| Literature DB >> 2942012 |
M Impicciatore, G Morini, M Chiavarini, P V Plazzi, F Bordi, F Vitali.
Abstract
The pharmacological properties of 2-aminohistamine and 2-amino-5-methylhistamine were studied and compared with those of histamine, 5-methylhistamine and dimaprit. The introduction of an amino group in position 2 of the histamine imidazole ring caused a reduction of histamine potency, mostly with respect to H1 receptors. Such disactivation was much more evident in its corresponding 5-methyl derivative. The pharmacological activity related to the chemical structure will be discussed in the paper.Entities:
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Year: 1986 PMID: 2942012 DOI: 10.1007/bf01988003
Source DB: PubMed Journal: Agents Actions ISSN: 0065-4299