Potent adenosine hA2A receptor antagonists are often accompanied by poor aqueous solubility, which presents issues for drug development. Herein we describe the early exploration of the structure-activity relationships of a lead pyrimidin-4-yl acetamide series to provide potent and selective 2-amino-N-pyrimidin-4-yl acetamides as hA2A receptor antagonists with excellent aqueous solubility. In addition, this series of compounds has demonstrated good bioavailability and in vivo efficacy in a rodent model of Parkinson's disease, despite having reduced potency for the rat A2A receptor versus the human A2A receptor.
Rate-limiting steps and transition state structure for the acylation stage of acetylcholinesterase-catalyzed hydrolysis of (acetylthio)choline have been characterized by measuring substrate and solvent isotope
effects and viscosity effects on the bimolecular rate constant k
E (=k
cat/K
m). Substrate and solvent isotope effects
have been measured for wild-type enzymes from Torpedo californica, human and mouse, and for various
active site mutants of these enzymes. Sizable solvent isotope effects, D
2
O
k
E ∼ 2, are observed when substrate
β-deuterium isotope effects are most inverse, βD
k
E = 0.95; conversely, reactions that have D
2
O
k
E ∼ 1 have
substrate isotope effects of βD
k
E = 1.00. Proton inventories of k
E provide a quantitative measure of the
contributions by the successive steps, diffusional encounter of substrate with the active site and consequent
chemical catalysis, to rate limitation of the acylation stage of catalysis. For reactions that have the largest
solvent isotope effects and most inverse substrate isotope effects, proton inventories are linear or nearly so,
consistent with prominent rate limitation by a chemical step whose transition state is stabilized by a single
proton bridge. Reactions that have smaller solvent isotope effects and less inverse substrate isotope effects
have nonlinear and upward bulging proton inventories, consistent with partial rate limitations by both diffusional
encounter and chemical catalysis. Curve fitting of such proton inventories provides a measure of the commitment
to catalysis that is in agreement with the effect of solvent viscosity on k
E and with the results of a double
isotope effect measurement, wherein βD
k
E is measured in both H2O and D2O. The results of these various
experiments not only provide a model for the structure of the acylation transition state but also establish the
validity of solvent isotope effects as a tool for quantitative characterization of rate limitation for acetylcholinesterase catalysis.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.