Novel H3 receptor antagonists with improved pharmacokinetic profiles
摘要:
A new series of H-3 antagonists derived from the natural product Conessine are presented. Several compounds from these new series retain the potency and selectivity of earlier diamine based analogs while exhibiting improved PK characteristics. One compound (3u) demonstrated functional antagonism of the H-3 receptor in an in vivo pharmacological model. (c) 2008 Elsevier Ltd. All rights reserved.