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.

9-Fluorenone-2-Carboxylic Acid as a Scaffold for Tubulin Interacting Compounds

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.
2013
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
antitumor agents; 2
7-disubstituted fluorenones; docking; 9-fluorenone-2-carboxylic acid; tubulins
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/263717
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