Further studies on the binding of N1-substituted tryptamines at h5-HT6 receptors

Bioorg Med Chem Lett. 2007 Mar 15;17(6):1691-4. doi: 10.1016/j.bmcl.2006.12.089. Epub 2007 Jan 4.

Abstract

N(1)-Arylsulfonyl-substituted analogs of N,N-dimethyltryptamine bind at 5-HT(6) receptors. Replacement of the aryl moiety with similarly hydrophobic alkyl substituents results in decreased affinity, as does replacement of a benzenesulfonyl moiety with a benzyl group. Current findings indicate that an aryl (or substituted aryl) sulfonyl (rather than alkylsulfonyl or benzyl) moiety is optimal for high-affinity binding, and further suggest that the N(1)-benzenesulfonyl- and their corresponding N(1)-benzyltryptamine counterparts bind in a different fashion.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Chromatography, Thin Layer
  • DNA, Complementary / biosynthesis
  • DNA, Complementary / genetics
  • Humans
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Receptors, Serotonin / metabolism*
  • Structure-Activity Relationship
  • Tryptamines / chemistry
  • Tryptamines / metabolism*

Substances

  • DNA, Complementary
  • Indicators and Reagents
  • Receptors, Serotonin
  • Tryptamines
  • serotonin 6 receptor