Sándor Kun

Synthesis and structure–activity relationships of C-glycosylated oxadiazoles as inhibitors of glycogen phosphorylase

Marietta Tóth, Sándor Kun, Éva Bokor et al. · Bioorganic & Medicinal Chemistry · 2009 · 65 citations · Full text

Medicinal Chemistry, Biochemistry, Natural Sciences +11

Synthesis of variously coupled conjugates of d-glucose, 1,3,4-oxadiazole, and 1,2,3-triazole for inhibition of glycogen phosphorylase

Sándor Kun, G. Nagy, Marietta Tóth et al. · Carbohydrate Research · 2011 · 55 citations · Full text

Glycogen Phosphorylase, Pharmaceutical Chemistry, Biomolecular Engineering +1

New synthesis of 3-(β-D-glucopyranosyl)-5-substituted-1,2,4-triazoles, nanomolar inhibitors of glycogen phosphorylase

Sándor Kun, Éva Bokor, Gergely Varga et al. · European Journal of Medicinal Chemistry · 2014 · 45 citations · Full text

Medicinal Chemistry, Medicine, New Synthesis +5

Glycogen phosphorylase inhibition improves beta cell function

Lilla Nagy, Judit Márton, András Vida et al. · British Journal of Pharmacology · 2017 · 45 citations · Full text

Synthetic, enzyme kinetic, and protein crystallographic studies of C -β- d -glucopyranosyl pyrroles and imidazoles reveal and explain low nanomolar inhibition of human liver glycogen phosphorylase

A.L. Kantsadi, Éva Bokor, Sándor Kun et al. · European Journal of Medicinal Chemistry · 2016 · 43 citations · Full text

Enzyme Kinetic, Low Nanomolar Inhibition, Biochemistry +7