kinetics of competitive inhibition in neurotransmitter receptor binding assays. Mol. Phannacol. 19:367-371 (1981). The kinetics of competitive inhibition was described by first-order differential equations, and the solution to these equations was derived numerically. The results of this analysis showed that the IC,o of a competitive inhibition curve decreases as equilibrium is approached if the dissociation rate constant of the nonlabeled ligand is equal to or less than that of the labeled ligand. The converse was true for competitive inhibition curves of a nonlabeled inhibitor with a dissociation rate constant greater than that of the labeled ligand. Nonequiibrium competitive inhibition experiments were performed using the muscarinic antag...
Binding kinetics is closely related to the efficacy of drugs. Several aspects of binding kinetics, s...
A theoretical analysis has been made of multiple inhibition systems involving a full and a partial i...
Equilibrium-binding affinities of ligands for a drug target do not always accurately reflect the suc...
<p>(A) Compounds <b>1</b> and <b>2</b> and the substrate do not competitively bind to the same site....
The hyperbolic parabola is commonly used to summarize kinetics for enzyme reactions and receptor bin...
Slow receptor dissociation kinetics has been implicated in the long clinical duration of action of t...
Binding expressions are derived and analytical procedures developed for the quantitative characteriz...
Abstract: Targeting receptor systems by competitive inhibition is the objective of various antibody ...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
N-Methyl-D-aspartate (NMDA) receptor ligands regulate the bind-ing of uncompetitive antagonists in m...
Antagonism of glutamate-receptor responses activated by N-methyl-D-aspartic acid (NMDA) was studied ...
Negative cooperativity is a phenomenon in which the binding of a first ligand or substrate molecule ...
A review of the single site receptor system is presented and the linear and nonlinear analysis that ...
Although there are several empirical approaches that enable the comparison of relative agonist effic...
<p>Because every state can bind up to 3 ligands, which are either agonists (red spheres) or antagoni...
Binding kinetics is closely related to the efficacy of drugs. Several aspects of binding kinetics, s...
A theoretical analysis has been made of multiple inhibition systems involving a full and a partial i...
Equilibrium-binding affinities of ligands for a drug target do not always accurately reflect the suc...
<p>(A) Compounds <b>1</b> and <b>2</b> and the substrate do not competitively bind to the same site....
The hyperbolic parabola is commonly used to summarize kinetics for enzyme reactions and receptor bin...
Slow receptor dissociation kinetics has been implicated in the long clinical duration of action of t...
Binding expressions are derived and analytical procedures developed for the quantitative characteriz...
Abstract: Targeting receptor systems by competitive inhibition is the objective of various antibody ...
Enzyme inhibition studies are conducted to characterize enzymes and to examine drug-drug interaction...
N-Methyl-D-aspartate (NMDA) receptor ligands regulate the bind-ing of uncompetitive antagonists in m...
Antagonism of glutamate-receptor responses activated by N-methyl-D-aspartic acid (NMDA) was studied ...
Negative cooperativity is a phenomenon in which the binding of a first ligand or substrate molecule ...
A review of the single site receptor system is presented and the linear and nonlinear analysis that ...
Although there are several empirical approaches that enable the comparison of relative agonist effic...
<p>Because every state can bind up to 3 ligands, which are either agonists (red spheres) or antagoni...
Binding kinetics is closely related to the efficacy of drugs. Several aspects of binding kinetics, s...
A theoretical analysis has been made of multiple inhibition systems involving a full and a partial i...
Equilibrium-binding affinities of ligands for a drug target do not always accurately reflect the suc...