Diaminopyrimidines, diaminopyridines and diaminopyridazines as histamine H4 receptor modulators
Histamine H4 receptor antagonists. [Display omitted] Previously disclosed H4 receptor modulators, the triamino substituted pyridines and pyrimidines, contain a free primary amino (–NH2) group. In this Letter we demonstrate that an exocyclic amine (NH2) is not needed to maintain affinity, and also sh...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2015-02, Vol.25 (4), p.956-959 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Histamine H4 receptor antagonists. [Display omitted]
Previously disclosed H4 receptor modulators, the triamino substituted pyridines and pyrimidines, contain a free primary amino (–NH2) group. In this Letter we demonstrate that an exocyclic amine (NH2) is not needed to maintain affinity, and also show a significant divergence in the SAR of the pendant diamine component. These des-NH2 azacycles also show a distinct functional spectrum, that appears to be influenced by the diamine component; in the case of the 1,3-amino pyrimidines, the preferred diamine is the amino pyrrolidine instead of the more common piperazines. Finally, we introduce 3,5-diamino pyridazines as novel histamine H4 antagonists. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2014.12.027 |