Synthesis and SAR studies of benzimidazolone derivatives as histamine H3-receptor antagonists-Reference-Cited by-同舟云学术

Synthesis and SAR studies of benzimidazolone derivatives as histamine H3-receptor antagonists

Published:2013-11 Issue:21 Volume:23 Page:6001-6003
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Zeng Qingbei,Rosenblum Stuart B.,Yang Zhaoxia,Jiang Yueheng,McCormick Kevin D.,Aslanian Robert G.,Duguma Luli,Kozlowski Joseph A.,Shih Neng-Yang,Hey John A.,West Robert E.,Korfmacher Walter A.,Berlin Michael,Boyce Christopher W.

Publisher

Elsevier BV

Subject

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

Reference22 articles.

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

2. Highly potent and selective ligands for histamine H3-receptors

3. Histamine inhibits dopamine release in the mouse striatum via presynaptic H3 receptors

4. Inhibition of noradrenaline release in the rat brain cortex via presynaptic H3 receptors

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