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Published on: September 21, 2017
Phenylpiperazinylmethylheterocycle derivatives: synthesis and dopamine receptor binding profiles
1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt. ahabadi@yahoo.com
Abstract:
Four series of phenylpiperazinylmethylimidazo[1, 2-a]pyridine, phenylpiperazinylmethylpyrrole, phenylpiperazinylmethylbenzofuran, and phenylpiperazinylmethylbenzothiophene derivatives were synthesized and investigated for their in vitro binding profiles for the dopamine receptor subtypes D(1), D2long, D2short, D(3) and D(4). All tested compounds showed selectivity towards the D(4) receptor subtype. Affinity and selectivity for D(4) follows the order imidazo[1, 2-a]pyridine > benzofuran > benzothiophene > pyrrole derivatives. The D(4)-related affinity and selectivity pattern seems to be dependent on the presence of a region of negative molecular electrostatic potential below the heterocyclic moiety.
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