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Furthermore, a study employing molecular docking techniques to evaluate the binding effects of luteolin, luteolin-4-O-glucoside and apigenin on TLR4 (93) found that these compounds interact with TLR4 through hydrophobic interactions and hydrogen bonding, with binding energy results less than-7 kcal/mol

doi: 10.1016/j.glohj.2020.01.004

M.ShukryM.et al

A., Kabir, M., Hossain, M
