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G J Riley

Showing results (31-40 of 49) with videos related to

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Journal of Medicinal Chemistry|September 1, 1991
Comparison of azabicyclic esters and oxadiazoles as ligands for the muscarinic receptorB S Orlek, F E Blaney, F Brown, et al.
Journal of Medicinal Chemistry|January 22, 1998
Design of [R-(Z)]-(+)-alpha-(methoxyimino)-1-azabicyclo[2.2.2]octane-3-acetonitri le (SB 202026), a functionally selective azabicyclic muscarinic M1 agonist incorporating the N-methoxy imidoyl nitrile group as a novel ester bioisostereS M Bromidge, F Brown, F Cassidy, et al.
Bioorganic & Medicinal Chemistry|September 26, 2000
Evaluation of a series of anticonvulsant 1,2,3,4-tetrahydroisoquinolinyl-benzamidesW N Chan, M S Hadley, J D Harling, et al.
Psychopharmacology|July 10, 2001
Central effects of urotensin-II following ICV administration in ratsJ Gartlon, F Parker, D C Harrison, et al.
Journal of Medicinal Chemistry|March 26, 1998
(R)-3,N-dimethyl-N-[1-methyl-3-(4-methyl-piperidin-1-yl) propyl]benzenesulfonamide: the first selective 5-HT7 receptor antagonistI T Forbes, S Dabbs, D M Duckworth, et al.
British Journal of Pharmacology|May 24, 2000
Characterization of SB-269970-A, a selective 5-HT(7) receptor antagonistJ J Hagan, G W Price, P Jeffrey, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Fused aminotetralins: novel antagonists with high selectivity for the dopamine D3 receptorK Y Avenell, I Boyfield, M C Coldwell, et al.
Journal of Medicinal Chemistry|February 12, 2000
A novel, potent, and selective 5-HT(7) antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl) phen ol (SB-269970)P J Lovell, S M Bromidge, S Dabbs, et al.
Bioorganic & Medicinal Chemistry Letters|November 22, 2000
Novel 2,3,4,5-tetrahydro-1H-3-benzazepines with high affinity and selectivity for the dopamine D3 receptorN E Austin, K Y Avenell, I Boyfield, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2000
1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonistsS M Bromidge, S Davies, D M Duckworth, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Journal of Medicinal Chemistry|September 1, 1991
Comparison of azabicyclic esters and oxadiazoles as ligands for the muscarinic receptorB S Orlek, F E Blaney, F Brown, et al.
Journal of Medicinal Chemistry|January 22, 1998
Design of [R-(Z)]-(+)-alpha-(methoxyimino)-1-azabicyclo[2.2.2]octane-3-acetonitri le (SB 202026), a functionally selective azabicyclic muscarinic M1 agonist incorporating the N-methoxy imidoyl nitrile group as a novel ester bioisostereS M Bromidge, F Brown, F Cassidy, et al.
Bioorganic & Medicinal Chemistry|September 26, 2000
Evaluation of a series of anticonvulsant 1,2,3,4-tetrahydroisoquinolinyl-benzamidesW N Chan, M S Hadley, J D Harling, et al.
Psychopharmacology|July 10, 2001
Central effects of urotensin-II following ICV administration in ratsJ Gartlon, F Parker, D C Harrison, et al.
Journal of Medicinal Chemistry|March 26, 1998
(R)-3,N-dimethyl-N-[1-methyl-3-(4-methyl-piperidin-1-yl) propyl]benzenesulfonamide: the first selective 5-HT7 receptor antagonistI T Forbes, S Dabbs, D M Duckworth, et al.
British Journal of Pharmacology|May 24, 2000
Characterization of SB-269970-A, a selective 5-HT(7) receptor antagonistJ J Hagan, G W Price, P Jeffrey, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Fused aminotetralins: novel antagonists with high selectivity for the dopamine D3 receptorK Y Avenell, I Boyfield, M C Coldwell, et al.
Journal of Medicinal Chemistry|February 12, 2000
A novel, potent, and selective 5-HT(7) antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl) phen ol (SB-269970)P J Lovell, S M Bromidge, S Dabbs, et al.
Bioorganic & Medicinal Chemistry Letters|November 22, 2000
Novel 2,3,4,5-tetrahydro-1H-3-benzazepines with high affinity and selectivity for the dopamine D3 receptorN E Austin, K Y Avenell, I Boyfield, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2000
1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonistsS M Bromidge, S Davies, D M Duckworth, et al.
Pageof 5