AP2412A - Phosphonate analogs of HIV inhibitor compounds. - Google Patents
Phosphonate analogs of HIV inhibitor compounds.Info
- Publication number
- AP2412A AP2412A AP2007003912A AP2007003912A AP2412A AP 2412 A AP2412 A AP 2412A AP 2007003912 A AP2007003912 A AP 2007003912A AP 2007003912 A AP2007003912 A AP 2007003912A AP 2412 A AP2412 A AP 2412A
- Authority
- AP
- ARIPO
- Prior art keywords
- inhibitor compounds
- hiv inhibitor
- phosphonate analogs
- phosphonate
- analogs
- Prior art date
Links
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 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
- C07H19/16—Purine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/662—Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/683—Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
-
- 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
-
- 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
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
-
- 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
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US59181104P | 2004-07-27 | 2004-07-27 | |
PCT/US2005/026504 WO2006110157A2 (fr) | 2004-07-27 | 2005-07-26 | Analogues phosphonates de composes inhibiteurs du vih |
Publications (2)
Publication Number | Publication Date |
---|---|
AP2007003912A0 AP2007003912A0 (en) | 2007-02-28 |
AP2412A true AP2412A (en) | 2012-06-01 |
Family
ID=35502668
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AP2007003912A AP2412A (en) | 2004-07-27 | 2005-07-26 | Phosphonate analogs of HIV inhibitor compounds. |
AP2007003899A AP2629A (en) | 2004-07-27 | 2005-07-27 | Nucleoside phosphonate conjugates as anti HIV agents |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AP2007003899A AP2629A (en) | 2004-07-27 | 2005-07-27 | Nucleoside phosphonate conjugates as anti HIV agents |
Country Status (36)
Country | Link |
---|---|
US (11) | US7871991B2 (fr) |
EP (4) | EP2258376B1 (fr) |
JP (3) | JP2008508291A (fr) |
KR (2) | KR101233824B1 (fr) |
CN (4) | CN101027062A (fr) |
AP (2) | AP2412A (fr) |
AR (1) | AR051922A1 (fr) |
AT (2) | ATE505196T1 (fr) |
AU (2) | AU2005330489B2 (fr) |
BR (2) | BRPI0512690A (fr) |
CA (2) | CA2574514A1 (fr) |
CY (2) | CY1111709T1 (fr) |
DE (2) | DE602005027466D1 (fr) |
DK (2) | DK1778251T3 (fr) |
EA (2) | EA019419B1 (fr) |
ES (3) | ES2363160T3 (fr) |
HK (2) | HK1103648A1 (fr) |
HR (4) | HRP20070078A2 (fr) |
HU (1) | HUE043207T2 (fr) |
IL (2) | IL180758A (fr) |
IS (2) | IS8595A (fr) |
LT (1) | LT2258376T (fr) |
ME (2) | ME03423B (fr) |
MX (2) | MX2007001053A (fr) |
NO (5) | NO339020B1 (fr) |
NZ (2) | NZ553405A (fr) |
PL (4) | PL1778251T3 (fr) |
PT (2) | PT1778251E (fr) |
RS (2) | RS58600B1 (fr) |
SG (1) | SG155164A1 (fr) |
SI (2) | SI1778251T1 (fr) |
TR (1) | TR201906416T4 (fr) |
TW (1) | TWI362934B (fr) |
UA (2) | UA88313C2 (fr) |
WO (2) | WO2006110157A2 (fr) |
ZA (2) | ZA200701465B (fr) |
Families Citing this family (142)
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 |
US7824851B2 (en) | 2002-11-15 | 2010-11-02 | Idenix Pharmaceuticals, Inc. | 2′-branched nucleosides and Flaviviridae mutation |
WO2004096286A2 (fr) | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Analogues de phosphonate antiviraux |
ES2363160T3 (es) * | 2004-07-27 | 2011-07-22 | Gilead Sciences, Inc. | Conjugados de fosfonato nucelosidico como agentes anti-vih. |
CA2616314A1 (fr) * | 2005-07-27 | 2007-02-01 | Gilead Sciences, Inc. | Composes antiviraux |
US8895531B2 (en) * | 2006-03-23 | 2014-11-25 | Rfs Pharma Llc | 2′-fluoronucleoside phosphonates as antiviral agents |
US8324179B2 (en) | 2007-02-09 | 2012-12-04 | Gilead Sciences, Inc. | Nucleoside analogs for antiviral treatment |
WO2008098374A1 (fr) * | 2007-02-16 | 2008-08-21 | Affinium Pharmaceuticals, Inc. | Sels, promédicaments et polymorphes d'inhibiteurs de fab 1 |
US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
US8173621B2 (en) * | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
AU2009268681B2 (en) | 2008-07-08 | 2014-10-02 | Gilead Sciences, Inc. | Salts of HIV inhibitor compounds |
TW201031675A (en) * | 2008-12-23 | 2010-09-01 | Pharmasset Inc | Synthesis of purine nucleosides |
US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
TWI598358B (zh) | 2009-05-20 | 2017-09-11 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
UY33311A (es) | 2010-03-31 | 2011-10-31 | Pharmasset Inc | Fosforamidatos de nucleosidos |
US8563530B2 (en) | 2010-03-31 | 2013-10-22 | Gilead Pharmassel LLC | Purine nucleoside phosphoramidate |
US8841275B2 (en) | 2010-11-30 | 2014-09-23 | Gilead Pharmasset Llc | 2′-spiro-nucleosides and derivatives thereof useful for treating hepatitis C virus and dengue virus infections |
CA2843324A1 (fr) | 2011-03-31 | 2012-11-15 | Idenix Pharmaceuticals, Inc. | Composes et compositions pharmaceutiques pour le traitement d'infections virales |
TWI635093B (zh) | 2011-05-19 | 2018-09-11 | 基利科學股份有限公司 | 用於製備抗hiv藥劑的方法與中間物 |
WO2013006738A1 (fr) | 2011-07-06 | 2013-01-10 | Gilead Sciences, Inc. | Composés pour traiter le vih |
EP2567961A1 (fr) | 2011-09-08 | 2013-03-13 | Straitmark Holding AG | Procédé pour la fabrication de composés contenant un groupe alpha-oxyphosphore en utilisant un activateur |
EP2755983B1 (fr) | 2011-09-12 | 2017-03-15 | Idenix Pharmaceuticals LLC. | Composés de carbonyloxyméthylphosphoramidate substitué et compositions pharmaceutiques servant à traiter les infections virales |
SI2709613T2 (sl) | 2011-09-16 | 2020-12-31 | Gilead Pharmasset LLC c/o Gilead Sciences, Inc. | Postopki za zdravljenje HCV |
MX353064B (es) * | 2011-10-07 | 2017-12-19 | Gilead Sciences Inc | Metodos para preparar analogos nucleotidicos antivirales. |
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 |
US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
CA2856722C (fr) | 2011-11-30 | 2022-11-22 | Emory University | Inhibiteurs de jak antiviraux utiles dans le traitement ou la prevention d'infections retrovirales et autres infections virales |
WO2013177195A1 (fr) | 2012-05-22 | 2013-11-28 | Idenix Pharmaceuticals, Inc. | Promédicaments de 3',5'-phosphate cyclique pour traiter une infection par le virus de l'hépatite c |
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. |
EP2861611B1 (fr) | 2012-05-25 | 2016-07-13 | Janssen Sciences Ireland UC | Nucléosides dýuracyle spirooxetane |
WO2014052638A1 (fr) | 2012-09-27 | 2014-04-03 | Idenix Pharmaceuticals, Inc. | Esters et malonates de promédicaments à base de s-acyl-2-thioéthyle (sate) |
