Аннотация:
3-Aminopropyl glycosides of Neu5Acα2-3Galβ, Neu5Acα2-3Galβ1-4GlcNAcβ, Neu5Acα2-3Galβ1-4(6-HSO3)GlcNAcβ, Neu5Acα2-3Galβ1-3GalNAcα, Neu5Acα2-3Galβ1-3(6-HSO3)GalNAcα, Neu5Acα2-3Galβ1-3GlcNAcβ, Neu5Acα2-3Galβ1- 3(6-HSO3)GlcNAcβ, Neu5Acα2-3Galβ1-3(Fucα1-4)GlcNAcβ and Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ were synthesized using protected Neu5Acα2-3Gal bromide as a glycosyl donor at the key stage.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
G. V. Pazynina, M. A. Sablina, A. B. Tuzikov, A. A. Chinarev, N. V. Bovin, “Synthesis of complex α2-3 sialooligosaccharides, including sulfated and fucosylated ones, using Neu5Acα2-3Gal as a building block”, Mendeleev Commun., 13:6 (2003), 245–248
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4045
https://www.mathnet.ru/rus/mendc/v13/i6/p245
Эта публикация цитируется в следующих 25 статьяx:
Leyu Tang, Jiaxu Zhang, Nassima Oumata, Nathalie Mignet, Matthieu Sollogoub, Yongmin Zhang, “Sialyl Lewis X (sLex):Biological Functions, Synthetic Methods and Therapeutic Implications”, European Journal of Medicinal Chemistry, 2025, 117315
Qiushi Chen, Han Liu, Xuechen Li, “Essential functions, syntheses and detection of sialyl Lewis X on glycoproteins”, Explor Drug Sci, 2023, 31
A. B. Tuzikov, E. V. Ryabukhina, A. S. Paramonov, A. O. Chizhov, N. V. Bovin, E. L. Vodovozova, “A convenient route to conjugates of 1,2-diglycerides with functionalized oligoethylene glycol spacer arms”, Mendeleev Commun., 31:4 (2021), 538–541
Marina O. Nagornaya, Anna V. Orlova, Elena V. Stepanova, Alexander I. Zinin, Tatiana V. Laptinskaya, Leonid O. Kononov, “The use of the novel glycosyl acceptor and supramer analysis in the synthesis of sialyl-α(2–3)-galactose building block”, Carbohydrate Research, 470 (2018), 27
Galina Pazynina, Marina Sablina, Tatiana Ovchinnikova, Tatiana Tyrtysh, Svetlana Tsygankova, Alexander Tuzikov, Kira Dobrochaeva, Nadezhda Shilova, Nailia Khasbiullina, Nicolai Bovin, “Synthetic glyco-O-sulfatome for profiling of human natural antibodies”, Carbohydrate Research, 445 (2017), 23
Abhishek Santra, Hai Yu, Nova Tasnima, Musleh M. Muthana, Yanhong Li, Jie Zeng, Nicholas J. Kenyon, Angelique Y. Louie, Xi Chen, “Systematic chemoenzymatic synthesis of O-sulfated sialyl Lewis x antigens”, Chem. Sci., 7:4 (2016), 2827
Alla Heider, Larisa Mochalova, Timm Harder, Alexander Tuzikov, Nicolai Bovin, Thorsten Wolff, Mikhail Matrosovich, Brunhilde Schweiger, A. García-Sastre, “Alterations in Hemagglutinin Receptor-Binding Specificity Accompany the Emergence of Highly Pathogenic Avian Influenza Viruses”, J Virol, 89:10 (2015), 5395
Tatsuya Kato, Takahiro Oizumi, Makoto Ogata, Akiko Murakawa, Taichi Usui, Enoch Y. Park, “Novel enzymatic synthesis of spacer-linked Pk trisaccharide targeting for neutralization of Shiga toxin”, Journal of Biotechnology, 209 (2015), 50
M. A. Sablina, A. B. Tuzikov, T. V. Ovchinnikova, I. V. Mikhura, N. V. Bovin, “Synthesis of mono- and di-O-sulfates of spacer-armed lactose”, Russ Chem Bull, 64:5 (2015), 1125
G. V. Pazynina, S. V. Tsygankova, N. V. Bovin, “Synthesis of glycoprotein N-chain core fragment GlcNAcβ1-4(Fucα1-6)GlcNAc”, Mendeleev Commun., 25:4 (2015), 250–251
Natalia R. Kuznetsova, Chantal Sevrin, David Lespineux, Nicolai V. Bovin, Elena L. Vodovozova, Tamás Mészáros, Janos Szebeni, Christian Grandfils, “Hemocompatibility of liposomes loaded with lipophilic prodrugs of methotrexate and melphalan in the lipid bilayer”, Journal of Controlled Release, 160:2 (2012), 394
E. L. Vodovozova, G. V. Pazynina, N. V. Bovin, “Synthesis of diglyceride conjugate of selectin ligand SiaLeX as a vector for targeting of drug-loaded liposomes”, Mendeleev Commun., 21:2 (2011), 69–71
Yulia Shtyrya, Larisa Mochalova, Galina Voznova, Irina Rudneva, Aleksandr Shilov, Nikolai Kaverin, Nicolai Bovin, “Adjustment of receptor-binding and neuraminidase substrate specificties in avian–human reassortant influenza viruses”, Glycoconj J, 26:1 (2009), 99
Sherry A. Hudson, Nicolai V. Bovin, Ronald L. Schnaar, Paul R. Crocker, Bruce S. Bochner, “Eosinophil-Selective Binding and Proapoptotic Effect in Vitro of a Synthetic Siglec-8 Ligand, Polymeric 6′-Sulfated Sialyl Lewis X”, J Pharmacol Exp Ther, 330:2 (2009), 608
G. Pazynina, M. Sablina, M. Mayzel, V. Nasonov, A. Tuzikov, N. Bovin, “Chemical synthesis of 6(GlcNAc)- and 6(Gal)-O-sulfated SiaLeX tetrasaccharides in spacer-armed form”, Glycobiology, 19:10 (2009), 1078
Alexandra S Gambaryan, Alexander B Tuzikov, Galina V Pazynina, Julia A Desheva, Nicolai V Bovin, Mikhail N Matrosovich, Alexander I Klimov, “6-sulfo sialyl Lewis X is the common receptor determinant recognized by H5, H6, H7 and H9 influenza viruses of terrestrial poultry”, Virol J, 5:1 (2008)
G. V. Pazynina, V. V. Severov, M. L. Maisel, I. M. Belyanchikov, N. V. Bovin, “Synthesis of mono-, di- and tri-O-sulfated N-acetyllactosamines in a form suitable for glycochip printing”, Mendeleev Commun., 18:5 (2008), 238–240
L. Mochalova, V. Kurova, Y. Shtyrya, E. Korchagina, A. Gambaryan, I. Belyanchikov, N. Bovin, “Oligosaccharide specificity of influenza H1N1 virus neuraminidases”, Arch Virol, 152:11 (2007), 2047
E. M. Rapoport, G. V. Pazynina, M. A. Sablina, P. R. Crocker, N. V. Bovin, “Probing sialic acid binding Ig-like lectins (siglecs) with sulfated oligosaccharides”, Biochemistry (Moscow), 71:5 (2006), 496
Alexandra Gambaryan, Alexander Tuzikov, Galina Pazynina, Nicolai Bovin, Amanda Balish, Alexander Klimov, “Evolution of the receptor binding phenotype of influenza A (H5) viruses”, Virology, 344:2 (2006), 432