Technologies

The Combretastatin A-4 (CA-4) Prodrug is a very promising compound now in phase II clinical trials against cancer. CA-4 is acting as a tubulin polymerization inhibitor, preventing cancerous cells from dividing.

While performing a structural activity relationship (SAR) study of the antineoplastic compound CA-4, ASU researchers discovered the Phenstatins family. Phenstatins are Combretastatins analogs with a modification of the double bond, which is replaced by a carbonyl group.

The first compound, Phenstatin, showed strong cytotoxicity and an antitubulin activity similar to that of CA-4. Phenstatin was also found to be as effective as CA-4 in competing with colchicine for binding site.

Phenstatin and its Prodrug were found to be essentially indistinguishable in potency (e.g. mean panel GI50 values) and differential cytotoxicity. Both were also quite similar to the CA-4 Prodrug both in terms of both potency and differential cytotoxicity, suggesting that their mechanism of action is similar to that of CA-4.

ASU researchers also investigated Hydroxyphenstatin, a compound possessing an additional hydroxy group, as found in Combretastatin A-1 (CA-1). Hydroxyphenstatin inhibition of tubulin polymerization appeared greater than that of both CA-4 and CA-1. A comparative testing of Hydroxyphenstatin and its Prodrug in the NCI 60-cell screen revealed a differential cytotoxicity profile and potency (mean-panel GI50 value of 1.7 x 10-7 M) that were essentially indistinguishable from each other or from those of CA-4.

In general, new discovered compounds disclose a potency and a differential cytotoxicity profile comparable to CA-4.