CA2887578A1 (fr) | 2012-10-08 | 2014-04-17 | Idenix Pharamaceuticals, Inc. | Analogues de nucleosides 2'-chloro pour traiter une infection par le virus de l'hepatite c |
US10723754B2 (en) | 2012-10-22 | 2020-07-28 | Idenix Pharmaceuticals Llc | 2′,4′-bridged nucleosides for HCV infection |
EP2935304A1 (fr) | 2012-12-19 | 2015-10-28 | IDENIX Pharmaceuticals, Inc. | 4'-fluoro-nucléosides pour le traitement du vhc |
SG11201504235UA (en) * | 2012-12-28 | 2015-07-30 | Blend Therapeutics Inc | Targeted conjugates encapsulated in particles and formulations thereof |
SG11201506021XA (en) | 2013-01-31 | 2015-08-28 | Gilead Pharmasset Llc | Combination formulation of two antiviral compounds |
US9309275B2 (en) | 2013-03-04 | 2016-04-12 | Idenix Pharmaceuticals Llc | 3′-deoxy 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 |
EP2970357A1 (fr) | 2013-03-13 | 2016-01-20 | IDENIX Pharmaceuticals, Inc. | Pronucléotides de phosphoramidate d'acide aminé de 2'-cyano, azido et amino nucléosides pour le traitement du virus de l'hépatite c (vhc) |
WO2014165542A1 (fr) | 2013-04-01 | 2014-10-09 | Idenix Pharmaceuticals, Inc. | 2',4'-fluoronucléosides pour le traitement du vhc |
EP3004130B1 (fr) | 2013-06-05 | 2019-08-07 | Idenix Pharmaceuticals LLC. | 1',4'-thio nucléosides pour le traitement du virus de l'hépatite c (vhc) |
US20150037282A1 (en) | 2013-08-01 | 2015-02-05 | Idenix Pharmaceuticals, Inc. | D-amino acid phosphoramidate pronucleotides of halogeno pyrimidine compounds for liver disease |
MX2016002185A (es) | 2013-08-27 | 2016-06-06 | Gilead Pharmasset Llc | Formulacion combinada de dos compuestos antivirales. |
EP3131914B1 (fr) | 2014-04-16 | 2023-05-10 | Idenix Pharmaceuticals LLC | Nucléosides méthyle ou alcynyle substitués en position 3 pour le traitement du virus de l'hépatite c |
EP3273028B1 (fr) * | 2014-05-28 | 2019-07-10 | Volvo Truck Corporation | Une unité de turborécupération |
NO2717902T3 (fr) | 2014-06-20 | 2018-06-23 | ||
TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
WO2016030863A1 (fr) | 2014-08-29 | 2016-03-03 | Glaxosmithkline Intellectual Property Development Limited | Composés et méthodes de traitement des infections virales |
US20160067255A1 (en) | 2014-09-04 | 2016-03-10 | Gilead Sciences, Inc. | Methods of treating or preventing hiv in patients using a combination of tenofovir alafenamide and dolutegravir |
TWI738321B (zh) | 2014-12-23 | 2021-09-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
PT3237397T (pt) | 2014-12-24 | 2019-02-08 | Gilead Sciences Inc | Compostos de isoquinolina para o tratamento de hiv |
MX2017008520A (es) | 2014-12-24 | 2018-03-01 | Gilead Sciences Inc | Compuestos de pirimidina fusionada para el tratamiento del virus de inmunodeficiencia humana (vih). |
TWI770552B (zh) | 2014-12-24 | 2022-07-11 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
RS62434B1 (sr) | 2014-12-26 | 2021-11-30 | Univ Emory | Antivirusni n4-hidroksicitidin derivati |
SI3097102T1 (en) | 2015-03-04 | 2018-02-28 | Gilead Sciences, Inc. | A TOOL RECEPTOR MODULING 4,6-DIAMINO-PYRIDO (3,2-D) PYRIMIDINE COMPOUNDS |
NZ735575A (en) | 2015-04-02 | 2018-11-30 | Gilead Sciences Inc | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
CA2995004A1 (fr) | 2015-08-26 | 2017-03-02 | Gilead Sciences, Inc. | Modulateurs deuteres du recepteur toll |
NZ741785A (en) | 2015-09-30 | 2019-07-26 | Gilead Sciences Inc | 3-cyano-1h-1,2,4-triazol-1-yl compounds and uses thereof for the treatment of hiv |
KR102165120B1 (ko) | 2015-12-15 | 2020-10-13 | 길리애드 사이언시즈, 인코포레이티드 | 인간 면역결핍 바이러스 중화 항체 |
TWI740910B (zh) * | 2016-03-09 | 2021-10-01 | 美商艾洛斯生物製藥公司 | 非環抗病毒劑 |
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 |
WO2017197036A1 (fr) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Dégronimères spirocycliques pour la dégradation de protéines cibles |
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 |
PL3597646T3 (pl) | 2016-08-19 | 2023-12-11 | Gilead Sciences, Inc. | Związki terapeutyczne użyteczne do profilaktycznego lub terapeutycznego leczenia zakażenia wirusem HIV |
WO2018042332A1 (fr) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinaisons, utilisations et traitements correspondants |
WO2018042331A1 (fr) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinaisons, utilisations et traitements correspondants |
US10370342B2 (en) | 2016-09-02 | 2019-08-06 | Gilead Sciences, Inc. | Toll like receptor modulator compounds |
ES2826748T3 (es) | 2016-09-02 | 2021-05-19 | Gilead Sciences Inc | Derivados de 4,6-diamino-pirido[3,2-d]pirimidina como moduladores de receptores de tipo Toll |
WO2018051250A1 (fr) | 2016-09-14 | 2018-03-22 | Viiv Healthcare Company | Combinaison comprenant du ténofovir alafénamide, du bictégravir et du 3tc |
EP3518935A1 (fr) | 2016-09-27 | 2019-08-07 | Gilead Sciences, Inc. | Compositions thérapeutiques pour le traitement du virus de l'immunodéficience humaine |
US10800772B2 (en) | 2016-09-28 | 2020-10-13 | Gilead Sciences, Inc. | Therapeutic compounds |
EP3532478B1 (fr) | 2016-10-27 | 2021-05-26 | Gilead Sciences, Inc. | Forme crystalline de darunavir base libre |
TWI820984B (zh) | 2017-01-31 | 2023-11-01 | 美商基利科學股份有限公司 | 替諾福韋埃拉酚胺(tenofovir alafenamide)之晶型 |
JOP20180009A1 (ar) | 2017-02-06 | 2019-01-30 | Gilead Sciences Inc | مركبات مثبط فيروس hiv |
US20190374557A1 (en) * | 2017-02-28 | 2019-12-12 | Alexandre Vasilievich Ivachtchenko | Cyclobutyl (S)-2-[[[(R)-2-(6-aminopurin-9-yl)-1-methyl-ethoxy]methyl-phenoxy-phosphoryl]amino]-propanoates, and production process and application thereof |
WO2018237148A1 (fr) | 2017-06-21 | 2018-12-27 | Gilead Sciences, Inc. | Anticorps multispécifiques ciblant gp120 et cd3 du vih |
WO2019027920A1 (fr) | 2017-08-01 | 2019-02-07 | Gilead Sciences, Inc. | Formes cristallines d'éthyl ((s)-((((2r,5r)-5-(6-amino-9h-purin-9-yl)-4-fluoro-2,5-dihydrofuran-2-yl)oxy)méthyl)(phénoxy)phosphoryl)-l-alaninate (gs-9131) pour le traitement d'infections virales |
TW202024061A (zh) | 2017-08-17 | 2020-07-01 | 美商基利科學股份有限公司 | Hiv蛋白質膜抑制劑之固體形式 |
AR112412A1 (es) | 2017-08-17 | 2019-10-23 | Gilead Sciences Inc | Formas de sal de colina de un inhibidor de la cápside del vih |
JOP20180092A1 (ar) | 2017-10-13 | 2019-04-13 | Gilead Sciences Inc | مثبطات hiv بروتياز |
US20190151307A1 (en) | 2017-10-24 | 2019-05-23 | Gilead Sciences, Inc. | Methods of treating patients co-infected with a virus and tuberculosis |
KR102626210B1 (ko) | 2017-12-07 | 2024-01-18 | 에모리 유니버시티 | N4-하이드록시사이티딘 및 유도체 및 이와 관련된 항-바이러스 용도 |
CN111566120B (zh) | 2017-12-20 | 2023-09-29 | 捷克共和国有机化学与生物化学研究所 | 活化sting转接蛋白的具有膦酸酯键的3’3’环状二核苷酸 |
JP7098748B2 (ja) | 2017-12-20 | 2022-07-11 | インスティチュート オブ オーガニック ケミストリー アンド バイオケミストリー エーエスシーアール,ヴイ.ヴイ.アイ. | Stingアダプタータンパク質を活性化するホスホン酸結合を有する2’3’環状ジヌクレオチド |
US10836746B2 (en) | 2018-02-15 | 2020-11-17 | Gilead Sciences, Inc. | Therapeutic compounds |
CA3175384A1 (fr) | 2018-02-16 | 2019-08-22 | Gilead Sciences, Inc. | Methodes et intermediaires pour preparer des composes therapeutiques utiles dans le traitement d'une infection virale des retroviridae |
TWI833744B (zh) | 2018-04-06 | 2024-03-01 | 捷克科學院有機化學與生物化學研究所 | 3'3'-環二核苷酸 |
TWI818007B (zh) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-環二核苷酸 |
TW202005654A (zh) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2,2,─環二核苷酸 |
WO2019211799A1 (fr) | 2018-05-03 | 2019-11-07 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | Analogue de dinucléotide 2'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle |
PE20210685A1 (es) | 2018-07-03 | 2021-04-08 | Gilead Sciences Inc | Anticuerpos que se dirigen al gp120 de vih y metodos de uso |
CN112423750A (zh) | 2018-07-16 | 2021-02-26 | 吉利德科学公司 | 用于治疗hiv的衣壳抑制剂 |
TWI829205B (zh) | 2018-07-30 | 2024-01-11 | 美商基利科學股份有限公司 | 抗hiv化合物 |
EP3860717A1 (fr) | 2018-10-03 | 2021-08-11 | Gilead Sciences, Inc. | Dérivés d'imidozopyrimidine |
SG11202103839UA (en) | 2018-10-31 | 2021-05-28 | Gilead Sciences Inc | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
AU2019373221B2 (en) | 2018-10-31 | 2022-05-26 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds having HPK1 inhibitory activity |
WO2020176505A1 (fr) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Agonistes de protéine kinase c |
WO2020176510A1 (fr) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Agonistes de protéine kinase c |
CA3129022C (fr) | 2019-03-07 | 2023-08-01 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | Dinucleotides cycliques en 2'3' et leurs promedicaments |
WO2020178768A1 (fr) | 2019-03-07 | 2020-09-10 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | Analogue du dinucléotide 3'3'-cyclique comprenant un nucléotide modifié par cyclopentanyle utilisé en tant que modulateur de sting |
EP3935066A1 (fr) | 2019-03-07 | 2022-01-12 | Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. | Dinucléotides 3'3'-cycliques et leurs promédicaments |
KR20210142711A (ko) | 2019-03-22 | 2021-11-25 | 길리애드 사이언시즈, 인코포레이티드 | 가교된 트리시클릭 카르바모일피리돈 화합물 및 그의 제약 용도 |
TWI751516B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
TW202104210A (zh) | 2019-04-17 | 2021-02-01 | 美商基利科學股份有限公司 | Hiv蛋白酶抑制劑 |
WO2020214647A1 (fr) | 2019-04-17 | 2020-10-22 | Gilead Sciences, Inc. | Formes solides d'un inhibiteur de protéase du vih |
TWI751517B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
TWI762925B (zh) | 2019-05-21 | 2022-05-01 | 美商基利科學股份有限公司 | 鑑別對使用gp120 v3聚醣導向之抗體的治療敏感之hiv病患的方法 |
WO2020237025A1 (fr) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1 |
RU2717101C1 (ru) | 2019-06-03 | 2020-03-18 | Андрей Александрович Иващенко | Анелированные 9-гидрокси-1,8-диоксо-1,3,4,8-тетрагидро-2Н-пиридо[1,2-a]пиразин-7-карбоксамиды - ингибиторы интегразы ВИЧ, способы их получения и применения |
CA3140708A1 (fr) | 2019-06-18 | 2020-12-24 | Helen Horton | Association de vaccins contre le virus de l'hepatite b (vhb) et de derives de pyridopyrimidine |
KR20220032568A (ko) | 2019-06-25 | 2022-03-15 | 길리애드 사이언시즈, 인코포레이티드 | Flt3l-fc 융합 단백질 및 사용 방법 |
AU2020315598A1 (en) | 2019-07-16 | 2022-03-03 | Gilead Sciences, Inc. | HIV vaccines and methods of making and using |
US20220257619A1 (en) | 2019-07-18 | 2022-08-18 | Gilead Sciences, Inc. | Long-acting formulations of tenofovir alafenamide |
US20220296619A1 (en) | 2019-08-19 | 2022-09-22 | Gilead Sciences, Inc. | Pharmaceutical formulations of tenofovir alafenamide |
EP4065116A1 (fr) | 2019-11-26 | 2022-10-05 | Gilead Sciences, Inc. | Inhibiteurs de capside pour la prévention du vih |
EP4081305B1 (fr) | 2019-12-24 | 2024-09-18 | Carna Biosciences, Inc. | Composés modulant la diacylglycérol kinase |
JP7453399B2 (ja) | 2020-02-24 | 2024-03-19 | ギリアード サイエンシーズ, インコーポレイテッド | Hiv感染症を治療するための四環式化合物及びその使用 |
AR121620A1 (es) | 2020-03-20 | 2022-06-22 | Gilead Sciences Inc | Profármacos de nucleósidos 4-c-sustituidos-2-halo-2-deoxiadenosina y métodos de preparación y uso de los mismos |
EP4153181A1 (fr) | 2020-05-21 | 2023-03-29 | Gilead Sciences, Inc. | Compositions pharmaceutiques contenant du bictégravir |
WO2021262990A1 (fr) | 2020-06-25 | 2021-12-30 | Gilead Sciences, Inc. | Inhibiteurs de capside pour le traitement du vih |
BR112023002164A2 (pt) | 2020-08-07 | 2023-03-14 | Gilead Sciences Inc | Profármacos de análogos de nucleotídeos de fosfonamida e seu uso farmacêutico |
EP4228656A4 (fr) * | 2020-08-18 | 2024-09-04 | Yeda Res & Dev | Composés anti-viraux et anti-tumoraux |
CN114262348A (zh) * | 2020-09-16 | 2022-04-01 | 上海本仁科技有限公司 | 环状核苷磷酸酯类化合物及其应用 |
CN116390924A (zh) | 2020-09-30 | 2023-07-04 | 吉利德科学公司 | 桥连三环氨基甲酰基吡啶酮化合物及其用途 |
TWI815194B (zh) | 2020-10-22 | 2023-09-11 | 美商基利科學股份有限公司 | 介白素2-Fc融合蛋白及使用方法 |
EP4244396A1 (fr) | 2020-11-11 | 2023-09-20 | Gilead Sciences, Inc. | Procédés d'identification des patients vih sensibles à la thérapie avec des anticorps visant le site de liaison cd4 de la gp120 |
US11613546B2 (en) | 2021-01-19 | 2023-03-28 | Gilead Sciences, Inc. | Substituted pyridotriazine compounds and uses thereof |
WO2022245814A1 (fr) * | 2021-05-17 | 2022-11-24 | Rome Therapeutics, Inc. | Méthodes de traitement d'états médicaux et d'inhibition de la transcriptase inverse de la line1 à l'aide d'un acide 4-fluoro-2,5-dihydrofuranyle phosphonique substitué ou d'un composé apparenté |
WO2022245671A1 (fr) | 2021-05-18 | 2022-11-24 | Gilead Sciences, Inc. | Méthodes d'utilisation de protéines de fusion flt3l-fc |
EP4359415A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés modulant les diacylglycérol kinases |
AU2022297367A1 (en) | 2021-06-23 | 2023-12-07 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
KR20240025616A (ko) | 2021-06-23 | 2024-02-27 | 길리애드 사이언시즈, 인코포레이티드 | 다이아실글리세롤 키나제 조절 화합물 |
EP4359411A1 (fr) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Composés modulant les diacylglycérol kinases |
IL312718A (en) | 2021-12-03 | 2024-07-01 | Gilead Sciences Inc | Therapeutic compounds for HIV infection |
CN118355020A (zh) | 2021-12-03 | 2024-07-16 | 吉利德科学公司 | Hiv病毒感染的治疗性化合物 |
TW202342447A (zh) | 2021-12-03 | 2023-11-01 | 美商基利科學股份有限公司 | 用於hiv病毒感染之治療性化合物 |
TWI843506B (zh) | 2022-04-06 | 2024-05-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
TW202402280A (zh) | 2022-07-01 | 2024-01-16 | 美商基利科學股份有限公司 | 可用於hiv病毒感染之疾病預防性或治療性治療的治療性化合物 |
WO2024015741A1 (fr) | 2022-07-12 | 2024-01-18 | Gilead Sciences, Inc. | Polypeptides immunogènes du vih et vaccins et utilisations de ceux-ci |
US20240083984A1 (en) | 2022-08-26 | 2024-03-14 | Gilead Sciences, Inc. | Dosing and scheduling regimen for broadly neutralizing antibodies |
WO2024076915A1 (fr) | 2022-10-04 | 2024-04-11 | Gilead Sciences, Inc. | Analogues de 4'-thionucléosides et leur utilisation pharmaceutique |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003091264A2 (fr) * | 2002-04-26 | 2003-11-06 | Gilead Sciences, Inc. | Inhibiteurs non nucleosidiques de la transcriptase inverse |
Family Cites Families (183)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4276351A (en) | 1980-06-30 | 1981-06-30 | E. I. Du Pont De Nemours And Company | Polyvinyl butyral plasticized with tetraethyleneglycol di-2-ethylhexanoate |
US4816570A (en) | 1982-11-30 | 1989-03-28 | The Board Of Regents Of The University Of Texas System | Biologically reversible phosphate and phosphonate protective groups |
US4649041A (en) | 1983-07-20 | 1987-03-10 | Warner-Lambert Company | Magnesium trisilicate suitable for preparation of medicament adsorbates of antinauseants |
DK159431C (da) | 1984-05-10 | 1991-03-18 | Byk Gulden Lomberg Chem Fab | 6-phenyl-3(2h)-pyridazinoner, fremgangsmaade til fremstilling deraf, laegemidler indeholdende disse samt anvendelse af forbindelserne til fremstilling af laegemidler |
US4724232A (en) | 1985-03-16 | 1988-02-09 | Burroughs Wellcome Co. | Treatment of human viral infections |
CS263952B1 (en) | 1985-04-25 | 1989-05-12 | Holy Antonin | Remedy with antiviral effect |
JPH035439Y2 (fr) | 1985-06-04 | 1991-02-12 | ||
WO1987001284A1 (fr) | 1985-08-26 | 1987-03-12 | United States Of America, Represented By The Unite | Inhibition du caractere infectieux et de l'effet cytopathique du htlv-iii/lav in vitro par la 2',3'-dideoxyinosine, 2',3'-dideoxyguanosine, ou 2',3'-dideoxyadenosine |
US6492352B1 (en) | 1985-10-31 | 2002-12-10 | Astra Lakemedel Aktiebolag | Method for the control and treatment of acquired immunodeficiency syndrome (AIDS) |
US4968788A (en) | 1986-04-04 | 1990-11-06 | Board Of Regents, The University Of Texas System | Biologically reversible phosphate and phosphonate protective gruops |
US5455339A (en) * | 1986-05-01 | 1995-10-03 | University Of Georgia Research Foundation, Inc. | Method for the preparation of 2',3'-dideoxy and 2',3'-dideoxydide-hydro nucleosides |
IE63869B1 (en) | 1986-11-06 | 1995-06-14 | Res Dev Foundation | Aerosols containing liposomes and method for their preparation |
US4978655A (en) | 1986-12-17 | 1990-12-18 | Yale University | Use of 3'-deoxythymidin-2'-ene (3'deoxy-2',3'-didehydrothymidine) in treating patients infected with retroviruses |
FR2611203B1 (fr) | 1987-02-20 | 1989-06-09 | Sturtz Georges | Analogues gem-diphosphoniques d'amethopterine (methotrexate) et de derives deaza-n-10 amethopterine. leur preparation et les compositions pharmaceutiques qui les contiennent |
US5028595A (en) | 1987-09-18 | 1991-07-02 | Hoffmann-La Roche Inc. | Method for preventing AIDS in a subject or treating a subject infected with the AIDS virus |
US5631370A (en) | 1988-01-20 | 1997-05-20 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
US5466793A (en) * | 1988-03-01 | 1995-11-14 | Ajinomoto Co., Inc. | Process for preparing 2', 3'- dideoxyinosine |
US5047407A (en) | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties |
ZA894534B (en) * | 1988-06-20 | 1990-03-28 | Merrell Dow Pharma | Novel neplanocin derivatives |
GB8815265D0 (en) | 1988-06-27 | 1988-08-03 | Wellcome Found | Therapeutic nucleosides |
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 |
CA2001715C (fr) | 1988-11-14 | 1999-12-28 | Muzammil M. Mansuri | Nucleosides et nucleotides carbocycliques |
US5202128A (en) | 1989-01-06 | 1993-04-13 | F. H. Faulding & Co. Limited | Sustained release pharmaceutical composition |
US5366972A (en) | 1989-04-20 | 1994-11-22 | Boehringer Ingelheim Pharmaceuticals, Inc. | 5,11-dihydro-6H-dipyrido(3,2-B:2',3'-E)(1,4)diazepines and their use in the prevention or treatment of HIV infection |
CA2297294C (fr) * | 1989-05-15 | 2005-11-08 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Derives de phosphonomethoxymethylpurine/pyrimidine |
US5539122A (en) | 1989-05-23 | 1996-07-23 | Abbott Laboratories | Retroviral protease inhibiting compounds |
JP2722673B2 (ja) | 1989-05-31 | 1998-03-04 | 住友化学工業株式会社 | 光学活性なアシルビフェニル誘導体の製造法 |
GB8927915D0 (en) | 1989-12-11 | 1990-02-14 | Hoffmann La Roche | Novel alcohols |
GB8927913D0 (en) | 1989-12-11 | 1990-02-14 | Hoffmann La Roche | Amino acid derivatives |
US5563142A (en) | 1989-12-28 | 1996-10-08 | The Upjohn Company | Diaromatic substituted compounds as anti-HIV-1 agents |
US6642245B1 (en) | 1990-02-01 | 2003-11-04 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
US5204466A (en) | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
DE4003574A1 (de) | 1990-02-07 | 1991-08-08 | Bayer Ag | Neue dipeptide, verfahren zu ihrer herstellung und ihre verwendung als renininhibitoren in arzneimitteln |
WO1991019721A1 (fr) | 1990-06-13 | 1991-12-26 | Arnold Glazier | Promedicaments phosphoreux |
EP0465297B1 (fr) | 1990-07-04 | 1996-01-31 | Merrell Dow Pharmaceuticals Inc. | Dérivés d'acides 9-purinyl phosphoniques |
US5177064A (en) | 1990-07-13 | 1993-01-05 | University Of Florida | Targeted drug delivery via phosphonate derivatives |
EP0468119A1 (fr) | 1990-07-24 | 1992-01-29 | Merrell Dow Pharmaceuticals Inc. | Nouveaux analogues carbocycliques de certains nucléosides |
US5223618A (en) | 1990-08-13 | 1993-06-29 | Isis Pharmaceuticals, Inc. | 4'-desmethyl nucleoside analog compounds |
EP0481214B1 (fr) * | 1990-09-14 | 1998-06-24 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Pro-médicaments dérivés de phosphonates |
US5672697A (en) * | 1991-02-08 | 1997-09-30 | Gilead Sciences, Inc. | Nucleoside 5'-methylene phosphonates |
DE4111730A1 (de) | 1991-04-10 | 1992-10-15 | Knoll Ag | Neue cytarabin-derivate, ihre herstellung und verwendung |
JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
EP0531597A1 (fr) | 1991-09-12 | 1993-03-17 | Merrell Dow Pharmaceuticals Inc. | Dérivés acycliques insaturés d'acides phosphoniques puriniques ou pyrimidimiques |
US5610294A (en) | 1991-10-11 | 1997-03-11 | The Du Pont Merck Pharmaceutical Company | Substituted cyclic carbonyls and derivatives thereof useful as retroviral protease inhibitors |
