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Design, Synthesis, In Vitro, and In Silico Insights of 5-(Substituted benzylidene)-2-phenylthiazol-4(5 H )-one Derivatives: A Novel Class of Anti-Melanogenic Compounds.

Dahye YoonMin Kyung KangHee Jin JungSultan UllahJieun LeeYeongmu JeongSang Gyun NohDongwan KangYujin ParkPusoon ChunHae Young ChungHyung Ryong Moon
Published in: Molecules (Basel, Switzerland) (2023)
( Z )-5-Benzylidene-2-phenylthiazol-4(5 H )-one (( Z )-BPT) derivatives were designed by combining the structural characteristics of two tyrosinase inhibitors. The double-bond geometry of trisubstituted alkenes, ( Z )-BPTs 1 - 14 , was determined based on the 3 J C,Hβ coupling constant of 1 H-coupled 13 C NMR spectra. Three ( Z )-BPT derivatives ( 1 - 3 ) showed stronger tyrosinase inhibitory activities than kojic acid; in particular, 2 was to be 189-fold more potent than kojic acid. Kinetic analysis using mushroom tyrosinase indicated that 1 and 2 were competitive inhibitors, whereas 3 was a mixed-type inhibitor. The in silico results revealed that 1 - 3 could strongly bind to the active sites of mushroom and human tyrosinases, supporting the kinetic results. Derivatives 1 and 2 decreased the intracellular melanin contents in a concentration-dependent manner in B16F10 cells, and their anti-melanogenic efficacy exceeded that of kojic acid. The anti-tyrosinase activity of 1 and 2 in B16F10 cells was similar to their anti-melanogenic effects, suggesting that their anti-melanogenic effects were primarily owing to their anti-tyrosinase activity. Western blotting of B16F10 cells revealed that the derivatives 1 and 2 inhibited tyrosinase expression, which partially contributes to their anti-melanogenic ability. Several derivatives, including 2 and 3 , exhibited potent antioxidant activities against ABTS cation radicals, DPPH radicals, ROS, and peroxynitrite. These results suggest that ( Z )-BPT derivatives 1 and 2 have promising potential as novel anti-melanogenic agents.
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