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  • Synthesis and biological evaluation of spin-labelled alkylphospholipid analogs
    Mravljak, Janez, 1978- ; Zeisig, Reiner ; Pečar, Slavko
    Alkylphospholipid analogues of perifosine and miltefosine bearing a nitroxide moiety at different positions on an alkyl chain were synthesized as electron paramagnetic resonance (EPR) probes. Their ... amphiphilic properties were characterized by determining their critical micelle concentration (cmc) and hemolytic activity on erythrocytes both in free and liposomal form. Spin-labeled analogues as membrane components of large unilamellar liposomes containing cholesterol and dicetyl phosphate or in free solution were evaluated using the MTT assay to determine growth inhibition on MT1, MT3, and MCF7 breast cancer cell lines. 4a (IC50 = 56.4 M) was found to be significantly more active than the perifosine against the MCF-7 cell line. Itshigh cmc (194.03 M) and low hemolytic activity shows that its cytotoxic activity might be more specificč therefore, 4a can be an important molecular tool for further EPR investigations.
    Source: Journal of medicinal chemistry. - ISSN 0022-2623 (Vol. 48, no. 20, 2005, str. 6393-6399)
    Type of material - article, component part
    Publish date - 2005
    Language - english
    COBISS.SI-ID - 1808497

source: Journal of medicinal chemistry. - ISSN 0022-2623 (Vol. 48, no. 20, 2005, str. 6393-6399)
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