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. 2018 Nov 9;9:4710. doi: 10.1038/s41467-018-07259-x

Fig. 5.

Fig. 5

Completion of the syntheses and cell growth inhibition data. a Four steps couple the ABCD* and EF fragments and produce the spongistatin 1 analogs 5a–c. b Cell growth inhibition assays with four human cancer cell lines establish that the D-ring modified analog 5a is approximately equipotent with spongistatin 1, while 5c represents a proof-of-concept result that the C(15) acetate may be structurally modified with only a minimal reduction in potency. LiHMDS lithium hexamethyldisilazide, HMPA hexamethylphosphoramide