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P129 QSAR and possible receptor binding sites of H1 agonistic 2-heteroaryl and 2-phenylhistamines

✍ Scribed by Dove, S.; Kühne, R.; Leschke, C.; Zingel, V.; Schunack, W.


Book ID
122737748
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
120 KB
Volume
2
Category
Article
ISSN
0928-0987

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N α -Alkylated Derivatives of 2-Phenylhistamines: Synthesis and in vitro Activity of Potent Histamine H 1 -Receptor Agonists. -In vitro study of new potent histamine H 1 -receptor agonists, e.g. (V), shows that the derivative (Va) is the most potent compound described in the literature until now. -