<?xml version="1.0"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=137879"><dc:title>Design and synthesis of novel 3-triazolyl-1-thiogalactosides as galectin-1, -3 and -8 inhibitors</dc:title><dc:creator>van Klaveren,	Sjors	(Avtor)
	</dc:creator><dc:creator>Dernovšek,	Jaka	(Avtor)
	</dc:creator><dc:creator>Jakopin,	Žiga	(Avtor)
	</dc:creator><dc:creator>Anderluh,	Marko	(Avtor)
	</dc:creator><dc:creator>Leffler,	Hakon	(Avtor)
	</dc:creator><dc:creator>Nilsson,	Ulf	(Avtor)
	</dc:creator><dc:creator>Tomašič,	Tihomir	(Avtor)
	</dc:creator><dc:description>Galectins are galactoside-binding proteins that play a role in various pathophysiological conditions, making them attractive targets in drug discovery. We have designed and synthesised a focused library of aromatic 3-triazolyl-1-thiogalactosides targeting their core site for binding of galactose and a subsite on its non-reducing side. Evaluation of their binding affinities for galectin-1, -3, and -8N identified acetamide-based compound 36 as a suitable compound for further affinity enhancement by adding groups at the reducing side of the galactose. Synthesis of its dichlorothiophenyl analogue 59 and the thiodigalactoside analogue 62 yielded promising pan-galectin inhibitors.</dc:description><dc:date>2022</dc:date><dc:date>2022-07-05 11:07:43</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>137879</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
