CY2036A - Substitued-1,3-oxathiolanes with antiviral properties - Google Patents

Substitued-1,3-oxathiolanes with antiviral properties

Info

Publication number
CY2036A
CY2036A CY203698A CY203698A CY2036A CY 2036 A CY2036 A CY 2036A CY 203698 A CY203698 A CY 203698A CY 203698 A CY203698 A CY 203698A CY 2036 A CY2036 A CY 2036A
Authority
CY
Cyprus
Prior art keywords
oxathiolanes
substitued
antiviral properties
antiviral
properties
Prior art date
Application number
CY203698A
Other languages
English (en)
Original Assignee
Iaf Biochem Int
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=25678044&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CY2036(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from CA002152269A external-priority patent/CA2152269C/fr
Application filed by Iaf Biochem Int filed Critical Iaf Biochem Int
Publication of CY2036A publication Critical patent/CY2036A/xx

Links

Classifications

    • 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
    • C07D411/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
    • C07D327/04—Five-membered rings
    • 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
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
    • 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
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
CY203698A 1989-02-08 1998-02-20 Substitued-1,3-oxathiolanes with antiviral properties CY2036A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/308,101 US5047407A (en) 1989-02-08 1989-02-08 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties
CA002152269A CA2152269C (fr) 1989-02-08 1992-12-21 Methode de preparation de derives de substitution de 1,3-oxathiolanes aux proprietes antivirales

Publications (1)

Publication Number Publication Date
CY2036A true CY2036A (en) 1998-02-20

Family

ID=25678044

Family Applications (1)

Application Number Title Priority Date Filing Date
CY203698A CY2036A (en) 1989-02-08 1998-02-20 Substitued-1,3-oxathiolanes with antiviral properties

Country Status (35)

Country Link
US (1) US5047407A (fr)
EP (2) EP0711771B1 (fr)
JP (4) JP2644357B2 (fr)
KR (1) KR960007531B1 (fr)
CN (1) CN1033640C (fr)
AP (1) AP136A (fr)
AT (2) ATE254125T1 (fr)
AU (1) AU630913B2 (fr)
CA (1) CA2009637C (fr)
CY (1) CY2036A (fr)
CZ (1) CZ282720B6 (fr)
DE (3) DE19675032I2 (fr)
DK (2) DK0711771T3 (fr)
ES (2) ES2206476T3 (fr)
FI (1) FI98065C (fr)
GR (1) GR3019919T3 (fr)
HK (2) HK51997A (fr)
HR (1) HRP940040B1 (fr)
HU (2) HU208134B (fr)
IE (1) IE72184B1 (fr)
IL (1) IL93318A (fr)
LU (1) LU88809I2 (fr)
MX (1) MX19437A (fr)
NL (1) NL960025I2 (fr)
NO (2) NO179518C (fr)
NZ (1) NZ232421A (fr)
OA (1) OA09193A (fr)
PL (1) PL164785B1 (fr)
PT (1) PT93094B (fr)
RU (1) RU2092485C1 (fr)
SG (2) SG48737A1 (fr)
SI (1) SI9010243B (fr)
SK (1) SK279175B6 (fr)
YU (1) YU48840B (fr)
ZA (1) ZA90943B (fr)

