Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure-Based Design of Inhibitors for Trypsin-Like Serine Proteases.

MLA

Furtmann, Norbert, et al. “Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure-Based Design of Inhibitors for Trypsin-Like Serine Proteases.” Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 22, no. 2, Jan. 2016, pp. 610–25. EBSCOhost, https://doi.org/10.1002/chem.201503534.

APA

Furtmann, N., Häußler, D., Scheidt, T., Stirnberg, M., Steinmetzer, T., Bajorath, J., & Gütschow, M. (2016). Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure-Based Design of Inhibitors for Trypsin-Like Serine Proteases. Chemistry (Weinheim an Der Bergstrasse, Germany), 22(2), 610–625. https://doi.org/10.1002/chem.201503534

Chicago

Furtmann, Norbert, Daniela Häußler, Tamara Scheidt, Marit Stirnberg, Torsten Steinmetzer, Jürgen Bajorath, and Michael Gütschow. 2016. “Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure-Based Design of Inhibitors for Trypsin-Like Serine Proteases.” Chemistry (Weinheim an Der Bergstrasse, Germany) 22 (2): 610–25. doi:10.1002/chem.201503534.