Marzullo Paola, Boiarska Zlata, Pérez-Peña Helena, Abel Anne-Catherine, Álvarez-Bernad Beatriz, Lucena-Agell Daniel, Vasile Francesca, Sironi Maurizio, Altmann Karl-Heinz, Prota Andrea E, Díaz J Fernando, Pieraccini Stefano, Passarella Daniele
Department of Chemistry, Università degli Studi di Milano, Via Golgi 19, 20133, Milan, Italy.
Laboratory of Biomolecular Research, Paul Scherrer Institute, Forschungsstrasse 111, 5232, Villigen PSI, Switzerland.
Chemistry. 2022 Jan 10;28(2):e202103520. doi: 10.1002/chem.202103520. Epub 2021 Nov 29.
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.
美登辛醇是制备美登素衍生物(称为美登素类化合物)的重要前体。受大环结构的吸引以及衍生物在靶向癌症治疗方面的成功启发,我们探索了美登辛醇的酰化反应。结果,我们获得了一系列对美登素骨架进行新型修饰的衍生物。我们通过对接研究、全面的生化评估以及测定它们与微管蛋白复合物的晶体结构来对这些分子进行表征。这些结果进一步揭示了美登素类化合物有趣的化学行为,并证实了这种特殊骨架在微管蛋白结合剂领域的相关性。