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P D Leeson

Showing results (21-30 of 42) with videos related to

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Molecular Pharmacology|May 1, 1992
Kynurenic acid analogues with improved affinity and selectivity for the glycine site on the N-methyl-D-aspartate receptor from rat brainA C Foster, J A Kemp, P D Leeson, et al.
British Journal of Pharmacology|November 1, 1994
The anticonvulsant and behavioural profile of L-687,414, a partial agonist acting at the glycine modulatory site on the N-methyl-D-aspartate (NMDA) receptor complexM D Tricklebank, L J Bristow, P H Hutson, et al.
Journal of Medicinal Chemistry|May 29, 1992
4-Amido-2-carboxytetrahydroquinolines. Structure-activity relationships for antagonism at the glycine site of the NMDA receptorP D Leeson, R W Carling, K W Moore, et al.
Journal of Medicinal Chemistry|May 10, 1996
5-(4-Chlorophenyl)-4-methyl-3-(1-(2-phenylethyl)piperidin-4-yl)isoxazole: a potent, selective antagonist at human cloned dopamine D4 receptorsM Rowley, H B Broughton, I Collins, et al.
Bioorganic & Medicinal Chemistry Letters|May 26, 1999
4-N-linked-heterocyclic piperidine derivatives with high affinity and selectivity for human dopamine D4 receptorsK W Moore, K Bonner, E A Jones, et al.
Journal of Medicinal Chemistry|October 29, 1993
3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory amino acid antagonists acting at glycine-site NMDA and (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptorsR W Carling, P D Leeson, K W Moore, et al.
Journal of Medicinal Chemistry|May 13, 1994
3'-(Arylmethyl)- and 3'-(aryloxy)-3-phenyl-4-hydroxyquinolin-2(1H)-ones: orally active antagonists of the glycine site on the NMDA receptorJ J Kulagowski, R Baker, N R Curtis, et al.
Annals of the New York Academy of Sciences|May 11, 1992
Neurotoxin-related research: from the laboratory to the clinicL Iversen, A C Foster, R G Hill, et al.
Journal of Medicinal Chemistry|February 1, 1989
Selective thyromimetics. Cardiac-sparing thyroid hormone analogues containing 3'-arylmethyl substituentsP D Leeson, J C Emmett, V P Shah, et al.
The Biochemical Journal|January 1, 1988
The dephosphorylation of inositol 1,4-bisphosphate to inositol in liver and brain involves two distinct Li+-sensitive enzymes and proceeds via inositol 4-phosphateC I Ragan, K J Watling, N S Gee, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Molecular Pharmacology|May 1, 1992
Kynurenic acid analogues with improved affinity and selectivity for the glycine site on the N-methyl-D-aspartate receptor from rat brainA C Foster, J A Kemp, P D Leeson, et al.
British Journal of Pharmacology|November 1, 1994
The anticonvulsant and behavioural profile of L-687,414, a partial agonist acting at the glycine modulatory site on the N-methyl-D-aspartate (NMDA) receptor complexM D Tricklebank, L J Bristow, P H Hutson, et al.
Journal of Medicinal Chemistry|May 29, 1992
4-Amido-2-carboxytetrahydroquinolines. Structure-activity relationships for antagonism at the glycine site of the NMDA receptorP D Leeson, R W Carling, K W Moore, et al.
Journal of Medicinal Chemistry|May 10, 1996
5-(4-Chlorophenyl)-4-methyl-3-(1-(2-phenylethyl)piperidin-4-yl)isoxazole: a potent, selective antagonist at human cloned dopamine D4 receptorsM Rowley, H B Broughton, I Collins, et al.
Bioorganic & Medicinal Chemistry Letters|May 26, 1999
4-N-linked-heterocyclic piperidine derivatives with high affinity and selectivity for human dopamine D4 receptorsK W Moore, K Bonner, E A Jones, et al.
Journal of Medicinal Chemistry|October 29, 1993
3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory amino acid antagonists acting at glycine-site NMDA and (RS)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptorsR W Carling, P D Leeson, K W Moore, et al.
Journal of Medicinal Chemistry|May 13, 1994
3'-(Arylmethyl)- and 3'-(aryloxy)-3-phenyl-4-hydroxyquinolin-2(1H)-ones: orally active antagonists of the glycine site on the NMDA receptorJ J Kulagowski, R Baker, N R Curtis, et al.
Annals of the New York Academy of Sciences|May 11, 1992
Neurotoxin-related research: from the laboratory to the clinicL Iversen, A C Foster, R G Hill, et al.
Journal of Medicinal Chemistry|February 1, 1989
Selective thyromimetics. Cardiac-sparing thyroid hormone analogues containing 3'-arylmethyl substituentsP D Leeson, J C Emmett, V P Shah, et al.
The Biochemical Journal|January 1, 1988
The dephosphorylation of inositol 1,4-bisphosphate to inositol in liver and brain involves two distinct Li+-sensitive enzymes and proceeds via inositol 4-phosphateC I Ragan, K J Watling, N S Gee, et al.
Pageof 5