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Amides derived from heteroaromatic amines and selected steryl hemiesters

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F13%3A33147873" target="_blank" >RIV/61989592:15310/13:33147873 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389030:_____/13:00398419 RIV/61388963:_____/13:00398419 RIV/61989592:15110/13:33147873 RIV/60461373:22330/13:43895382

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0039128X13002171" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0039128X13002171</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.steroids.2013.10.003" target="_blank" >10.1016/j.steroids.2013.10.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Amides derived from heteroaromatic amines and selected steryl hemiesters

  • Original language description

    The current interest of the team has been focused on investigation of novel amides with potential cytotoxicity. The presented series of compounds was synthesized from selected steryl hemiesters and hetero-aromatic amines. The synthetic protocol was designed in a simple and economic way, and divided into several general methodologies applicable to the compounds synthesized. The cytotoxicity was tested on cells derived from human T-Iymphoblastic leukemia, breast adenocarcinoma and cervical cancer, and compared with tests on normal human fibroblasts. Most of the lanosterol-based compounds (3-5 and 7-10) showed medium to good cytotoxicity, while only two derivatives of cholesterol (18 and 19) showed medium cytotoxicity on human T-Iymphoblastic leukemia cell line. The compounds 8 and 9 displayed the reasonable cytotoxicity among this series of amides, tested on the cell lines of T-Iymphoblastic leukemia [14.5 +/- 0.4 mu M (8) and 18.5 +/- 3.9 mu M (9)], breast adenocarcinoma [19.5 +/- 2.1 m

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    ED - Physiology

  • 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

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Steroids

  • ISSN

    0039-128X

  • e-ISSN

  • Volume of the periodical

    78

  • Issue of the periodical within the volume

    14

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    1347-1352

  • UT code for WoS article

    000328303300006

  • EID of the result in the Scopus database