Synthesis of substituted N-[3-(3-methoxyphenyl)propyl] amides as highly potent MT sub(2)-selective melatonin ligands
A series of substituted N-[3-(3-methoxyphenyl)propyl] amides were synthesized and their binding affinities towards human melatonin MT sub(1) and MT sub(2) receptors were evaluated. It was discovered that a benzyloxyl substituent incorporated at C6 position of the 3-methoxyphenyl ring dramatically en...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2010-04, Vol.20 (8), p.2582-2585 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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