Synthesis and Preliminary Evaluation of Biological Activity of Glycoconjugates Analogues of Acyclic Uridine Derivatives. 2018

Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Faculty of Chemistry, Silesian University of Technology, Krzywoustego 4, 44-100 Gliwice, Poland. roman.m.komor@gmail.com.

Herein we present the methodology for obtaining glycosyltransferase inhibitors, analogues of natural enzyme substrates of donor-type: UDP-glucose and UDP-galactose. The synthesis concerned glycoconjugates, nucleoside analogues containing an acyclic ribose mimetic linked to a uracil moiety in their structure. The biological activity of the synthesised compounds was determined on the basis of their ability to inhibit the model enzyme action of β-1,4-galactosyltransferase from bovine milk. The obtained results allowed to expand and supplement the existing library of synthetic compounds that are able to regulate the biological activity of enzymes from the GT class.

UI MeSH Term Description Entries
D004791 Enzyme Inhibitors Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. Enzyme Inhibitor,Inhibitor, Enzyme,Inhibitors, Enzyme
D006001 Glycoconjugates Carbohydrates covalently linked to a nonsugar moiety (lipids or proteins). The major glycoconjugates are glycoproteins, glycopeptides, peptidoglycans, glycolipids, and lipopolysaccharides. (From Biochemical Nomenclature and Related Documents, 2d ed; From Principles of Biochemistry, 2d ed) Glycoconjugate
D014529 Uridine A ribonucleoside in which RIBOSE is linked to URACIL. Allo-Uridine,Allouridine,Allo Uridine
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular
D016695 Glycosyltransferases Enzymes that catalyze the transfer of glycosyl groups to an acceptor. Most often another carbohydrate molecule acts as an acceptor, but inorganic phosphate can also act as an acceptor, such as in the case of PHOSPHORYLASES. Some of the enzymes in this group also catalyze hydrolysis, which can be regarded as transfer of a glycosyl group from the donor to water. Subclasses include the HEXOSYLTRANSFERASES; PENTOSYLTRANSFERASES; SIALYLTRANSFERASES; and those transferring other glycosyl groups. EC 2.4. Glycosyltransferase,Glycoside Transferases,Transferases, Glycoside

Related Publications

Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
January 1987, Journal of medicinal chemistry,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
May 1997, Farmaco (Societa chimica italiana : 1989),
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
December 2003, Chemical & pharmaceutical bulletin,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
January 2013, Nucleosides, nucleotides & nucleic acids,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
May 2004, Bioorganic & medicinal chemistry letters,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
March 1992, Journal of medicinal chemistry,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
September 1992, Journal of medicinal chemistry,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
September 1981, Journal of medicinal chemistry,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
March 1995, Journal of medicinal chemistry,
Roman Komor, and Gabriela Pastuch-Gawolek, and Ewelina Krol, and Wieslaw Szeja
July 2013, Molecules (Basel, Switzerland),
Copied contents to your clipboard!