Publication Date:
2013
abstract:
The introduction of a hydrophobic group at position7 of 9-fluorenone-2-carboxylic acid generates new tubulin binders, the design of which is suggested by modeling studies. The synthesis is based on the use of 2,7-dibromo-fluorenone as starting material. The antiproliferative activity on two different cell lines, fluorescent microscopy, flow cytometry, and sedimentation assay tests confirmed the supposed mechanism.
Iris type:
01.01 Articolo in rivista
Keywords:
antitumor agents; 2; 7-disubstituted fluorenones; docking; 9-fluorenone-2-carboxylic acid; tubulins
List of contributors: