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_168
Snippet: In one study, an in vitro assay related to hyaluronidase inhibition by phlorotannins was evaluated. The E. bicyclis and E. kurome phlorotannins exhibited potent inhibition in comparison to the popular inhibitors catechins and sodium cromoglycate. Phloroglucinol, eckol (trimer), phlorofucofuroeckol-A (pentamer), dieckol, 8,8'-bieckol (hexamers), and an unknown tetramer showed IC 50 values of 280, >800, 140, 120, 40, and 650 µM, respectively, wher.....
Document: In one study, an in vitro assay related to hyaluronidase inhibition by phlorotannins was evaluated. The E. bicyclis and E. kurome phlorotannins exhibited potent inhibition in comparison to the popular inhibitors catechins and sodium cromoglycate. Phloroglucinol, eckol (trimer), phlorofucofuroeckol-A (pentamer), dieckol, 8,8'-bieckol (hexamers), and an unknown tetramer showed IC 50 values of 280, >800, 140, 120, 40, and 650 µM, respectively, whereas catechin, epigallocatechin gallate, and sodium cromoglycate had an IC 50 value of 620, 190, and 270 µM, respectively. According to the results, eckol (IC 50 > 800 µM) showed no inhibitory effect on hyaluronidase activity [74] .
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