Abstract
Pyridazinone 1 was recently reported as a potent H(3)R antagonist with good drug-like properties and in vivo activity. A series of constrained amine analogs of 1 was synthesized to identify compounds with improved pharmacokinetic profiles. From these efforts, a new class of (S)-2-pyrrolidin-1-ylmethyl-1-pyrrolidinyl amides was identified.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
-
Amines / chemistry*
-
Animals
-
Dose-Response Relationship, Drug
-
Histamine H3 Antagonists / chemical synthesis
-
Histamine H3 Antagonists / chemistry
-
Histamine H3 Antagonists / pharmacology*
-
Humans
-
Molecular Structure
-
Pyridazines / chemical synthesis
-
Pyridazines / chemistry
-
Pyridazines / pharmacology*
-
Rats
-
Receptors, Histamine H3 / metabolism
-
Stereoisomerism
-
Structure-Activity Relationship
Substances
-
Amines
-
Histamine H3 Antagonists
-
Pyridazines
-
Receptors, Histamine H3