FI20030932A - Förfarande för upplösning av cis-enatiomerer av FTC - Google Patents
Förfarande för upplösning av cis-enatiomerer av FTCInfo
- Publication number
- FI20030932A FI20030932A FI20030932A FI20030932A FI20030932A FI 20030932 A FI20030932 A FI 20030932A FI 20030932 A FI20030932 A FI 20030932A FI 20030932 A FI20030932 A FI 20030932A FI 20030932 A FI20030932 A FI 20030932A
- Authority
- FI
- Finland
- Prior art keywords
- cis
- ftc
- enantiomers
- separation
- oxathiolane
- Prior art date
Links
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)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Genetics & Genomics (AREA)
- Communicable Diseases (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (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 |
---|---|
FI20030932A true FI20030932A (sv) | 2003-06-24 |
Family
ID=35276919
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI933684A FI114915B (sv) | 1991-02-22 | 1993-08-20 | Förfarande för framställning av terapeutiskt användbara enantiomerer av beta-2-hydroximetyl-5-(5-fluorcytosin-1-yl)-1,3-oxatiolan |
FI20030932A FI20030932A (sv) | 1991-02-22 | 2003-06-24 | Förfarande för upplösning av cis-enatiomerer av FTC |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI933684A FI114915B (sv) | 1991-02-22 | 1993-08-20 | Förfarande för framställning av terapeutiskt användbara enantiomerer av beta-2-hydroximetyl-5-(5-fluorcytosin-1-yl)-1,3-oxatiolan |
Country Status (25)
Country | Link |
---|---|
EP (3) | EP0984013B1 (sv) |
JP (2) | JP2901160B2 (sv) |
KR (1) | KR0172590B1 (sv) |
CN (4) | CN1037682C (sv) |
AT (2) | ATE469147T1 (sv) |
AU (2) | AU679649B2 (sv) |
BG (1) | BG62053B1 (sv) |
BR (1) | BR9205661A (sv) |
CA (2) | CA2104399C (sv) |
CZ (1) | CZ295074B6 (sv) |
DE (2) | DE69233786D1 (sv) |
DK (2) | DK1439177T3 (sv) |
ES (2) | ES2224547T3 (sv) |
FI (2) | FI114915B (sv) |
HK (1) | HK1026419A1 (sv) |
HU (2) | HU227823B1 (sv) |
IE (1) | IE920545A1 (sv) |
IL (1) | IL100965A (sv) |
MX (1) | MX9200747A (sv) |
MY (1) | MY114350A (sv) |
NO (3) | NO312399B1 (sv) |
NZ (2) | NZ241625A (sv) |
PT (1) | PT100151B (sv) |
RO (2) | RO122814B1 (sv) |
WO (1) | WO1992014743A2 (sv) |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5466806A (en) * | 1989-02-08 | 1995-11-14 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
US5684164A (en) | 1988-04-11 | 1997-11-04 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
ES2196004T3 (es) * | 1989-02-08 | 2003-12-16 | Iaf Biochem Int | Procedimiento para preparar 1,3-oxatiolanos sustituidos con propiedades antivirales. |
US5914331A (en) * | 1990-02-01 | 1999-06-22 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
US5728575A (en) | 1990-02-01 | 1998-03-17 | 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 |
US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
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 (- |
US6812233B1 (en) | 1991-03-06 | 2004-11-02 | Emory University | Therapeutic nucleosides |
PT100198B (pt) * | 1991-03-06 | 2000-03-31 | Univ Emory | Utilizacao de nucleosido oxatiolano para a preparacao de composicoes para fins terapeuticos |
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 |
ZA923640B (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 |
US6177435B1 (en) | 1992-05-13 | 2001-01-23 | Glaxo Wellcome Inc. | Therapeutic combinations |
WO1993023021A2 (en) * | 1992-05-13 | 1993-11-25 | The Wellcome Foundation Limited | 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 |
WO1995007086A1 (en) * | 1993-09-10 | 1995-03-16 | Emory University | Nucleosides with anti-hepatitis b virus activity |
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 |
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 |
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 |
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 |
US6391859B1 (en) | 1995-01-27 | 2002-05-21 | Emory University | [5-Carboxamido or 5-fluoro]-[2′,3′-unsaturated or 3′-modified]-pyrimidine nucleosides |
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 |
WO1996040164A1 (en) | 1995-06-07 | 1996-12-19 | Emory University | Nucleosides with anti-hepatitis b virus activity |
PL330747A1 (en) * | 1996-06-25 | 1999-05-24 | Glaxo Group Ltd | Vx478, zidovudin, ftc and/or 3tc containing combinations for use in treating hiv infections |
US5753789A (en) * | 1996-07-26 | 1998-05-19 | Yale University | Oligonucleotides containing L-nucleosides |
EP0970078B1 (en) * | 1997-03-19 | 2004-05-19 | Emory University | Synthesis, anti-human immunodeficiency virus and anti-hepatitis b virus activities of 1,3-oxaselenolane nucleosides |
IT1290447B1 (it) | 1997-03-28 | 1998-12-03 | Zambon Spa | Derivati 1,3-ossatiolanici ad attivita' antivirale |
EP0986375A2 (en) | 1997-04-07 | 2000-03-22 | Triangle Pharmaceuticals Inc. | Use of 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 |
CA2340214C (en) | 1998-08-12 | 2007-10-30 | Triangle Pharmaceuticals, Inc. | Method of manufacture of 1,3-oxathiolane nucleosides |
US6979561B1 (en) | 1998-10-09 | 2005-12-27 | Gilead Sciences, Inc. | Non-homogeneous systems for the resolution of enantiomeric mixtures |
EA004767B1 (ru) | 1998-12-23 | 2004-08-26 | Шайре Байокем Инк. | Аналоги нуклеозида (варианты) и их применение, комбинация и способ лечения вирусных инфекций, фармацевтическая композиция |
KR100339786B1 (ko) * | 1999-04-02 | 2002-06-07 | 안용현 | 라세미 혼합물 상태로 존재하는 뉴클레오시드로부터 거울상 이성질체의 분리 방법 |
EP1600452A3 (en) | 1999-11-12 | 2008-09-10 | 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 |
KR101005299B1 (ko) | 2000-10-18 | 2011-01-04 | 파마셋 인코포레이티드 | 바이러스 감염 및 비정상적인 세포 증식의 치료를 위한 변형된 뉴클레오시드 |
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 |
CA2788498C (en) * | 2001-03-01 | 2016-02-16 | Gilead Sciences, Inc. | Polymorphic and other crystalline forms of cis-ftc |
AU2008202336B2 (en) * | 2001-03-01 | 2011-11-10 | Abbvie Inc. | Polymorphic and other crystalline forms of cis-FTC |
CN1329407C (zh) * | 2002-04-12 | 2007-08-01 | 阿奇林医药品公司 | 合成β-L-5-氟-2′,3′-双脱氧-2′,3′-双脱氢胞嘧啶核苷的方法 |
WO2004048590A1 (en) * | 2002-11-18 | 2004-06-10 | Shire Biochem Inc. | Stereoselective process for the production of dioxolane nucleoside analogues |
CN105596356A (zh) | 2003-01-14 | 2016-05-25 | 吉里德科学公司 | 用于联合抗病毒治疗的组合物和方法 |
ITMI20030578A1 (it) * | 2003-03-24 | 2004-09-25 | Clariant Lsm Italia Spa | Processo ed intermedi per la preparazione di emtricitabina |
JP5001254B2 (ja) * | 2005-03-14 | 2012-08-15 | シャイアー カナダ インコーポレイテッド | 光学的に活性なcis−2−ヒドロキシメチル−4−(シトシン−1’−イル)−1,3−オキサチオランまたはその薬学的に許容される塩の製造方法 |
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 |
TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
BRPI0808089A2 (pt) | 2007-02-28 | 2014-07-15 | Conatus Pharmaceuticals Inc | Método para tratar uma doença do fígado, para diminuir um nível elevado de uma enzima do fígado, para inibir uma cascata de sinalização de tnf-alfa e uma cascata de sinalização de alfa-faz, para reduzir um dano ao fígado, para suprimir a apoptose excessiva em uma célula de fígado, e para inibir a replicação do vírus da hepatite c. |
US8236797B2 (en) | 2007-06-18 | 2012-08-07 | 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 |
JPWO2009107692A1 (ja) * | 2008-02-29 | 2011-07-07 | 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 |
PA8855601A1 (es) | 2008-12-23 | 2010-07-27 | Forformidatos de nucleósidos | |
US8551973B2 (en) | 2008-12-23 | 2013-10-08 | Gilead Pharmasset Llc | Nucleoside analogs |
KR20110104074A (ko) | 2008-12-23 | 2011-09-21 | 파마셋 인코포레이티드 | 퓨린 뉴클레오시드의 합성 |
EP2377862A1 (en) | 2010-03-29 | 2011-10-19 | Esteve Química, S.A. | Process for obtaining emtricitabine |
CA2794671C (en) | 2010-03-31 | 2018-05-01 | Gilead Pharmasset Llc | Stereoselective synthesis of phosphorus containing actives |
BR112013012245B1 (pt) | 2010-11-19 | 2022-09-27 | Janssen Sciences Ireland Uc | Comprimido compreendendo hcl de rilpivirina e fumarato de tenofovir disoproxila seu uso no tratamento profilático ou terapêutico de uma infecção por hiv |
EP2846788A1 (en) | 2012-05-11 | 2015-03-18 | Akron Molecules AG | Use of compounds for the treatment of pain |
WO2014068265A1 (en) | 2012-10-29 | 2014-05-08 | Cipla Limited | 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 |
WO2021209563A1 (en) | 2020-04-16 | 2021-10-21 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
CN114190092B (zh) * | 2020-07-14 | 2023-07-18 | 四川大学 | 3-去氧-2-酮糖酸含氮衍生物及其制备方法和用途 |
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 |
CA2095613C (en) * | 1990-11-13 | 2001-01-02 | Bernard Belleau | Substituted 1, 3-oxathiolanes and substituted 1, 3-dithiolanes with antiviral properties |
PT100198B (pt) | 1991-03-06 | 2000-03-31 | Univ Emory | Utilizacao de nucleosido oxatiolano para a preparacao de composicoes para fins terapeuticos |
-
1992
- 1992-02-17 NZ NZ241625A patent/NZ241625A/en not_active IP Right Cessation
- 1992-02-17 IL IL10096592A patent/IL100965A/en not_active IP Right Cessation
- 1992-02-17 NZ NZ250842A patent/NZ250842A/en not_active IP Right Cessation
- 1992-02-20 DE DE69233786T patent/DE69233786D1/de not_active Expired - Lifetime
- 1992-02-20 ES ES99203367T patent/ES2224547T3/es 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 CA CA002104399A patent/CA2104399C/en not_active Expired - Lifetime
- 1992-02-20 CZ CS1992497A patent/CZ295074B6/cs not_active IP Right Cessation
- 1992-02-20 AT AT99203367T patent/ATE270291T1/de active
- 1992-02-20 BR BR9205661A patent/BR9205661A/pt not_active Application Discontinuation
- 1992-02-20 EP EP99203367A patent/EP0984013B1/en not_active Expired - Lifetime
- 1992-02-20 KR KR1019930702516A patent/KR0172590B1/ko not_active IP Right Cessation
- 1992-02-20 DK DK04076245.2T patent/DK1439177T3/da active
- 1992-02-20 RO ROA200400584A patent/RO122814B1/ro unknown
- 1992-02-20 JP JP4507549A patent/JP2901160B2/ja not_active Expired - Lifetime
- 1992-02-20 RO RO93-01137A patent/RO119365B1/ro unknown
- 1992-02-20 CA CA2513440A patent/CA2513440C/en not_active Expired - Lifetime
- 1992-02-20 EP EP19920908027 patent/EP0575482A1/en not_active Ceased
- 1992-02-20 DK DK99203367T patent/DK0984013T3/da active
- 1992-02-20 EP EP04076245A patent/EP1439177B1/en not_active Expired - Lifetime
- 1992-02-20 HU HU9302377A patent/HU227823B1/hu active Protection Beyond IP Right Term
- 1992-02-20 WO PCT/US1992/001339 patent/WO1992014743A2/en active IP Right Grant
- 1992-02-20 DE DE69233379T patent/DE69233379T2/de not_active Expired - Lifetime
- 1992-02-21 IE IE054592A patent/IE920545A1/en not_active Application Discontinuation
- 1992-02-21 PT PT100151A patent/PT100151B/pt not_active IP Right Cessation
- 1992-02-21 MY MYPI92000287A patent/MY114350A/en unknown
- 1992-02-21 MX MX9200747A patent/MX9200747A/es active IP Right Grant
- 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/sv 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
- 1998-12-28 HK HK00105566A patent/HK1026419A1/xx not_active IP Right Cessation
-
2002
- 2002-09-30 CN CNB021440336A patent/CN100396785C/zh not_active Expired - Lifetime
-
2003
- 2003-06-24 FI FI20030932A patent/FI20030932A/sv 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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