AR056327A1 - Compuestos de nucleosidos para el tratamiento de infecciones virales - Google Patents
Compuestos de nucleosidos para el tratamiento de infecciones viralesInfo
- Publication number
- AR056327A1 AR056327A1 ARP060101650A ARP060101650A AR056327A1 AR 056327 A1 AR056327 A1 AR 056327A1 AR P060101650 A ARP060101650 A AR P060101650A AR P060101650 A ARP060101650 A AR P060101650A AR 056327 A1 AR056327 A1 AR 056327A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- hydrogen
- group
- compounds
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- 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
-
- 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
-
- 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
- C07H19/14—Pyrrolo-pyrimidine radicals
Abstract
Se exponen compuestos y uso de estos compuestos para preparar medicamentos. Estos compuestos son utiles para tratar infecciones virales causadas por un virus de la familia Flaviviridae, tal como el virus de la hepatitis C. Reivindicacion 1: Un compuesto de la formula (1) caracterizado porque: Y es O o CH2; X se selecciona de halo y O-W2; cada W, W1 y W2 se selecciona del grupo que consiste de hidrogeno, alquilo C1-4, y un grupo prodroga farmacéuticamente aceptable, previsto que cuando X es -O-W2, uno de W, W1 y W2 sea alquilo C1-4; R3 se selecciona del grupo que consiste de hidrogeno, OH, acilo, alquilo C1-4, y alcoxi C1-4; T se selecciona del grupo que consiste de: a) -C:::C-R, en donde R se selecciona del grupo que consiste de: i) hidrogeno; ii) tri-alquilsililoC1-4, -C(O)NR1R2, alcoxialquilo, heteroarilo, heteroarilo sustituido, fenilo, y fenilo sustituido; en donde R1 y R2 se seleccionan independientemente del grupo que consiste de hidrogeno, alquilo, alquilo sustituido, amino, amino sustituido, arilo, arilo sustituido, heteroarilo, heteroarilo sustituido, heterocíclico y heterocíclico sustituido previsto que solo uno de R1 y R2 es amino o amino sustituido, y además en donde R1 y R2, junto con el átomo de nitrogeno pendiente de este, forman un heterocíclico o heterocíclico sustituido; y iii) -C(O)OR14 , en donde R14 es hidrogeno, alquilo o alquilo sustituido; b) -CH=CH-Q2, en donde Q2 se selecciona de hidrogeno o cis-alcoxi; c) -C(O)H; d) -CH=NNHR15, en donde R15 es hidrogeno o alquilo C1-4; e) -CH=N(OR15), en donde R15 es como se definio anteriormente; f) -CH(OR16)2, en donde R16 es alquilo C3-6; g) -B(OR15)2, en donde R15 es como se definio anteriormente; y h) -NO2; o sales farmacéuticamente aceptables o sales parciales de éstos; previsto que cuando R3 es hidrogeno, OH, o alcoxi C1-3, entonces X es halo o -OalquiloC1-4.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67473105P | 2005-04-25 | 2005-04-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR056327A1 true AR056327A1 (es) | 2007-10-03 |
Family
ID=36764686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060101650A AR056327A1 (es) | 2005-04-25 | 2006-04-25 | Compuestos de nucleosidos para el tratamiento de infecciones virales |
Country Status (4)
Country | Link |
---|---|
US (1) | US7405204B2 (es) |
AR (1) | AR056327A1 (es) |
TW (1) | TW200720285A (es) |
WO (1) | WO2006116557A1 (es) |
Families Citing this family (77)
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 |
EP1294735A2 (en) | 2000-05-26 | 2003-03-26 | Novirio Pharmaceuticals Limited | Methods and compositions for treating flaviviruses and pestiviruses |
US7608600B2 (en) | 2002-06-28 | 2009-10-27 | Idenix Pharmaceuticals, Inc. | Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections |
KR20050035194A (ko) | 2002-06-28 | 2005-04-15 | 이데닉스 (케이만) 리미티드 | 플라비비리다에 감염 치료용 2'-c-메틸-3'-o-l-발린에스테르 리보푸라노실 사이티딘 |
