Long chain amines and long chain ammonium salts as novel inhibitors of dynamin GTPase activity.

نویسندگان

  • Timothy A Hill
  • Luke R Odell
  • Annie Quan
  • Ruben Abagyan
  • Gemma Ferguson
  • Phillip J Robinson
  • Adam McCluskey
چکیده

We examined a number of ligands with the view of inhibiting the GTPase activity of dynamin. Dynamin contains a pleckstrin homology (PH) domain that interacts with lipids. We report a series of simple lipid-like molecules that display moderate inhibitory activity. Inhibitory activity is linked to chain length and quaternarization of the terminal amine. A change in the counterion, Cl versus Br or I, had little effect on potency. However, introduction of a hydrophobic collar proximal to the charged site was beneficial to dynamin GTPase inhibitory action. The most potent compound was myristoyl trimethyl ammonium bromide (MTMAB, IC(50) 3.15 microM).

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عنوان ژورنال:
  • Bioorganic & medicinal chemistry letters

دوره 14 12  شماره 

صفحات  -

تاریخ انتشار 2004