MX9603510A - (-)-liarozol enantiomericamente puro. - Google Patents

(-)-liarozol enantiomericamente puro.

Info

Publication number
MX9603510A
MX9603510A MX9603510A MX9603510A MX9603510A MX 9603510 A MX9603510 A MX 9603510A MX 9603510 A MX9603510 A MX 9603510A MX 9603510 A MX9603510 A MX 9603510A MX 9603510 A MX9603510 A MX 9603510A
Authority
MX
Mexico
Prior art keywords
compounds
liarozole
enantiomerically pure
novel
formula
Prior art date
Application number
MX9603510A
Other languages
English (en)
Inventor
Marc Gaston Venet
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of MX9603510A publication Critical patent/MX9603510A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Abstract

Esta invencion se refiere al isomero levogiro enantioméricamente puro novedoso de la formula I (Ver Formula) y las formas de sal ácida de adicion farmacéuticamente aceptable del mismo; estos compuestos son particularmente utiles para tratar trastornos que se caracterizan por una proliferacion incrementada y/o diferenciacion anormal de células epiteliales normales, preneoplásticas o neoplásticas; los compuestos de la formula (I) son particularmente utiles en el campo de la oncología; también se describen composiciones que contienen dichos compuestos novedosos, métodos para preparar dichos compuestos novedosos así como métodos para usar los compuestos mencionados para tratar los trastornos mencionados.
MX9603510A 1994-02-18 1995-02-10 (-)-liarozol enantiomericamente puro. MX9603510A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP94200418 1994-02-18
PCT/EP1995/000491 WO1995022541A1 (en) 1994-02-18 1995-02-10 Enantiomerically pure(-)-liarozole

Publications (1)

Publication Number Publication Date
MX9603510A true MX9603510A (es) 1997-03-29

Family

ID=8216651

Family Applications (1)

Application Number Title Priority Date Filing Date
MX9603510A MX9603510A (es) 1994-02-18 1995-02-10 (-)-liarozol enantiomericamente puro.

Country Status (11)

Country Link
EP (1) EP0745078A1 (es)
JP (1) JPH09508915A (es)
CN (1) CN1141041A (es)
AU (1) AU688852B2 (es)
IL (1) IL112689A0 (es)
MX (1) MX9603510A (es)
NZ (1) NZ279228A (es)
SG (1) SG47122A1 (es)
TW (1) TW418203B (es)
WO (1) WO1995022541A1 (es)
ZA (1) ZA951342B (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1992228A1 (en) * 2007-05-14 2008-11-19 Bayer CropScience AG Insecticidal substituted thiourea derivatives

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ221729A (en) * 1986-09-15 1989-07-27 Janssen Pharmaceutica Nv Imidazolyl methyl-substituted benzimidazole derivatives and pharmaceutical compositions
CA2002859C (en) * 1988-11-29 1998-12-29 Jean P. F. Van Wauwe Method of treating epithelial disorders

Also Published As

Publication number Publication date
AU688852B2 (en) 1998-03-19
EP0745078A1 (en) 1996-12-04
SG47122A1 (en) 1998-03-20
TW418203B (en) 2001-01-11
JPH09508915A (ja) 1997-09-09
CN1141041A (zh) 1997-01-22
NZ279228A (en) 1997-11-24
AU1578895A (en) 1995-09-04
WO1995022541A1 (en) 1995-08-24
IL112689A0 (en) 1995-05-26
ZA951342B (en) 1996-08-19

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