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. 2019 Nov 19;15(1):50–67. doi: 10.1002/cmdc.201900576

Figure 1.

Figure 1

Molecular docking of 4 in the sEH active site (PDB‐ID: 3OTQ23) and the ligand binding site of FXR (PDB‐ID: 4QE824) particularly suggested potential for structural optimization in the terminal cyclopentylurethane moiety. Docking was performed in MOE and visualized using UCSF Chimera.