US5413999A (en) | 1991-11-08 | 1995-05-09 | Merck & Co., Inc. | HIV protease inhibitors useful for the treatment of AIDS |
DE4138584A1 (de) | 1991-11-23 | 1993-05-27 | Hoechst Ag | Carbocyclische phosphonat-nucleotidanaloge, deren herstellung und verwendung |
GB9126144D0 (en) | 1991-12-10 | 1992-02-12 | British Bio Technology | Compounds |
FR2692265B1 (fr) | 1992-05-25 | 1996-11-08 | Centre Nat Rech Scient | Composes biologiquement actifs de type phosphotriesters. |
US5665720A (en) | 1992-08-07 | 1997-09-09 | Merck & Co., Inc. | Benzoxazinones as inhibitors of HIV reverse transcriptase |
IS2334B (is) | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
US5484926A (en) | 1993-10-07 | 1996-01-16 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
DE4308096A1 (de) | 1993-03-13 | 1994-09-15 | Hoechst Ag | Prodrug-Derivate von Enzyminhibitoren mit Hydroxylgruppen, Verfahren zu deren Herstellung und ihre Verwendung |
US5654286A (en) | 1993-05-12 | 1997-08-05 | Hostetler; Karl Y. | Nucleotides for topical treatment of psoriasis, and methods for using same |
CA2126601A1 (fr) | 1993-06-29 | 1994-12-30 | Mitsubishi Chemical Corporation | Derives d'ester phosphonate de nucleotide |
US5670497A (en) | 1993-07-14 | 1997-09-23 | Ciba-Geigy Corporation | Cyclic hydrazine compounds |
US5656745A (en) | 1993-09-17 | 1997-08-12 | Gilead Sciences, Inc. | Nucleotide analogs |
WO1995007920A1 (fr) | 1993-09-17 | 1995-03-23 | Gilead Sciences, Inc. | Analogues de nucleotides |
US5446137B1 (en) | 1993-12-09 | 1998-10-06 | Behringwerke Ag | Oligonucleotides containing 4'-substituted nucleotides |
US5493030A (en) | 1994-02-18 | 1996-02-20 | Syntex (U.S.A.) Inc. | 5-substituted derivatives of mycophenolic acid |
US5854227A (en) | 1994-03-04 | 1998-12-29 | Hartmann; John F. | Therapeutic derivatives of diphosphonates |
WO1997011092A1 (fr) | 1994-04-07 | 1997-03-27 | Nippon Shinyaku Co., Ltd. | Derives de phosphates de cyclosporine et composition medicinale |
BR9509024A (pt) | 1994-09-26 | 1997-09-30 | Shionogi & Co | Derivados de imidazol |
JP2002515849A (ja) | 1994-11-04 | 2002-05-28 | ギリアード サイエンシーズ,インコーポレイテッド | Hivプロテアーゼを阻害および検出するチエパン化合物 |
US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
ES2097703B1 (es) | 1995-04-12 | 1997-12-01 | Decox S L | Una nueva composicion estimulante de la actividad cerebral basada en alcaloides de nucleo de eburnamenina, y sus metodos de preparacion. |
US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
AU6299496A (en) | 1995-06-29 | 1997-01-30 | Novo Nordisk A/S | Novel substituted azabicyclic compounds |
US5750493A (en) | 1995-08-30 | 1998-05-12 | Raymond F. Schinazi | Method to improve the biological and antiviral activity of protease inhibitors |
US5646180A (en) | 1995-12-05 | 1997-07-08 | Vertex Pharmaceuticals Incorporated | Treatment of the CNS effects of HIV |
US5914332A (en) | 1995-12-13 | 1999-06-22 | Abbott Laboratories | Retroviral protease inhibiting compounds |
RU2106353C1 (ru) | 1996-03-19 | 1998-03-10 | Корпорация "С энд Ти Сайенс энд Текнолоджи Инк." | Соли 5'-н-фосфоната 3'- азидо-3'-дезокситимидина, являющиеся специфическими ингибиторами продукции вируса иммунодефицита человека вич-1 и вич-2 |
US5874577A (en) | 1996-04-03 | 1999-02-23 | Medichem Research, Inc. | Method for the preparing 9-12-(Diethoxyphosphonomethoxy)ethyl!adenine and analogues thereof |
US5849911A (en) | 1996-04-22 | 1998-12-15 | Novartis Finance Corporation | Antivirally active heterocyclic azahexane derivatives |
US5795909A (en) | 1996-05-22 | 1998-08-18 | Neuromedica, Inc. | DHA-pharmaceutical agent conjugates of taxanes |
CA2261619C (fr) | 1996-07-26 | 2006-05-23 | Gilead Sciences, Inc. | Analogues de nucleotides |
US6194398B1 (en) | 1996-08-13 | 2001-02-27 | Mitsubishi Chemical Corporation | Phosphonate nucleotide compound |
CA2266404A1 (fr) | 1996-09-17 | 1998-03-26 | Amur Pharmaceuticals, Inc. | Derives de medicaments phospholipidiques |
BR9712285A (pt) | 1996-10-09 | 2001-11-20 | Pharmasset Ltd | Tetrafosfonato bicìclico de trianidridas |
US6018049A (en) | 1996-12-26 | 2000-01-25 | Shionogi & Co., Ltd. | Process for the preparation of carbamoylated imidazole derivatives |
WO1999029702A2 (fr) | 1997-12-10 | 1999-06-17 | The Government Of The United States Of America Reppresented By The Secretary, Department Of Health And Human Services | PROCEDE DE SYNTHESE DE LA 9-(2,3-DIDEOXY -2-FLUORO-β-D-THREO-PENTOFLURANOSYL)ADENINE (β-FddA) |
US6436989B1 (en) | 1997-12-24 | 2002-08-20 | Vertex Pharmaceuticals, Incorporated | Prodrugs of aspartyl protease inhibitors |
US6312662B1 (en) * | 1998-03-06 | 2001-11-06 | Metabasis Therapeutics, Inc. | Prodrugs phosphorus-containing compounds |
US6174888B1 (en) | 1998-05-28 | 2001-01-16 | Novartis Ag | 2-amino-7-(1-substituted-2-hydroxyethyl)-3,5-dihydropyrrolo[3,2-D]pyrimidin-4-ones |
WO1999062921A1 (fr) | 1998-06-01 | 1999-12-09 | S & T Science And Technology Inc. | Derives phosphores de la 4'-thio-5-ethyl-2'-deoxyuridine comme antiviraux |
GB9815567D0 (en) | 1998-07-18 | 1998-09-16 | Glaxo Group Ltd | Antiviral compound |
US6319946B1 (en) | 1999-02-12 | 2001-11-20 | Vertex Pharmaceuticals Incorporated | Inhibitors of aspartyl protease |
US6761903B2 (en) | 1999-06-30 | 2004-07-13 | Lipocine, Inc. | Clear oil-containing pharmaceutical compositions containing a therapeutic agent |
CZ20013180A3 (cs) | 1999-03-05 | 2002-02-13 | Metabasis Therapeutics, Inc. | Nové cyklické fosforamidáty, způsob jejich přípravy a farmaceutické kompozice, které je obsahují |
DE19912636A1 (de) | 1999-03-20 | 2000-09-21 | Aventis Cropscience Gmbh | Bicyclische Heterocyclen, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und pharmazeutische Mittel |
US6258831B1 (en) | 1999-03-31 | 2001-07-10 | The Procter & Gamble Company | Viral treatment |
US6608027B1 (en) | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
DE19927689A1 (de) | 1999-06-17 | 2000-12-21 | Gruenenthal Gmbh | Orale Darreichungsformen zur Verabreichung einer fixen Kombination von Tramadol und Diclofenac |
ATE248835T1 (de) | 1999-06-25 | 2003-09-15 | Vertex Pharma | Prodrugs von impdh-inhibierenden carbamaten |
US6581606B2 (en) | 1999-07-06 | 2003-06-24 | The Rx Files Corporation | Method, apparatus and system for use in treating patient with a drug having an antineoplastic effect to optimize therapy and prevent an adverse drug response |
WO2001013957A2 (fr) | 1999-08-24 | 2001-03-01 | Cellgate, Inc. | Compositions et procedes ameliorant la diffusion de medicaments a travers et dans des tissus epitheliaux |
GB9920872D0 (en) | 1999-09-04 | 1999-11-10 | Glaxo Group Ltd | Benzophenones as inhibitors of reverse transcriptase |
IL131887A0 (en) | 1999-09-14 | 2001-03-19 | Dpharm Ltd | Phospholipid prodrugs of anti-proliferative drugs |
WO2001039724A2 (fr) | 1999-12-03 | 2001-06-07 | The Regents Of The University Of California, San Diego | Composes de phosphonate |
US6448429B1 (en) | 1999-12-22 | 2002-09-10 | Merck Frosst Canada & Co. | Protein tyrosine phosphatase 1B (PTP-1B) inhibitors containing two ortho-substituted aromatic phosphonates |
AU2001234174A1 (en) | 2000-02-29 | 2001-09-12 | Mitsubishi Pharma Corporation | Phosphonate nucleotide compound |
MY164523A (en) * | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
CZ20023940A3 (cs) | 2000-06-13 | 2003-05-14 | Shionogi & Co., Ltd. | Lékařské směsi zahrnující propenonové deriváty |
FR2810322B1 (fr) | 2000-06-14 | 2006-11-10 | Pasteur Institut | PRODUCTION COMBINATOIRE D'ANALOGUES DE NUCLEOTIDES ET NUCLEOTIDES (XiTP) |
UA72612C2 (en) | 2000-07-06 | 2005-03-15 | Pyrido[2.3-d]pyrimidine and pyrimido[4.5-d]pyrimidine nucleoside analogues, prodrugs and method for inhibiting growth of neoplastic cells | |
US6617310B2 (en) | 2000-07-19 | 2003-09-09 | Bristol-Myers Squibb Pharma Company | Phosphate esters of bis-amino acid sulfonamides containing substituted benzyl amines |
CN1291994C (zh) | 2000-07-21 | 2006-12-27 | 吉里德科学公司 | 核苷酸膦酸酯类似物前药及其筛选和制备方法 |
US6420586B1 (en) | 2000-08-15 | 2002-07-16 | University Of Kansas | Amino acid-derived cyclic phosphonamides and methods of synthesizing the same |
ATE343384T1 (de) | 2000-09-08 | 2006-11-15 | Zeria Pharm Co Ltd | Pharmazeutische zusammensetzungen enthaltend aminothiazole derivate zur behandlung von motorischen störungen des dickdarms |
RU2188203C2 (ru) | 2000-10-05 | 2002-08-27 | Государственный научный центр вирусологии и биотехнологии "Вектор" | 2',3'-дидегидро-2',3'-дидезокситимидин-5'[(этоксикарбонил)(этил)фосфонат]- ингибитор репродукции вируса иммунодефицита человека |
GB0028429D0 (en) | 2000-11-22 | 2001-01-10 | Astrazeneca Ab | Therapy |
WO2002048165A2 (fr) | 2000-12-15 | 2002-06-20 | Pharmasset Ltd. | Agents antiviraux utilises dans le traitement des infections par les flaviviridae |
BRPI0116607B8 (pt) | 2000-12-28 | 2021-05-25 | Kissei Pharmaceutical | derivados de glicopiranosiloxipirazol , composições farmacêuticas que os contêm e usos dos mesmos |
EP2399588B1 (fr) | 2001-01-22 | 2020-04-29 | Merck Sharp & Dohme Corp. | Dérivés de nucléosides en tant qu'inhibiteurs de polymérase virale d'arn dépendante de l'arn |
PL363321A1 (en) | 2001-01-31 | 2004-11-15 | Warner-Lambert Company Llc | Method for carbamoylating alcohols |
EP1360169B2 (fr) | 2001-02-12 | 2017-05-24 | Wyeth LLC | Sel de succinate de o-desmethyl-venlafaxine |
DE60225374T2 (de) | 2001-05-31 | 2009-03-26 | Sumitomo Chemical Co., Ltd. | Verfahren zur Herstellung eines aktivierten Aluminiumoxid-Formkörpers |
GB0114286D0 (en) | 2001-06-12 | 2001-08-01 | Hoffmann La Roche | Nucleoside Derivatives |
KR20020097384A (ko) | 2001-06-20 | 2002-12-31 | 미쯔비시 도꾜 세이야꾸 가부시끼가이샤 | 기존의 약제에 내성변이를 가지는 바이러스에 유효한 약제 |
ATE371026T1 (de) | 2001-06-20 | 2007-09-15 | Nuevolution As | Eine methode zur synthese von matrizenabhängigen molekülen |
DK1408984T3 (da) | 2001-07-20 | 2009-02-09 | Bioagency Ag | Organofosforforbindelser til aktivering af gamma/delta T celler |
ES2330089T3 (es) * | 2001-08-17 | 2009-12-04 | Mitsui Chemicals Agro, Inc. | Derivado de 3-fenoxi-4-piridazinol y composicion herbicida que lo contiene. |
JP2005508924A (ja) | 2001-08-30 | 2005-04-07 | 三菱ウェルファーマ株式会社 | 抗ウイルス剤 |
KR20040066140A (ko) | 2001-11-29 | 2004-07-23 | 화이자 프로덕츠 인크. | 5,8,14-트리아자테트라시클로[10.3.1.0(2,11).0(4,9)]헥사데카-2(11),3,5,7,9-펜타엔의 숙신산염 및 그의 제약 조성물 |
JP2005511749A (ja) | 2001-12-07 | 2005-04-28 | 三菱ウェルファーマ株式会社 | B型肝炎ウィルス感染症を治療するためのホスホネートヌクレオチド類似体の使用 |
PL370858A1 (en) | 2001-12-12 | 2005-05-30 | Pfizer Products Inc. | Salt forms of e-2-methoxy-n-(3-{4-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenylamino]-quinazolin-6-yl}-allyl)-acetamide and method of production |
US7229978B2 (en) | 2001-12-21 | 2007-06-12 | Mgi Gp, Inc. | Process for preparing water soluble phosphonooxymethyl derivatives of alcohol and phenol |
US20030198666A1 (en) | 2002-01-07 | 2003-10-23 | Richat Abbas | Oral insulin therapy |
EA008379B1 (ru) | 2002-02-01 | 2007-04-27 | Ариад Джин Терапьютикс, Инк. | Фосфорсодержащие соединения и их применения |
WO2003066005A2 (fr) | 2002-02-08 | 2003-08-14 | Conforma Therapeutics Corporation | Ansamycines a proprietes pharmacologiques et biologiques ameliorees |
US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
WO2003080078A1 (fr) | 2002-03-18 | 2003-10-02 | Mitsubishi Pharma Corporation | Traitement d'infections mutants de la region pre-c du virus de l'hepatite b |
CA2481855A1 (fr) * | 2002-04-10 | 2003-10-23 | Ortho-Mcneil Pharmaceutical, Inc. | Nouveaux derives heteroarylalkylamide utiles en tant que modulateurs du recepteur de la bradykinine |
US6872827B2 (en) | 2002-04-26 | 2005-03-29 | Chembridge Research Laboratories, Inc. | Somatostatin analogue compounds |
US20050239054A1 (en) | 2002-04-26 | 2005-10-27 | Arimilli Murty N | Method and compositions for identifying anti-HIV therapeutic compounds |
CA2499819A1 (fr) | 2002-09-30 | 2004-04-08 | A/S Gea Farmaceutisk Fabrik | Nouveaux sels d'addition acides de raloxifene et/ou solvates de ceux-ci, procede ameliore permettant la purification de ces sels d'addition acides et/ou de ces solvates, et compositions pharmaceutiques les contenant |
US20040157793A1 (en) * | 2002-11-12 | 2004-08-12 | Stuyver Lieven J. | Modified nucleosides as antiviral agents |
AU2004260630B2 (en) | 2003-02-19 | 2009-12-10 | Masanori Baba | Anti-viral nucleoside analogs and methods for treating viral infections, especially HIV infections |
US7470724B2 (en) | 2003-04-25 | 2008-12-30 | Gilead Sciences, Inc. | Phosphonate compounds having immuno-modulatory activity |
WO2004096237A2 (fr) | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Analogues de phosphonates convenant au traitement d'affections du metabolisme |
MXPA05011289A (es) | 2003-04-25 | 2006-01-24 | Gilead Sciences Inc | Compuestos de fosfato que tienen actividad inmunomoduladora. |
WO2004096285A2 (fr) | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Analogues anti-infectieux du phosphonate |
US7407965B2 (en) | 2003-04-25 | 2008-08-05 | Gilead Sciences, Inc. | Phosphonate analogs for treating metabolic diseases |
MXPA05011294A (es) | 2003-04-25 | 2006-03-15 | Gilead Sciences Inc | Compuestos de fosfonato anti-inflamatorios. |