CN1849142A (zh) | 2002-11-15 | 2006-10-18 | 埃迪尼克斯(开曼)有限公司 | 2′-支链核苷和黄病毒突变 |
EP1976382B1 (en) | 2005-12-23 | 2013-04-24 | IDENIX Pharmaceuticals, Inc. | Process for preparing a synthetic intermediate for preparation of branched nucleosides |
GB0623493D0 (en) * | 2006-11-24 | 2007-01-03 | Univ Cardiff | Chemical compounds |
US7951789B2 (en) * | 2006-12-28 | 2011-05-31 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
JP2010515680A (ja) * | 2007-01-05 | 2010-05-13 | メルク・シャープ・エンド・ドーム・コーポレイション | Rna依存性rnaウイルス感染症の治療用としてのヌクレオシドアリールホスホロアミデート |
AU2012241173B2 (en) * | 2007-03-30 | 2014-09-25 | Gilead Pharmasset Llc | Nucleoside Phosphoramidate Prodrugs |
AU2014233579B2 (en) * | 2007-03-30 | 2016-06-23 | Gilead Pharmasset Llc | Nucleoside phosphoramidate prodrugs |
US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
CA2711384C (en) * | 2008-01-18 | 2016-07-26 | Institute Of Organic Chemistry And Biochemistry As Cr, V.V.I. | Cytostatic 7-deazapurine nucleosides |
US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
WO2010015637A1 (en) * | 2008-08-06 | 2010-02-11 | Novartis Ag | New antiviral modified nucleosides |
AU2009329872B2 (en) | 2008-12-23 | 2016-07-07 | Gilead Pharmasset Llc | Synthesis of purine nucleosides |
SG172361A1 (en) | 2008-12-23 | 2011-07-28 | Pharmasset Inc | Nucleoside analogs |
AR074897A1 (es) | 2008-12-23 | 2011-02-23 | Pharmasset Inc | Fosforamidatos de nucleosidos |
CA3033133C (en) | 2009-03-25 | 2021-11-09 | The Board Of Regents Of The University Of Texas System | Compositions for stimulation of mammalian innate immune resistance to pathogens |
WO2010114905A1 (en) * | 2009-03-31 | 2010-10-07 | Arqule, Inc. | Peri-fused pyrazolo-pyrimidine compounds |
US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
TWI583692B (zh) | 2009-05-20 | 2017-05-21 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
PE20210668A1 (es) * | 2009-09-21 | 2021-04-05 | Gilead Sciences Inc | Analogos de carba-nucleosidos sustituidos con 2'-fluoro antivirales |
SI2480559T1 (sl) | 2009-09-21 | 2013-10-30 | Gilead Sciences, Inc. | Postopki in intermediati za pripravo 1'-ciano-karbanukleozidnih analogov |
WO2011123672A1 (en) | 2010-03-31 | 2011-10-06 | Pharmasset, Inc. | Purine nucleoside phosphoramidate |
US8563530B2 (en) | 2010-03-31 | 2013-10-22 | Gilead Pharmassel LLC | Purine nucleoside phosphoramidate |
EP2752422B1 (en) | 2010-03-31 | 2017-08-16 | Gilead Pharmasset LLC | Stereoselective synthesis of phosphorus containing actives |
KR20200052384A (ko) | 2010-07-19 | 2020-05-14 | 길리애드 사이언시즈, 인코포레이티드 | 부분입체 이성질성으로 순수한 포스포라미데이트 전구약물의 제조 방법 |
PT2595980E (pt) | 2010-07-22 | 2014-11-27 | Gilead Sciences Inc | Métodos e compostos para tratar infeções pelo vírus da família paramyxoviridae |
NZ607996A (en) | 2010-09-22 | 2014-07-25 | Alios Biopharma Inc | Substituted nucleotide analogs |
ES2716158T3 (es) | 2010-11-30 | 2019-06-10 | Gilead Pharmasset Llc | 2'-spiro-nucleótidos para el tratamiento de hepatitis C |
WO2012154321A1 (en) | 2011-03-31 | 2012-11-15 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
AU2012242978A1 (en) | 2011-04-13 | 2013-10-24 | Merck Sharp & Dohme Corp. | 2'-Cyano Substituted Nucleoside Derivatives and methods of use thereof for the treatment of viral diseases |
JP2014515023A (ja) * | 2011-04-13 | 2014-06-26 | メルク・シャープ・アンド・ドーム・コーポレーション | 2’−置換ヌクレオシド誘導体およびウイルス疾患の処置のためのその使用方法 |
EP2697242B1 (en) | 2011-04-13 | 2018-10-03 | Merck Sharp & Dohme Corp. | 2'-azido substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
US9408863B2 (en) | 2011-07-13 | 2016-08-09 | Merck Sharp & Dohme Corp. | 5′-substituted nucleoside analogs and methods of use thereof for the treatment of viral diseases |
