Bioorganic & Medicinal Chemistry Letters 2010-11-01

Investigation of 4-piperidinols as novel H3 antagonists.

James T Anderson, Michael Campbell, Jianmin Wang, Kurt R Brunden, John J Harrington, Alain Stricker-Krongrad, Jianping Song, Chris Doucette, Steven Murphy, Youssef L Bennani

Index: Bioorg. Med. Chem. Lett. 20(21) , 6246-9, (2010)

Full Text: HTML

Abstract

Compounds containing a substituted 4-piperidinol core have been found to be potent antagonists of the human H(3) receptor. The compounds exhibited up to a 60-fold preference for inhibiting the human H(3) receptor over the mouse and showed a low binding affinity for the hERG channel.Copyright © 2010 Elsevier Ltd. All rights reserved.


Related Compounds

  • 4-Piperidinol

Related Articles:

Synthesis of novel IP agonists via N-aminoethyl cyclic amines prepared by decarboxylative ring-opening reactions.

2012-01-01

[Molecules 17(2) , 1233-46, (2012)]

N- versus O-arylation of aminoalcohols: orthogonal selectivity in copper-based catalysts.

2007-03-28

[J. Am. Chem. Soc. 129 , 3490, (2007)]

The spectroscopic (FT-IR, FT-IR gas phase, FT-Raman and UV) and NBO analysis of 4-Hydroxypiperidine by density functional method.

2010-03-01

[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 75(3) , 941-52, (2010)]

More Articles...