Fig. 5

3D representations of the compound at the binding pocket of dihydropteroate synthase of S. aureus (PDB: ID 1AD4). (a and b) luteolin 7-O-glucopyransoide, (c and d) Myricetin 3-O-rhamnoside, (e and f) Quercetin 3-O-rhamnoside and (g and h) ciprofloxacin.