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N R Curtis

Showing results (1-10 of 7) with videos related to

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Organic Letters|March 22, 2001
Stereocontrolled syntheses of epimeric 3-aryl-6-phenyl-1-oxa-7-azaspiro(4.5)decane NK-1 receptor antagonist precursorsJ J Kulagowski, N R Curtis, C J Swain, et al.
British Journal of Pharmacology|January 1, 1987
Effects of tachykinins on inositol phospholipid hydrolysis in slices of hamster urinary bladderD R Bristow, N R Curtis, N Suman-Chauhan, et al.
Journal of Medicinal Chemistry|January 8, 1993
Cyclic peptides as selective tachykinin antagonistsB J Williams, N R Curtis, A T McKnight, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 1999
Synthesis and sar of 2- and 3-substituted 7-azaindoles as potential dopamine D4 ligandsN R Curtis, J J Kulagowski, P D Leeson, et al.
Molecular Pharmacology|December 1, 1996
Identification and pharmacological characterization of [125I]L-750,667, a novel radioligand for the dopamine D4 receptorS Patel, S Patel, R Marwood, et al.
Molecular Pharmacology|January 1, 1986
Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding siteM A Cascieri, G G Chicchi, R M Freidinger, et al.
Journal of Medicinal Chemistry|April 1, 1991
Kynurenic acid derivatives. Structure-activity relationships for excitatory amino acid antagonism and identification of potent and selective antagonists at the glycine site on the N-methyl-D-aspartate receptorP D Leeson, R Baker, R W Carling, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Organic Letters|March 22, 2001
Stereocontrolled syntheses of epimeric 3-aryl-6-phenyl-1-oxa-7-azaspiro(4.5)decane NK-1 receptor antagonist precursorsJ J Kulagowski, N R Curtis, C J Swain, et al.
British Journal of Pharmacology|January 1, 1987
Effects of tachykinins on inositol phospholipid hydrolysis in slices of hamster urinary bladderD R Bristow, N R Curtis, N Suman-Chauhan, et al.
Journal of Medicinal Chemistry|January 8, 1993
Cyclic peptides as selective tachykinin antagonistsB J Williams, N R Curtis, A T McKnight, et al.
Bioorganic & Medicinal Chemistry Letters|March 31, 1999
Synthesis and sar of 2- and 3-substituted 7-azaindoles as potential dopamine D4 ligandsN R Curtis, J J Kulagowski, P D Leeson, et al.
Molecular Pharmacology|December 1, 1996
Identification and pharmacological characterization of [125I]L-750,667, a novel radioligand for the dopamine D4 receptorS Patel, S Patel, R Marwood, et al.
Molecular Pharmacology|January 1, 1986
Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding siteM A Cascieri, G G Chicchi, R M Freidinger, et al.
Journal of Medicinal Chemistry|April 1, 1991
Kynurenic acid derivatives. Structure-activity relationships for excitatory amino acid antagonism and identification of potent and selective antagonists at the glycine site on the N-methyl-D-aspartate receptorP D Leeson, R Baker, R W Carling, et al.
Pageof 1