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Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R

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Popova I. S. et al. Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 578-580.
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Popova I. S., Korchagina E. Y., Sablina M. A., Paramonov A. S., Hult A. K., Henry S. M., Bovin N. V. Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 578-580.
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TY - JOUR
DO - 10.1016/j.mencom.2019.09.034
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.034
TI - Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R
T2 - Mendeleev Communications
AU - Popova, Inna Stanislavovna
AU - Korchagina, Elena Yuryevna
AU - Sablina, Marina Aleksandrovna
AU - Paramonov, Alexander Sergeyevich
AU - Hult, Annika K
AU - Henry, Stephen M
AU - Bovin, Nicolai Vladimirovich
PY - 2019
DA - 2019/09/04
PB - Mendeleev Communications
SP - 578-580
IS - 5
VL - 29
ER -
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@article{2019_Popova,
author = {Inna Stanislavovna Popova and Elena Yuryevna Korchagina and Marina Aleksandrovna Sablina and Alexander Sergeyevich Paramonov and Annika K Hult and Stephen M Henry and Nicolai Vladimirovich Bovin},
title = {Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.034},
number = {5},
pages = {578--580},
doi = {10.1016/j.mencom.2019.09.034}
}
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Popova, Inna Stanislavovna, et al. “Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R.” Mendeleev Communications, vol. 29, no. 5, Sep. 2019, pp. 578-580. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.034.

Abstract

Synthesis of the glycan part of Forssman glycolipid GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glc–Cer in the form of 2-aminoethyl glycoside has been carried out. The glycoside has been converted into a lipophilic derivative capable of controlled inserting into erythrocytes. The obtained surface-modified cells, termed kodecytes, revealed a high level of the blood group system FORS serological activity.

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