ATE320813T1 - Methoden zur reduktion der toxizität von 5- fluorouracil mittels acylierter pyrimidinnukleoside - Google Patents
Methoden zur reduktion der toxizität von 5- fluorouracil mittels acylierter pyrimidinnukleosideInfo
- Publication number
- ATE320813T1 ATE320813T1 AT04023557T AT04023557T ATE320813T1 AT E320813 T1 ATE320813 T1 AT E320813T1 AT 04023557 T AT04023557 T AT 04023557T AT 04023557 T AT04023557 T AT 04023557T AT E320813 T1 ATE320813 T1 AT E320813T1
- Authority
- AT
- Austria
- Prior art keywords
- fluorouracil
- toxicity
- reducing
- methods
- pyrimidine nucleosides
- Prior art date
Links
- 239000002718 pyrimidine nucleoside Substances 0.000 title abstract 3
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 title 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 229960002949 fluorouracil Drugs 0.000 title 1
- 230000001988 toxicity Effects 0.000 title 1
- 231100000419 toxicity Toxicity 0.000 title 1
- KSPDSMOWMQFPBL-UHFFFAOYSA-N 5-fluoropyrimidine Chemical compound FC1=CN=CN=C1 KSPDSMOWMQFPBL-UHFFFAOYSA-N 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 201000011510 cancer Diseases 0.000 abstract 2
- 229940127073 nucleoside analogue Drugs 0.000 abstract 2
- 102100022334 Dihydropyrimidine dehydrogenase [NADP(+)] Human genes 0.000 abstract 1
- 108010066455 Dihydrouracil Dehydrogenase (NADP) Proteins 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 150000003230 pyrimidines Chemical class 0.000 abstract 1
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
-
- 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
- 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
-
- 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
- A61K31/33—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
- A61K31/515—Barbituric acids; Derivatives thereof, e.g. sodium pentobarbital
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
-
- 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
-
- 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
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/472,210 US5968914A (en) | 1987-10-28 | 1995-06-07 | Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE320813T1 true ATE320813T1 (de) | 2006-04-15 |
Family
ID=23874595
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT04023557T ATE320813T1 (de) | 1995-06-07 | 1996-06-06 | Methoden zur reduktion der toxizität von 5- fluorouracil mittels acylierter pyrimidinnukleoside |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US5968914A (de) |
| EP (2) | EP0831849A4 (de) |
| JP (3) | JPH10511689A (de) |
| KR (1) | KR19990022804A (de) |
| CN (1) | CN1192149A (de) |
| AT (1) | ATE320813T1 (de) |
| AU (1) | AU724805B2 (de) |
| CA (1) | CA2223640A1 (de) |
| DE (1) | DE69635941T2 (de) |
| DK (1) | DK1491201T3 (de) |
| ES (1) | ES2257721T3 (de) |
| PT (1) | PT1491201E (de) |
| WO (1) | WO1996040165A1 (de) |
Families Citing this family (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5691320A (en) * | 1987-10-28 | 1997-11-25 | Pro-Neuron, Inc. | Acylated pyrimidine nucleosides for treatment of systemic inflammation and inflammatory hepatitis |
| US7776838B1 (en) * | 1987-10-28 | 2010-08-17 | Wellstat Therapeutics Corporation | Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides |
| CA2213385A1 (en) * | 1997-08-20 | 1999-02-20 | Eng-Hong Lee | Method of protecting against coccidiosis infections in poultry |
| WO1999008686A1 (en) * | 1997-08-21 | 1999-02-25 | Basf Aktiengesellschaft | Use of uridine to counter 5-fluorouracil toxicity |