Families Citing this family (149)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7119202B1 (en) 1989-02-08 2006-10-10 Glaxo Wellcome Inc. Substituted-1,3-oxathiolanes and substituted-1,3-dioxolanes with antiviral properties
US5047407A (en) 1989-02-08 1991-09-10 Iaf Biochem International, Inc. 2-substituted-5-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
US6350753B1 (en) 1988-04-11 2002-02-26 Biochem Pharma Inc. 2-Substituted-4-substituted-1,3-dioxolanes and use thereof
US5466806A (en) * 1989-02-08 1995-11-14 Biochem Pharma Inc. Processes for preparing substituted 1,3-oxathiolanes with antiviral properties
US5270315A (en) * 1988-04-11 1993-12-14 Biochem Pharma Inc. 4-(purinyl bases)-substituted-1,3-dioxlanes
US6903224B2 (en) * 1988-04-11 2005-06-07 Biochem Pharma Inc. Substituted 1,3-oxathiolanes
AU3154993A (en) * 1989-02-08 1994-07-19 Biochem Pharma Inc. Process for preparing substituted 1,3-oxathiolanes with antiviral properties
UA45942A (uk) * 1989-02-08 2002-05-15 Біокем Фарма, Інк. 1,3-оксатіолан, його похідні, спосіб (варіанти) його одержання та фармацевтична композиція
US6703396B1 (en) 1990-02-01 2004-03-09 Emory University Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers
US5700937A (en) * 1990-02-01 1997-12-23 Emory University Method for the synthesis, compositions and use of 2'-deoxy-5-fluoro-3'-thiacytidine and related compounds
US5276151A (en) * 1990-02-01 1994-01-04 Emory University Method of synthesis of 1,3-dioxolane nucleosides
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
US5728575A (en) * 1990-02-01 1998-03-17 Emory University Method of resolution of 1,3-oxathiolane nucleoside enantiomers
GB9009861D0 (en) * 1990-05-02 1990-06-27 Glaxo Group Ltd Chemical compounds
US6228860B1 (en) 1990-11-13 2001-05-08 Biochem Pharma Inc. Substituted 1,3-oxathiolanes with antiviral properties
ATE143016T1 (de) * 1990-11-13 1996-10-15 Iaf Biochem Int Substituierte 1,3-oxathiolane mit antiviralen eigenschaften
US5587480A (en) * 1990-11-13 1996-12-24 Biochem Pharma, Inc. Substituted 1,3-oxathiolanes and substituted 1,3-dithiolanes with antiviral properties
US6369066B1 (en) 1990-11-13 2002-04-09 Biochem Pharma, Inc. Substituted 1,3-oxathiolanes with antiviral properties
US5179104A (en) * 1990-12-05 1993-01-12 University Of Georgia Research Foundation, Inc. Process for the preparation of enantiomerically pure β-D-(-)-dioxolane-nucleosides
US5248776A (en) * 1990-12-05 1993-09-28 University Of Georgia Research Foundation, Inc. Process for enantiomerically pure β-L-1,3-oxathiolane nucleosides
US5925643A (en) * 1990-12-05 1999-07-20 Emory University Enantiomerically pure β-D-dioxolane-nucleosides
WO1992010496A1 (fr) * 1990-12-05 1992-06-25 University Of Georgia Research Foundation, Inc. NUCLEOSIDES DE β-L-(-)-1,3-OXATHIOLANE ENANTIOMERIQUEMENT PURS
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 (-
NZ250842A (en) * 1991-02-22 1996-03-26 Univ Emory Resolution of a racemic mixture of nucleoside enantiomers such as 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane (ftc)
GB9104740D0 (en) * 1991-03-06 1991-04-17 Wellcome Found Antiviral nucleoside combination
US6812233B1 (en) * 1991-03-06 2004-11-02 Emory University Therapeutic nucleosides
ATE361293T1 (de) * 1991-03-06 2007-05-15 Univ Emory Salze und amide von (-) cis 5-fluoro-2'-deoxy-3'- thiacytidine geeignet für die behandlung von hepatitis b
WO1992018517A1 (fr) * 1991-04-17 1992-10-29 Yale University Procede de traitement ou de prevention du virus de l'hepatite b
US5817667A (en) * 1991-04-17 1998-10-06 University Of Georgia Research Foudation Compounds and methods for the treatment of cancer
GB9109506D0 (en) * 1991-05-02 1991-06-26 Wellcome Found Therapeutic nucleosides
DK0513917T4 (da) * 1991-05-16 2001-06-25 Glaxo Group Ltd Antivirale kombinationer indeholdende nukleosidanaloger
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
GB9111902D0 (en) * 1991-06-03 1991-07-24 Glaxo Group Ltd Chemical compounds
GB9116601D0 (en) * 1991-08-01 1991-09-18 Iaf Biochem Int 1,3-oxathiolane nucleoside analogues
EP0530407B1 (fr) * 1991-09-04 1996-06-05 Stichting REGA V.Z.W. Dérivés substitués de nucléosides, leurs méthodes de préparation et compositions pharmaceutiques les contenant
US20050192299A1 (en) * 1992-04-16 2005-09-01 Yung-Chi Cheng Method of treating or preventing hepatitis B virus
US6177435B1 (en) 1992-05-13 2001-01-23 Glaxo Wellcome Inc. Therapeutic combinations
DK0639971T3 (da) * 1992-05-13 2000-03-20 Wellcome Found Terapeutiske kombinationer
US6444656B1 (en) 1992-12-23 2002-09-03 Biochem Pharma, Inc. Antiviral phosphonate nucleotides
US6005107A (en) 1992-12-23 1999-12-21 Biochem Pharma, Inc. Antiviral compounds
GB9226879D0 (en) * 1992-12-23 1993-02-17 Iaf Biochem Int Anti-viral compounds
GB9311709D0 (en) * 1993-06-07 1993-07-21 Iaf Biochem Int Stereoselective synthesis of nucleoside analogues using bicycle intermediate
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 (fr) * 1993-09-10 1995-03-16 Emory University Nucleosides a activite contre le virus de l'hepatite b
US5587362A (en) * 1994-01-28 1996-12-24 Univ. Of Ga Research Foundation L-nucleosides
IL113432A (en) * 1994-04-23 2000-11-21 Glaxo Group Ltd Process for the diastereoselective synthesis of nucleoside analogues
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
MY115461A (en) 1995-03-30 2003-06-30 Wellcome Found Synergistic combinations of zidovudine, 1592u89 and 3tc
AU5527196A (en) * 1995-04-04 1996-10-23 Brigham And Women's Hospital Inhibiting retroviral replication
JP4413996B2 (ja) 1995-06-07 2010-02-10 エモリー・ユニバーシティ 抗ｂ型肝炎ウィルス活性を有するヌクレオシド
GB9605293D0 (en) * 1996-03-13 1996-05-15 Glaxo Group Ltd Medicaments
FR2746396B1 (fr) * 1996-03-20 1998-06-05 Inst Nat Sante Rech Med 1,3-thiazolidin-4-ones et 1,3-thiazolidines substituees, procede d'obtention de ces composes et leurs utilisations comme medicaments
US6544961B1 (en) 1996-06-25 2003-04-08 Smithkline Beecham Corporation Combinations comprising VX478, zidovudine, FTC and/or 3TC for use in the treatments of HIV
US5753789A (en) * 1996-07-26 1998-05-19 Yale University Oligonucleotides containing L-nucleosides
US6113920A (en) * 1996-10-31 2000-09-05 Glaxo Wellcome Inc. Pharmaceutical compositions
US6022876A (en) * 1996-11-15 2000-02-08 Yale University L-β-dioxolane uridine analogs and methods for treating and preventing Epstein-Barr virus infections
US5792773A (en) * 1996-11-15 1998-08-11 Yale University L-β-dioxolane uridine analog administration for treating Epstein-Barr virus infection
US20040044016A1 (en) * 1997-01-31 2004-03-04 Mitsubishi Chemical Corporation Antiviral agents
ES2221164T3 (es) 1997-03-19 2004-12-16 Emory University Sintesis y actividad de la inmunodeficiencia humana y antivirus de la hepatitis b de nucleosidos de 1,3-oxaselenolano.
TW536403B (en) * 1997-03-24 2003-06-11 Glaxo Group Ltd An ethanol and ethylenediaminetetraacetic acid free pharmaceutical composition comprising lamivudine and exhibiting antimicrobial preservative efficacy
IT1290447B1 (it) * 1997-03-28 1998-12-03 Zambon Spa Derivati 1,3-ossatiolanici ad attivita' antivirale
AU6898498A (en) 1997-04-07 1998-10-30 Triangle Pharmaceuticals, Inc. Use of mkc-442 in combination with other antiviral agents
CA2322008C (fr) 1998-02-25 2011-06-28 Emory University 2'-fluoronucleosides
EP1754710A3 (fr) 1998-02-25 2007-12-19 Emory University 2'-Fluoronucleosides
US6215004B1 (en) 1998-08-12 2001-04-10 Emory University 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
DE69942042D1 (de) 1998-11-02 2010-04-01 Gilead Sciences Inc Kombinationstherapie zur Behandlung von Hepatitis B Infektionen
KR100618028B1 (ko) 1998-11-05 2006-08-30 쌍트르 나쉬오날 드 라 르쉐르스 쉬앙티피끄 항-ｂ형 간염 활성을 가진 뉴클레오시드
NZ513094A (en) 1998-12-23 2004-05-28 Shire Biochem Inc Antiviral nucleoside analogues
US6630480B1 (en) * 1999-03-29 2003-10-07 Biochem Pharma Inc. Methods of treating leukemia
AU756295B2 (en) 1999-05-26 2003-01-09 Johnson Matthey Pharmaceutical Materials, Inc. Methods of separating FTC isomers and derivatives thereof
US6752929B1 (en) * 1999-05-26 2004-06-22 Johnson Matthey Pharmaceutical Materials, Inc. Methods of separating FTC isomers and derivatives thereof
US6653318B1 (en) * 1999-07-21 2003-11-25 Yale University 5-(E)-Bromovinyl uracil analogues and related pyrimidine nucleosides as anti-viral agents and methods of use
US6432966B2 (en) * 1999-10-29 2002-08-13 Smithkline Beecham Corporation Antiviral combinations
WO2001034618A2 (fr) * 1999-11-12 2001-05-17 Pharmasset Limited Synthese de 2'-deoxy-l-nucleosides
EP1600452A3 (fr) 1999-11-12 2008-09-10 Pharmasset, Inc. Synthèse de 2'-déoxy-L-nucléosides
US6436948B1 (en) 2000-03-03 2002-08-20 University Of Georgia Research Foundation Inc. Method for the treatment of psoriasis and genital warts
GB0016845D0 (en) * 2000-07-07 2000-08-30 Leuven K U Res & Dev Pharmaceutical composition for treatment of HIV infection
WO2002051852A1 (fr) * 2000-12-27 2002-07-04 Mitsui Chemicals, Inc. Procede de production d'un derive de saccharide non naturel
PT1574512E (pt) 2001-03-01 2008-03-05 Abbott Lab Formas polimórficas e outras formas cristalinas de cis-ftc
CA2351049C (fr) 2001-06-18 2007-03-13 Brantford Chemicals Inc. Procede pour separer des nucleosides cis-1,3-oxathiolaniques recherches de leurs isomeres trans non desires
JP2003039582A (ja) * 2001-07-19 2003-02-13 Three M Innovative Properties Co 湿潤防滑性シート及び湿潤防滑構造体
MY169670A (en) 2003-09-03 2019-05-08 Tibotec Pharm Ltd Combinations of a pyrimidine containing nnrti with rt inhibitors
US6855346B2 (en) * 2001-10-05 2005-02-15 Tzu-Sheng Wu Pharmaceutical composition having prophylactic effects on lamivudine-related disease relapse and drug resistance and methods of using the same
EP1441735B1 (fr) * 2001-10-26 2006-02-22 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Inhibiteurs de l'integrase du vih a base d'hydroxypyrimidinone carboxamide n-substitue
BR0214940A (pt) * 2001-12-14 2006-05-30 Pharmasset Ltd preparação de intermediários úteis na sìntese de nucleosìdeos antivirais
KR20040088519A (ko) 2002-02-22 2004-10-16 뉴 리버 파마슈티칼스, 인크. 활성 제제 전달 시스템 및 활성 제제의 보호 및 투여 방법
ES2360096T3 (es) 2002-08-06 2011-05-31 Pharmasset, Inc. Procedimientos de preparación de nucleosidos de 1,3-dioxolano.
DE10238722A1 (de) 2002-08-23 2004-03-11 Bayer Ag Selektive Phosphodiesterase 9A-Inhibitoren als Arzneimittel zur Verbesserung kognitiver Prozesse
DE10238724A1 (de) 2002-08-23 2004-03-04 Bayer Ag Alkyl-substituierte Pyrazolpyrimidine
DE10238723A1 (de) * 2002-08-23 2004-03-11 Bayer Ag Phenyl-substituierte Pyrazolyprimidine
JP2006508134A (ja) * 2002-11-08 2006-03-09 グラクソ　グループ　リミテッド 医薬組成物
CA2502625A1 (fr) * 2002-12-09 2004-06-24 The University Of Georgia Research Foundation, Inc. Dioxolane thymine et combinaisons utilisables contre les souches resistantes du vih
KR20080032014A (ko) * 2003-01-14 2008-04-11 길리애드 사이언시즈, 인코포레이티드 복합 항바이러스 치료를 위한 조성물 및 방법
DE10320785A1 (de) * 2003-05-09 2004-11-25 Bayer Healthcare Ag 6-Arylmethyl-substituierte Pyrazolopyrimidine
US8044060B2 (en) 2003-05-09 2011-10-25 Boehringer Ingelheim International Gmbh 6-cyclylmethyl- and 6-alkylmethyl pyrazolo[3,4-D]pyrimidines, methods for their preparation and methods for their use to treat impairments of perception, concentration learning and/or memory
DE102004001873A1 (de) * 2004-01-14 2005-09-29 Bayer Healthcare Ag Cyanopyrimidinone
ES2363160T3 (es) 2004-07-27 2011-07-22 Gilead Sciences, Inc. Conjugados de fosfonato nucelosidico como agentes anti-vih.
JP2006214695A (ja) * 2005-02-07 2006-08-17 Sanken Setsubi Kogyo Co Ltd 空調システム
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
US20070059360A1 (en) * 2005-07-29 2007-03-15 Ashish Jaiswal Water-dispersible anti-retroviral pharmaceutical compositions
CN1328240C (zh) * 2005-08-31 2007-07-25 四川大学 苯甲酰氧基乙醛的制备方法
US20080241265A1 (en) * 2005-08-31 2008-10-02 Amar Lulla Pharmaceutical Combinations Containing Lamivudine, Stavudine and Nevirapine
CA2904692A1 (fr) 2005-09-26 2007-04-05 Gilead Pharmasset Llc 4'-nucleosides modifies comme agents antiviraux
US20080317852A1 (en) * 2005-12-14 2008-12-25 Amar Lulla Pharmaceutical Combination
US8895531B2 (en) * 2006-03-23 2014-11-25 Rfs Pharma Llc 2′-fluoronucleoside phosphonates as antiviral agents
WO2007119248A1 (fr) * 2006-04-18 2007-10-25 Lupin Limited Nouvelle forme cristalline de la lamivudine
EP2086955A2 (fr) * 2006-10-30 2009-08-12 Lupin Ltd. Procédé amélioré de fabrication de lamivudine
KR100840495B1 (ko) 2007-04-13 2008-06-23 한미약품 주식회사 라미부딘을 입체선택적으로 제조하는 방법
CN101328171A (zh) 2007-06-18 2008-12-24 张中能 一种溴苯基-取代的噻唑二氢嘧啶
WO2009037538A2 (fr) * 2007-09-17 2009-03-26 Aurobindo Pharma Ltd Procédé de préparation de lamivudine de forme i
BRPI0820224A2 (pt) * 2007-11-29 2015-06-16 Ranbaxy Lab Ltd Composto de fórmula iii ou seus estereoisômeros; processo para sua preparação e seu uso; uso de um composto de formula iii(a) ou iii(b) em um processo para a preparação de lamivudina de fórmula i(a) ou um composto de fórmula i(c); processo para preparação de lamivudina de fórmula i(a)
BRPI0820226A2 (pt) * 2007-11-29 2015-06-16 Ranbaxy Lab Ltd Processo para o preparo de um 1,3-oxatiolana, para o preparo de lamivudina e para isolar lamivudina, lamivudina e composição farmacêutica
EP2217602B1 (fr) * 2007-11-30 2018-08-29 Boehringer Ingelheim International GmbH Dérivés 1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one et leur utilisation comme modulateurs de pde9a pour le traitement de troubles cns
UA105362C2 (en) 2008-04-02 2014-05-12 Бьорингер Ингельхайм Интернациональ Гмбх 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their use as pde9a modulators
TW201010692A (en) 2008-06-19 2010-03-16 Public Univ Corp Nagoya City Univ Pharmaceutical composition for treatment or prevention of hbv infection
PE20110383A1 (es) 2008-09-08 2011-07-15 Boehringer Ingelheim Int Pirazolopirimidinonas como inhibidores de la fosfodiesterasa 9a (pde9a)
CN103497192B (zh) 2008-12-09 2015-09-23 吉里德科学公司 Toll样受体调节剂
US20110282046A1 (en) * 2009-01-19 2011-11-17 Rama Shankar Process for preparation of cis-nucleoside derivative
WO2010112437A1 (fr) 2009-03-31 2010-10-07 Boehringer Ingelheim International Gmbh Dérivés 1-hétérocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one et leur utilisation en tant que modulateurs de pde9a
KR101474570B1 (ko) 2009-04-13 2014-12-19 주식회사 대희화학 라미부딘의 신규한 중간체 및 이의 제조방법
TW201118099A (en) * 2009-08-12 2011-06-01 Boehringer Ingelheim Int New compounds for the treatment of CNS disorders
EP2488516B1 (fr) 2009-10-14 2015-04-01 Mylan Laboratories Limited Procédé pour la préparation de lamivudine et nouveaux sels dans sa fabrication
SG10201707183TA (en) 2010-01-27 2017-10-30 Viiv Healthcare Co Antiviral therapy
US20120295930A1 (en) 2010-02-03 2012-11-22 Shankar Rama Novel process for the preparation of cis-nucleoside derivative
US20110223131A1 (en) 2010-02-24 2011-09-15 Gilead Sciences, Inc. Antiviral compounds
CN102234269B (zh) * 2010-04-29 2015-09-16 重庆医药工业研究院有限责任公司 拉米夫定的工业化制备方法
WO2011141805A2 (fr) 2010-05-14 2011-11-17 Lupin Limited Procédé de production amélioré de lamivudine
US20130115237A1 (en) 2010-06-09 2013-05-09 Vaccine Technologies, Incorporated Therapeutic immunization in hiv infected subjects to augment antiretroviral treatment
EP2603511B1 (fr) 2010-08-12 2017-03-15 Boehringer Ingelheim International GmbH Dérivés 6-cycloalkyle-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one et leur utilisation en tant qu'inhibiteurs de pde9a
US8809345B2 (en) 2011-02-15 2014-08-19 Boehringer Ingelheim International Gmbh 6-cycloalkyl-pyrazolopyrimidinones for the treatment of CNS disorders
US20130296562A1 (en) 2011-08-05 2013-11-07 Lupin Limited Stereoselective process for preparation of 1,3-oxathiolane nucleosides
WO2013168066A1 (fr) 2012-05-05 2013-11-14 Lupin Limited Procédé amélioré de fabrication de lamivudine de forme i
CN103694231A (zh) * 2013-11-28 2014-04-02 安徽一帆香料有限公司 一种拉米夫定中间体hdms的合成制备方法
WO2016001907A1 (fr) 2014-07-02 2016-01-07 Prendergast Patrick T Mogroside iv et mogroside v utilisables en tant qu'agonistes/stimulateurs/agents de déblocage des récepteurs toll 4 et adjuvant destiné à être utilisé dans un vaccin humain/animal et pour stimuler l'immunité contre des agents pathologiques
WO2016007765A1 (fr) 2014-07-11 2016-01-14 Gilead Sciences, Inc. Modulateurs de récepteurs de type toll pour le traitement du vih
WO2016033164A1 (fr) 2014-08-26 2016-03-03 Enanta Pharmaceuticals, Inc. Dérivés de nucléosides et de nucléotides
JP2018527366A (ja) 2015-09-15 2018-09-20 ギリアード サイエンシーズ， インコーポレイテッド ＨＩＶを処置するためのｔｏｌｌ様レセプターのモジュレーター
RU2736941C2 (ru) 2015-12-02 2020-11-23 Мерк Шарп энд Доум Корп. Фармацевтические композиции, содержащие доравирин, тенофовира дизопроксила фумарат и ламивудин
JP2020515607A (ja) * 2017-03-31 2020-05-28 ザ ユニバーシティー オブ リヴァプール プロドラッグ組成物

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4000137A (en) * 1975-06-10 1976-12-28 American Home Products Corporation Antitumor derivatives of periodate-oxidized nucleosides
JPS5259171A (en) * 1975-11-10 1977-05-16 Asahi Chem Ind Co Ltd Preparation of uracil derivatives
JPS6045196B2 (ja) * 1976-08-09 1985-10-08 株式会社興人 １−（２−テトラヒドロフリル）ウラシル類の製造方法
JPS5668674A (en) * 1979-11-08 1981-06-09 Shionogi & Co Ltd 5-fluorouracil derivative
JPS56167685A (en) * 1980-05-28 1981-12-23 Taiho Yakuhin Kogyo Kk 1- 2-tetrahydrothiophene-1,1-dioxide -5-fluorouracil and its preparation
JPS56169689A (en) * 1980-06-02 1981-12-26 Taiho Yakuhin Kogyo Kk 3-substituted-5-fluorouracil derivative and its preparation
JPS5738774A (en) * 1980-08-19 1982-03-03 Chugai Pharmaceut Co Ltd Uracil derivative and its preparation
SU1035023A1 (ru) * 1982-03-23 1983-08-15 Ордена Трудового Красного Знамени Институт Органической И Физической Химии Им.А.Е.Арбузова Способ получени 3-(тииранил-2-метил)-6-метилурацилов
DE3324769A1 (de) * 1983-07-08 1985-01-17 Bayer Ag, 5090 Leverkusen 5-aminomethyl-1,3-oxathiolane
DE3689976T2 (de) * 1985-05-15 1995-03-16 Wellcome Found Therapeutische Nucleoside und deren Herstellung.
CA1294960C (fr) * 1986-10-24 1992-01-28 Thomas C. Malone 7-deazaguanines en tant qu'immunomodulateurs
DE3712735A1 (de) * 1987-04-15 1988-11-10 Boehringer Mannheim Gmbh Neue pyrazolo(3,4-d)pyrimidine, verfahren zu ihrer herstellung und verwendung als arzneimittel
ZA891076B (en) * 1988-02-16 1990-10-31 Lilly Co Eli 2',3'-dideoxy-2',2'-difluoronucleosides
NZ228645A (en) * 1988-04-11 1991-09-25 Iaf Biochem Int 1,3-dioxolane derivatives substituted in the 5th position by a purine or pyrimidine radical; treatment of viral infections
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

Also Published As

Publication number Publication date
FI98065B (fi) 1996-12-31
SG77215A1 (en) 2000-12-19
SI9010243B (sl) 1998-08-31
DE69026971T2 (de) 1996-09-12
GR3019919T3 (en) 1996-08-31
IL93318A (en) 1995-07-31
HK1009270A1 (en) 1999-05-28
CA2009637C (fr) 1997-10-07
CA2009637A1 (fr) 1990-08-08
ZA90943B (en) 1990-10-31
JPH08119967A (ja) 1996-05-14
EP0382526A3 (fr) 1992-01-02
EP0711771A3 (fr) 1996-07-10
KR960007531B1 (ko) 1996-06-05
US5047407A (en) 1991-09-10
PT93094B (pt) 1995-12-29
NL960025I2 (nl) 1997-03-03
OA09193A (en) 1992-06-30
HUT53362A (en) 1990-10-28
KR900012932A (ko) 1990-09-03
EP0711771B1 (fr) 2003-11-12
AP136A (en) 1991-08-05
DE69026971D1 (de) 1996-06-20
FI98065C (fi) 1997-04-10
AU4920190A (en) 1990-08-16
SG48737A1 (en) 1998-05-18
NO2001002I1 (no) 2001-02-12
NO900619L (no) 1990-08-09
FI900631A0 (fi) 1990-02-08
DE69034119T2 (de) 2004-08-26
NO900619D0 (no) 1990-02-08
SI9010243A (en) 1996-10-31
CZ282720B6 (cs) 1997-09-17
DK0711771T3 (da) 2004-03-22
AU630913B2 (en) 1992-11-12
MX19437A (es) 1993-05-01
CS410991A3 (en) 1992-07-15
YU24390A (en) 1991-10-31
HRP940040B1 (en) 2002-04-30
NO179518C (no) 2000-09-11
JP2000143662A (ja) 2000-05-26
LU88809I2 (fr) 1997-01-03
ATE254125T1 (de) 2003-11-15
HU900708D0 (en) 1990-04-28
EP0382526A2 (fr) 1990-08-16
NZ232421A (en) 1993-10-26
HK51997A (en) 1997-05-02
CN1033640C (zh) 1996-12-25
AP9000163A0 (en) 1990-04-30
JPH037282A (ja) 1991-01-14
RU2092485C1 (ru) 1997-10-10
ES2206476T3 (es) 2004-05-16
ATE138065T1 (de) 1996-06-15
DE69034119D1 (de) 2003-12-18
DK0382526T3 (da) 1996-08-05
NL960025I1 (nl) 1997-01-06
EP0711771A2 (fr) 1996-05-15
HU208134B (en) 1993-08-30
JP2001226373A (ja) 2001-08-21
YU48840B (sh) 2002-06-19
PL164785B1 (en) 1994-10-31
IE72184B1 (en) 1997-03-26
IE960758L (en) 1990-08-08
JP2644357B2 (ja) 1997-08-25
ES2086371T3 (es) 1996-07-01
EP0382526B1 (fr) 1996-05-15
PT93094A (pt) 1990-08-31
SK279175B6 (sk) 1998-07-08
DE19675032I2 (de) 2007-11-08
IE900452L (en) 1990-08-08
CN1044817A (zh) 1990-08-22
HRP940040A2 (en) 1997-04-30
JP3105154B2 (ja) 2000-10-30
HU210537A9 (en) 1995-04-28
NO179518B (no) 1996-07-15

Similar Documents

Publication Publication Date Title
CY2036A (en) Substitued-1,3-oxathiolanes with antiviral properties
MD809B2 (en) (-)-Enantiomer cis-4-amino-1-(2-hydroxymethil-1,3-oxathiolan-5-yl)-
GR3022463T3 (en) 1-H-3-aryl-pyrrolidin-2,4-dion-derivatives
HU9201701D0 (en) Chemically stable, non-immunogenous haemoglobine substituting platelets
GB2265314B (en) Protective articles.
EG19674A (en) Antiviral tetrahydroimidazol (1,4) denzodiazepin -2-thiones
ZA898608B (en) 14alpha,17alpha-ethanoestratrienes
ZA903177B (en) N-sulfenyl-and n-sulfinyl-n,n'-diacylhydrazides
DE4092638D2 (en) Mappe, insbesondere muster-, werbe- oder angebotsmappe
GB8911158D0 (en) Antiviral pyridazinamines
NO903036L (no) Gjenstander belagt med vinyldispersjonsharpikser.
GR3015270T3 (en) Antiviral tetrahydroimidazo (1,4)-benzodiazepines.
BA96097A (bs) Supstituirani 1,3-oksatiolani s antivirusnim svojstvima
DE69002365D1 (de) Antivirale zusammensetzung.
CS275339B2 (en) N,o-dimethacryloylhydroxylamine
IE893635L (en) 14ó,17ó-ethanoestratrienes
ZA909616B (en) 14alpha,17alpha-ethano-16alpha-hydroxy-estratrienes
GB8904962D0 (en) Antiviral uses
HU896204D0 (en) Coloured, collapsible, plain toyfamily
IE900821L (en) 3-keto-16ó,17ó-dihydroxysteroids
GB8919038D0 (en) Q,c,safegrip
IE883828L (en) Acylating n, n-diallylanilines
GB8926126D0 (en) Transition piece
GB9024371D0 (en) Putting,perceptor
GB8903983D0 (en) Sporting article