128395-47-1Relevant academic research and scientific papers
Toward biophysical probes for the 5-HT3 receptor: Structure-activity relationship study of granisetron derivatives
Vernekar, Sanjeev Kumar V.,Hallaq, Hasan Y.,Clarkson, Guy,Thompson, Andrew J.,Silvestr, Linda,Lummis, Sarah C. R.,Lochner, Martin
supporting information; experimental part, p. 2324 - 2328 (2010/07/17)
This report describes the synthesis and biological characterization of novel granisetron derivatives that are antagonists of the human serotonin (5-HT3A) receptor. Some of these substituted granisetron derivatives showed low nanomolar binding affinity and allowed the identification of positions on the granisetron core that might be used as attachment points for biophysical tags. A BODIPY fluorophore was appended to one such position and specifically bound to 5-HT3A receptors in mammalian cells.
Synthesis and gastrointestinal prokinetic activity of novel benzamide derivatives with amphoteric side chains
Sakaguchi,Iwasaki,Iwanaga,Saito,Takahara,Kato,Hanaoka
, p. 424 - 436 (2007/10/03)
Novel benzamide derivatives (19-24, 32a-c, 43d-f), each possessing a cycloaminoalkanecarboxylic acid side chain, were synthesized and their gastrointestinal prokinetic and dopamine D2 receptor antagonist activities were evaluated. 4-[(4-Amino-5
