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
| Autor: | 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, Psarra, Anna-Maria G., Somsák, László, Leonidas, Demetres D. |
|---|---|
| Zdroj: | In Bioorganic & Medicinal Chemistry 1 January 2020 28(1) |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect