Novel Histamine H3-Receptor Antagonists with Benzyl Ether Structure or Related Moieties: Synthesis and Structure-Activity Relationships-Reference-Cited by-同舟云学术

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Novel Histamine H3-Receptor Antagonists with Benzyl Ether Structure or Related Moieties: Synthesis and Structure-Activity Relationships

Published:1996 Issue:8-9 Volume:329 Page:379-385
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:de
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Hüls Annette,Purand Katja,Stark Holger,Reidemeister Sibylle,Ligneau Xavier,Arrang Jean-Michel,Schwartz Jean-Charles,Schunack Walter

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference36 articles.

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

2. Autoregulation of histamine release in brain by presynaptic H3-receptors

3. Autoinhibition of histamine synthesis mediated by presynaptic H3-receptors

4. Histamine H3 receptor-mediated inhibition of serotonin release in the rat brain cortex

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

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Molecular and cellular analysis of human histamine receptor subtypes;Trends in Pharmacological Sciences;2013-01

2. The Histamine H3 Receptor as a Therapeutic Drug Target for Metabolic Disorders: Status, Challenges and Opportunities;Current Topics in Medicinal Chemistry;2011-06-01

3. ChemInform Abstract: Novel Histamine H3-Receptor Antagonists with Benzyl Ether Structure or Related Moieties: Synthesis and Structure-Activity Relationships.;ChemInform;2010-08-04

4. Exploration of Structure-Activity Relationships for Dual Serotonin Transporter Reuptake Inhibitors-Histamine H3 Receptor Antagonists;Current Topics in Medicinal Chemistry;2010-04-01

5. No Evidence for Functional Selectivity of Proxyfan at the Human Histamine H3 Receptor Coupled to Defined Gi/Go Protein Heterotrimers;Journal of Pharmacology and Experimental Therapeutics;2009-12-03

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