| US6136339A (en) * | 1998-08-21 | 2000-10-24 | Gardiner; Paul T. | Food supplements and methods comprising lipoic acid and creatine |
| US7807654B2 (en) | 1998-08-31 | 2010-10-05 | Wellstat Therapeutics Corporation | Compositions and methods for treatment of mitochondrial diseases |
| US6472378B2 (en) | 1998-08-31 | 2002-10-29 | Pro-Neuron, Inc. | Compositions and methods for treatment of mitochondrial diseases |
| US7915233B1 (en) | 1998-08-31 | 2011-03-29 | Wellstat Therapeutics Corporation | Compositions and methods for treatment of mitochondrial diseases |
| EP1808177B1 (de) | 1999-02-23 | 2018-08-08 | The Regents of The University of California | Behandlungsmethoden für mitochondriale Erkrankungen |
| US6875751B2 (en) * | 2000-06-15 | 2005-04-05 | Idenix Pharmaceuticals, Inc. | 3′-prodrugs of 2′-deoxy-β-L-nucleosides |
| WO2002011668A2 (en) * | 2000-08-09 | 2002-02-14 | Kolon Industries, Inc. | 5'-deoxy-n-(substituted oxycarbonyl)-5-fluorocytosine and derivatives thereof, method of preparing same, and anticancer composition comprising same as active ingredients |
| US6613753B2 (en) * | 2001-02-21 | 2003-09-02 | Supergen, Inc. | Restore cancer-suppressing functions to neoplastic cells through DNA hypomethylation |
| AU2002306551A1 (en) * | 2001-03-01 | 2002-09-19 | Eli Lilly And Company | Tumor treatement with a combination of a substrate of mrp5 and modulators of mrp5 |
| DE10110355A1 (de) * | 2001-03-03 | 2002-09-12 | Ulrich Walker | Bekämpfung von Nebenwirkungen |
| US6905669B2 (en) * | 2001-04-24 | 2005-06-14 | Supergen, Inc. | Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase |
| US20030082228A1 (en) * | 2001-05-09 | 2003-05-01 | Inex Pharmaceuticals Corporation | Anti-angiogenic therapy using liposome-encapsulated chemotherapeutic agents |
| SE521676C2 (sv) * | 2002-01-02 | 2003-11-25 | Dilafor Ab | Användning av glykosaminoglykaner för prevention och behandling av värksvaghet vid fullgången graviditet |
| US6998391B2 (en) * | 2002-02-07 | 2006-02-14 | Supergen.Inc. | Method for treating diseases associated with abnormal kinase activity |
| US20030147813A1 (en) * | 2002-02-07 | 2003-08-07 | John Lyons | Method for treating chronic myelogenous leukemia |
| EP1352910A1 (de) * | 2002-04-10 | 2003-10-15 | Grünenthal GmbH | Neue Analoga von Nitrobenzylthioinosine |
| US6982253B2 (en) * | 2002-06-05 | 2006-01-03 | Supergen, Inc. | Liquid formulation of decitabine and use of the same |
| US20040162263A1 (en) * | 2002-10-31 | 2004-08-19 | Supergen, Inc., A Delaware Corporation | Pharmaceutical formulations targeting specific regions of the gastrointesinal tract |
| WO2004104022A2 (en) * | 2003-05-16 | 2004-12-02 | The General Hospital Corporation | Compositions comprising pathogen elicited epithelial chemoattractant (eicosanoid hepoxilin a3), inhibitors thereof and methods of use thereof |
| US20050037992A1 (en) * | 2003-07-22 | 2005-02-17 | John Lyons | Composition and method for treating neurological disorders |
| US20050059682A1 (en) * | 2003-09-12 | 2005-03-17 | Supergen, Inc., A Delaware Corporation | Compositions and methods for treatment of cancer |
| ATE540679T1 (de) * | 2004-04-29 | 2012-01-15 | Taiho Pharmaceutical Co Ltd | Verfahren zur verringerung der gastrointestinalen toxizität durch verabreichung von tegafur |
| US20080214606A1 (en) * | 2004-06-18 | 2008-09-04 | The Government of the United States of America as represented by The Secretary of the Dept. of ..... | Methods for the Identification and Use of Compounds Suitable for the Treatment of Drug Resistant Cancer Cells |
