[a]<p>The measurements were performed using 1 mM L-aspartate, 3 µM ADC, and 1 mM compound (potential inhibitor) in D<sub>2</sub>O at 25°C.</p>[b]<p>The conversion percentage corresponds to the product formed by integration of the <sup>1</sup>H NMR signals corresponding to substrate and product of the enzymatic reaction after ca. 30 min upon addition of the enzyme. The time was adjusted to correspond to 50% conversion in the <i>absence</i> of inhibitor (reference). The absolute values were averaged from at least two independent assays.</p>[c]<p>The relative inhibitory effect, <i>k</i><sub>rel</sub>, was calculated as the ratio of the conversion percentages in the presence and absence of compound.</p>[d]<p>While full inhibition was also obser...
<p>The <i>k</i><sub>inact</sub> and <i>K</i><sub>I</sub> values for the covalent inhibitors were obt...
a<p>The NAT activity was measured by the NAT-inhibition assay using 150 µM HLZ and 120 µM Ac-CoA as ...
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>The different points correspond to conversion percentages of the individual <sup>1</sup>H NMR spe...
<p>Bars indicate the difference between the percentage inhibition observed using 0.11 mM GAL as subs...
(A, B) Kinetics analysis of MsCS for oxaloacetate (A) and acetyl-CoA (B). (C, D) Inhibition kinetic ...
<p>The enzymatic activity assay with inhibitors was performed by using d,l-glyceraldehyde as a subst...
<p>The concentration of the inhibitor was kept at 100 µM and the readings were taken under two subst...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
<p>Percentage residual activity was determined at various inhibitor concentrations using the followi...
<p>Relative nucleotidase activities expressed as percentage of available substrate dephosphorylated,...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
[a]Assays were performed in duplicate (errors were less than 5%) with CENTA as reporter substrate (1...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
<p>NT<i>Hi</i> Nuc was incubated with 2 μM FRET substrate and increasing concentrations of inhibitor...
<p>The <i>k</i><sub>inact</sub> and <i>K</i><sub>I</sub> values for the covalent inhibitors were obt...
a<p>The NAT activity was measured by the NAT-inhibition assay using 150 µM HLZ and 120 µM Ac-CoA as ...
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>The different points correspond to conversion percentages of the individual <sup>1</sup>H NMR spe...
<p>Bars indicate the difference between the percentage inhibition observed using 0.11 mM GAL as subs...
(A, B) Kinetics analysis of MsCS for oxaloacetate (A) and acetyl-CoA (B). (C, D) Inhibition kinetic ...
<p>The enzymatic activity assay with inhibitors was performed by using d,l-glyceraldehyde as a subst...
<p>The concentration of the inhibitor was kept at 100 µM and the readings were taken under two subst...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
<p>Percentage residual activity was determined at various inhibitor concentrations using the followi...
<p>Relative nucleotidase activities expressed as percentage of available substrate dephosphorylated,...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
[a]Assays were performed in duplicate (errors were less than 5%) with CENTA as reporter substrate (1...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
<p>NT<i>Hi</i> Nuc was incubated with 2 μM FRET substrate and increasing concentrations of inhibitor...
<p>The <i>k</i><sub>inact</sub> and <i>K</i><sub>I</sub> values for the covalent inhibitors were obt...
a<p>The NAT activity was measured by the NAT-inhibition assay using 150 µM HLZ and 120 µM Ac-CoA as ...
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...