WO2004096286A2 (fr) | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Analogues de phosphonate antiviraux |
MXPA05011287A (es) * | 2003-04-25 | 2006-01-24 | Gilead Sciences Inc | Analogos de fosfonato anti-cancer. |
KR20060022647A (ko) | 2003-04-25 | 2006-03-10 | 길리애드 사이언시즈, 인코포레이티드 | 키나아제 억제 포스포네이트 유사체 |
CN101410120A (zh) | 2003-04-25 | 2009-04-15 | 吉里德科学公司 | 抗炎的膦酸酯化合物 |
US7432261B2 (en) | 2003-04-25 | 2008-10-07 | Gilead Sciences, Inc. | Anti-inflammatory phosphonate compounds |
WO2004096233A2 (fr) * | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Analogues d'un phosphonate nucleosidique |
US7452901B2 (en) * | 2003-04-25 | 2008-11-18 | Gilead Sciences, Inc. | Anti-cancer phosphonate analogs |
WO2004096287A2 (fr) | 2003-04-25 | 2004-11-11 | Gilead Sciences, Inc. | Composes de phosphonate inhibiteurs de l'inosine monophosphate deshydrogenase |
EP1617848A2 (fr) | 2003-04-25 | 2006-01-25 | Gilead Sciences, Inc. | Conjugues phosphonate anti-cancereux |
WO2005002626A2 (fr) | 2003-04-25 | 2005-01-13 | Gilead Sciences, Inc. | Composes de phosphonate therapeutiques |
JP2007502329A (ja) | 2003-05-23 | 2007-02-08 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | セルトラリン組成物 |
KR100985013B1 (ko) * | 2003-06-16 | 2010-10-04 | 아지노모토 가부시키가이샤 | 이노신 유도체 및 이의 제조방법 |
AU2004260789B2 (en) | 2003-07-30 | 2011-06-30 | Gilead Sciences, Inc. | Nucleobase phosphonate analogs for antiviral treatment |
WO2005016900A1 (fr) | 2003-08-18 | 2005-02-24 | H. Lundbeck A/S | Sel de succinate et de malonate de trans-4-((1r,3s)-6-chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine et son utilisation en tant que medicament |
EP1678321A1 (fr) | 2003-10-24 | 2006-07-12 | Gilead Sciences, Inc. | Procedes et compositions permettant d'identifier des composes therapeutiques |
US7427624B2 (en) | 2003-10-24 | 2008-09-23 | Gilead Sciences, Inc. | Purine nucleoside phosphorylase inhibitory phosphonate compounds |
US7432273B2 (en) | 2003-10-24 | 2008-10-07 | Gilead Sciences, Inc. | Phosphonate analogs of antimetabolites |
AU2004308974A1 (en) | 2003-12-22 | 2005-07-14 | Gilead Sciences, Inc. | Kinase inhibitor phosphonate conjugates |
WO2005063751A1 (fr) | 2003-12-22 | 2005-07-14 | Gilead Sciences, Inc. | Derives de carbovir et d'abacavir 4'-substitues et composes associes dotes d'une activite antivirale dirigee contre le vih et le vhc |
US20050171126A1 (en) * | 2003-12-26 | 2005-08-04 | Ajinomoto Co., Inc. | Process for the production of purine nucleoside compounds |
US7404949B2 (en) | 2004-03-15 | 2008-07-29 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Methods and compositions useful to prevent in-grown hair arising from shaving |
US20090035315A1 (en) | 2004-06-17 | 2009-02-05 | Stephan Christgau | Method of Improving Treatments in Rheumatic and Arthritic Diseases |
ES2363160T3 (es) * | 2004-07-27 | 2011-07-22 | Gilead Sciences, Inc. | Conjugados de fosfonato nucelosidico como agentes anti-vih. |
WO2006015262A2 (fr) | 2004-07-29 | 2006-02-09 | Coherix, Inc. | Procede pour traiter des donnees d'imagerie interferometriques a longueurs d'ondes multiples |
US20060069060A1 (en) | 2004-09-27 | 2006-03-30 | Sanjeev Redkar | Salts of decitabine |
US7154505B2 (en) | 2004-11-11 | 2006-12-26 | Stonecube Limited | Method of and apparatus for generating a representation of an object |
KR20060080817A (ko) | 2005-01-06 | 2006-07-11 | 씨제이 주식회사 | 시부트라민의 디카복실산염 |
MY148074A (en) | 2005-05-10 | 2013-02-28 | Novartis Ag | Pharmaceutical compositions comprising imatinib and a release retardant |
EP1912938A2 (fr) | 2005-08-04 | 2008-04-23 | Novartis AG | Sels de vildagliptin |
DE102005041860A1 (de) | 2005-09-02 | 2007-03-08 | Schering Ag | Nanopartikulärer Einschluss- und Ladungskomplex für pharmazeutische Formulierungen |
JP2009519952A (ja) | 2005-12-16 | 2009-05-21 | ワイス | トリアゾロピリミジン化合物の凍結乾燥組成物 |
US20060223820A1 (en) | 2006-03-21 | 2006-10-05 | Chemagis Ltd. | Crystalline aripiprazole salts and processes for preparation and purification thereof |
US8895531B2 (en) * | 2006-03-23 | 2014-11-25 | Rfs Pharma Llc | 2′-fluoronucleoside phosphonates as antiviral agents |
PT2487163T (pt) * | 2007-02-23 | 2016-11-21 | Gilead Sciences Inc | Moduladores de propriedades farmacocinéticas de agentes terapêuticos |
US20090163449A1 (en) | 2007-12-20 | 2009-06-25 | Eastman Chemical Company | Sulfo-polymer powder and sulfo-polymer powder blends with carriers and/or additives |
AU2009268681B2 (en) | 2008-07-08 | 2014-10-02 | Gilead Sciences, Inc. | Salts of HIV inhibitor compounds |
JP4330086B1 (ja) | 2009-02-09 | 2009-09-09 | 株式会社テクネス | 非酸化物セラミックス製品の製造方法 |
EP2305680A3 (fr) | 2009-09-30 | 2011-05-18 | Aurobindo Pharma Limited | Nouveaux sels de (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-méthanol |
US20140094485A1 (en) | 2012-10-03 | 2014-04-03 | Gilead Sciences, Inc. | Solid state forms of hiv inhibitor |
US20140094609A1 (en) | 2012-10-03 | 2014-04-03 | Gilead Sciences, Inc. | Process for the preparation of an hiv integrase inhibitor |
-
2005
- 2005-07-26 ES ES05857701T patent/ES2363160T3/es active Active
- 2005-07-26 JP JP2007523730A patent/JP2008508291A/ja active Pending
- 2005-07-26 ME MEP-2019-115A patent/ME03423B/fr unknown
- 2005-07-26 AR ARP050103101 patent/AR051922A1/es active IP Right Grant
- 2005-07-26 SI SI200531308T patent/SI1778251T1/sl unknown
- 2005-07-26 PT PT05857701T patent/PT1778251E/pt unknown
- 2005-07-26 EP EP10178348.8A patent/EP2258376B1/fr active Active
- 2005-07-26 RS RS20190476A patent/RS58600B1/sr unknown
- 2005-07-26 PL PL05857701T patent/PL1778251T3/pl unknown
- 2005-07-26 PT PT10178348T patent/PT2258376T/pt unknown
- 2005-07-26 KR KR1020077004805A patent/KR101233824B1/ko active IP Right Grant
- 2005-07-26 SI SI200532247T patent/SI2258376T1/sl unknown
- 2005-07-26 UA UAA200701987A patent/UA88313C2/ru unknown
- 2005-07-26 CN CNA2005800325676A patent/CN101027062A/zh active Pending
- 2005-07-26 AP AP2007003912A patent/AP2412A/xx active
- 2005-07-26 DK DK05857701.6T patent/DK1778251T3/da active
- 2005-07-26 TR TR2019/06416T patent/TR201906416T4/tr unknown
- 2005-07-26 RS RSP20110303 patent/RS51799B/en unknown
- 2005-07-26 EA EA200700363A patent/EA019419B1/ru not_active IP Right Cessation
- 2005-07-26 EP EP05857701A patent/EP1778251B1/fr active Active
- 2005-07-26 ME MEP-2011-303A patent/ME01945B/fr unknown
- 2005-07-26 AU AU2005330489A patent/AU2005330489B2/en active Active
- 2005-07-26 DK DK10178348.8T patent/DK2258376T3/en active
- 2005-07-26 AT AT05857701T patent/ATE505196T1/de active
