FI20030932A7 - Menetelmä cis-FTC:n enantiomeerien erottamiseksi - Google Patents
Menetelmä cis-FTC:n enantiomeerien erottamiseksi Download PDFInfo
- Publication number
- FI20030932A7 FI20030932A7 FI20030932A FI20030932A FI20030932A7 FI 20030932 A7 FI20030932 A7 FI 20030932A7 FI 20030932 A FI20030932 A FI 20030932A FI 20030932 A FI20030932 A FI 20030932A FI 20030932 A7 FI20030932 A7 FI 20030932A7
- Authority
- FI
- Finland
- Prior art keywords
- ftc
- cis
- separating enantiomers
- enantiomers
- separating
- Prior art date
Links
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Virology (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/659,760 US5210085A (en) | 1990-02-01 | 1991-02-22 | Method for the synthesis, compositions and use of 2'-deoxy-5-fluoro-3'-thiacytidine and related compounds |
| US73608991A | 1991-07-26 | 1991-07-26 | |
| US83115392A | 1992-02-12 | 1992-02-12 | |
| PCT/US1992/001339 WO1992014743A2 (en) | 1991-02-22 | 1992-02-20 | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FI20030932A7 true FI20030932A7 (fi) | 2003-06-24 |
Family
ID=35276919
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI933684A FI114915B (fi) | 1991-02-22 | 1993-08-20 | Menetelmä terapeuttisesti käyttökelpoisten beta-2-hydroksimetyyli-5-(5-fluorisytosin-1-yyli)-1,3-oksatiolaanin enantiomeerien valmistamiseksi |
| FI20030932A FI20030932A7 (fi) | 1991-02-22 | 2003-06-24 | Menetelmä cis-FTC:n enantiomeerien erottamiseksi |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI933684A FI114915B (fi) | 1991-02-22 | 1993-08-20 | Menetelmä terapeuttisesti käyttökelpoisten beta-2-hydroksimetyyli-5-(5-fluorisytosin-1-yyli)-1,3-oksatiolaanin enantiomeerien valmistamiseksi |
Country Status (24)
| Country | Link |
|---|---|
| EP (3) | EP0575482A1 (fi) |
| JP (2) | JP2901160B2 (fi) |
| KR (1) | KR0172590B1 (fi) |
| CN (4) | CN1037682C (fi) |
| AT (2) | ATE270291T1 (fi) |
| AU (2) | AU679649B2 (fi) |
| BG (1) | BG62053B1 (fi) |
| BR (1) | BR9205661A (fi) |
| CA (2) | CA2104399C (fi) |
| CZ (1) | CZ295074B6 (fi) |
| DE (2) | DE69233786D1 (fi) |
| DK (2) | DK1439177T3 (fi) |
| ES (2) | ES2345102T3 (fi) |
| FI (2) | FI114915B (fi) |
| HU (2) | HU227823B1 (fi) |
| IE (1) | IE920545A1 (fi) |
| IL (1) | IL100965A (fi) |
| MX (1) | MX9200747A (fi) |
| MY (1) | MY114350A (fi) |
| NO (3) | NO312399B1 (fi) |
| NZ (2) | NZ241625A (fi) |
| PT (1) | PT100151B (fi) |
| RO (2) | RO122814B1 (fi) |
| WO (1) | WO1992014743A2 (fi) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6175008B1 (en) | 1988-04-11 | 2001-01-16 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
| US5466806A (en) * | 1989-02-08 | 1995-11-14 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
| CA2152269C (en) * | 1989-02-08 | 1999-09-21 | Bernard Belleau (Deceased) | Process for preparing substituted 1,3-oxathiolanes with antiviral properties |
| US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
| US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
| 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 |
| US5827727A (en) * | 1990-02-01 | 1998-10-27 | Emory University | Method of resolution of 1,3-oxathiolane nucleoside enantiomers |
| US5276151A (en) * | 1990-02-01 | 1994-01-04 | Emory University | Method of synthesis of 1,3-dioxolane nucleosides |
| US5444063A (en) * | 1990-12-05 | 1995-08-22 | Emory University | Enantiomerically pure β-D-dioxolane nucleosides with selective anti-Hepatitis B virus activity |
| IL100502A (en) * | 1991-01-03 | 1995-12-08 | Iaf Biochem Int | PHARMACEUTICAL PREPARATIONS CONTAINING CIS-4-AMINO-1-) 2-HYDROXIMETHIL-1,3-OXETYOLEN-5-IL (- |
| CA2105486C (en) * | 1991-03-06 | 2003-10-28 | George Robert Painter Iii | Therapeutic nucleosides |
| US6812233B1 (en) | 1991-03-06 | 2004-11-02 | Emory University | Therapeutic nucleosides |
| US5817667A (en) * | 1991-04-17 | 1998-10-06 | University Of Georgia Research Foudation | Compounds and methods for the treatment of cancer |
| GB9110874D0 (en) * | 1991-05-20 | 1991-07-10 | Iaf Biochem Int | Medicaments |
| ZA923641B (en) * | 1991-05-21 | 1993-02-24 | Iaf Biochem Int | Processes for the diastereoselective synthesis of nucleosides |
| GB9116601D0 (en) * | 1991-08-01 | 1991-09-18 | Iaf Biochem Int | 1,3-oxathiolane nucleoside analogues |
| WO1993023021A2 (en) * | 1992-05-13 | 1993-11-25 | The Wellcome Foundation Limited | Therapeutic combinations |
| US6177435B1 (en) | 1992-05-13 | 2001-01-23 | Glaxo Wellcome Inc. | Therapeutic combinations |
| GB9226927D0 (en) * | 1992-12-24 | 1993-02-17 | Iaf Biochem Int | Dideoxy nucleoside analogues |
| TW374087B (en) * | 1993-05-25 | 1999-11-11 | Univ Yale | L-2',3'-dideoxy nucleotide analogs as anti-hepatitis B(HBV) and anti-HIV agents |
| US5627160A (en) * | 1993-05-25 | 1997-05-06 | Yale University | L-2',3'-dideoxy nucleoside analogs as anti-hepatitis B (HBV) and anti-HIV agents |
| US20020120130A1 (en) | 1993-09-10 | 2002-08-29 | Gilles Gosselin | 2' or 3' -deoxy and 2', 3' -dideoxy-beta-L-pentofuranonucleo-side compounds, method of preparation and application in therapy, especially as anti- viral agents |
| WO1995007086A1 (en) * | 1993-09-10 | 1995-03-16 | Emory University | Nucleosides with anti-hepatitis b virus activity |
| GB9320316D0 (en) * | 1993-10-01 | 1993-11-17 | Smithkline Beecham Plc | Pharmaceuticals |
| US5587362A (en) * | 1994-01-28 | 1996-12-24 | Univ. Of Ga Research Foundation | L-nucleosides |
| FR2720397B1 (fr) * | 1994-05-24 | 1996-08-23 | Laphal Laboratoires Sa | Nouveaux oxathiolanes, leur procédé de préparation et les compositions pharmaceutiques qui en renferment. |
| IL115156A (en) | 1994-09-06 | 2000-07-16 | Univ Georgia | Pharmaceutical compositions for the treatment of cancer comprising 1-(2-hydroxymethyl-1,3-dioxolan-4-yl) cytosines |
| US6391859B1 (en) | 1995-01-27 | 2002-05-21 | Emory University | [5-Carboxamido or 5-fluoro]-[2′,3′-unsaturated or 3′-modified]-pyrimidine nucleosides |
| US5703058A (en) * | 1995-01-27 | 1997-12-30 | Emory University | Compositions containing 5-fluoro-2',3'-didehydro-2',3'-dideoxycytidine or a mono-, di-, or triphosphate thereof and a second antiviral agent |
| US5808040A (en) * | 1995-01-30 | 1998-09-15 | Yale University | L-nucleosides incorporated into polymeric structure for stabilization of oligonucleotides |
| US5869461A (en) * | 1995-03-16 | 1999-02-09 | Yale University | Reducing toxicity of L-nucleosides with D-nucleosides |
| AU722214B2 (en) * | 1995-06-07 | 2000-07-27 | Centre National De La Recherche Scientifique (Cnrs) | Nucleosides with anti-hepatitis B virus activity |
| JP2000515852A (ja) * | 1996-06-25 | 2000-11-28 | グラクソ、グループ、リミテッド | Hivの治療に使用するためのvx478、ジドブジン、ftcおよび/または3tcを含んでなる組合わせ |
| US5753789A (en) * | 1996-07-26 | 1998-05-19 | Yale University | Oligonucleotides containing L-nucleosides |
| EA005097B1 (ru) | 1997-03-19 | 2004-10-28 | Эмори Юниверсити | Синтез 1,3-оксаселеноланнуклеозидов, обладающих активностью против вируса иммунодефицита человека и против вируса гепатита-b |
| IT1290447B1 (it) | 1997-03-28 | 1998-12-03 | Zambon Spa | Derivati 1,3-ossatiolanici ad attivita' antivirale |
| WO1998044913A2 (en) | 1997-04-07 | 1998-10-15 | Triangle Pharmaceuticals, Inc. | Compositions containing mkc-442 in combination with other antiviral agents |
| WO1999037754A2 (en) * | 1998-01-26 | 1999-07-29 | Pharm-Eco Laboratories, Inc. | Enzyme activated supports for enantiomeric separations |
| EA200700564A1 (ru) | 1998-02-25 | 2007-08-31 | Эмори Юниверсити | 2`-фторнуклеозиды |
| RU2244712C2 (ru) * | 1998-08-12 | 2005-01-20 | Гайлид Сайенсиз, Инк. | Способ получения 1,3-оксатиоланового нуклеозида, способ получения производного 1,3-оксатиоланил-5-она |
| US6979561B1 (en) | 1998-10-09 | 2005-12-27 | Gilead Sciences, Inc. | Non-homogeneous systems for the resolution of enantiomeric mixtures |
| DE69912842T2 (de) | 1998-12-23 | 2004-05-13 | Shire Biochem Inc., Laval | Antivirale nukleosidanaloga |
| KR100339786B1 (ko) * | 1999-04-02 | 2002-06-07 | 안용현 | 라세미 혼합물 상태로 존재하는 뉴클레오시드로부터 거울상 이성질체의 분리 방법 |
| EP1634888A3 (en) | 1999-11-12 | 2007-11-21 | Pharmasset, Inc. | Synthesis of 2'-deoxy-L-nucleosides |
| US6436948B1 (en) | 2000-03-03 | 2002-08-20 | University Of Georgia Research Foundation Inc. | Method for the treatment of psoriasis and genital warts |
| CA2308559C (en) | 2000-05-16 | 2005-07-26 | Brantford Chemicals Inc. | 1,3-oxathiolan-5-ones useful in the production of antiviral nucleoside analogues |
| CA2426187C (en) | 2000-10-18 | 2011-08-16 | Pharmasset Limited | Modified nucleosides for the treatment of viral infections and abnormal cellular proliferation |
| US6828119B2 (en) * | 2001-01-04 | 2004-12-07 | Bristol Myers Squibb Company | Enzymatic deprotection of amines and hydroxides |
| DE10104231A1 (de) | 2001-01-31 | 2002-08-08 | Consortium Elektrochem Ind | Verfahren zur enzymatischen Herstellung von enantiomerenreinen 1,3-Dioxolan-4-on-Derivaten |
| DK1574512T3 (da) | 2001-03-01 | 2008-03-03 | Abbott Lab | Polymorfe og andre krystallinske former af cis-FTC |
| AU2008202336B2 (en) * | 2001-03-01 | 2011-11-10 | Abbvie Inc. | Polymorphic and other crystalline forms of cis-FTC |
| WO2003087119A1 (en) * | 2002-04-12 | 2003-10-23 | Achillion Pharmaceuticals, Inc. | METHOD FOR SYNTHESIZING β-L-FLUORO-2´,3´DIDEHYDROCYTIDINE (β-L-FD4C) |
| WO2004048590A1 (en) * | 2002-11-18 | 2004-06-10 | Shire Biochem Inc. | Stereoselective process for the production of dioxolane nucleoside analogues |
| JP4996241B2 (ja) | 2003-01-14 | 2012-08-08 | ギリアード サイエンシーズ, インコーポレイテッド | 組み合わせ抗ウイルス治療のための組成物および方法 |
| ITMI20030578A1 (it) * | 2003-03-24 | 2004-09-25 | Clariant Lsm Italia Spa | Processo ed intermedi per la preparazione di emtricitabina |
| MX2007011274A (es) * | 2005-03-14 | 2008-03-13 | Shire Canada Inc | Procesos y metodos para la preparacion de cis-2-hidroximetil-4-(ci tosin-1-il)-1,3-oxatiolano opticamente activas o sales aceptables farmaceuticamente del mismo. |
| TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
| TWI375560B (en) | 2005-06-13 | 2012-11-01 | Gilead Sciences Inc | Composition comprising dry granulated emtricitabine and tenofovir df and method for making the same |
| PL2144604T3 (pl) | 2007-02-28 | 2012-02-29 | Conatus Pharmaceuticals Inc | Sposoby leczenia przewlekłego zapalenia wątroby typu C z zastosowaniem RO 113-0830 |
| AU2008265397C1 (en) | 2007-06-18 | 2013-08-29 | Sunshine Lake Pharma Co., Ltd. | Bromo-phenyl substituted thiazolyl dihydropyrimidines |
| WO2009084033A2 (en) | 2007-12-07 | 2009-07-09 | Matrix Laboratories Limited | Process for producing 5-fluoro-1-(2r,5s)-[2-(hydroxymethyl)-1,3-oxathiolan-5-yi]cytosine |
| WO2009107692A1 (ja) * | 2008-02-29 | 2009-09-03 | 株式会社カネカ | 2’-水酸基が保護されたリボヌクレオシド誘導体およびその製造方法 |
| US8716263B2 (en) | 2008-12-23 | 2014-05-06 | Gilead Pharmasset Llc | Synthesis of purine nucleosides |
| US8551973B2 (en) | 2008-12-23 | 2013-10-08 | Gilead Pharmasset Llc | Nucleoside analogs |
| PA8855601A1 (es) | 2008-12-23 | 2010-07-27 | Forformidatos de nucleósidos | |
| EP2377862A1 (en) | 2010-03-29 | 2011-10-19 | Esteve Química, S.A. | Process for obtaining emtricitabine |
| WO2011123668A2 (en) | 2010-03-31 | 2011-10-06 | Pharmasset, Inc. | Stereoselective synthesis of phosphorus containing actives |
| EA201691695A1 (ru) | 2010-11-19 | 2017-11-30 | Джилид Сайэнс, Инк. | Терапевтические композиции, содержащие рилпивирин hcl и тенофовира дизопроксилфумарат |
| WO2013167743A1 (en) | 2012-05-11 | 2013-11-14 | Akron Molecules Gmbh | Use of compounds for the treatment of pain |
| CA2889903C (en) | 2012-10-29 | 2021-03-09 | Manjinder Singh Phull | Antiviral phosphonate analogues and process for preparation thereof |
| CN102911167B (zh) * | 2012-11-09 | 2014-06-25 | 合肥工业大学 | 一种高光学纯度的核苷类中间体的制备方法 |
| CN104059057A (zh) * | 2014-01-03 | 2014-09-24 | 石家庄龙泽制药有限公司 | 拉米夫定杂质3-tu的制备方法 |
| CN108285895B (zh) * | 2018-01-26 | 2020-06-23 | 中国科学院南海海洋研究所 | 一种酯酶EstC11及其编码基因和应用 |
| KR102069443B1 (ko) | 2018-08-31 | 2020-01-22 | (주)대한뷰티산업진흥원 | 울금, 비트 및 무 추출물을 포함하는 바이오셀룰로오스 및 이의 제조방법 |
| US20230218644A1 (en) | 2020-04-16 | 2023-07-13 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
| JP2023542455A (ja) * | 2020-07-14 | 2023-10-10 | スーチュワン ユニバーシティ | 3-デオキシ-2-ケトアルドン酸窒素含有誘導体、その製造方法及びその使用 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4914028A (en) * | 1988-02-10 | 1990-04-03 | Eli Lilly And Company | Method of preparing beta-2',2'-difluoronucleosides |
| US5047407A (en) * | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties |
| US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
| WO1992008717A1 (en) * | 1990-11-13 | 1992-05-29 | Biochem Pharma Inc. | Substituted 1,3-oxathiolanes and substituted 1,3-dithiolanes with antiviral properties |
| CA2105486C (en) | 1991-03-06 | 2003-10-28 | George Robert Painter Iii | Therapeutic nucleosides |
-
1992
- 1992-02-17 IL IL10096592A patent/IL100965A/en not_active IP Right Cessation
- 1992-02-17 NZ NZ241625A patent/NZ241625A/en not_active IP Right Cessation
- 1992-02-17 NZ NZ250842A patent/NZ250842A/en not_active IP Right Cessation
- 1992-02-20 WO PCT/US1992/001339 patent/WO1992014743A2/en not_active Ceased
- 1992-02-20 CA CA002104399A patent/CA2104399C/en not_active Expired - Lifetime
- 1992-02-20 BR BR9205661A patent/BR9205661A/pt not_active Application Discontinuation
- 1992-02-20 DK DK04076245.2T patent/DK1439177T3/da active
- 1992-02-20 DK DK99203367T patent/DK0984013T3/da active
- 1992-02-20 EP EP19920908027 patent/EP0575482A1/en not_active Ceased
- 1992-02-20 KR KR1019930702516A patent/KR0172590B1/ko not_active Expired - Lifetime
- 1992-02-20 AT AT99203367T patent/ATE270291T1/de active
- 1992-02-20 HU HU9302377A patent/HU227823B1/hu active Protection Beyond IP Right Term
- 1992-02-20 JP JP4507549A patent/JP2901160B2/ja not_active Expired - Lifetime
- 1992-02-20 AT AT04076245T patent/ATE469147T1/de active
- 1992-02-20 ES ES04076245T patent/ES2345102T3/es not_active Expired - Lifetime
- 1992-02-20 DE DE69233786T patent/DE69233786D1/de not_active Expired - Lifetime
- 1992-02-20 DE DE69233379T patent/DE69233379T2/de not_active Expired - Lifetime
- 1992-02-20 ES ES99203367T patent/ES2224547T3/es not_active Expired - Lifetime
- 1992-02-20 RO ROA200400584A patent/RO122814B1/ro unknown
- 1992-02-20 EP EP99203367A patent/EP0984013B1/en not_active Expired - Lifetime
- 1992-02-20 RO RO93-01137A patent/RO119365B1/ro unknown
- 1992-02-20 EP EP04076245A patent/EP1439177B1/en not_active Expired - Lifetime
- 1992-02-20 CZ CS1992497A patent/CZ295074B6/cs not_active IP Right Cessation
- 1992-02-20 CA CA2513440A patent/CA2513440C/en not_active Expired - Lifetime
- 1992-02-21 MY MYPI92000287A patent/MY114350A/en unknown
- 1992-02-21 PT PT100151A patent/PT100151B/pt not_active IP Right Cessation
- 1992-02-21 MX MX9200747A patent/MX9200747A/es active IP Right Grant
- 1992-02-21 IE IE054592A patent/IE920545A1/en not_active Application Discontinuation
- 1992-02-22 CN CN92101981A patent/CN1037682C/zh not_active Expired - Lifetime
-
1993
- 1993-08-20 BG BG98062A patent/BG62053B1/bg unknown
- 1993-08-20 FI FI933684A patent/FI114915B/fi not_active IP Right Cessation
- 1993-08-20 NO NO19932980A patent/NO312399B1/no active IP Right Maintenance
-
1995
- 1995-06-28 HU HU95P/P00510P patent/HU211344A9/hu unknown
- 1995-08-18 CN CN95109814A patent/CN1109108C/zh not_active Expired - Lifetime
- 1995-11-20 AU AU37943/95A patent/AU679649B2/en not_active Withdrawn - After Issue
-
1997
- 1997-11-06 JP JP34046997A patent/JP3292830B2/ja not_active Expired - Lifetime
-
1998
- 1998-05-15 CN CN98108905A patent/CN1084745C/zh not_active Expired - Lifetime
- 1998-08-17 AU AU80773/98A patent/AU8077398A/en not_active Abandoned
-
2002
- 2002-09-30 CN CNB021440336A patent/CN100396785C/zh not_active Expired - Lifetime
-
2003
- 2003-06-24 FI FI20030932A patent/FI20030932A7/fi unknown
-
2005
- 2005-07-01 NO NO2005015C patent/NO2005015I2/no not_active Application Discontinuation
-
2008
- 2008-06-13 NO NO2008010C patent/NO2008010I1/no unknown
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