Synthesis and SAR of 1,3-disubstituted cyclohexylmethyl urea and amide derivatives as non-peptidic motilin receptor antagonists

A novel and potent motilin antagonist series was derived based on an understanding of the key binding elements of a known motilin antagonist. A series of 1,3-disubstituted cyclohexylmethyl urea and amide derivatives were synthesized as motilin receptor antagonists. Starting from known motilin antago...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2006-07, Vol.16 (13), p.3362-3366
Hauptverfasser: Johnson, Sigmond G., Gunnet, Joseph W., Moore, John B., Miller, William, Wines, Pam, Rivero, Ralph A., Combs, Don, Demarest, Keith T.
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Sprache:eng
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Zusammenfassung:A novel and potent motilin antagonist series was derived based on an understanding of the key binding elements of a known motilin antagonist. A series of 1,3-disubstituted cyclohexylmethyl urea and amide derivatives were synthesized as motilin receptor antagonists. Starting from known motilin antagonists, 1a and 1b, the cyclopentene scaffold was replaced and the four recognition elements optimized to arrive at a potent novel series.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2006.04.017