HK1009599A1 - Crystalline oxathiolane derivatives - Google Patents

Crystalline oxathiolane derivatives

Info

Publication number
HK1009599A1
HK1009599A1 HK98110312A HK98110312A HK1009599A1 HK 1009599 A1 HK1009599 A1 HK 1009599A1 HK 98110312 A HK98110312 A HK 98110312A HK 98110312 A HK98110312 A HK 98110312A HK 1009599 A1 HK1009599 A1 HK 1009599A1
Authority
HK
Hong Kong
Prior art keywords
oxathiolane derivatives
crystalline
crystalline oxathiolane
derivatives
oxathiolane
Prior art date
Application number
HK98110312A
Other languages
English (en)
Inventor
Tony Gordon Roberts
Paul Evans
Original Assignee
Glaxo Group Ltd
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=10696001&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HK1009599(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of HK1009599A1 publication Critical patent/HK1009599A1/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
    • C07D411/02—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
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
  • Secondary Cells (AREA)
  • Medicinal Preparation (AREA)
HK98110312A 1991-06-03 1998-08-31 Crystalline oxathiolane derivatives HK1009599A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB919111902A GB9111902D0 (en) 1991-06-03 1991-06-03 Chemical compounds

Publications (1)

Publication Number Publication Date
HK1009599A1 true HK1009599A1 (en) 1999-06-04

Family

ID=10696001

Family Applications (1)

Application Number Title Priority Date Filing Date
HK98110312A HK1009599A1 (en) 1991-06-03 1998-08-31 Crystalline oxathiolane derivatives

Country Status (31)

Country Link
US (1) US5905082A (xx)
EP (2) EP1099700A1 (xx)
JP (1) JP2851480B2 (xx)
KR (1) KR100244008B1 (xx)
AP (1) AP300A (xx)
AT (1) ATE212630T1 (xx)
AU (2) AU656379B2 (xx)
BG (1) BG60914B1 (xx)
CA (2) CA2311988C (xx)
CZ (1) CZ284513B6 (xx)
DE (1) DE69232387T2 (xx)
DK (1) DK0517145T3 (xx)
ES (1) ES2171158T3 (xx)
GB (1) GB9111902D0 (xx)
GE (1) GEP19991834B (xx)
HK (1) HK1009599A1 (xx)
IE (2) IE921780A1 (xx)
IL (1) IL102073A (xx)
IS (2) IS1867B (xx)
MX (1) MX9202619A (xx)
NO (1) NO301713B1 (xx)
NZ (1) NZ242981A (xx)
OA (1) OA09913A (xx)
PT (1) PT517145E (xx)
RU (1) RU2102393C1 (xx)
SG (1) SG52455A1 (xx)
SK (1) SK281249B6 (xx)
TW (1) TW254939B (xx)
UA (1) UA41265C2 (xx)
WO (1) WO1992021676A1 (xx)
ZA (1) ZA924007B (xx)

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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
US5728575A (en) 1990-02-01 1998-03-17 Emory University Method of resolution of 1,3-oxathiolane nucleoside enantiomers
US5204466A (en) * 1990-02-01 1993-04-20 Emory University Method and compositions for the synthesis of bch-189 and related compounds
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
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
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
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
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
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
ES2276404T3 (es) 1995-06-07 2007-06-16 Emory University Nucleosidos con actividad antivirus de la hepatitis-b.
US5914332A (en) * 1995-12-13 1999-06-22 Abbott Laboratories Retroviral protease inhibiting compounds
ID19490A (id) 1996-06-25 1998-07-16 Glaxo Group Ltd Kombinasi-kombinasi antiviral
US5753789A (en) * 1996-07-26 1998-05-19 Yale University Oligonucleotides containing L-nucleosides
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
US6436948B1 (en) 2000-03-03 2002-08-20 University Of Georgia Research Foundation Inc. Method for the treatment of psoriasis and genital warts
CA2788498C (en) * 2001-03-01 2016-02-16 Gilead Sciences, Inc. Polymorphic and other crystalline forms of cis-ftc
US6600044B2 (en) 2001-06-18 2003-07-29 Brantford Chemicals Inc. Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers
WO2003027106A1 (en) * 2001-09-25 2003-04-03 Cadila Healthcar Limited Process for the preparation of crystalline polymorph ii of lamivudine
JP4625637B2 (ja) 2002-02-22 2011-02-02 シャイア エルエルシー 活性物質送達系及び活性物質を保護し投与する方法
CA2505130C (en) * 2002-11-08 2009-10-06 Glaxo Group Limited Pharmaceutical compositions
DE602004014470D1 (de) 2003-01-14 2008-07-31 Gilead Sciences Inc Zusammensetzungen und verfahren zur antiviralen kombinationstherapie
JP4891250B2 (ja) * 2004-11-10 2012-03-07 ノバルティス ヴァクシンズ アンド ダイアグノスティクス， インコーポレイテッド 脱アミドされたインターフェロンβ
US20060242012A1 (en) * 2005-04-22 2006-10-26 Sumit Agarwal Determining or scoring properties to solicit to join ad network using advertiser or aggregated advertiser interest
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
ES2357159T3 (es) * 2006-04-18 2011-04-19 Lupin Ltd. Forma cristalina novedosa de lamivudina.
WO2009031026A2 (en) * 2007-09-06 2009-03-12 Combino Pharm, S.L. Novel pharmaceutical compositions
WO2009037538A2 (en) * 2007-09-17 2009-03-26 Aurobindo Pharma Ltd Process for the preparation of lamivudine form i
CN101918393A (zh) * 2007-11-29 2010-12-15 兰贝克赛实验室有限公司 拉米夫定的晶形i及其制备方法
AU2008331167A1 (en) * 2007-11-29 2009-06-04 Ranbaxy Laboratories Limited Process and intermediates for the preparation of substituted 1, 3-oxathiolanes, especially lamivudine
WO2009069011A1 (en) * 2007-11-29 2009-06-04 Ranbaxy Laboratories Limited Process for the preparation of substituted 1,3-oxathiolanes
WO2009127996A1 (en) * 2008-04-17 2009-10-22 Ranbaxy Laboratories Limited Novel crystalline form of lamivudine
WO2010023676A2 (en) * 2008-09-01 2010-03-04 Hetero Research Foundation Process for preparing lamivudine polymorph form
US20110288298A1 (en) * 2008-11-12 2011-11-24 Lupin Limited novel polymorph of emtricitabine and a process for preparing of the same
CN101531656B (zh) * 2009-03-24 2010-12-08 福建广生堂药业有限公司 拉米夫定晶型及其制备方法
CN101993439B (zh) * 2009-03-24 2013-04-24 福建广生堂药业股份有限公司 拉米夫定晶型及其制备方法
US8481554B2 (en) * 2009-05-27 2013-07-09 Hetero Research Foundation Solid oral dosage forms of lamivudine
WO2011007367A1 (en) 2009-07-15 2011-01-20 Lupin Limited An improved process for preparation of efavirenz
DK2488516T3 (en) 2009-10-14 2015-05-26 Mylan Lab Ltd Method of producing lamivudine and novel salts in the preparation thereof
DK3494972T3 (da) 2010-01-27 2024-01-29 Viiv Healthcare Co Kombinationer af dolutegravir og lamivudin til behandling af HIV-infektion
US20120295930A1 (en) * 2010-02-03 2012-11-22 Shankar Rama Novel process for the preparation of cis-nucleoside derivative
US8796452B2 (en) * 2010-02-12 2014-08-05 Merck Sharp & Dohme Corp. Preparation of lamivudine form I
WO2011156594A2 (en) 2010-06-09 2011-12-15 Vaccine Technologies, Incorporated Therapeutic immunization in hiv infected subjects receiving stable antiretroviral treatment
WO2013021290A1 (en) 2011-08-05 2013-02-14 Lupin Limited A stereoselective process for preparation of 1,3-oxathiolane nucleosides
WO2013168066A1 (en) 2012-05-05 2013-11-14 Lupin Limited An improved process for the manufacture of lamivudine form i.
CN114099454B (zh) * 2020-08-31 2023-06-27 长春海悦药业股份有限公司 一种拉米夫定片及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
GB9009861D0 (en) * 1990-05-02 1990-06-27 Glaxo Group Ltd Chemical compounds
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

Also Published As

Publication number Publication date
SK281249B6 (sk) 2001-01-18
PT517145E (pt) 2002-07-31
EP0517145B1 (en) 2002-01-30
IL102073A0 (en) 1993-01-14
CA2311988C (en) 2005-11-15
BG60914B1 (bg) 1996-06-28
AP9200395A0 (en) 1992-07-31
ATE212630T1 (de) 2002-02-15
CA2070230A1 (en) 1992-12-04
DE69232387D1 (de) 2002-03-14
IE921780A1 (en) 1992-12-16
MX9202619A (es) 1992-12-01
GEP19991834B (en) 1999-11-05
JP2851480B2 (ja) 1999-01-27
JPH06211848A (ja) 1994-08-02
TW254939B (xx) 1995-08-21
AU656379B2 (en) 1995-02-02
OA09913A (en) 1994-09-15
SG52455A1 (en) 1998-09-28
EP1099700A1 (en) 2001-05-16
NO922182D0 (no) 1992-06-02
DK0517145T3 (da) 2002-05-06
NZ242981A (en) 1994-04-27
IE20020782A1 (en) 2003-04-02
WO1992021676A1 (en) 1992-12-10
DE69232387T2 (de) 2002-09-26
CA2070230C (en) 2004-08-03
NO922182L (no) 1992-12-04
KR930000511A (ko) 1993-01-15
BG98254A (bg) 1994-07-29
NO301713B1 (no) 1997-12-01
US5905082A (en) 1999-05-18
AP300A (en) 1994-01-20
AU1881092A (en) 1993-01-08
CZ261293A3 (en) 1994-04-13
EP0517145A1 (en) 1992-12-09
SK125793A3 (en) 1994-11-09
IS4268A (is) 1995-02-27
GB9111902D0 (en) 1991-07-24
KR100244008B1 (ko) 2000-03-02
CZ284513B6 (cs) 1998-12-16
CA2311988A1 (en) 1992-12-04
IS3873A (is) 1992-12-04
IL102073A (en) 1996-05-14
IS1867B (is) 2003-05-02
UA41265C2 (uk) 2001-09-17
AU1736192A (en) 1993-03-11
RU2102393C1 (ru) 1998-01-20
ES2171158T3 (es) 2002-09-01
ZA924007B (en) 1993-04-28

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PE Patent expired

Effective date: 20120601