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

Tricyclic
DOI: 10.1002/cmdc.200800416 Publication Date: 2009-02-18T07:27:35Z
ABSTRACT
Abstract A panel of new potential Ras ligands was generated by decorating a tricyclic levoglucosenone‐derived scaffold with aromatic moieties. Some members the show in vitro inhibitory activity toward nucleotide exchange process on and are toxic to some human cancer cell lines. magnified image
SUPPLEMENTAL MATERIAL
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