| Literature DB >> 11133071 |
G I Stevenson1, A L Smith, S Lewis, S G Michie, J G Neduvelil, S Patel, R Marwood, S Patel, J L Castro.
Abstract
A series of 2-aryl tryptamines have been identified as high-affinity h5-HT2A antagonists. Structure-activity relationship studies have shown that h5-HT2A affinity can be attained via modifications to the tryptamine side chain and that selectivity over h5-HT2C and hD2 receptors can be controlled by suitable C-2 aryl groups.Entities:
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Year: 2000 PMID: 11133071 DOI: 10.1016/s0960-894x(00)00557-6
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823