1. Human exposure to magnolol can reach a high dose in daily life. Our previous studies indicated that magnolol showed high affinities to several UDP-glucuronosyltransferases (UGTs) This study was designed to examine the in vitro inhibitory effects of magnolol on UGTs, and further to evaluate the possibility of the in vivo inhibition that might happen
Inhibition of UDP-glucuronosyltransferase (UGT) isoforms can result in severe clinical results, incl...
<p>Cells were treated with 10 ng/mL of IL-1β for different time periods (A) or were treated with mag...
Relatively few selective substrate and inhibitor probes have been identified for human UDP-glucurono...
Background: Magnolol, a biphenyl phenol, is a major active component in Magnolia Officinalis (also k...
Substrates that are specific for certain UDP-glucuronosyltrans-ferase (UGT) isoforms are usually use...
Magnolol, the most abundant bioactive constituent of the Chinese herb Magnolia officinalis, has been...
In this study we investigated the antimicrobial activity of magnolol on Staphylococcus aureus. The m...
UDP-glucuronosyltransferases (UGTs), the most important phase II drug metabolizing enzymes (DMEs), c...
Inhibition of UDP-glucuronosyltransferases (UGTs) can result in many undesired side effects. Diethyl...
The aim of the present study was to investigate arbidol's inhibition towards UDP-glucuronosyltransfe...
Magnolol, a major active constituent in herbal medicine, potently inhibits propofol glucuronidation ...
Magnolol and luteolin are two natural compounds recognized in several medicinal plants widely used i...
Herb-drug interaction strongly limits the clinical application of herbs and drugs, and the inhibitio...
Magnofluorine, a secondary metabolite commonly found in various plants, has pharmacological potentia...
Uridine-diphosphate glucuronosyltransferase 1A1 (UGT1A1) is an important conjugative enzyme in mamma...
Inhibition of UDP-glucuronosyltransferase (UGT) isoforms can result in severe clinical results, incl...
<p>Cells were treated with 10 ng/mL of IL-1β for different time periods (A) or were treated with mag...
Relatively few selective substrate and inhibitor probes have been identified for human UDP-glucurono...
Background: Magnolol, a biphenyl phenol, is a major active component in Magnolia Officinalis (also k...
Substrates that are specific for certain UDP-glucuronosyltrans-ferase (UGT) isoforms are usually use...
Magnolol, the most abundant bioactive constituent of the Chinese herb Magnolia officinalis, has been...
In this study we investigated the antimicrobial activity of magnolol on Staphylococcus aureus. The m...
UDP-glucuronosyltransferases (UGTs), the most important phase II drug metabolizing enzymes (DMEs), c...
Inhibition of UDP-glucuronosyltransferases (UGTs) can result in many undesired side effects. Diethyl...
The aim of the present study was to investigate arbidol's inhibition towards UDP-glucuronosyltransfe...
Magnolol, a major active constituent in herbal medicine, potently inhibits propofol glucuronidation ...
Magnolol and luteolin are two natural compounds recognized in several medicinal plants widely used i...
Herb-drug interaction strongly limits the clinical application of herbs and drugs, and the inhibitio...
Magnofluorine, a secondary metabolite commonly found in various plants, has pharmacological potentia...
Uridine-diphosphate glucuronosyltransferase 1A1 (UGT1A1) is an important conjugative enzyme in mamma...
Inhibition of UDP-glucuronosyltransferase (UGT) isoforms can result in severe clinical results, incl...
<p>Cells were treated with 10 ng/mL of IL-1β for different time periods (A) or were treated with mag...
Relatively few selective substrate and inhibitor probes have been identified for human UDP-glucurono...