Synthesis and in Vitro Pharmacology of a Series of New Chiral Histamine H3-Receptor Ligands: 2-(R and S)-Amino-3-(1H-imidazol-4(5)-yl)propyl Ether Derivatives-Reference-Cited by-同舟云学术

Synthesis and in Vitro Pharmacology of a Series of New Chiral Histamine H3-Receptor Ligands: 2-(R and S)-Amino-3-(1H-imidazol-4(5)-yl)propyl Ether Derivatives

Published:1999-03-13 Issue:7 Volume:42 Page:1193-1202
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Kovalainen Jari T.¹,Christiaans Johannes A. M.¹,Kotisaari Sanna¹,Laitinen Jarmo T.¹,Männistö Pekka T.¹,Tuomisto Leena¹,Gynther Jukka¹

Affiliation:

1. University of Kuopio, P.O. Box 1627, FIN-70211 Kuopio, Finland

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm980408v

Reference43 articles.

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

2. Modulation of neurotransmitter releaseviahistamine H3heteroreceptors

3. Effects of clobenpropit (VUF-9153), a histamine H3-receptor antagonist, on learning and memory, and on cholinergic and monoaminergic systems in mice

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