Discovery and optimization of 2-phenyloxazole derivatives as diacylglycerol acyltransferase-1 inhibitors
The discovery and SAR studies of a phenyloxazole based diacylglycerol acyltransferase-1 inhibitor are reported. The optimized compound 25 is orally available and demonstrated in vivo efficacy in a diet-induced obesity (DIO) rat model. In a discovery effort to find safe and effective DGAT-1 inhibitor...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2011-12, Vol.21 (23), p.7205-7209 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The discovery and SAR studies of a phenyloxazole based diacylglycerol acyltransferase-1 inhibitor are reported. The optimized compound
25 is orally available and demonstrated in vivo efficacy in a diet-induced obesity (DIO) rat model.
In a discovery effort to find safe and effective DGAT-1 inhibitors, we have identified 2-phenyloxazole 4-carboxamide
1 as a conformationally constrained analog of a hydrazide hit, which was previously identified from high-throughput screening. Further optimization of this series has led to chemically more stable 2-phenyloxazole-based DGAT-1 inhibitor
25 with improved solubility, cell-based activity, and pharmacokinetic properties. Compound
25 also demonstrated in vivo efficacy in a diet-induced obesity (DIO) rat model. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2011.09.039 |