Characterization of the binding site of the histamine H3 receptor. 2. Synthesis, in vitro pharmacology, and QSAR of a series of monosubstituted benzyl analogues of thioperamide

Albert D. Windhorst*, Henk Timmerman, Edward A. Worthington, Greetje J. Bijloo, Paul H.J. Nederkoorn, Wiro M.P.B. Menge, Rob Leurs, Jacobus D.M. Herscheid

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A series of monosubstituted benzyl analogues of the histamine H3 receptor antagonist thioperamide were synthesized and evaluated for their histamine H3 receptor activity on the guinea pig jejunum. Incorporation of Cl, Br, and I at the ortho position of the benzyl moiety led to an increase of the pA2 value, whereas the same substituents at the para position led to a decrease. However, a fluorine substituent gave a strong decrease in pA2, regardless of the position. Molecular modeling revealed a QSAR with a correlation (r = 0.93) between the pA2 and the dihedral angle between the thiourea and the benzyl moiety and the calculated electron density on the substituted carbon atom. To verify whether this QSAR model had a predictive value, the ortho tert-butyl and methyl analogues were synthesized and evaluated. Indeed it was shown that the predicted pA2 values of these two compounds were in accordance with the measured pA2 values.

Original languageEnglish
Pages (from-to)1754-1761
Number of pages8
JournalJournal of Medicinal Chemistry
Volume43
Issue number9
DOIs
Publication statusPublished - 30 May 2000

Cite this