mandelalide-a and Neoplasms

Recollection of the tunicate source of the mandelalides has provided new and known analogues that have facilitated expanded analyses of the disputed cancer cytotoxicity of mandelalide A following a number of recent reported total syntheses. Using newly characterized mandelalide E, reisolated natural mandelalides B and C, and synthetic mandelalide A, the cytotoxicity of the mandelalides is demonstrated to be strongly influenced by compound glycosylation and assay cell density. Glycosylated mandelalides reduced the viability of human cancer cells cultured at a high starting density with a rank order of potency A > B ≫ E, yet display dramatically reduced cytotoxic efficacy against low density cultures.

Topics: Animals; Antineoplastic Agents; Drug Screening Assays, Antitumor; Glycosylation; HCT116 Cells; HeLa Cells; Humans; Macrolides; Molecular Structure; Neoplasms; Stereoisomerism; Urochordata