- 2005-07-26 HU HUE10178348A patent/HUE043207T2/hu unknown
- 2005-07-26 PL PL10178348T patent/PL2258376T3/pl unknown
- 2005-07-26 WO PCT/US2005/026504 patent/WO2006110157A2/fr active Application Filing
- 2005-07-26 US US11/190,225 patent/US7871991B2/en active Active
- 2005-07-26 EP EP19155831.1A patent/EP3539546A1/fr not_active Withdrawn
- 2005-07-26 MX MX2007001053A patent/MX2007001053A/es not_active Application Discontinuation
- 2005-07-26 ES ES10178348T patent/ES2720618T3/es active Active
- 2005-07-26 PL PL382846A patent/PL216369B1/pl not_active IP Right Cessation
- 2005-07-26 CA CA002574514A patent/CA2574514A1/fr not_active Abandoned
- 2005-07-26 LT LTEP10178348.8T patent/LT2258376T/lt unknown
- 2005-07-26 BR BRPI0512690-8A patent/BRPI0512690A/pt not_active IP Right Cessation
- 2005-07-26 US US11/658,419 patent/US8318701B2/en active Active
- 2005-07-26 DE DE602005027466T patent/DE602005027466D1/de active Active
- 2005-07-26 NZ NZ553405A patent/NZ553405A/xx unknown
- 2005-07-27 NZ NZ553406A patent/NZ553406A/en unknown
- 2005-07-27 AU AU2005267800A patent/AU2005267800B2/en active Active
- 2005-07-27 MX MX2007001059A patent/MX2007001059A/es active IP Right Grant
- 2005-07-27 UA UAA200701991A patent/UA91688C2/ru unknown
- 2005-07-27 DE DE602005021506T patent/DE602005021506D1/de active Active
- 2005-07-27 CA CA2574121A patent/CA2574121C/fr active Active
- 2005-07-27 EP EP05777315A patent/EP1778249B1/fr active Active
- 2005-07-27 CN CN2010102437749A patent/CN101914124B/zh active Active
- 2005-07-27 CN CN2010102437734A patent/CN101935333A/zh active Pending
- 2005-07-27 CN CN2005800325568A patent/CN101031306B/zh active Active
- 2005-07-27 EA EA200700362A patent/EA019559B1/ru not_active IP Right Cessation
- 2005-07-27 AT AT05777315T patent/ATE469163T1/de not_active IP Right Cessation
- 2005-07-27 KR KR1020077004803A patent/KR101233823B1/ko active IP Right Grant
- 2005-07-27 WO PCT/US2005/027088 patent/WO2006015261A2/fr active Application Filing
- 2005-07-27 ES ES05777315T patent/ES2346454T3/es active Active
- 2005-07-27 JP JP2007523866A patent/JP4954877B2/ja active Active
- 2005-07-27 AP AP2007003899A patent/AP2629A/xx active
- 2005-07-27 SG SG200905022-0A patent/SG155164A1/en unknown
- 2005-07-27 PL PL382843A patent/PL230036B1/pl unknown
- 2005-07-27 TW TW94125503A patent/TWI362934B/zh active
- 2005-07-27 BR BRPI0512683-5A patent/BRPI0512683A/pt active Search and Examination
- 2005-07-27 US US11/658,628 patent/US8329926B2/en active Active
-
2007
- 2007-01-17 IL IL180758A patent/IL180758A/en active IP Right Grant
- 2007-01-18 IL IL180781A patent/IL180781A/en active IP Right Grant
- 2007-01-23 IS IS8595A patent/IS8595A/is unknown
- 2007-01-23 IS IS8594A patent/IS2840B/is unknown
- 2007-02-20 ZA ZA200701465A patent/ZA200701465B/xx unknown
- 2007-02-20 ZA ZA2007/01466A patent/ZA200701466B/en unknown
- 2007-02-26 NO NO20071078A patent/NO339020B1/no unknown
- 2007-02-26 NO NO20071077A patent/NO339222B1/no unknown
- 2007-02-27 HR HR20070078A patent/HRP20070078A2/xx not_active Application Discontinuation
- 2007-02-27 HR HR20070079A patent/HRP20070079A2/xx not_active Application Discontinuation
- 2007-11-02 HK HK07111940.1A patent/HK1103648A1/xx unknown
- 2007-11-02 HK HK07111941.0A patent/HK1103649A1/xx unknown
-
2011
- 2011-06-03 JP JP2011125822A patent/JP2011201911A/ja not_active Withdrawn
- 2011-07-06 CY CY20111100662T patent/CY1111709T1/el unknown
- 2011-07-13 HR HR20110527T patent/HRP20110527T1/hr unknown
-
2012
- 2012-09-25 US US13/626,687 patent/US8697861B2/en active Active
- 2012-10-17 US US13/653,982 patent/US9579332B2/en active Active
-
2014
- 2014-02-11 US US14/178,237 patent/US9457035B2/en active Active
-
2016
- 2016-09-01 US US15/254,684 patent/US20170088576A1/en not_active Abandoned
- 2016-09-23 NO NO20161521A patent/NO342132B1/no unknown
- 2016-10-07 NO NO20161612A patent/NO342571B1/no unknown
-
2017
- 2017-01-10 US US15/402,857 patent/US20170210770A1/en not_active Abandoned
- 2017-07-06 US US15/643,168 patent/US20180086784A1/en not_active Abandoned
-
2018
- 2018-02-16 NO NO20180243A patent/NO20180243A1/no not_active Application Discontinuation
- 2018-11-19 US US16/195,152 patent/US20190315785A1/en not_active Abandoned
- 2018-11-20 US US16/196,075 patent/US20190345190A1/en not_active Abandoned
-
2019
- 2019-04-16 HR HRP20190712TT patent/HRP20190712T1/hr unknown
- 2019-05-14 CY CY20191100518T patent/CY1121623T1/el unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003091264A2 (fr) * | 2002-04-26 | 2003-11-06 | Gilead Sciences, Inc. | Inhibiteurs non nucleosidiques de la transcriptase inverse |
WO2003090690A2 (fr) * | 2002-04-26 | 2003-11-06 | Gilead Sciences, Inc. | Accumulation cellulaire d'analogues de phosphonate de composes inhibiteurs de la protease du vih |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AP2412A (en) | Phosphonate analogs of HIV inhibitor compounds. | |
HK1114832A1 (en) | 12-aryl prostaglandin analogs 12- | |
NO20055590D0 (no) | Kinaseinhiberende fosfonatanaloger | |
IL179161A0 (en) | Hiv integrase inhibitors: cyclic pyrimidinone compounds | |
ZA200605354B (en) | Prostaglandin nitrooxyderivatives | |
EP1771453A4 (fr) | Analogues dipeptidiques d'inhibiteurs de l'hepatite c | |
ZA200700357B (en) | Tetrapetide analogs | |
EP1910378A4 (fr) | Analogues de peptides inhibiteurs de l'hepatite c | |
WO2004096235A8 (fr) | Analogues de phosphonate anticancereux | |
IL189933A0 (en) | Rna antagonist compounds for the inhibition of apo-b100 expression | |
EP1763531A4 (fr) | Analogues peptidiques d'inhibiteurs de l'hepatite c | |
IL180495A0 (en) | Benzyltriazolone compounds as nin-nucleoside reverse transcriptase inhibitors | |
HK1129679A1 (en) | Enantiomerically pure phosphoindole as hiv inhibitor hiv | |
PL1776090T3 (pl) | Stabilizowana kompozycja prostaglandyny | |
TWI365876B (en) | Prodrugs of hiv protease inhibitors | |
ZA200904053B (en) | Phosphonate compounds | |
ZA200804607B (en) | Substituted aminophenylsulfonamide compounds as HIV protease inhibitor | |
ZA200710861B (en) | Uses of prostacyclin analogs | |
HK1099203A1 (en) | Piperidinyl prostaglandin e analogs | |
TH0501003440A (th) | สิ่งเทียบเคียงฟอสฟอเนตของสารประกอบสารยับยั้ง hiv | |
PL371824A1 (pl) | Nowe inhibitory integrazy HIV, ich prekursory oraz ich stosowanie | |
PL376515A1 (pl) | Nowe związki α₁-aminoalkano-karbamoiloalkano-fosfinowe użyteczne jako inhibitory aminopeptydazy N oraz sposób ich wytwarzania | |
ZA200702390B (en) | S-triazolyl α-mercaptoacetanildes as inhibitors of HIV reverse transciptase |