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Bioorganic & Medicinal Chemistry Letters|January 2, 2001
Solid-phase synthesis of 2,3-disubstituted indoles: discovery of a novel, high-affinity, selective h5-HT2A antagonistA L Smith, G I Stevenson, S Lewis, et al.The Journal of Biological Chemistry|August 15, 1990
Purification of the 5-hydroxytryptamine 5-HT3 receptor from NCB20 cellsR M McKernan, N P Gillard, K Quirk, et al.Journal of Medicinal Chemistry|March 20, 1992
Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)-oxazoles)C J Swain, R Baker, C Kneen, et al.Bioorganic & Medicinal Chemistry Letters|January 2, 2001
2-Aryl tryptamines: selective high-affinity antagonists for the h5-HT2A receptorG I Stevenson, A L Smith, S Lewis, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 2: A pharmacophore model for arylsulfonamide bindingJ M Elliott, H Broughton, M A Cascieri, et al.Journal of Medicinal Chemistry|October 29, 1993
3-Acyl-4-hydroxyquinolin-2(1H)-ones. Systemically active anticonvulsants acting by antagonism at the glycine site of the N-methyl-D-aspartate receptor complexM Rowley, P D Leeson, G I Stevenson, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Serine derived NK1 antagonists. 1: The effect of modifications to the serine substituentsJ M Elliott, M A Cascieri, G Chicchi, et al.Journal of Medicinal Chemistry|December 24, 1997
Effect of plasma protein binding on in vivo activity and brain penetration of glycine/NMDA receptor antagonistsM Rowley, J J Kulagowski, A P Watt, et al.Journal of Medicinal Chemistry|November 7, 1998
4,4-Disubstituted piperidine high-affinity NK1 antagonists: structure-activity relationships and in vivo activityG I Stevenson, I Huscroft, A M MacLeod, et al.Pageof 1