Enantioselective Synthesis of Clavaminol A, Xestoaminol C and their Stereoisomers Exhibiting Cytotoxic Activity
ČlánekOmezený přístuppeer-reviewedpublished versionDatum publikování
2020
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Wiley-VCH
Abstrakt
The simple preparation of the natural sphingoid bases possessing cytotoxic activity - the marine drugs Clavaminol A and Xestoaminol C and all their unnatural stereoisomers - in high enantiomeric purity (ca. 95 % of major enantiomer) was described. The individual enantiomers were obtained by the utilization of asymmetric Henry reaction. The diastereomers of target compounds were separated by column chromatography after transformation into corresponding 2-phenyloxazoline derivatives. The individual stereoisomers of Clavaminol A and Xestoaminol C were evaluated for antiproliferative activity in cancer cell lines (A-549; Jurkat; SH-SY5Y, MG-63). From the obtained IC50 values is obvious, that the stereoisomers of Xestoaminol C are more potent inhibitors of cell proliferation than the stereoisomers of Clavaminol A. Further, it was found, that stereoisomers with syn-configuration exhibited larger antiproliferative effects in comparison with the stereoisomers having anti-configuration, in both sphingoid bases. Nevertheless, the values of IC50 found for individual enantiomers in each of the enantiomeric pairs are rather comparable implying a possibility of using racemic mixtures for induction of cytotoxicity.
Rozsah stran
p. 3671-3679
ISSN
1434-193X
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Zdrojový dokument
European Journal of Organic Chemistry, volume 2020, issue: 24
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https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000353
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cytotoxicity, enantioselective catalysis, Henry reaction, Clavaminol A, Xestoaminol C, cytotoxicita, enantioselektivní katylýza, Henryho reakce, Clavaminol A, Xestoaminol C