Abstract
A synthesis of four new analogs of bacterial undecaprenyldiphosphate galactose, in which the oligoisoprenoid moiety is replaced with a linear hydrocarbon chain, was accomplished. These compounds contain a fluorescent anthracenyl group at the ω-end of the lipophilic chain variable in length. A comparative analysis of their ability to serve as substrates-acceptors of the mannose moiety in the enzymatic reactions catalyzed by mannosyltransferase from bacteria Salmonella newport cell membranes was performed.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 0202–0209, January, 2015.
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Vinnikova, A.N., Demirova, K.A., Druzhinina, T.N. et al. New fluorescent analogs of bacterial undecaprenyldiphosphate galactose. Russ Chem Bull 64, 202–209 (2015). https://doi.org/10.1007/s11172-015-0843-4
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DOI: https://doi.org/10.1007/s11172-015-0843-4