US9416154B2 (en) | 2011-07-13 | 2016-08-16 | Merck Sharp & Dohme Corp. | 5′-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
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 |
MD4589C1 (ro) | 2011-09-16 | 2019-03-31 | Gilead Pharmasset Llc | Compoziţie farmaceutică cu conţinut de sofosbuvir şi utilizarea acesteia în tratamentul hepatitei virale C |
US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
NZ702744A (en) * | 2012-05-22 | 2016-12-23 | Idenix Pharmaceuticals Llc | D-amino acid compounds for liver disease |
EP2852604B1 (en) | 2012-05-22 | 2017-04-12 | Idenix Pharmaceuticals LLC | 3',5'-cyclic phosphoramidate prodrugs for hcv infection |
WO2013177195A1 (en) | 2012-05-22 | 2013-11-28 | Idenix Pharmaceuticals, Inc. | 3',5'-cyclic phosphate prodrugs for hcv infection |
UY34824A (es) | 2012-05-25 | 2013-11-29 | Janssen R & D Ireland | Nucleósidos de espirooxetano de uracilo |
US9192621B2 (en) | 2012-09-27 | 2015-11-24 | Idenix Pharmaceuticals Llc | Esters and malonates of SATE prodrugs |
EA030189B8 (ru) * | 2012-10-08 | 2018-10-31 | Иденикс Фармасьютикалз Ллс | Аналоги 2'-хлоронуклеозидов для инфекции вгс |
AR092959A1 (es) * | 2012-10-17 | 2015-05-06 | Merck Sharp & Dohme | Derivados de nucleosidos 2-metil sustituidos y metodos de uso de los mismos para el tratamiento de enfermedades virales |
US10723754B2 (en) | 2012-10-22 | 2020-07-28 | Idenix Pharmaceuticals Llc | 2′,4′-bridged nucleosides for HCV infection |
WO2014099941A1 (en) | 2012-12-19 | 2014-06-26 | Idenix Pharmaceuticals, Inc. | 4'-fluoro nucleosides for the treatment of hcv |
NZ625087A (en) | 2013-01-31 | 2017-05-26 | Gilead Pharmasset Llc | Combination formulation of two antiviral compounds |
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 |
WO2014135107A1 (zh) | 2013-03-08 | 2014-09-12 | 南京圣和药业有限公司 | 新的核苷氨基磷酸酯化合物及其应用 |
EP2970357A1 (en) | 2013-03-13 | 2016-01-20 | IDENIX Pharmaceuticals, Inc. | Amino acid phosphoramidate pronucleotides of 2'-cyano, azido and amino nucleosides for the treatment of hcv |
US9187515B2 (en) | 2013-04-01 | 2015-11-17 | 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 |
ES2900570T3 (es) | 2013-08-27 | 2022-03-17 | Gilead Pharmasset Llc | Formulación de combinación de dos compuestos antivirales |
WO2015161137A1 (en) | 2014-04-16 | 2015-10-22 | Idenix Pharmaceuticals, Inc. | 3'-substituted methyl or alkynyl nucleosides for the treatment of hcv |
WO2016015638A1 (zh) * | 2014-07-30 | 2016-02-04 | 南京圣和药业股份有限公司 | 丙型肝炎病毒抑制剂及其应用 |
US10286065B2 (en) | 2014-09-19 | 2019-05-14 | Board Of Regents, The University Of Texas System | Compositions and methods for treating viral infections through stimulated innate immunity in combination with antiviral compounds |
TWI698444B (zh) | 2014-10-29 | 2020-07-11 | 美商基利科學股份有限公司 | 製備核糖苷的方法 |
CN107771179A (zh) | 2015-06-22 | 2018-03-06 | 桑多斯股份公司 | 氨基磷酸酯的合成 |
CA2998189C (en) | 2015-09-16 | 2021-08-03 | Gilead Sciences, Inc. | Methods for treating arenaviridae and coronaviridae virus infections |
US10202412B2 (en) | 2016-07-08 | 2019-02-12 | Atea Pharmaceuticals, Inc. | β-D-2′-deoxy-2′-substituted-4′-substituted-2-substituted-N6-substituted-6-aminopurinenucleotides for the treatment of paramyxovirus and orthomyxovirus infections |
US20190169221A1 (en) * | 2016-08-12 | 2019-06-06 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
CN110869028B (zh) | 2017-03-14 | 2023-01-20 | 吉利德科学公司 | 治疗猫冠状病毒感染的方法 |
CN115403626A (zh) | 2017-05-01 | 2022-11-29 | 吉利德科学公司 | 新结晶形式 |
US10675296B2 (en) | 2017-07-11 | 2020-06-09 | Gilead Sciences, Inc. | Compositions comprising an RNA polymerase inhibitor and cyclodextrin for treating viral infections |