| US20060024376A1 (en) * | 2004-07-30 | 2006-02-02 | The University Of Chicago | Methods and compositions for reducing toxicity associated with leflunomide treatment |
| US20080255168A1 (en) * | 2004-12-03 | 2008-10-16 | Adherex Technologies, Inc. | Methods for administering dpd inhibitors in combination with 5-fu and 5-fu prodrugs |
| US20060128653A1 (en) * | 2004-12-10 | 2006-06-15 | Chunlin Tang | Pharmaceutical formulation of decitabine |
| US20060128654A1 (en) * | 2004-12-10 | 2006-06-15 | Chunlin Tang | Pharmaceutical formulation of cytidine analogs and derivatives |
| US7250416B2 (en) * | 2005-03-11 | 2007-07-31 | Supergen, Inc. | Azacytosine analogs and derivatives |
| US7700567B2 (en) | 2005-09-29 | 2010-04-20 | Supergen, Inc. | Oligonucleotide analogues incorporating 5-aza-cytosine therein |
| US20070105792A1 (en) * | 2005-11-04 | 2007-05-10 | Dimartino Jorge F | Administration Of DNA Methylation Inhibitors For Treating Epigenetic Diseases |
| US20070117776A1 (en) * | 2005-11-04 | 2007-05-24 | John Lyons | Low Dose Therapy Of DNA Methylation Inhibitors |
| CN101384623B (zh) * | 2005-12-22 | 2013-07-24 | 常山凯捷健生物药物研发(河北)有限公司 | 白蛋白与治疗剂的预成型偶联物的制备方法 |
| US7906518B2 (en) | 2006-06-27 | 2011-03-15 | Cbt Development Limited | Therapeutic compounds |
| BRPI0713902A2 (pt) | 2006-06-27 | 2012-11-27 | Biovitrum Ab | compostos terapêuticos |
| JO2778B1 (en) | 2007-10-16 | 2014-03-15 | ايساي انك | Certain Compounds, Compositions and Methods |
| US20100316655A1 (en) * | 2008-02-11 | 2010-12-16 | Hall Matthew D | Compounds with mdr1-inverse activity |
| CN102014919B (zh) * | 2008-03-03 | 2015-02-25 | 托斯克公司 | 减少毒性的甲氨蝶呤佐剂及其使用方法 |
| US9265785B2 (en) | 2008-12-22 | 2016-02-23 | The Board Of Trustees Of The University Of Illinois | Compositions comprising decitabine and tetrahydrouridine and uses thereof |
| US9259469B2 (en) | 2008-12-22 | 2016-02-16 | The Board Of Trustees Of The University Of Illinois | Compositions comprising decitabine and tetrahydrouridine and uses thereof |
| US8609631B2 (en) | 2009-04-06 | 2013-12-17 | Eisai Inc. | Compositions and methods for treating cancer |
| AU2010234637B2 (en) * | 2009-04-06 | 2016-05-12 | Taiho Pharmaceutical Co., Ltd. | (2 ' -deoxy-ribofuranosyl) -1,3,4, 7-tetrahydro- (1,3) iazepin-2-0ne derivatives for treating cancer |
| AR076263A1 (es) * | 2009-04-06 | 2011-06-01 | Eisai Inc | Composiciones y metodos para tratar cancer. uso. |
| AU2010234562B2 (en) * | 2009-04-06 | 2016-05-12 | Taiho Pharmaceutical Co., Ltd. | Combination of cytidine-based antineoplastic drugs with cytidine deaminase inhibitor and use thereof in the treatment of cancer |
| US8617540B2 (en) * | 2009-04-15 | 2013-12-31 | Fox Chase Cancer Center | Combinational chemotherapy treatment |
| EP2455787A1 (de) | 2009-07-15 | 2012-05-23 | Asahi Glass Company, Limited | Verfahren zur herstellung von laminat und laminat |
| EP2348131A1 (de) | 2010-01-22 | 2011-07-27 | Institut Curie | Niedrige Mengen von Cytidindeaminase als Marker für genetische Prädisposition zur Entwicklung von Krebs |
| CN102775458B (zh) * | 2011-05-09 | 2015-11-25 | 中国人民解放军军事医学科学院毒物药物研究所 | β-D-(2’R)-2’-脱氧—2’-氟-2’-C-甲基胞苷衍生物的制备及用途 |
| EP3431142B1 (de) | 2011-08-30 | 2020-06-17 | Astex Pharmaceuticals, Inc. | Decitabinderivatformulierungen |
| BR102013022567B1 (pt) * | 2013-09-03 | 2021-09-21 | Uniao Brasileira De Educacão E Assistência | Uso de 6-hidroxi-2-piridonas e seus derivados na preparação de uma composição farmacêutica que atue pela inibição da enzima uridina fosforilase humana |
| CN104496972A (zh) * | 2014-12-04 | 2015-04-08 | 浙江大学 | 一种新型替加氟药物共晶及其制备方法 |
| JP7381190B2 (ja) | 2014-12-26 | 2023-11-15 | エモリー・ユニバーシテイ | N4-ヒドロキシシチジン及び誘導体並びにそれに関連する抗ウイルス用途 |
| SG11201707513QA (en) * | 2015-05-29 | 2017-10-30 | Univ Leland Stanford Junior | Nucleoside agents for the reduction of the deleterious activity of extended nucleotide repeat containing genes |
| AU2016287585B2 (en) | 2015-07-02 | 2020-12-17 | Otsuka Pharmaceutical Co., Ltd. | Lyophilized pharmaceutical compositions |
| CA3027118C (en) * | 2016-06-28 | 2023-08-15 | Cellix Bio Private Limited | Compositions and methods for the treatment of cancer |
| RU2020108580A (ru) | 2017-08-03 | 2021-09-03 | Оцука Фармасьютикал Ко., Лтд. | Лекарственное соединение и способы его очистки |
| AU2019215105B2 (en) | 2018-02-01 | 2024-12-19 | Pharma Cinq, Llc | Compositions and devices for systemic delivery of uridine |
| WO2020036982A1 (en) | 2018-08-14 | 2020-02-20 | Tosk, Inc. | Methods and compositions for treating mucositis |
| WO2020036975A1 (en) | 2018-08-14 | 2020-02-20 | Tosk, Inc. | Methods and compositions for reducing fluorouracil induced toxicity |
| WO2020036974A1 (en) * | 2018-08-14 | 2020-02-20 | Tosk, Inc. | Methods and compositions for reducing radiation induced toxicity |
| WO2020226889A1 (en) * | 2019-05-07 | 2020-11-12 | Wellstat Therapeutics Corporation | Formulations of uridine triacetate in triacetin |
| US11446303B2 (en) | 2019-06-21 | 2022-09-20 | Tosk, Inc. | Uridine phosphorylase (UPase) inhibitors for treatment of liver conditions |
| US11116737B1 (en) | 2020-04-10 | 2021-09-14 | University Of Georgia Research Foundation, Inc. | Methods of using probenecid for treatment of coronavirus infections |
| KR20230012572A (ko) * | 2020-05-19 | 2023-01-26 | 셀릭스 바이오 프라이빗 리미티드 | 암을 치료하기 위한 약학 제형 및 이의 제조 |
| EP4178581A4 (de) | 2020-07-07 | 2024-06-05 | Tosk, Inc. | Uridinphosphorylasehemmer zur behandlung oder prävention von lungenerkrankungen |
| PT4210709T (pt) | 2020-09-14 | 2026-02-04 | Pharma Cinq Llc | 2¿,3¿‐diacetiluridina substituída com acetoacetilo na posição 5¿ |
| WO2022226312A1 (en) * | 2021-04-22 | 2022-10-27 | Clear Creek Bio, Inc. | Combination nucleotide pool depletion for treatment of viral infections and cancers |
| CN113332305B (zh) * | 2021-06-03 | 2022-08-16 | 中国医学科学院医药生物技术研究所 | 胞苷类化合物的脂质组合物 |
| CN113336816B (zh) * | 2021-06-03 | 2022-05-17 | 中国医学科学院医药生物技术研究所 | 胞苷类化合物及其抗肿瘤用途 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1297398A (de) * | 1969-08-06 | 1972-11-22 | ||
| US4017606A (en) * | 1973-10-04 | 1977-04-12 | The Upjohn Company | Organic compounds and process |
| GB1473148A (de) * | 1974-09-16 | 1977-05-11 | ||
| DE3100478A1 (de) * | 1981-01-09 | 1982-08-12 | Dr. Thilo & Co GmbH, 8021 Sauerlach | 5'ester von pyrimidinnucleosiden mit antiviraler wirksamkeit, verfahren zur herstellung und daraus hergestellte arzneimittel |
| DE3481191D1 (de) * | 1983-07-20 | 1990-03-08 | Teijin Ltd | Antineoplastisches mittel. |
| JPS60174797A (ja) * | 1984-02-21 | 1985-09-09 | Funai Corp | Ν−アロイルチミジン誘導体ならびに抗腫瘍活性物質の毒性低下剤 |
| US5736531A (en) * | 1987-10-28 | 1998-04-07 | Pro-Neuron, Inc. | Compositions of chemotherapeutic agent or antiviral agent with acylated pyrimidine nucleosides |
| EP0712629B1 (de) * | 1987-10-28 | 2003-06-18 | Wellstat Therapeutics Corporation | Acyldeoxyribonukleosid-Derivate und Verwendungen davon |
| CA1321994C (en) * | 1987-10-28 | 1993-09-07 | Reid Von Borstel | Acylated uridine and cytidine and uses thereof |
| US4874602A (en) * | 1988-02-22 | 1989-10-17 | Paul Calabresi | Reduction of the severity 3'-azido-3'-deoxythymidine-induced anemia using benzylacyclouridine |
| US5077280A (en) * | 1988-04-12 | 1991-12-31 | Brown University Research Foundation | Treatment of viral infections |
| US4950466A (en) * | 1988-06-22 | 1990-08-21 | Paul Calabresi | Reduction of the severity of 3'-azido-3'-deoxythymidine-induced anemia using a combination of benzylacyclouridine and dipyridamole |
| US5132291A (en) * | 1989-01-24 | 1992-07-21 | Gensia Pharmaceuticals, Inc. | Antivirals and methods for increasing the antiviral activity of azt |
| DE69014562T2 (de) * | 1989-01-24 | 1995-06-22 | Gensia Pharma | Verfahren und verbindungen zur verabreichung von aica ribosiden und zur erniedrigung des blutglucose gehaltes. |
| US5141943A (en) * | 1990-04-12 | 1992-08-25 | Brown University Research Foundation | 5-benzyl barbiturate derivatives |
| CA2111571C (en) * | 1991-07-05 | 2005-08-23 | Reid W. Von Borstel | Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides |
| WO1994026761A1 (en) * | 1993-05-14 | 1994-11-24 | Pro-Neuron, Inc. | Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides |
-
1995
- 1995-06-07 US US08/472,210 patent/US5968914A/en not_active Expired - Lifetime
-
1996
- 1996-06-06 AT AT04023557T patent/ATE320813T1/de active
- 1996-06-06 JP JP9502184A patent/JPH10511689A/ja not_active Withdrawn
- 1996-06-06 KR KR1019970709273A patent/KR19990022804A/ko not_active Ceased
- 1996-06-06 WO PCT/US1996/010067 patent/WO1996040165A1/en not_active Ceased
- 1996-06-06 DK DK04023557T patent/DK1491201T3/da active
- 1996-06-06 PT PT04023557T patent/PT1491201E/pt unknown
- 1996-06-06 CN CN96195929A patent/CN1192149A/zh active Pending
- 1996-06-06 EP EP96918461A patent/EP0831849A4/de not_active Ceased
- 1996-06-06 DE DE69635941T patent/DE69635941T2/de not_active Expired - Lifetime
- 1996-06-06 ES ES04023557T patent/ES2257721T3/es not_active Expired - Lifetime
- 1996-06-06 CA CA002223640A patent/CA2223640A1/en not_active Abandoned
- 1996-06-06 EP EP04023557A patent/EP1491201B1/de not_active Expired - Lifetime
- 1996-06-06 AU AU61114/96A patent/AU724805B2/en not_active Expired
-
1999
- 1999-02-16 US US09/249,790 patent/US6344447B2/en not_active Expired - Lifetime
-
2003
- 2003-01-06 JP JP2003000721A patent/JP2003201240A/ja not_active Withdrawn
-
2009
- 2009-04-28 JP JP2009110077A patent/JP2009167213A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE69635941D1 (de) | 2006-05-11 |
| EP1491201B1 (de) | 2006-03-22 |
| DK1491201T3 (da) | 2006-07-31 |
| JP2003201240A (ja) | 2003-07-18 |
| HK1072897A1 (en) | 2005-09-16 |
| DE69635941T2 (de) | 2006-11-23 |
| CA2223640A1 (en) | 1996-12-19 |
| JPH10511689A (ja) | 1998-11-10 |
| WO1996040165A1 (en) | 1996-12-19 |
| US6344447B2 (en) | 2002-02-05 |
| EP0831849A4 (de) | 2003-03-26 |
| EP1491201A1 (de) | 2004-12-29 |
| PT1491201E (pt) | 2006-08-31 |
| JP2009167213A (ja) | 2009-07-30 |
| CN1192149A (zh) | 1998-09-02 |
| EP0831849A1 (de) | 1998-04-01 |
| AU6111496A (en) | 1996-12-30 |
| US20010025032A1 (en) | 2001-09-27 |
| US5968914A (en) | 1999-10-19 |
| ES2257721T3 (es) | 2006-08-01 |
| KR19990022804A (ko) | 1999-03-25 |
| AU724805B2 (en) | 2000-09-28 |
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