Identification of a novel selective H1-antihistamine with optimized pharmacokinetic properties for clinical evaluation in the treatment of insomnia

Identification of a novel selective H1-antihistamine with optimized pharmacokinetic properties for clinical evaluation in the treatment of insomnia Characterization of Novel Selective H₁-Antihistamines for Clinical Evaluation in the Treatment of Insomnia Design, synthesis and biological activity evaluation of desloratadine analogues as H1 receptor antagonists Norpiperidine Imidazoazepines as a New Class of Potent, Selective, and Nonsedative H₁ Antihistamines Benzo- and pyrido-1,4-oxazepin-5-ones and -thiones: synthesis and structure-activity relationships of a new series of H1-antihistamines Structure−Activity Relationships of Dimethindene Derivatives as New M₂-Selective Muscarinic Receptor Antagonists Synthesis and Structure−Activity Relationships of Novel Histamine H₁ Antagonists:  Indolylpiperidinyl Benzoic Acid Derivatives Synthesis and antihistamine evaluations of novel loratadine analogues Stereoselective synthesis of desloratadine derivatives as antagonist of histamine Identification and profiling of 3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)phenyl] amide as histamine H3 receptor antagonist for the treatment of depression