Design, Synthesis, and Biological Evaluation of Levoglucosenone‐Derived Ras Activation Inhibitors
Tricyclic
DOI:
10.1002/cmdc.200800416
Publication Date:
2009-02-18T07:27:35Z
AUTHORS (12)
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
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