2-Aryl tryptamines: selective high-affinity antagonists for the h5-HT2A receptor-Reference-Cited by-同舟云学术

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2-Aryl tryptamines: selective high-affinity antagonists for the h5-HT2A receptor

Published:2000-12 Issue:24 Volume:10 Page:2697-2699
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Stevenson Graeme I,Smith Adrian L,Lewis Stephen,Michie Stephen G,Neduvelil Joseph G,Patel Smita,Marwood Rosemarie,Patel Shil,Castro José L

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. Kane, J. M. In Schizophrenia From Mind to Molecule; Andreasen, N. C., Ed.; American Psychiatric, 1994, pp 173–187.

2. Stereoselective blockade of central [3H]5-hydroxytryptamine binding to multiple sites (5-HT1A, 5-HT1B and 5-HT1C) by mianserin and propranolol

4. Solid-phase synthesis of 2,3-disubstituted indoles: discovery of a novel, high-affinity, selective h5-HT2A antagonist

5. 2-Substituted Tryptamines: Agents with Selectivity for 5-HT6 Serotonin Receptors

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