Аннотация:
The docking study of ferrocene-substituted bispidines to binding sites of thrombin and factor Xa has shown that bispidine scaffold provides a 3D-arranegment of all substituents and a direction for the ferrocene group to fill the S4 pocket for both thrombin and factor Xa.
Образец цитирования:
S. Z. Vatsadze, D. A. Shulga, Yu. D. Loginova, I. A. Vatsadze, L. Wang, H. Yu, K. V. Kudryavtsev, “Computer modeling of ferrocene-substituted 3,7-diazabicyclo[3.3.1]nonanes as serine protease inhibitors”, Mendeleev Commun., 26:3 (2016), 212–213