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Potential utilization Naphthoquinones in a medicine

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F05%3A00086674" target="_blank" >RIV/62156489:43210/05:00086674 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    čeština

  • Original language name

    Potencionální využití naftochinonu v medicíně

  • Original language description

    Naphthoquinones, compounds of natural origin, mostly appeared as chromatic pigments. They are deposited in cells vacuoles, where they are dissolved (in glycoside form). They are synthesised by range of chemical reactions, where shikimate acid, L-alanine,parahydroxybenzoic acid and C10 isoprenoid unit are initial substrates for biosynthesis of juglone, droserone, plumbagin and 7-methyljuglone [1]. In nature they occur in wide range of plants species and also in fungi and microorganisms as group of secondary metabolites. Naphthoquinones are very toxic, their antimicrobial, antifungal, antiviral and antiparasitic effects were observed [2]. An anticancer effect of naphthoquinones awakes an interest in determination and characterization of single derivatesof 1,2 and 1,4 quinone in biological samples. The aim of our work was to optimize the high performance liquid chromatography coupled with diode array detector for the determination of naphtoquinones (1,4-naphtoquinone, lawsone, juglone a

  • Czech name

    Potencionální využití naftochinonu v medicíně

  • Czech description

    Naphthoquinones, compounds of natural origin, mostly appeared as chromatic pigments. They are deposited in cells vacuoles, where they are dissolved (in glycoside form). They are synthesised by range of chemical reactions, where shikimate acid, L-alanine,parahydroxybenzoic acid and C10 isoprenoid unit are initial substrates for biosynthesis of juglone, droserone, plumbagin and 7-methyljuglone [1]. In nature they occur in wide range of plants species and also in fungi and microorganisms as group of secondary metabolites. Naphthoquinones are very toxic, their antimicrobial, antifungal, antiviral and antiparasitic effects were observed [2]. An anticancer effect of naphthoquinones awakes an interest in determination and characterization of single derivatesof 1,2 and 1,4 quinone in biological samples. The aim of our work was to optimize the high performance liquid chromatography coupled with diode array detector for the determination of naphtoquinones (1,4-naphtoquinone, lawsone, juglone a

Classification

  • Type

    D - Article in proceedings

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GP525%2F04%2FP132" target="_blank" >GP525/04/P132: Study of protection mechanisms for stress-induced by heavy metals</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2005

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    Dny diagnosticke, prediktivni a experimentalni onkologie

  • ISBN

    80-239-6302-3

  • ISSN

  • e-ISSN

  • Number of pages

    2

  • Pages from-to

    39-40

  • Publisher name

    Solen

  • Place of publication

    Olomouc

  • Event location

  • Event date

  • Type of event by nationality

  • UT code for WoS article