WO2021154687A1 (en) | 2020-01-27 | 2021-08-05 | Gilead Sciences, Inc. | Methods for treating sars cov-2 infections |
CN115298181A (zh) | 2020-03-12 | 2022-11-04 | 吉利德科学公司 | 制备1’-氰基核苷的方法 |
EP4132651A1 (en) | 2020-04-06 | 2023-02-15 | Gilead Sciences, Inc. | Inhalation formulations of 1'-cyano substituted carbanucleoside analogs |
CA3179226A1 (en) | 2020-05-29 | 2021-12-02 | Tomas Cihlar | Remdesivir treatment methods |
CN115996928A (zh) | 2020-06-24 | 2023-04-21 | 吉利德科学公司 | 1’-氰基核苷类似物及其用途 |
CN114057814B (zh) * | 2020-08-05 | 2023-12-08 | 广州市恒诺康医药科技有限公司 | 核苷类似物及其应用 |
PE20231983A1 (es) | 2020-08-27 | 2023-12-12 | Gilead Sciences Inc | Compuestos y metodos para el tratamiento de infecciones virales |
WO2023167944A1 (en) | 2022-03-02 | 2023-09-07 | Gilead Sciences, Inc. | Compounds and methods for treatment of viral infections |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4107288A (en) * | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
AU7675491A (en) * | 1990-04-04 | 1991-10-30 | Chiron Corporation | Hepatitis c virus protease |
US5145684A (en) * | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
DE69332105T2 (de) * | 1992-09-29 | 2003-03-06 | Inhale Therapeutic Systems San | Pulmonale abgabe von aktiven fragmenten des parathormons |
EP0693126B9 (en) * | 1993-04-02 | 2007-09-12 | Rigel Pharmaceuticals, Inc. | Method for selective inactivation of viral replication |
IT1272179B (it) * | 1994-02-23 | 1997-06-16 | Angeletti P Ist Richerche Bio | Metodologia per riprodurre in vitro l'attivita' proteolitica della proteasi ns3 del virus hcv. |
US6150510A (en) * | 1995-11-06 | 2000-11-21 | Aventis Pharma Deutschland Gmbh | Modified oligonucleotides, their preparation and their use |
US5861267A (en) * | 1995-05-01 | 1999-01-19 | Vertex Pharmaceuticals Incorporated | Methods, nucleotide sequences and host cells for assaying exogenous and endogenous protease activity |
AU719122B2 (en) | 1995-09-27 | 2000-05-04 | Emory University | Recombinant hepatitis C virus RNA replicase |
US5759795A (en) * | 1996-03-08 | 1998-06-02 | Schering Corporation | Assay for determining inhibitors of ATPase |
KR20000075983A (ko) * | 1997-03-05 | 2000-12-26 | 엘. 데이예를 카렌. | 헤파타이티스 c 바이러스 복제를 선택적으로 저해하는 물질을 확인하기 위한 새로운 스크리닝 방법 |
DE69838513T2 (de) * | 1997-12-11 | 2008-07-03 | Smithkline Beecham Corp. | Verkürztes hepatitis-c-virus protein nsb5 und methoden, um antivirale substanzen zu identifizieren |
RS50236B (sr) * | 2001-01-22 | 2009-07-15 | Merck & Co.Inc., | Nukleozidni derivati kao inhibitori rnk-zavisne rnk virusne polimeraze |
JP2005533108A (ja) | 2002-07-16 | 2005-11-04 | メルク エンド カムパニー インコーポレーテッド | Rna依存性rnaウイルスポリメラーゼの阻害剤としてのヌクレオシド誘導体 |
AU2003261434A1 (en) | 2002-08-12 | 2004-02-25 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of hcv replication |
US7094768B2 (en) * | 2002-09-30 | 2006-08-22 | Genelabs Technologies, Inc. | Nucleoside derivatives for treating hepatitis C virus infection |
NZ538457A (en) | 2002-09-30 | 2008-04-30 | Genelabs Tech Inc | Nucleoside derivatives for treating hepatitis C virus infection |
EP2345661A1 (en) | 2003-05-30 | 2011-07-20 | Pharmasset, Inc. | Modified fluorinated nucleoside analogues |
WO2005024268A1 (en) | 2003-09-08 | 2005-03-17 | Scott Ronald Thomas | Line tensioning device and methods |
US7144868B2 (en) * | 2003-10-27 | 2006-12-05 | Genelabs Technologies, Inc. | Nucleoside compounds for treating viral infections |
AU2004295291A1 (en) * | 2003-10-27 | 2005-06-16 | Smithkline Beecham Corporation | Nucleoside compounds for treating viral infections |
CA2542776A1 (en) * | 2003-10-27 | 2005-05-12 | Genelabs Technologies, Inc. | Nucleoside compounds for treating viral infections |
US7169918B2 (en) * | 2003-10-27 | 2007-01-30 | Genelabs Technologies, Inc. | Methods for preparing 7-(2′-substituted-β-D-ribofuranosyl)-4-(NR2R3)-5-(substituted ethyn-1-yl)-pyrrolo[2,3-d]pyrimidine derivatives |
US7202223B2 (en) * | 2003-10-27 | 2007-04-10 | Genelabs Technologies, Inc. | Nucleoside compounds for treating viral infections |
US7414031B2 (en) * | 2004-11-22 | 2008-08-19 | Genelabs Technologies, Inc. | 5-nitro-nucleoside compounds for treating viral infections |
EP1853617A1 (en) * | 2005-02-28 | 2007-11-14 | Genelabs Technologies, Inc. | Tricyclic-nucleoside prodrugs for treating viral infections |
-
2006
- 2006-04-25 WO PCT/US2006/015940 patent/WO2006116557A1/en active Application Filing
- 2006-04-25 AR ARP060101650A patent/AR056327A1/es not_active Application Discontinuation
- 2006-04-25 TW TW095114793A patent/TW200720285A/zh unknown
- 2006-04-25 US US11/411,434 patent/US7405204B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US20060241064A1 (en) | 2006-10-26 |
WO2006116557A1 (en) | 2006-11-02 |
US7405204B2 (en) | 2008-07-29 |
TW200720285A (en) | 2007-06-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR056327A1 (es) | Compuestos de nucleosidos para el tratamiento de infecciones virales | |
RU2500680C2 (ru) | Новые замещенные пиридин-2-оны и пиридазин-3-оны | |
AR057023A1 (es) | Compuestos heterociclicos con propiedades inhibidoras de hiv-integrasa | |
ECSP055815A (es) | Composición para el tratamiento de la infección por virus flaviviridae | |
AR052458A1 (es) | Amino-imidazolonas para la inhibicion de beta-secretasa | |
AR085327A1 (es) | Inhibidores del virus de la hepatitis c | |
EA200970478A1 (ru) | Аналоги тиофена для лечения или предупреждения флавивирусных инфекций | |
NZ630259A (en) | Heterobicyclic compounds as beta-lactamase inhibitors | |
AR067105A1 (es) | Moleculas pequenas que contienen boro | |
EA200970493A1 (ru) | Макроциклические ингибиторы вируса гепатита с | |
CO6231002A2 (es) | Compuestos utiles como ligandos para tomar imagenes de inervacion cardiaca | |
HRP20120523T1 (hr) | Inhibitori virusa hepatitisa c | |
AR053120A1 (es) | Aminopiridinas como inhibidores de beta secretasa | |
PE20130375A1 (es) | Compuestos de triazolopiridinas y triazolopirazinas inhibidores de c-met y composiciones de los mismos | |
EA200800476A1 (ru) | Макроциклические ингибиторы вируса гепатита с | |
AR078157A1 (es) | Derivados de pirazol-[4,5-d]pirrolo[2,3-b]piridina inhibidores de tirosinquinasas jak 2, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del cancer | |
AR064319A1 (es) | Compuestos y composiciones farmaceuticas derivadas de sulfonamida ciclicos, proceso de preparacion y usos en el tratamiento de trastornos vasomotrices, sexuales, gastrointestinales y otros | |
DE602004031258D1 (de) | Polycyclische mittel zur behandlung von infektione | |
TW200635585A (en) | Monocyclic substituted methanones | |
EA201000017A1 (ru) | Предварительная композиция серного цемента и способ приготовления предварительной композиции серного цемента | |
ECSP077402A (es) | Derivados de 2-amido-4-feniltiazol, su preparación y su aplicación en terapéutica | |
AR080185A1 (es) | Derivados de acido boronico y benzofurano, composiciones farmaceuticas que los contienen,y uso de los mismos en el tratamiento y/o prevencion de infecciones virales, en particular por el virus de hepatitis c(hcv). | |
RU2009146124A (ru) | Дигидрохиноновые и дигидронафтиридиновые ингибиторы киназы jnk | |
CO6321159A2 (es) | Compuestos pirazina fusionados utiles para el tratamiento de enfermedades degenerativas e inflamatorias | |
PE20220252A1 (es) | Compuestos de pirrol |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |