Rc. Vollinga et al., HOMOLOGS OF HISTAMINE AS HISTAMINE H-3 RECEPTOR ANTAGONISTS - A NEW POTENT AND SELECTIVE H-3 ANTAGONIST, 4(5)-(5-AMINOPENTYL)-1H-IMIDAZOLE, Journal of medicinal chemistry, 38(2), 1995, pp. 266-271
The influence of alkyl chain length variation on the histamine H-3 rec
eptor activity of histamine homologs 1 was investigated. A series of 4
(5)-(omega-aminoalkyl)-1H-imidazoles 1 was prepared with an alkyl chai
n length varying from one methylene group to 10 methylene groups. Besi
des the H-3 activity, the affinities of these compounds for the H-1 an
d H-2 receptors were determined. The ethylene chain of histamine is op
timal for agonistic activity on all three histamine receptor subtypes.
For the H-3 receptor, elongation of the alkyl chain from three methyl
ene groups on leads to compounds with antagonistic properties. 4(5)-(5
-Aminopentyl)-1H-imidazole (impentamine, 1e) is the most potent and se
lective H-3 antagonist from this series of 4(5)-(omega-aminoalkyl)-1H-
imidazoles 1, with a pA(2) value of 8.4 (on guinea pig jejunum). A spe
cific antagonistic binding site for this compound is proposed.