The synthesis and biological activity of N-epsilon-Z-[Lys(3)]didemnin B are
reported. This novel analogue retains antiproliferative, cytotoxic, and pr
otein biosynthesis inhibition activities, but at reduced levels. This resul
t suggests the use of [Lys(3)]didemnin derivatives as potential affinity pr
obes for studying the molecular target(s) of the didemnin class of natural
products. (C) 2000 Elsevier Science Ltd. All rights reserved.