Combretastatin A-4 inspired heterocyclic derivatives were synthesized and evaluated for their biological activities on tubulin polymerization and cell proliferation. Among the 19 described sulfur-containing compounds, derivatives (Z)-4h and (Z)-4j exhibited interesting in cellulo tubulin polymerization inhibition and antiproliferative activities with IC50 values for six different cell lines between 8 and 27 nM. Furthermore, in silico docking studies within the colchicine/CA-4 binding site of tubulin were carried out to understand the interactions of our products with the protein target. The effects on the cell cycle of follicular lymphoma cells were also investigated at 1-10 nM concentrations showing that apoptotic processes occurred
International audienceA novel series of tubulin polymerization inhibitors, based on fluorinated deri...
A series of colchicine site binding tubulin inhibitors were synthesized by the modification of the c...
Cancer is the second most common cause of death in the USA. Among the known classes of anticancer ag...
Combretastatin A-4 inspired heterocyclic derivatives were synthesized and evaluated for their biolog...
International audienceA novel series of combretastatin A-4 heterocyclic analogues was prepared by re...
A series of combretastatin derivatives were designed and synthesised by a two-step stereoselective s...
There is a clear need for anti-cancer therapies that have effective cytotoxic efficiency and margin...
International audienceA series of novel combretastatin A4 analogues, in which the cis-olefinic bridg...
ABSTRACT: A series of novel pyridine-bridged analogues of combretastatin-A4 (CA-4) were designed and...
A series of novel pyridine-bridged analogues of combretastatin-A4 (CA-4) were designed and synthesiz...
A novel class of combretastatins, modified at A-ring or both A- and B-rings, mainly by replacement w...
International audienceA novel series of tubulin polymerization inhibitors, based on fluorinated deri...
A series of colchicine site binding tubulin inhibitors were synthesized by the modification of the c...
Cancer is the second most common cause of death in the USA. Among the known classes of anticancer ag...
Combretastatin A-4 inspired heterocyclic derivatives were synthesized and evaluated for their biolog...
International audienceA novel series of combretastatin A-4 heterocyclic analogues was prepared by re...
A series of combretastatin derivatives were designed and synthesised by a two-step stereoselective s...
There is a clear need for anti-cancer therapies that have effective cytotoxic efficiency and margin...
International audienceA series of novel combretastatin A4 analogues, in which the cis-olefinic bridg...
ABSTRACT: A series of novel pyridine-bridged analogues of combretastatin-A4 (CA-4) were designed and...
A series of novel pyridine-bridged analogues of combretastatin-A4 (CA-4) were designed and synthesiz...
A novel class of combretastatins, modified at A-ring or both A- and B-rings, mainly by replacement w...
International audienceA novel series of tubulin polymerization inhibitors, based on fluorinated deri...
A series of colchicine site binding tubulin inhibitors were synthesized by the modification of the c...
Cancer is the second most common cause of death in the USA. Among the known classes of anticancer ag...