Design, Synthesis, and Biological Evaluation of Levoglucosenone‐Derived Ras Activation Inhibitors

ChemMedChem - Tập 4 Số 4 - Trang 524-528 - 2009
Christian Müller1, María Antonia Gómez-Zurita Frau1, Dario Ballinari1, Sonia Colombo2, Alessandro Bitto2, Enzo Martegani2, Cristina Airoldi2, Anske Stephanie van Neuren3, Matthias Stein3, Jörg Weiser3, C Battistini1, Francesco Peri2
1B. U. Oncology, Nerviano Medical Sciences, Viale Pasteur 10, 20014 Nerviano, MI (Italy), Fax: (+39) 03-3158-1347
2Department of Biotechnology and Biosciences, University of Milan‐Bicocca, Piazza della Scienza 2, 20126 Milan (Italy), Fax: (+39) 02‐6448‐3565
3Anterio Consulting & Research GmbH, Augustaanlage 23, 68165 Mannheim (Germany)

Tóm tắt

AbstractA panel of new potential Ras ligands was generated by decorating a tricyclic levoglucosenone‐derived scaffold with aromatic moieties. Some members of the panel show in vitro inhibitory activity toward the nucleotide exchange process on Ras and are toxic to some human cancer cell lines.magnified image

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