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Synthesis and evaluation of potent pyrrolidine H(3) antagonists
Authors:Vasudevan Anil  Conner Scott E  Gentles Robert G  Faghih Ramin  Liu Huaqing  Dwight Wesley  Ireland Lynne  Kang Chae Hee  Esbenshade Timothy A  Bennani Youssef L  Hancock Arthur A
Affiliation:Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60031, USA. anil.vasudevan@abbott.com
Abstract:The synthesis and biological evaluation of novel antagonists of the rat H(3) receptor are described. These compounds differ from prototypical H(3) antagonists in that they do not contain an imidazole moiety, but rather a substituted aminopyrrolidine moiety. A systematic modification of the substituents on the aminopyrrolidine ring was performed using pre-formatted precursor sets, where applicable, to afford several compounds with high affinity and selectivity for the H(3) receptor.
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