As part of the research endeavors to combat cancer, a non-symmetric bis-isatin derivative (compound
3) was synthesized and showed a significant anti-proliferative potency. The current study provides a comprehensive characterization of the interaction of compound
3 with the drug-transporting protein bovine serum
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As part of the research endeavors to combat cancer, a non-symmetric bis-isatin derivative (compound
3) was synthesized and showed a significant anti-proliferative potency. The current study provides a comprehensive characterization of the interaction of compound
3 with the drug-transporting protein bovine serum albumin (BSA) via the use of spectroscopic tools along with molecular docking studies. Fluorescence spectral measurements showed that the BSA intrinsic fluorescence can be significantly quenched by the addition of compound
3 and the formation of a non-fluorescent complex. Further measurements revealed a static type of quenching with Stern–Volmer and Linweaver–Burk constants of 10
5. The thermodynamic parameters of the binding were calculated to be Δ
S° 105.09 ± 5.32 with Δ
H° of −0.72 ± 0.71 and negative Δ
G° values. In addition, synchronous fluorescence and 3D fluorescence spectroscopy suggested that compound
3 did not induce conformational changes in BSA. Site competition experiments revealed that compound
3 competes with warfarin within the BSA binding domain (Sudlow site I). This was further confirmed by the molecular docking results showing a binding energy of −25.93 kJ/mol for compound
3-BSA. Hence, the observed results in the present study assumed that the compound
3-BSA binding is spontaneous, involving electrostatic forces and hydrogen bonding.
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