Highly efficient and rapid lead compound evaluation for estimation of inhibition parameters and type of inhibition is proposed. This is based on a single progress-curve measurement in the presence of each candidate compound, followed by the simultaneous analysis of all of these curves using the ENZO enzyme kinetics suite, which can be implemented as a web application. In the first step, all of the candidate ligands are tested as competitive inhibitors. Where the theoretical curves do not correspond to the experimental data, minimal additional measurements are added, with subsequent processing according to modified reaction mechanisms
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
Poster abstracts: "Classical Drug Discovery" is a discovery process wherein screening is done for a ...
<p>(<b>Left</b>) Simulated progress curves for competitive (blue trace), uninhibited (black trace) r...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
<div><p>A difficulty associated with high throughput screening for enzyme inhibitors is to establish...
Click on the DOI link below to access the article (may not be free).The efficiency of suicide inhibi...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
A procedure is proposed for determining whether an inhibitor of an enzyme-catalyzed reaction is comp...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
Poster abstracts: "Classical Drug Discovery" is a discovery process wherein screening is done for a ...
<p>(<b>Left</b>) Simulated progress curves for competitive (blue trace), uninhibited (black trace) r...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
A difficulty associated with high throughput screening for enzyme inhibitors is to establish reactio...
<div><p>A difficulty associated with high throughput screening for enzyme inhibitors is to establish...
Click on the DOI link below to access the article (may not be free).The efficiency of suicide inhibi...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Starting with the development of an enzymatic assay, where an enzyme in solution hydrolysed a solid-...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
A procedure is proposed for determining whether an inhibitor of an enzyme-catalyzed reaction is comp...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
simple graphical method for the determination of reversible inhibition type,inhibitio constant(Ki) ...
Poster abstracts: "Classical Drug Discovery" is a discovery process wherein screening is done for a ...
<p>(<b>Left</b>) Simulated progress curves for competitive (blue trace), uninhibited (black trace) r...