Аннотация:
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.
Образец цитирования:
I. S. Popova, E. Yu. Korchagina, M. A. Sablina, A. S. Paramonov, A. K. Hult, S. M. Henry, N. V. Bovin, “Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R”, Mendeleev Commun., 29:5 (2019), 578–580
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1597
https://www.mathnet.ru/rus/mendc/v29/i5/p578
Эта публикация цитируется в следующих 2 статьяx:
Inna S. Popova, Marina A. Sablina, Ivan M. Ryzhov, Darya O. Anisimova, Tatyana V. Ovchinnikova, Tatiana V. Tyrtysh, Elena Yu. Korchagina, Alexander O. Chizhov, Alexander S. Paramonov, Nicolai V. Bovin, “Block synthesis of Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ in the form of 3-aminopropyl glycoside”, Carbohydrate Research, 2024, 109370
T. D. Melikhova, N. V. Bovin, A. D. Antipov, M. N. Tereshin, R. H. Ziganshin, A. B. Tuzikov, “Sortase-promoted synthesis of homooligomers from a monomeric protein”, Mendeleev Commun., 33:5 (2023), 624–626