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Antioxidative succinobucol-sterol conjugates: Crystal structures and pseudosymmetry in the crystals

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F12%3A43894012" target="_blank" >RIV/60461373:22330/12:43894012 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389030:_____/12:00380688

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.molstruc.2011.12.016" target="_blank" >http://dx.doi.org/10.1016/j.molstruc.2011.12.016</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.molstruc.2011.12.016" target="_blank" >10.1016/j.molstruc.2011.12.016</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antioxidative succinobucol-sterol conjugates: Crystal structures and pseudosymmetry in the crystals

  • Original language description

    An extensive study to attach succinobucol to sterols has provided conjugates which comprise two pharmaceutically important compounds into one entity where the components are expected to have a synergistic effect. The motivation to design these novel conjugates was the need to broaden the armamentarium of current agents used in the treatment of atherosclerotic diseases and type 2 diabetes. In desire for detailed information of these compounds in solid state, which also have an influence to their physiological activity, systematic crystallization experiments were performed and as a result, X-ray quality single crystals were obtained from four succinobucol-sterol conjugates. All of these compounds crystallized in space group P1 with two or four moleculesin an asymmetric unit and the crystallographically independent molecules were found to be related by pseudosymmetry (i.e. by pseudoinversion in 1-3 and by pseudoinversion plus pseudotranslation in 4).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

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

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Molecular Structure

  • ISSN

    0022-2860

  • e-ISSN

  • Volume of the periodical

    1011

  • Issue of the periodical within the volume

    03 2012

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    25-33

  • UT code for WoS article

    000301316600005

  • EID of the result in the Scopus database