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
Kyriakis, Efthimios, Karra, Aikaterini G., Papaioannou, Olga, Solovou, Theodora, Skamnaki, Vassiliki T., Liggri, Panagiota G.V., Zographos, Spyros E., Szennyes, Eszter, Bokor, Éva, Kun, Sándor, PsarraМова:
english
Журнал:
Bioorganic & Medicinal Chemistry
DOI:
10.1016/j.bmc.2019.115196
Date:
November, 2019
Файл:
PDF, 10.60 MB
english, 2019
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