Article ID Journal Published Year Pages File Type
1375342 Bioorganic & Medicinal Chemistry Letters 2010 5 Pages PDF
Abstract

A series of aryloxyazetidines, aryloxypyrrolidines and aryloxypiperidines were designed based on structural overlap with previously reported arylpyrazine Oxytocin antagonists. Similarly high levels of Oxytocin antagonism were achievable in these new series. Several aryloxyazetidines also showed high levels of selectivity, with one compound, 25, displaying promising in vivo pharmacokinetics and significantly improved aqueous solubility over related compounds containing a biaryl substituent.

Graphical abstractSeveral potent aryl ether/triazole Oxytocin antagonists are described. One of these compounds, 25, has excellent potency and selectivity, as well as promising in vivo pharmacokinetics and significantly improved aqueous solubility over related systems containing a biaryl substituent.Figure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Chemistry Organic Chemistry
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