The discovery of phenylbenzamide derivatives as Grb7-based antitumor agents

Nigus Dessalew Ambaye, Menachem Joseph Gunzburg, Reece Chih Chian Lim, John Timothy Price, Matthew Charles James Wilce, Jacqueline Anne Wilce

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10 Citations (Scopus)


Grb7 is a non-catalytic protein, the overexpression of which has been associated with the proliferative and migratory potentials of cancer cells. Virtual screening strategies involving a shape-based similarity search, molecular docking, and 2D-similarity searches complemented by experimental binding studies (Thermofluor and isothermal titration calorimetry) resulted in the identification of nine novel phenylbenzamide-based antagonists of the Grb7 SH2 domain. Moderate binding affinities were observed, ranging from K(d)=32.3 muM for lead phenylbenzamide NSC 104999 (1) to K(d)=1.1 muM for a structurally related compound, NSC 57148 (2). Deconvolution of the affinity data into its components revealed differences in lead binding, from being entropy based (lead 1) to enthalpically driven (NSC 100874 (3), NSC 55158 (4), and compound 2). Finally, the lead compound 1 was found to decrease the growth of MDA-MB-468 breast cancer cells, with an IC(50) value of 39.9 muM. It is expected that these structures will serve as novel leads in the development of Grb7-based anticancer therapeutics.
Original languageEnglish
Pages (from-to)280 - 288
Number of pages9
Issue number2
Publication statusPublished - 2013

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