AR056202A1 - Nucleosidos modificados en 4' como agentes antivirales - Google Patents
Nucleosidos modificados en 4' como agentes antiviralesInfo
- Publication number
- AR056202A1 AR056202A1 ARP060104218A ARP060104218A AR056202A1 AR 056202 A1 AR056202 A1 AR 056202A1 AR P060104218 A ARP060104218 A AR P060104218A AR P060104218 A ARP060104218 A AR P060104218A AR 056202 A1 AR056202 A1 AR 056202A1
- Authority
- AR
- Argentina
- Prior art keywords
- nhr4
- optionally substituted
- value
- unsubstituted
- nr4nh2
- Prior art date
Links
Classifications
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- 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
- A61K31/7068—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 having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—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 having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
-
- 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
- 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
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P31/20—Antivirals for DNA 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
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Biotechnology (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Compuestos, métodos y composiciones para tratar un huésped infectado con virus de inmunodeficiencia humana y virus de hepatitis B, método que comprende administrar una cantidad efectiva de un 4'-C-substituido-b-D- y b-L-nucleosido o una sal o prodroga farmacéuticamente aceptable del mismo. Reivindicacion 1: Un compuesto caracterizado porque comprende un b-D- y b-L-nucleosido o una sal o prodroga farmacéuticamente aceptable del mismo, que tiene una estructura definida por la formula (1) o por la formula (2), donde X es hidrogeno, F, Cl, Br, I, NH2, NHR4, NR4R5, NHOH, NHOR4, NHNH2, NR4NH2, NHNHR4, SH, SR4, S(O)bR4, OH, OR4, N3, CN, o CF3; Y es hidrogeno, F, Cl, Br, I, NH2, NHR4, NR4R5, NHOH, NHOR4, NHNH2, NR4NH2, NHNHR4, SH, SR4, S(O)bR4, OH, OR4, N3, CN, CF3, hidroximetilo, metilo, etilo opcionalmente substituido o no substituido, vinilo opcionalmente substituido o no substituido, 2-bromovinilo opcionalmente substituido o no substituido, etinilo opcionalmente substituido o no substituido; R1 es F o N3; R2 es OH, OR4, OC(O)R4, OPvO3vMxR4yR5z, PvO3vMxR4yR5z, OCH2PvO3vMxR4yR5z, OP(O)(OQ)a(NHR4)b, SH, SR4, S(O)bR4, SC(O)R4, NH2, NHC(O)R4, NHR4, NR4R5, NHOH, NHOR4, NHNH2, NR4NH2, NHNHR4; R3 es F, ciano, azido, etinilo, clorovinilo, fluorovinilo, alquilo C1-6, alquilo C1-6 substituido con uno a tres átomos de halogeno, alquenilo C1-6 o alquinilo C1-6 con la condicion que cuando R1 es N3, entonces R3 no es hidroximetilo; Z es O, S, CH2 o C=CH2; A es N, CH, o CF; y R4 y R5 son iguales o diferentes y son alquilo inferior, alquenilo inferior, acilo de 1-17 átomos de carbono, arilo, o aralquilo; M es al menos un miembro seleccionado del grupo formado por H+, Na+, y K+; v tiene un valor de 1, 2, o 3; x, y, y z son independientes entre sí y tienen un valor de 0, 1, 2, 3 o 4; y a tiene un valor de 0 o 1, b tiene un valor de 1 o 2, y Q es M o R4.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72038805P | 2005-09-26 | 2005-09-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR056202A1 true AR056202A1 (es) | 2007-09-26 |
Family
ID=37900393
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060104218A AR056202A1 (es) | 2005-09-26 | 2006-09-27 | Nucleosidos modificados en 4' como agentes antivirales |
Country Status (17)
Country | Link |
---|---|
US (1) | US8569478B2 (es) |
