ES2081192T3 - Inhibidor de timidina quinasa viral del herpes simple. - Google Patents

Inhibidor de timidina quinasa viral del herpes simple.

Info

Publication number
ES2081192T3
ES2081192T3 ES93402128T ES93402128T ES2081192T3 ES 2081192 T3 ES2081192 T3 ES 2081192T3 ES 93402128 T ES93402128 T ES 93402128T ES 93402128 T ES93402128 T ES 93402128T ES 2081192 T3 ES2081192 T3 ES 2081192T3
Authority
ES
Spain
Prior art keywords
thymidine kinase
inhibitor
thymid
thymin
kinase inhibitor
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES93402128T
Other languages
English (en)
Inventor
Choung Un Kim
Bing Yu Luh
Peter F Misco
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Squibb Co
Original Assignee
Bristol Myers Squibb Co
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
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Application granted granted Critical
Publication of ES2081192T3 publication Critical patent/ES2081192T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06Pyrimidine radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

INHIBIDOR DE TIMIDINA QUINASA DE FORMULA I EN LA CUAL R ES ALQUILO C1-6 O AR(CH2)N-, EN DONDE AR REPRESENTA FENILO OPCIONALMENTE SUSTITUIDO CON DE UNO A CINCO HALOGENOS IGUALES O DIFERENTES, ALQUILO C1-6 O ALQUILOOXILO C1-6; Y N ES IGUAL A DE UNO A SEIS. UN ASPECTO ADICIONAL DE LA PRESENTE INVENCION ES EL USO DE TALES INHIBIDORES DE TIMIDINA QUINASA EN LA FABRICACION DE UNA COMPOSICION PARA INHIBIR TIMIDINA QUINASA VIRICA. ADEMAS OTRO ASPECTO DE LA INVENCION ES RELATIVA AL USO DE TAL INHIBIDOR DE TIMIDINA QUINASA EN LA FABRICACION DE UN MEDICAMENTO PARA TRATAR INFECCIONES DE HERPES SIMPLE VIRICO EN MAMIFEROS. ADEMAS OTRO ASPECTO DE LA INVENCION PROVEE UNA FORMULACION FARMACEUTICA.
ES93402128T 1992-09-02 1993-08-31 Inhibidor de timidina quinasa viral del herpes simple. Expired - Lifetime ES2081192T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/939,232 US5306722A (en) 1992-09-02 1992-09-02 Thymidine derivatives and therapeutic method of use

Publications (1)

Publication Number Publication Date
ES2081192T3 true ES2081192T3 (es) 1996-02-16

Family

ID=25472788

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93402128T Expired - Lifetime ES2081192T3 (es) 1992-09-02 1993-08-31 Inhibidor de timidina quinasa viral del herpes simple.

Country Status (9)

Country Link
US (1) US5306722A (es)
EP (1) EP0586298B1 (es)
JP (1) JPH06172349A (es)
AT (1) ATE130618T1 (es)
CA (1) CA2104895A1 (es)
DE (1) DE69300857T2 (es)
DK (1) DK0586298T3 (es)
ES (1) ES2081192T3 (es)
GR (1) GR3019075T3 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5550132A (en) * 1994-06-22 1996-08-27 University Of North Carolina Hydroxyalkylammonium-pyrimidines or purines and nucleoside derivatives, useful as inhibitors of inflammatory cytokines
US5643893A (en) * 1994-06-22 1997-07-01 Macronex, Inc. N-substituted-(Dihydroxyboryl)alkyl purine, indole and pyrimidine derivatives, useful as inhibitors of inflammatory cytokines

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE147775C (es) * 1900-01-01
JPS5699478A (en) * 1980-01-11 1981-08-10 Taiho Yakuhin Kogyo Kk 5-fluorouracil derivative and its preparation
US4782142A (en) * 1982-01-05 1988-11-01 The Research Foundation Of State University Of New York Novel 5-substituted 2-pyrimidinone nucleosides and methods of use
US4468384A (en) * 1982-01-05 1984-08-28 The Research Foundation Of State University Of New York Method for the inhibition of the replication of DNA viruses with 5-substituted 2-pyrimidinone nucleosides
DK363987A (da) * 1986-08-08 1988-02-09 Hoffmann La Roche Pyrimidinderivater
DK163128C (da) * 1986-08-12 1992-06-15 Hoffmann La Roche Pyrimidinnucleosider, fremgangsmaade til fremstilling deraf, farmaceutiske praeparater indeholdende pyrimidinnucleosiderne og anvendelse af pyrimidinnucleosiderne
NO170884C (no) * 1986-08-18 1992-12-23 Hoffmann La Roche Analogifremgangsmaate ved fremstilling av terapeutisk aktive pyrimidinderivater
US5008252A (en) * 1987-03-20 1991-04-16 The University Of North Carolina At Chapel Hill Process for inhibiting herpes simplex virus-specified thymidine kinase
US4782062A (en) * 1987-05-11 1988-11-01 Merck & Co., Inc. 9-(2-hydroxymethyl)cycloalkylmethyl) guanines
US4863927A (en) * 1987-05-11 1989-09-05 Merck & Co., Inc. 1-(2-hydroxymethyl)cycloalkylmethyl)-5-substituted uracils
DE68917479D1 (de) * 1988-02-24 1994-09-15 Inst Rech Chim Biolog Derivate von deoxy-2'-uridin substituiert in der 5, 3' oder 5' stellung durch acylierte alpha-amino-gruppen, verfahren zur herstellung und arzneimittel daraus.
US5091375A (en) * 1988-02-29 1992-02-25 Bayer Ag Nikkomycin derivatives

Also Published As

Publication number Publication date
JPH06172349A (ja) 1994-06-21
EP0586298A1 (en) 1994-03-09
DK0586298T3 (da) 1996-03-04
EP0586298B1 (en) 1995-11-22
CA2104895A1 (en) 1994-03-03
DE69300857D1 (de) 1996-01-04
ATE130618T1 (de) 1995-12-15
US5306722A (en) 1994-04-26
GR3019075T3 (en) 1996-05-31
DE69300857T2 (de) 1996-07-04

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