Binding Affinity of a Newly Synthesized 5-HT2 Antagonist, AT-1015 (N-[2-[4-(5H-Dibenzo[a,d]cyclohepten-5-ylidene)-piperidino]ethyl]-1-formyl-4-piperidinecarboxamide Monohydrochloride Monohydrate), in the Rabbit Platelet Membrane.
Author:
Affiliation:
1. Department of Pharmacology, Niigata College of Pharmacy
2. Department of Public Health, Niigata College of Medical Technology
3. Department of Medical Technology, School of Health Sciences, Faculty of Medicine, Niigata University
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology,General Medicine
Link
http://www.jstage.jst.go.jp/article/bpb/24/10/24_10_1188/_pdf
Reference15 articles.
1. Evidence for functional 5-HT2 receptor sites on human blood platelets
2. Platelet-mediated vascular permeability in the rat: A predominant role for 5-hydroxytryptamine
3. Stimulation of aortic smooth muscle cell mitogenesis by serotonin.
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1. Identification of Amino Acid Residues Important for Sarpogrelate Binding to the Human 5-Hydroxytryptamine2A Serotonin Receptor;Journal of Pharmacological Sciences;2006
2. Functions of 5-HT2A receptor and its antagonists in the cardiovascular system;Pharmacology & Therapeutics;2004-10
3. AT-1015, a newly synthesized 5-HT2 receptor antagonist, dissociates slowly from the 5-HT2 receptor sites in rabbit cerebral cortex membrane;Journal of Pharmacy and Pharmacology;2002-08
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