Author: Manandhar, Bandana; Paudel, Pradeep; Seong, Su Hui; Jung, Hyun Ah; Choi, Jae Sue
Title: Characterizing Eckol as a Therapeutic Aid: A Systematic Review Document date: 2019_6_18
ID: 0dpv85od_184
Snippet: In a similar study of tyrosinase inhibition, eckol derived from E. cava was evaluated on melanogenesis and its binding capacity using a molecular docking simulation. The impact of eckol on melanin synthesis was evaluated in B16F10 melanoma cells induced by the α-melanocyte stimulating hormone. Eckol (25-100 µM) suppressed melanin synthesis and tyrosinase activity by inhibiting tyrosinase, both TRP1 and TRP2, expression in α-MSH-stimulated B16F.....
Document: In a similar study of tyrosinase inhibition, eckol derived from E. cava was evaluated on melanogenesis and its binding capacity using a molecular docking simulation. The impact of eckol on melanin synthesis was evaluated in B16F10 melanoma cells induced by the α-melanocyte stimulating hormone. Eckol (25-100 µM) suppressed melanin synthesis and tyrosinase activity by inhibiting tyrosinase, both TRP1 and TRP2, expression in α-MSH-stimulated B16F10 cells. As compared to 50-100 µM eckol, 350 µM of arbutin (positive control) presented a weaker inhibition on tyrosinase activity [148] .
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