
|
2002-09-30 |
2006-08-22 |
Genelabs Technologies, Inc. |
Nucleoside derivatives for treating hepatitis C virus infection
|
|
TW200418498A
(en)
|
2002-09-30 |
2004-10-01 |
Genelabs Tech Inc |
Nucleoside derivatives for treating hepatitis C virus infection
|
|
JP2006519753A
(ja)
*
|
2002-11-15 |
2006-08-31 |
イデニクス(ケイマン)リミテツド |
2’−分枝ヌクレオシドおよびフラビウイルス科ウイルス突然変異
|
|
TWI332507B
(en)
*
|
2002-11-19 |
2010-11-01 |
Hoffmann La Roche |
Antiviral nucleoside derivatives
|
|
MXPA05006230A
(es)
*
|
2002-12-12 |
2005-09-20 |
Idenix Cayman Ltd |
Proceso para la produccion de nucleosidos ramificados-2'.
|
|
KR20060008297A
(ko)
|
2003-03-20 |
2006-01-26 |
마이크로 바이올로지카 퀴미카 이 파마슈티카 리미티드 |
2'-데옥시-β-L-뉴클레오시드의 제조방법
|
|
US20040259934A1
(en)
|
2003-05-01 |
2004-12-23 |
Olsen David B. |
Inhibiting Coronaviridae viral replication and treating Coronaviridae viral infection with nucleoside compounds
|
|
US20040229839A1
(en)
|
2003-05-14 |
2004-11-18 |
Biocryst Pharmaceuticals, Inc. |
Substituted nucleosides, preparation thereof and use as inhibitors of RNA viral polymerases
|
|
PL3521297T3
(pl)
*
|
2003-05-30 |
2022-04-04 |
Gilead Pharmasset Llc |
Zmodyfikowane fluorowane analogi nukleozydów
|
|
JP2006527719A
(ja)
*
|
2003-06-19 |
2006-12-07 |
エフ.ホフマン−ラ ロシュ アーゲー |
4’−アジドヌクレオシド誘導体の調製方法
|
|
CA2531412A1
(en)
*
|
2003-06-30 |
2005-01-13 |
Idenix (Cayman) Limited |
Synthesis of .beta.-l-2'-deoxy nucleosides
|
|
US7144868B2
(en)
*
|
2003-10-27 |
2006-12-05 |
Genelabs Technologies, Inc. |
Nucleoside compounds for treating viral infections
|
|
US20050137141A1
(en)
*
|
2003-10-24 |
2005-06-23 |
John Hilfinger |
Prodrug composition
|
|
CA2543090A1
(en)
|
2003-10-27 |
2005-06-16 |
Genelabs Technologies, Inc. |
Nucleoside compounds for treating viral infections
|
|
WO2005042556A1
(en)
*
|
2003-10-27 |
2005-05-12 |
Genelabs Technologies, Inc. |
Nucleoside compounds for treating viral infections
|
|
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
|
|
EP1794172B1
(en)
*
|
2004-08-23 |
2009-07-15 |
F.Hoffmann-La Roche Ag |
Antiviral 4'-azido-nucleosides
|
|
JP5001842B2
(ja)
*
|
2004-09-14 |
2012-08-15 |
ギリアド ファーマセット エルエルシー |
2’−フルオロ−2’−アルキル−置換又は他の置換されていてもよいリボフラノシルピリミジン類及びプリン類並びにそれらの誘導体の製造
|
|
WO2006121468A1
(en)
*
|
2004-11-22 |
2006-11-16 |
Genelabs Technologies, Inc. |
5-nitro-nucleoside compounds for treating viral infections
|
|
EA200701669A1
(ru)
|
2005-02-09 |
2008-02-28 |
Мидженикс Инк. |
Композиции и способы лечения или предотвращения инфекций, вызванных вирусами семейства flaviviridae
|
|
DE102005012681A1
(de)
|
2005-03-18 |
2006-09-21 |
Weber, Lutz, Dr. |
Neue 1,5-Dihydro-pyrrol-2-one
|
|
US7405204B2
(en)
|
2005-04-25 |
2008-07-29 |
Genelabs Technologies, Inc. |
Nucleoside compounds for treating viral infections
|
|
EP1976382B1
(en)
|
2005-12-23 |
2013-04-24 |
IDENIX Pharmaceuticals, Inc. |
Process for preparing a synthetic intermediate for preparation of branched nucleosides
|