Zobrazeno 1 - 6
of 6
pro vyhledávání: '"R. J. Powel"'
Publikováno v:
Journal of Neurochemistry. 59:2087-2093
Neomycin appears as a full agonist and spermidine as a partial agonist at the site where polyamines enhance 1-[1-(2-thienyl)cyclohexyl][3H]piperidine ([3H]TCP) binding on the N-methyl-D-aspartate (NMDA) receptor. Other aminoglycosides also enhance [3
Autor:
Andre I. Salama, D. LaMonte, Thomas J. Mangano, Jitendra Patel, P. J. Warwick, William C. Zinkand, R. J. Powel, Richard A. Keith, M. Britt, Linda M. Pullan, Robert J. Stumpo, M. J. Chapdelaine
Publikováno v:
Journal of Neurochemistry. 55:1346-1351
HA-966 (1-hydroxy-3-aminopyrrolidone-2) is an antagonist at the glycine allosteric site of the N-methyl-D-aspartate receptor ionophore complex. Unlike presently known glycine antagonists, HA-966 is chiral. We report stereoselectivity for the (R)-enan
Autor:
L M, Pullan, R J, Powel
Publikováno v:
Neuroscience letters. 148(1-2)
We compared, for a number of ligands to the two receptors, the displacement of [3H]strychnine binding to the glycine-gated chloride channel of spinal cord and brainstem synaptic membranes to the displacement of [3H]glycine binding to the NMDA recepto
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 262(2)
The effects of N-(3-aminopropyl)-1,10-diaminodecane (APDA10) on the N-methyl-D-aspartate (NMDA) receptor/ion channel complex were investigated. In the presence of 100 microM glutamate and 100 microM glycine, APDA10 had biphasic effects on the binding
Publikováno v:
Research communications in chemical pathology and pharmacology. 75(3)
We studied the influence of chronic moricizine hydrochloride (MRZ) treatment on the drug's pharmacokinetics and on drug metabolizing enzyme activities in rats. Separate groups of 8 rats (4 males and 4 females) were treated with 40 and 100 mg/kg oral
Autor:
L M, Pullan, M, Britt, M J, Chapdelaine, R A, Keith, D, LaMonte, T J, Mangano, J, Patel, R J, Powel, R J, Stumpo, P J, Warwick
Publikováno v:
Journal of neurochemistry. 55(4)
HA-966 (1-hydroxy-3-aminopyrrolidone-2) is an antagonist at the glycine allosteric site of the N-methyl-D-aspartate receptor ionophore complex. Unlike presently known glycine antagonists, HA-966 is chiral. We report stereoselectivity for the (R)-enan