British journal of medicine type 2 diabetes
Tartalom
Such files may be downloaded by article for research use if there is a public use license linked to the relevant article, that license may permit other uses.
Cited By This article is cited by 25 publications. ACS Catalysis11 15 Davies, Rachel T. Mathomes, Timothy J. ACS Chemical Biology14 7 Solovou, Csenge Koppány, Anastassia L. Kantsadi, Katalin E. Szabó, Andrea Szakács, George A. Stravodimos, Tibor Docsa, Vassiliki T.
Skamnaki, Spyros E. Zographos, Pál Gergely, Demetres D. Leonidas, and László Somsák. Journal of Medicinal Chemistry60 22 Organic Letters19 13 Chemical Reviews3 Synthesis of non-classical C-acyl-glycosides via Liebeskind—Srogl coupling: Scope, limitation, improved synthesis and antioxidant activity of scleropentaside A.
Tetrahedron92 Pharmaceuticals14 4 Mavreas, Dionysios D. Neofytos, Evangelia D. Chrysina, Alessandro Venturini, Thanasis Gimisis.
Synthesis, Kinetic and Conformational Studies of 2-Substituted β-d-glucopyranosyl -pyrimidinones as Potential Inhibitors of Glycogen Phosphorylase. Molecules25 22 N- and C-Glycopyranosyl heterocycles as glycogen phosphorylase inhibitors.
Skamnaki, Panagiota G. Liggri, Spyros E. Psarra, László Somsák, Demetres D. The architecture of hydrogen and sulfur σ-hole interactions explain differences in the inhibitory potency of C-β-d-glucopyranosyl thiazoles, imidazoles and an N-β-d glucopyranosyl tetrazole for human liver glycogen phosphorylase and offer new insights to structure-based design.
New syntheses towards C -glycosyl type glycomimetics. Pure and Applied Chemistry91 7 Chrysina, Thanasis Gimisis.
Molecules24 12 Carbohydrate Research, Synthesis of C-β-d-glucopyranosyl derivatives of some fused azoles for the inhibition of glycogen phosphorylase.