https://www.selleckchem.com/products/GDC-0449.html
The compound and some positive controls act as ligand were subject binding to PrgQ, PrgX, PrgZ, and CcfA as proteins target, the ligands were free for blind docking. A framework was presented potency of phenolic compounds to inhibit the protein's target from its affinity binding scores. It was found thatcompound was potential to inhibit all of the tested protein and gave the highest binding affinity to PrgX (-9.2 kcal.mol ; the site at Phe59B, Phe59B, Asn63A, and Asn63B residue) and PrgZ (-7.4 kcal.mol ; the site at Leu4B, Thr65A, Thr8
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