Synthesis and structure–activity relationships of 2-(1,4′-bipiperidin-1′-yl)thiazolopyridine as H3 receptor antagonists-Reference-Cited by-同舟云学术

Synthesis and structure–activity relationships of 2-(1,4′-bipiperidin-1′-yl)thiazolopyridine as H3 receptor antagonists

Published:2009-11 Issue:21 Volume:19 Page:6176-6180
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Rao Ashwin U.,Palani Anandan,Chen Xiao,Huang Ying,Aslanian Robert G.,West Robert E.,Williams Shirley M.,Wu Ren-Long,Hwa Joyce,Sondey Christopher,Lachowicz Jean

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference41 articles.

1. Genomics Meets Histamine Receptors: New Subtypes, New Receptors

2. Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor

3. Modulation of neurotransmitter releaseviahistamine H3heteroreceptors

4. Histamine H3 receptors modulate the release of [3H]-acetylcholine from slices of rat entorhinal cortex: evidence for the possible existence of H3 receptor subtypes

5. Histamine H3 Receptor Antagonists: Preclinical Promise for Treating Obesity and Cognitive Disorders

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