<p>Fig 4 A shows the inhibitory effects of phenylbutazone on the 7-O-glucuronide of diosmetin in HLMs and UGT1A6. Fig 4 B displays the inhibitory effects of carvacrol on the 3′-O-glucuronide of diosmetin in HLMs and UGT1A9. Fig 4 C presents the inhibitory effects of carvacrol on the 7-O-glucuronide of chrysoeriol in HLMs and UGT1A9. Fig 4 D shows the inhibitory effects of bilirubin on the 4′-O-glucuronides of chrysoeriol in HLMs and UGT1A1. Each column corresponds to the average of three determinations with error bars representing the S.D. The “*” symbol means a statistically significant difference compared with control at p < 0.05; “**” means p < 0.01; “***” means p < 0.001.</p
Enzyme selective inhibitors represent the most valuable experi-mental tool for reaction phenotyping....
Bavachalcone and corylin are two major bioactive compounds isolated from Psoralea corylifolia L., wh...
: Biochim Biophys Acta 2001 Jul 9;1548(1):23-8 Related Articles, Books, LinkOut Inhibition of human ...
UDP-glucuronosyltransferases (UGTs), the most important phase II drug metabolizing enzymes (DMEs), c...
<p>Note: The concentrations of CHL was 5 µM and that for the other specific inhibitors was 1 µM. The...
<p>5 μM Ko143, 10 μM Ko143, 10 μM diosmetin, 10 μM diosmetin with 5 μM Ko143 or 10 μM Ko143, 10μM ch...
<p>Sigmoidal plot of HPA relative enzyme inhibition (%) versus varying concentration gedunin and aza...
This study aimed to determine the reaction kinetics of the regioselective glucuronidation of diosmet...
Context: Glutaredoxins (GRX) are involved in the regulation of thiol redox state. GRX-1 is a cytosol...
Isoliquiritigenin, a herbal ingredient with chalcone structure, has been speculated to be able to in...
<p>Diosmetin (10 μM) was incubated with recombinant CYP1A1 (1mg/ml) and CYP1B1 (1mg/ml) at various t...
The aim of this study was to assess the effects of diosmetin and hesperetin, two flavonoids present ...
Summary: Herein, we report the experimental results of the inhibition effects of some phenolic compo...
Tolcapone and entacapone are two potent catechol-O-methyltransferase (COMT) inhibitors with a simila...
<p>The enzymatic activity assay with inhibitors was performed by using d,l-glyceraldehyde as a subst...
Enzyme selective inhibitors represent the most valuable experi-mental tool for reaction phenotyping....
Bavachalcone and corylin are two major bioactive compounds isolated from Psoralea corylifolia L., wh...
: Biochim Biophys Acta 2001 Jul 9;1548(1):23-8 Related Articles, Books, LinkOut Inhibition of human ...
UDP-glucuronosyltransferases (UGTs), the most important phase II drug metabolizing enzymes (DMEs), c...
<p>Note: The concentrations of CHL was 5 µM and that for the other specific inhibitors was 1 µM. The...
<p>5 μM Ko143, 10 μM Ko143, 10 μM diosmetin, 10 μM diosmetin with 5 μM Ko143 or 10 μM Ko143, 10μM ch...
<p>Sigmoidal plot of HPA relative enzyme inhibition (%) versus varying concentration gedunin and aza...
This study aimed to determine the reaction kinetics of the regioselective glucuronidation of diosmet...
Context: Glutaredoxins (GRX) are involved in the regulation of thiol redox state. GRX-1 is a cytosol...
Isoliquiritigenin, a herbal ingredient with chalcone structure, has been speculated to be able to in...
<p>Diosmetin (10 μM) was incubated with recombinant CYP1A1 (1mg/ml) and CYP1B1 (1mg/ml) at various t...
The aim of this study was to assess the effects of diosmetin and hesperetin, two flavonoids present ...
Summary: Herein, we report the experimental results of the inhibition effects of some phenolic compo...
Tolcapone and entacapone are two potent catechol-O-methyltransferase (COMT) inhibitors with a simila...
<p>The enzymatic activity assay with inhibitors was performed by using d,l-glyceraldehyde as a subst...
Enzyme selective inhibitors represent the most valuable experi-mental tool for reaction phenotyping....
Bavachalcone and corylin are two major bioactive compounds isolated from Psoralea corylifolia L., wh...
: Biochim Biophys Acta 2001 Jul 9;1548(1):23-8 Related Articles, Books, LinkOut Inhibition of human ...