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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: Cancer Chemother Pharmacol. 2015 Jan 24;75(4):671–682. doi: 10.1007/s00280-015-2675-1

Figure 1.

Figure 1

Structures of compounds used in this study. Marcrocycle analogs of Largazole were synthesized to replace the thiazole in the parent compound Largazole with a pyridyl group, to substitute a peptide isostere for the depsipeptide, and to replace the thioester prodrug with a pyridyl-disulfide.