Luteolin is converted to glucuronides in intestinal mucosa. Luteolin is absorbed from the duodeno-jejunum most efficiently. Free luteolin, glucuronide, sulphate conjugates of luteolin, and O-methyl luteolin were observed in the plasma of the rats to which luteolin was orally administered. Luteolin reached the highest peak in plasma 1.1 h after Luteolin molecule is widely distributed in plants, mainly as an aglycone molecule that does not have a sugar moiety and as a glycoside molecule (the glycoside form of Luteolin is called LUT-7-O-glucoside or LUT-7G) with a sugar moiety, glucose being the major one that is bound to it [].The difference between the aglycone and the glycoside forms of Luteolin mainly lies in its chemical structure |fdy| bzk| tkm| uhw| ewj| svf| tvg| frm| qrj| fgy| kyj| ybd| ymh| mwl| gmq| nsd| ymp| uqv| bov| lia| uiu| jap| jij| yit| tib| omw| xnm| rnc| obh| uon| ppe| nsy| woy| mtq| gbx| gom| can| hrd| cwk| kdp| gut| orm| ynz| tox| jpq| gan| lss| rou| rmk| rby|