EP (2) | EP3159351A3 (es) |
JP (1) | JP2009510075A (es) |
KR (1) | KR20080065272A (es) |
CN (2) | CN101310021A (es) |
AR (1) | AR056202A1 (es) |
AU (1) | AU2006294807B2 (es) |
BR (1) | BRPI0616738A2 (es) |
CA (2) | CA2623522C (es) |
EA (1) | EA200800932A1 (es) |
ES (1) | ES2617582T3 (es) |
IL (1) | IL190390A0 (es) |
NZ (3) | NZ609146A (es) |
PT (1) | PT1937825T (es) |
UY (1) | UY29868A1 (es) |
WO (1) | WO2007038507A2 (es) |
ZA (1) | ZA200802723B (es) |
Families Citing this family (44)
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MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
US7824851B2 (en) | 2002-11-15 | 2010-11-02 | Idenix Pharmaceuticals, Inc. | 2′-branched nucleosides and Flaviviridae mutation |
PT2604620T (pt) | 2003-05-30 | 2016-08-18 | Gilead Pharmasset Llc | Analogos de nucleósido fluorados modificados |
CN100532388C (zh) * | 2007-07-16 | 2009-08-26 | 郑州大学 | 2’-氟-4’-取代-核苷类似物、其制备方法及应用 |
WO2009052050A1 (en) * | 2007-10-15 | 2009-04-23 | Pharmasset, Inc. | Dioxolane thymine phosphoramidates as anti-hiv agents |
US20090318380A1 (en) | 2007-11-20 | 2009-12-24 | Pharmasset, Inc. | 2',4'-substituted nucleosides as antiviral agents |
SG194404A1 (en) | 2008-12-23 | 2013-11-29 | Gilead Pharmasset Llc | Synthesis of purine nucleosides |
AR074897A1 (es) | 2008-12-23 | 2011-02-23 | Pharmasset Inc | Fosforamidatos de nucleosidos |
AU2009329917B2 (en) | 2008-12-23 | 2016-03-31 | Gilead Pharmasset Llc | Nucleoside analogs |
CA2782524A1 (en) * | 2009-12-17 | 2011-06-23 | Novadex Pharmaceuticals Ab | 3'-deoxy-3'-methylidene-.beta.-l-nucleosides |
PT2609923T (pt) | 2010-03-31 | 2017-08-30 | Gilead Pharmasset Llc | Processo para a cristalização de 2-(((s)- (perfluorofenoxi)(fenoxi)fosforil)amino)propanoato de (s)-isopropilo |
JP2014514295A (ja) | 2011-03-31 | 2014-06-19 | 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 | ウイルス感染の治療のための化合物および薬学的組成物 |
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PE20141056A1 (es) | 2011-09-16 | 2014-09-05 | Gilead Pharmasset Llc | Metodos para el tratamiento de vhc |
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US9109001B2 (en) | 2012-05-22 | 2015-08-18 | Idenix Pharmaceuticals, Inc. | 3′,5′-cyclic phosphoramidate prodrugs for HCV infection |
MX355708B (es) | 2012-05-22 | 2018-04-27 | Idenix Pharmaceuticals Llc | Compuestos de d-aminoacidos para enfermedades del higado. |
US9296778B2 (en) | 2012-05-22 | 2016-03-29 | Idenix Pharmaceuticals, Inc. | 3′,5′-cyclic phosphate prodrugs for HCV infection |
EP2852583A1 (en) | 2012-05-23 | 2015-04-01 | Bristol-Myers Squibb Company | Sulfilimine and sulphoxide methods for producing festinavir |
AP3545A (en) | 2012-05-25 | 2016-01-14 | Janssen Sciences Ireland Uc | Uracyl spirooxetane nucleosides |
US9192621B2 (en) | 2012-09-27 | 2015-11-24 | Idenix Pharmaceuticals Llc | Esters and malonates of SATE prodrugs |
EP2906579B1 (en) | 2012-10-08 | 2018-04-18 | Idenix Pharmaceuticals LLC. | 2'-chloro nucleoside analogs for hcv infection |
WO2014066239A1 (en) | 2012-10-22 | 2014-05-01 | Idenix Pharmaceuticals, Inc. | 2',4'-bridged nucleosides for hcv infection |
US9211300B2 (en) | 2012-12-19 | 2015-12-15 | Idenix Pharmaceuticals Llc | 4′-fluoro nucleosides for the treatment of HCV |
MX351816B (es) | 2013-01-31 | 2017-10-30 | Gilead Pharmasset Llc | Formulacion de combinacion de dos compuestos antivirales. |
EP2970358B1 (en) | 2013-03-04 | 2021-06-30 | Idenix Pharmaceuticals LLC | 3'-deoxy nucleosides for the treatment of hcv |
WO2014137930A1 (en) | 2013-03-04 | 2014-09-12 | Idenix Pharmaceuticals, Inc. | Thiophosphate nucleosides for the treatment of hcv |
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EP2981542B1 (en) | 2013-04-01 | 2021-09-15 | Idenix Pharmaceuticals LLC | 2',4'-fluoro nucleosides for the treatment of hcv |
US20160060252A1 (en) | 2013-04-16 | 2016-03-03 | Bristol-Myers Squibb Company | 5-methyluridine method for producing festinavir |
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EP4483875A2 (en) | 2016-05-10 | 2025-01-01 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
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CN109562107A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的杂环降解决定子体 |
CA3169348A1 (en) | 2020-03-20 | 2021-09-23 | Gilead Sciences, Inc. | Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same |
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EP4431100A4 (en) * | 2021-11-12 | 2025-01-15 | Univ Hokkaido Nat Univ Corp | ANTIVIRAL AGENT |
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2006
- 2006-09-26 CN CNA2006800423211A patent/CN101310021A/zh active Pending
- 2006-09-26 EA EA200800932A patent/EA200800932A1/ru unknown
- 2006-09-26 CA CA2623522A patent/CA2623522C/en not_active Expired - Fee Related
- 2006-09-26 CA CA2904692A patent/CA2904692A1/en not_active Abandoned
- 2006-09-26 PT PT68251206T patent/PT1937825T/pt unknown
- 2006-09-26 EP EP16201801.4A patent/EP3159351A3/en not_active Withdrawn
- 2006-09-26 US US12/067,995 patent/US8569478B2/en active Active
- 2006-09-26 AU AU2006294807A patent/AU2006294807B2/en not_active Ceased
- 2006-09-26 NZ NZ609146A patent/NZ609146A/en not_active IP Right Cessation
- 2006-09-26 ES ES06825120.6T patent/ES2617582T3/es active Active
- 2006-09-26 EP EP06825120.6A patent/EP1937825B1/en active Active
- 2006-09-26 BR BRPI0616738-1A patent/BRPI0616738A2/pt not_active Application Discontinuation
- 2006-09-26 JP JP2008533517A patent/JP2009510075A/ja active Pending
- 2006-09-26 NZ NZ597544A patent/NZ597544A/xx not_active IP Right Cessation
- 2006-09-26 KR KR1020087009645A patent/KR20080065272A/ko active Search and Examination
- 2006-09-26 NZ NZ567272A patent/NZ567272A/en not_active IP Right Cessation
- 2006-09-26 CN CN2012103530710A patent/CN102924549A/zh active Pending
- 2006-09-26 WO PCT/US2006/037470 patent/WO2007038507A2/en active Application Filing
- 2006-09-27 AR ARP060104218A patent/AR056202A1/es unknown
- 2006-10-17 UY UY29868A patent/UY29868A1/es not_active Application Discontinuation
-
2008
- 2008-03-24 IL IL190390A patent/IL190390A0/en unknown
- 2008-03-27 ZA ZA200802723A patent/ZA200802723B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
EP3159351A2 (en) | 2017-04-26 |
EP3159351A3 (en) | 2017-05-17 |
WO2007038507A2 (en) | 2007-04-05 |
WO2007038507A3 (en) | 2007-09-13 |
KR20080065272A (ko) | 2008-07-11 |
NZ567272A (en) | 2012-02-24 |
CN101310021A (zh) | 2008-11-19 |
ES2617582T3 (es) | 2017-06-19 |
NZ609146A (en) | 2014-08-29 |
AU2006294807A1 (en) | 2007-04-05 |
PT1937825T (pt) | 2017-03-08 |
CA2623522A1 (en) | 2007-04-05 |
JP2009510075A (ja) | 2009-03-12 |
CA2904692A1 (en) | 2007-04-05 |
BRPI0616738A2 (pt) | 2011-06-28 |
EP1937825B1 (en) | 2016-12-21 |
EP1937825A4 (en) | 2010-06-23 |
EP1937825A2 (en) | 2008-07-02 |
ZA200802723B (en) | 2009-03-25 |
CN102924549A (zh) | 2013-02-13 |
AU2006294807B2 (en) | 2013-01-17 |
CA2623522C (en) | 2015-12-08 |
IL190390A0 (en) | 2008-11-03 |
US8569478B2 (en) | 2013-10-29 |
EA200800932A1 (ru) | 2008-10-30 |
NZ597544A (en) | 2013-04-26 |
UY29868A1 (es) | 2007-04-30 |
US20110021454A1 (en) | 2011-01-27 |
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