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Maytansinol Derivatives: Side Reactions as a Chance for New Tubulin Binders.

Paola MarzulloZlata BoiarskaHelena Pérez-PeñaAnne-Catherine AbelBeatriz Álvarez-BernadDaniel Lucena-AgellFrancesca VasileMaurizio SironiKarl-Heinz AltmannAndrea E ProtaJ Fernando DíazStefano PieracciniDaniele Passarella
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2021)
Maytansinol is a valuable precursor for the preparation of maytansine derivatives (known as maytansinoids). Inspired by the intriguing structure of the macrocycle and the success in targeted cancer therapy of the derivatives, we explored the maytansinol acylation reaction. As a result, we were able to obtain a series of derivatives with novel modifications of the maytansine scaffold. We characterized these molecules by docking studies, by a comprehensive biochemical evaluation, and by determination of their crystal structures in complex with tubulin. The results shed further light on the intriguing chemical behavior of maytansinoids and confirm the relevance of this peculiar scaffold in the scenario of tubulin binders.
Keyphrases
  • cancer therapy
  • structure activity relationship
  • drug delivery
  • molecular dynamics simulations
  • mass spectrometry
  • small molecule
  • tandem mass spectrometry