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. Author manuscript; available in PMC: 2010 Oct 25.
Published in final edited form as: Chem Biol Drug Des. 2009 Aug 18;74(4):358–368. doi: 10.1111/j.1747-0285.2009.00866.x

Figure 1. Design and synthesis of pironetin analogs.

Figure 1

A. Covalent tubulin modification by αLys352 conjugate addition to bound (−)-pironetin and a pironetin derivative designed to mimic interaction with αLys352 without covalent binding. B, Synthesis of pironetin derivatives 3 and 4.